Page last updated: 2024-08-17

galactose and Malabsorption Syndromes

galactose has been researched along with Malabsorption Syndromes in 138 studies

Research

Studies (138)

Timeframe	Studies, this research(%)	All Research%
pre-1990	102 (73.91)	18.7374
1990's	16 (11.59)	18.2507
2000's	13 (9.42)	29.6817
2010's	5 (3.62)	24.3611
2020's	2 (1.45)	2.80

Authors

Authors	Studies
Prasad, BS; Yachha, SK	1
Chen, L; Pan, J; Wang, D; Yuan, T; Zhang, F	1
Chen, F; Chen, L; Long, Q; Lu, M; Ma, M; Wang, W; Zhang, T	1
Chai, PF; Lee, WS; Nazrul, N; Paed, M; Tay, CG	1
Wang, H; Xin, B	1
Kinne, RK; Raja, M	1
Cornette, L; De Bruyn, G; Loeys, B; Moring, AS; Vallaeys, L; Van Biervliet, S; Van Deynse, E	1
Chailloux, E; Chedane-Girault, C; Colin, E; Dabadie, A; Giniès, JL; Maurage, C; Pelatan, C; Piloquet, H	1
Martin, MG; Turk, E; Wright, EM	3
Kanai, Y	1
Milla, PJ; Pahari, A; van't Hoff, WG	1
DESAI, HG; JEEJEEBHOY, KN; VERGHESE, RV	1
AMMANN, R; AURICCHIO, S; HAEMMERLI, UP; KISTLER, H; MARTHALER, T; PRADER, A; SEMENZA, G	1
EVANS, PR	1
BARTHELMAI, W; LINNEWEH, F; SCHAUMLOEFFEL, E	1
Blau, N; Santer, R; Slaveska, N; Tasic, V	1
Aydin, HI; Gok, F; Gokcay, E; Kasahara, M; Kurt, I; Maeda, M	1
Balfe, JW; Barbar, M; El-Naggar, W; Taha, D	1
Brook, A; Davachi, B; Esmaili, M; Kianifar, HR; Talebi, S; Tavakkol-Afshari, J	1
Altinöz, S; Ecevit, C; Kasahara, M; Maeda, M; Oztürk, AA; Soylu, OB; Temizkan, AK	1
Faloon, WW; Paes, IC; Rubert, MW; Searl, P	1
Anderson, GJ; Giday, Z; Liu, HY; Moore, BF; Tsao, MU	1
Aperia, A; Bergqvist, G; Linné, T; Zetterström, R	1
Bayless, TM; Ravich, WJ	1
Lentze, MJ; Rossi, E	1
Desjeux, JF; Grasset, E; Heyman, M	1
Iancu, TC; Nitzan, M; Steinherz, R	1
Harries, JT	1
Cario, WR; Höck, S; Hübschmann, K; Lindenau, E; Michel, A	1
Beau, JP; Desjeux, JF; Dumontier, AM; Evans, LA; Faverge, B; Grasset, E; Heyman, M	1
Bangstad, HJ	1
Fredrikzon, B; Keston, AS; Meeuwisse, GW	1
Desjeux, JF; Dumontier, AM; Grasset, E; Heyman, M; Lestradet, H	1
Beyreiss, K; Hoepffner, W; Müller, F; Scheerschmidt, G	2
Bijleveld, CM; Desjeux, JF; Douwes, AC; Fernandes, J; van Caillie, M	1
Desjeux, JF; Wright, EM	2
Kerner, C; Lostao, MP; Martín, MG; Turk, E; Wright, EM	1
Carroccio, A; Cavataio, F; Iacono, G; Montalto, G; Soresi, M	1
Kerner, C; Martín, MG; Turk, E; Wirth, S; Wright, EM; Zabel, B	1
Abdullah, AM; al Mazyad, A; el Shiekh, OK; el-Mouzan, MI	1
Castro, M; Diamanti, A; Ferretti, F; Gambarara, M; Papadatou, B; Pirozzi, N; Rivosecchi, M; Rupi, E	1
Abad-Sinden, A; Borowitz, S; Meyers, R; Sutphen, J	1
Bamba, T; Fukuda, M	1
Wright, EM	1
Bosshard, NU; Hirayama, BA; Lam, JT; Martín, MG; Steinmann, B; Turk, E; Wright, EM	1
Boisen, KA; Hjelt, K	1
Abe, T; Hayashi, S; Kasahara, M; Maeda, M; Mori, Y	1
Lalani, HA; Lamabadusuriya, SP; Wickramasinghe, P	1
Rosensweig, NS	1
Cohn, RM; Segal, S; Yudkoff, M	1
Sunshine, P	1
Bloch, R	1
Castro Gómez, A; de la Rosa, A; Gayoso Gómez, F; Gómez de Terreros, I; Muñóz Conde, J; Senín Sánchez, J	1
Kovács, BJ; Nagy, I; Németh, L	1
Shibuya, S	1
Clark, ML; Dawson, AM; Fairclough, PD; Harries, JT; Milla, PJ; Silk, DB	1
Clifton, JA	1
McMichael, HB	1
Cornblath, M; Schwartz, R	1
Gray, GM	2
Hughes, WS; Senior, JR	1
Abdullah, AM; Abdullah, MA; Abdurrahman, MB; al Husain, MA	1
Dyer, J; Mundlos, S; Turk, E; Wright, EM; Zabel, B	2
Biller, JA; Grand, RJ; Mobassaleh, M; Montgomery, RK	1
Chong, AS; Low, PS; Quak, SH	1
Beyreiss, K; Booth, IW; Brown, GA; Buick, R; Patel, PB; Sule, D	1
Buentello, G; Listernick, R; Lloyd-Still, JD	1
Coignet, J; Faverge, B; Garcia, P	1
Gellért, M; Hajdi, G	1
Duquesne, A; Gueho, A; Guibaud, P; La Selve, P; Larbre, F; Regent, P	1
Beau, JP; Desjeux, JF; Dumontier, AM; Evans, L; Grasset, E; Heyman, M	1
Arnaud-Battandier, F; Bresson, JL; Collard, Y; Rey, J; Ricour, C; Sarles, J; Schmitz, J	1
Cook, GC	2
Chmelík, V; Fric, P; Jodl, J; Lojda, Z	1
Johnson, JD; Kretchmer, N; Simoons, FJ	1
Bartsocas, CS; Crawford, JD	1
Madge, DS	1
Harries, JT; Wimberely, PD	1
Ament, ME	1
Bickel, H; Schmidt, H; Schürrle, L	1
Poley, JR	1
Bernhardt, W	1
Elsas, LJ; Lambe, DW	1
McGill, DB; Phillips, SF	1
Kesäniemi, YA; Salaspuro, MP	1
Habte, D; Hyvarinen, A; Sterky, G	1
Dorca, N; Faur, A; Ghircoiaşu, T; Păsculescu, G; Toma, C	1
Peternel, WW	1
Lindquist, B; Meeuwisse, G	2
Eggermont, E	1
Linneweh, F	2
Kinter, WB; Schneider, AJ; Stirling, CE; Wong, MD	1
Bond, JH; Levitt, MD	1
Bilir, S	1
Lugo-de-Rivera, C; Rodriguez, H; Torres-Pinedo, R	1
Berger, H	1
Beyreiss, K; Künzel, R; Liebe, S	1
Meeuwisse, GW; Melin, K	1
Lindquist, B	1
Gitzelmann, R	1
Elsas, LJ; Hillman, RE; Patterson, JH; Rosenberg, LE	1
Meeuwisse, GW	1
Kaijser, K; Ockerman, PA	1
Fiehring, C; Koslowski, H	1
Elsas, LJ	1
Davidson, AG; Mullinger, M	1
Desjeux, JF; Lestradet, H; Sandler, L; Sassier, P	1
Swoboda, W	1
Grävinghoff, J	1
Cohen, BE; Garti, R; Katzenelson, D; Lebenthal, E; Mathoth, Y	1
Grimmel, K; Rommel, K	1
Graul, EH; Linneweh, F; Schaumlöffel, E	1
Adam, WE; Grimmel, K; Rommel, K	1
Althausen, TL; Doig, RK; Uyeyama, K; Weiden, S	1
Göthe, S; Linneweh, F	1
Dahlqvist, A; Meeuwisse, GW	1
Francis, DE; Harries, JT	1
Waldenström, J; Zetterström, R	1
Holzel, A	1
Achord, JL; Fales, FW; Patterson, JH; Pruitt, AW	1
Kinter, WB; Schneider, AJ; Stirling, CE	1
Bode, HH; Graul, EH; Linneweh, F; Schaumlöffel, E	1
Buddington, RK; Burrin, DG; Chang, X; Cottrell, JJ; Cui, L; Stephens, JE; Stoll, B	1
Levin, RJ	1
Danon, F; Hurez, D; Mihaesco, E; Preud'homme, JL; Seligmann, M	1
Brown, MS; Gardner, JD; Laster, L	1
Hurez, D; Mihaesco, C; Mihaesco, E; Preud'homme, JL; Rambaud, JC; Seligmann, M	1
Frangione, B; Mihaesco, E; Seligmann, M	1

Reviews

23 review(s) available for galactose and Malabsorption Syndromes

Article	Year
Molecular basis for glucose-galactose malabsorption. Cell biochemistry and biophysics, 2002, Volume: 36, Issue:2-3 Topics: Carbohydrate Metabolism, Inborn Errors; Chromosomes, Human, Pair 22; Female; Galactose; Glucose; Humans; Infant, Newborn; Intestinal Absorption; Malabsorption Syndromes; Male; Membrane Glycoproteins; Monosaccharide Transport Proteins; Mutation; Sodium-Glucose Transporter 1	2002
[Molecular mechanisms of glucose transport in renal proximal tubules]. Nihon rinsho. Japanese journal of clinical medicine, 2002, Volume: 60 Suppl 7 Topics: Animals; Galactose; Glucose; Glucose Transporter Type 1; Glucose Transporter Type 2; Humans; Hypoglycemic Agents; Kidney Tubules, Proximal; Malabsorption Syndromes; Membrane Glycoproteins; Monosaccharide Transport Proteins; Sodium-Glucose Transporter 1	2002
Intestinal absorption in health and disease--sugars. Best practice & research. Clinical gastroenterology, 2003, Volume: 17, Issue:6 Topics: Animals; Carbohydrate Metabolism; Dietary Carbohydrates; Fructose; Galactose; Glucose; Glucose Transporter Type 2; Glucose Transporter Type 5; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intestinal Absorption; Malabsorption Syndromes; Microvilli; Monosaccharide Transport Proteins; Mutation	2003
Carbohydrate absorption and malabsorption. Clinics in gastroenterology, 1983, Volume: 12, Issue:2 Topics: Dietary Carbohydrates; Digestion; Fructose; Fructose Intolerance; Galactose; Glucose; Humans; Intestinal Absorption; Intestinal Mucosa; Intestines; Lactose Intolerance; Malabsorption Syndromes; Microvilli; Oligo-1,6-Glucosidase; Starch; Sucrase; Trehalase	1983
Clinical significance of enzymatic deficiencies in the gastrointestinal tract with particular reference to lactase deficiency. Annals of allergy, 1984, Volume: 53, Issue:6 Pt 2 Topics: Adult; Aging; Amino Acid Sequence; Animals; beta-Galactosidase; Child, Preschool; Digestion; Digestive System; Disaccharidases; Enteropeptidase; Enzyme Activation; Epithelium; Exocrine Pancreatic Insufficiency; Forecasting; Galactose; Gastrointestinal Motility; Glucose; Humans; Hydrolases; Infant; Infant, Newborn; Lactose Intolerance; Malabsorption Syndromes; Microvilli; Oligo-1,6-Glucosidase; Sucrase	1984
Disorders of carbohydrate absorption. Clinics in gastroenterology, 1982, Volume: 11, Issue:1 Topics: Carbohydrate Metabolism, Inborn Errors; Galactose; Glucose; Humans; Hydrolysis; Intestinal Absorption; Lactose Intolerance; Malabsorption Syndromes; Starch; Sucrase-Isomaltase Complex; Trehalase	1982
[30 years' work on congenital glucose and galactose malabsorption: from phenotype to genotype]. Annales de gastroenterologie et d'hepatologie, 1993, Volume: 29, Issue:5 Topics: Galactose; Genotype; Glucose; Humans; Intestinal Absorption; Malabsorption Syndromes; Phenotype	1993
[Selective congenital glucose, galactose malabsorption in the small intestine]. Ryoikibetsu shokogun shirizu, 1998, Issue:19 Pt 2 Topics: Animals; Carbohydrate Metabolism, Inborn Errors; Diagnosis, Differential; Galactose; Glucose; Humans; Intestinal Absorption; Malabsorption Syndromes; Membrane Glycoproteins; Monosaccharide Transport Proteins; Mutation; Sodium-Glucose Transporter 1	1998
I. Glucose galactose malabsorption. The American journal of physiology, 1998, Volume: 275, Issue:5 Topics: Animals; Biological Transport; Cell Membrane; Galactose; Glucose; Humans; Intestinal Mucosa; Malabsorption Syndromes; Membrane Glycoproteins; Microvilli; Models, Molecular; Monosaccharide Transport Proteins; Point Mutation; Protein Structure, Secondary; Sodium-Glucose Transporter 1	1998
Absorption and malabsorption of carbohydrates. Mead Johnson Symposium on Perinatal and Developmental Medicine, 1977, Issue:11 Topics: alpha-Glucosidases; beta-Galactosidase; Carbohydrate Metabolism; Disaccharides; Fructose; Galactose; Glucose; Humans; Hydrolysis; Infant, Newborn; Infant, Premature; Intestinal Absorption; Intestines; Malabsorption Syndromes; Monosaccharides	1977
Disorders of carbohydrate digestion and absorption. Clinics in endocrinology and metabolism, 1976, Volume: 5, Issue:3 Topics: Aging; Blood Glucose; Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Colon; Dietary Carbohydrates; Digestion; Disaccharides; Galactose; Glucose; Humans; Infant, Newborn; Intestinal Absorption; Intestinal Mucosa; Intestines; Lactose; Lactose Intolerance; Malabsorption Syndromes; Models, Biological; Monosaccharides; Pharmaceutical Preparations; Starch	1976
Carbohydrate digestion and absorption. Role of the small intestine. The New England journal of medicine, 1975, Jun-05, Volume: 292, Issue:23 Topics: Amylases; Animals; Biological Transport; Carbohydrate Metabolism; Digestion; Disaccharidases; Epithelial Cells; Epithelium; Fructose; Galactose; Glucose; Humans; Hydrolysis; Infant; Intestinal Absorption; Intestine, Small; Kinetics; Malabsorption Syndromes; Monosaccharides; Oligosaccharides; Starch	1975
Molecular genetics of intestinal glucose transport. The Journal of clinical investigation, 1991, Volume: 88, Issue:5 Topics: Animals; Cloning, Molecular; Galactose; Glucose; Humans; Intestinal Mucosa; Kinetics; Malabsorption Syndromes; Models, Biological; Monosaccharide Transport Proteins	1991
Cytochemistry of the human jejunal mucosa in the norm and in malabsorption syndrome. Current topics in pathology. Ergebnisse der Pathologie, 1970, Volume: 52 Topics: Abetalipoproteinemia; Acid Phosphatase; Adenosine Triphosphatases; Amino Acids; Biopsy; Celiac Disease; Esterases; Galactose; Glucose; Histocytochemistry; Humans; Intestinal Mucosa; Jejunum; Malabsorption Syndromes; Microscopy, Electron; Mitochondria; Oxidoreductases; Sprue, Tropical; Whipple Disease	1970
Lactose malabsorption: its biology and history. Advances in pediatrics, 1974, Volume: 21 Topics: Africa; Animals; Asia; Dairying; Europe; Galactose; Galactosidases; Hexosyltransferases; History, 20th Century; History, Ancient; History, Medieval; Humans; Intestinal Absorption; Intestines; Lactose; Lactose Intolerance; Lactose Synthase; Malabsorption Syndromes; Milk; United States	1974
Malabsorption syndromes in infancy and childhood. I. The Journal of pediatrics, 1972, Volume: 81, Issue:4 Topics: Caseins; Child, Preschool; Chlorides; Diarrhea; Dietary Carbohydrates; Dietary Fats; Endopeptidases; Feces; Galactose; Glucose; Humans; Hydrogen-Ion Concentration; Hypersensitivity; Immunologic Deficiency Syndromes; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intestinal Diseases, Parasitic; Intestines; Lactose Intolerance; Malabsorption Syndromes; Metabolism, Inborn Errors; Sucrase	1972
Dietary treatment of inborn errors of amino acid and carbohydrate metabolism. Bibliotheca nutritio et dieta, 1973, Issue:18 Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Child; Child Development; Child Nutritional Physiological Phenomena; Child, Preschool; Cystinosis; Diet Therapy; Galactose; Glucose; Histidine; Homocystinuria; Humans; Infant; Infant Nutrition Disorders; Infant, Newborn; Lactose Intolerance; Malabsorption Syndromes; Maple Syrup Urine Disease; Phenylketonurias; Sucrose; Tyrosine	1973
Chronic diarrhea in infants and children. I. Southern medical journal, 1973, Volume: 66, Issue:9 Topics: Adolescent; Bile Acids and Salts; Child; Child, Preschool; Chronic Disease; Cystic Fibrosis; Diarrhea; Dietary Carbohydrates; Dietary Proteins; Fatty Acids; Food Hypersensitivity; Galactose; Gastrointestinal Motility; Glucose; Glutens; Glycoside Hydrolases; Humans; Infant; Intestinal Absorption; Intestines; Lipase; Malabsorption Syndromes; Metabolism, Inborn Errors; Pancreas	1973
Disaccharidase deficiency. The Medical clinics of North America, 1968, Volume: 52, Issue:6 Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Celiac Disease; Colitis, Ulcerative; Crohn Disease; Deficiency Diseases; Diarrhea; Galactose; Glucose; Glycoside Hydrolases; Humans; Intestinal Absorption; Intestinal Mucosa; Kwashiorkor; Lactose Intolerance; Malabsorption Syndromes; Monosaccharides; Peptic Ulcer; Sprue, Tropical; Sucrase	1968
Glucose-galactose malabsorption. Bibliotheca paediatrica, 1968, Volume: 87 Topics: Diarrhea; Diet Therapy; Galactose; Glucose; Glycosuria; Humans; Intestinal Absorption; Kidney; Malabsorption Syndromes; Pedigree	1968
The genetics of intestinal carbohydrate intolerance. Progress in medical genetics, 1969, Volume: 6 Topics: Carbohydrate Metabolism, Inborn Errors; Fructose; Galactose; Glucose; Glycoside Hydrolases; Humans; Intestinal Absorption; Intestinal Mucosa; Lactose Intolerance; Malabsorption Syndromes; Starch; Sucrose	1969
Intestinal digestion and maldigestion of dietary carbohydrates. Annual review of medicine, 1971, Volume: 22 Topics: Biological Transport, Active; Deficiency Diseases; Dextranase; Dietary Carbohydrates; Digestion; Galactose; Glucose; Glycoside Hydrolases; Humans; Hydrolysis; Intestinal Absorption; Intestine, Small; Lactose Intolerance; Malabsorption Syndromes; Metabolism, Inborn Errors; Oligosaccharides; Sucrase	1971
The columnar epithelial cell of the small intestine: digestion and transport. II. The New England journal of medicine, 1970, Dec-03, Volume: 283, Issue:23 Topics: Amino Acids; Animals; Bacteria; Biological Transport; Biological Transport, Active; Carbohydrate Metabolism; Cell Membrane Permeability; Digestion; Epithelial Cells; Epithelium; Hexoses; Humans; Intestinal Absorption; Intestinal Mucosa; Intestine, Small; Kinetics; Malabsorption Syndromes; Potassium; Sodium	1970

Other Studies

115 other study(ies) available for galactose and Malabsorption Syndromes

Article	Year
Congenital Glucose-Galactose Malabsorption in a Child. Indian pediatrics, 2022, 10-15, Volume: 59, Issue:10 Topics: Carbohydrate Metabolism, Inborn Errors; Child; Galactose; Glucose; Humans; Malabsorption Syndromes; Metabolism, Inborn Errors	2022
Congenital Glucose-Galactose Malabsorption in a Neonate with Hyperbilirubinemia and Hypernatremia. Indian journal of pediatrics, 2023, Volume: 90, Issue:7 Topics: Carbohydrate Metabolism, Inborn Errors; Galactose; Glucose; Humans; Hyperbilirubinemia; Hypernatremia; Infant, Newborn; Malabsorption Syndromes; Metabolism, Inborn Errors	2023
Nutrition management of congenital glucose-galactose malabsorption: Case report of a Chinese infant. Medicine, 2019, Volume: 98, Issue:33 Topics: Carbohydrate Metabolism, Inborn Errors; China; Diet, Carbohydrate-Restricted; Female; Galactose; Glucose; Humans; Infant Formula; Infant, Newborn; Malabsorption Syndromes; Mutation; Sodium-Glucose Transporter 1	2019
A case of neonatal diarrhoea caused by congenital glucose-galactose malabsorption. The Medical journal of Malaysia, 2009, Volume: 64, Issue:1 Topics: Consanguinity; Diarrhea; Female; Galactose; Glucose; Humans; Infant; Malabsorption Syndromes; Prognosis	2009
Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish. Clinical genetics, 2011, Volume: 79, Issue:1 Topics: Adolescent; Adult; Child; Child, Preschool; DNA Mutational Analysis; Female; Founder Effect; Galactose; Genetic Predisposition to Disease; Genetic Variation; Glucose; Humans; Infant; Infant, Newborn; Intestinal Absorption; Malabsorption Syndromes; Male; Mutation; Pedigree; Sodium-Glucose Transporter 1; Young Adult	2011
Structural insights into genetic variants of Na(+)/glucose cotransporter SGLT1 causing glucose-galactose malabsorption: vSGLT as a model structure. Cell biochemistry and biophysics, 2012, Volume: 63, Issue:2 Topics: Amino Acid Motifs; Amino Acid Sequence; Amino Acid Substitution; Bacterial Proteins; Galactose; Genetic Variation; Glucose; Humans; Hydrogen Bonding; Intestinal Absorption; Malabsorption Syndromes; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation, Missense; Protein Structure, Tertiary; Sequence Homology, Amino Acid; Sodium-Glucose Transporter 1; Structural Homology, Protein	2012
Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene. European journal of pediatrics, 2013, Volume: 172, Issue:3 Topics: Base Sequence; Female; Galactose; Genetic Markers; Glucose; Homozygote; Humans; Infant, Newborn; Malabsorption Syndromes; Sequence Deletion; Sodium-Glucose Transporter 1	2013
[Neonatal diarrhea due to congenital glucose-galactose malabsorption: report of seven cases]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2012, Volume: 19, Issue:12 Topics: Child, Preschool; Diarrhea, Infantile; Female; Galactose; Glucose; Humans; Infant; Infant, Newborn; Malabsorption Syndromes; Male	2012
Neonatal nephrocalcinosis in association with glucose-galactose malabsorption. Pediatric nephrology (Berlin, Germany), 2003, Volume: 18, Issue:7 Topics: Calcium; Diarrhea; Galactose; Glucose; Growth Disorders; Humans; Hypercalcemia; Infant, Newborn; Karyotyping; Kidney; Malabsorption Syndromes; Male; Nephrocalcinosis; Oxalates; Polyuria; Ultrasonography	2003
MILK INTOLERANCE IN TROPICAL MALABSORPTION SYNDROME. ROLE OF LACTOSE MALABSORPTION. Lancet (London, England), 1964, Sep-26, Volume: 2, Issue:7361 Topics: Carbohydrate Metabolism; Celiac Disease; Diarrhea; Galactose; Glucose; Glucose Tolerance Test; Humans; Lactose; Lactose Intolerance; Malabsorption Syndromes; Milk; Peptic Ulcer; Sprue, Tropical; Statistics as Topic	1964
ACQUIRED MILK INTOLERANCE IN THE ADULT CAUSED BY LACTOSE MALABSORPTION DUE TO A SELECTIVE DEFICIENCY OF INTESTINAL LACTASE ACTIVITY. The American journal of medicine, 1965, Volume: 38 Topics: Adult; beta-Galactosidase; Carbohydrate Metabolism; Galactose; Geriatrics; Glucose Tolerance Test; Glycoside Hydrolases; Humans; Intestinal Absorption; Intestines; Lactose; Lactose Intolerance; Malabsorption Syndromes; Maltose; Metabolic Diseases	1965
HYPOGLYCAEMIA INDUCED BY LACTOSE OR GALACTOSE. Lancet (London, England), 1965, Apr-03, Volume: 1, Issue:7388 Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Consanguinity; Diarrhea; Diarrhea, Infantile; Galactose; Glucose Tolerance Test; Hemiplegia; Humans; Hypoglycemia; Infant; Infant, Newborn; Lactose; Lactose Intolerance; Malabsorption Syndromes; Seizures	1965
[CONGENITAL GLUCOSE AND GALACTOSE MALABSORPTION]. Klinische Wochenschrift, 1965, Apr-15, Volume: 43 Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Diet; Diet Therapy; Fructose; Galactose; Glucose; Humans; Intestinal Absorption; Malabsorption Syndromes	1965
Nephrolithiasis in a child with glucose-galactose malabsorption. Pediatric nephrology (Berlin, Germany), 2004, Volume: 19, Issue:2 Topics: Amino Acid Transport Systems, Basic; Chronic Disease; Codon, Nonsense; Cytosine; Diarrhea; Female; Galactose; Gene Deletion; Glucose; Humans; Infant, Newborn; Kidney Calculi; Malabsorption Syndromes; Thymine; Ultrasonography	2004
A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption. Journal of pediatric gastroenterology and nutrition, 2005, Volume: 40, Issue:4 Topics: Carbohydrate Metabolism, Inborn Errors; Exons; Female; Galactose; Glucose; Humans; Immunohistochemistry; Infant, Newborn; Malabsorption Syndromes; Monosaccharide Transport Proteins; Mutation, Missense; Pedigree	2005
Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis. Pediatric nephrology (Berlin, Germany), 2005, Volume: 20, Issue:9 Topics: Acidosis, Renal Tubular; Female; Galactose; Glucose; Glucose Metabolism Disorders; Humans; Infant; Infant, Newborn; Malabsorption Syndromes; Male; Nephrocalcinosis	2005
D28G mutation in congenital glucose-galactose malabsorption. Archives of Iranian medicine, 2007, Volume: 10, Issue:4 Topics: Aspartic Acid; Female; Galactose; Glucose; Glycine; Humans; Infant, Newborn; Malabsorption Syndromes; Male; Mutation; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Sodium-Glucose Transporter 1	2007
Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1. European journal of pediatrics, 2008, Volume: 167, Issue:12 Topics: Fanconi Syndrome; Female; Galactose; Glucose; Glucose Metabolism Disorders; Humans; Infant; Malabsorption Syndromes; Mutation, Missense; Nephrocalcinosis; Sodium-Glucose Transporter 1	2008
Intestinal lactase deficiency and saccharide malabsorption during oral neomycin administration. Gastroenterology, 1967, Volume: 53, Issue:1 Topics: Chromatography, Thin Layer; Disaccharides; Feces; Galactose; Glucose; Glucose Tolerance Test; Humans; Intestinal Mucosa; Jejunum; Kanamycin; Lactose; Lactose Intolerance; Malabsorption Syndromes; Monosaccharides; Neomycin	1967
Tm glucose in a case of congenital intestinal and renal malabsorption of monosaccharides. Pediatric research, 1967, Volume: 1, Issue:5 Topics: Absorption; Female; Galactose; Glucose; Glycosuria; Humans; Infant; Intestinal Diseases; Kidney Function Tests; Kidney Tubules; Malabsorption Syndromes	1967
Familial Fanconi syndrome with malabsorption and galactose intolerance, normal kinase and transferase activity. A report on two siblings. Acta paediatrica Scandinavica, 1981, Volume: 70, Issue:4 Topics: Carbohydrate Metabolism, Inborn Errors; Fanconi Syndrome; Female; Galactose; Humans; Infant; Kidney; Malabsorption Syndromes; Male; Phosphotransferases; Renal Aminoacidurias; Transferases	1981
[Systems of membrane transport, genetics and nutrition; the example of congenital anomalies of intestinal transport in children]. Reproduction, nutrition, developpement, 1984, Volume: 24, Issue:5B Topics: Amino Acids; Biological Transport; Cell Membrane; Child; Epithelium; Galactose; Genes; Genes, Regulator; Glucose; Humans; Intestinal Absorption; Intestinal Mucosa; Intestines; Malabsorption Syndromes	1984
Hypernatremic dehydration as a sign leading to the diagnosis of glucose-galactose malabsorption in breast-fed neonates. Helvetica paediatrica acta, 1984, Volume: 39, Issue:3 Topics: Carbohydrate Metabolism, Inborn Errors; Dehydration; Female; Galactose; Glucose; Humans; Hypernatremia; Infant, Newborn; Malabsorption Syndromes	1984
[Glucose-galactose malabsorption]. Kinderarztliche Praxis, 1982, Volume: 50, Issue:8 Topics: Diarrhea; Galactose; Glucose; Humans; Infant; Infant Nutritional Physiological Phenomena; Malabsorption Syndromes; Male	1982
[Intestinal malabsorption of glucose and galactose. Study of a family]. Archives francaises de pediatrie, 1982, Volume: 39 Suppl 2 Topics: Adult; Alanine; Electrophysiology; Female; Galactose; Glucose; Glycosuria; Humans; Infant; Intestinal Absorption; Intestinal Mucosa; Malabsorption Syndromes; Male; Microvilli	1982
[Life-threatening diarrhea in the neonatal period. A case of congenital glucose-galactose malabsorption]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1982, Nov-30, Volume: 102, Issue:33 Topics: Diarrhea, Infantile; Female; Galactose; Glucose; Humans; Infant, Newborn; Malabsorption Syndromes	1982
Evidence for participation of mutarotase in sugar transport: absence of the enzyme in a case of glucose galactose malabsorption. Biochemical and biophysical research communications, 1982, Oct-29, Volume: 108, Issue:4 Topics: Adult; Biological Transport; Carbohydrate Epimerases; Child; Female; Galactose; Glucose; Humans; Infant; Intestinal Mucosa; Jejunum; Kinetics; Malabsorption Syndromes; Male; Syndrome	1982
Relationship between transport of D-xylose and other monosaccharides in jejunal mucosa of children. Gastroenterology, 1981, Volume: 80, Issue:4 Topics: Adolescent; Child; Child, Preschool; Electrophysiology; Fructose; Galactose; Humans; Infant; Intestinal Absorption; Intestinal Mucosa; Jejunum; Malabsorption Syndromes; Ouabain; Sodium; Xylose	1981
[Glucose-galactose malabsorption: quantitative determination of digestion and absorption of carbohydrates by continuing perfusion of small intestine]. Kinderarztliche Praxis, 1981, Volume: 49, Issue:8 Topics: Female; Galactose; Glucose; Humans; Infant; Intestinal Absorption; Malabsorption Syndromes	1981
Interval breath hydrogen test in glucose-galactose malabsorption. European journal of pediatrics, 1981, Volume: 137, Issue:3 Topics: Air; Female; Galactose; Glucose; Humans; Hydrogen; Infant, Newborn; Malabsorption Syndromes	1981
Structure of the human Na+/glucose cotransporter gene SGLT1. The Journal of biological chemistry, 1994, May-27, Volume: 269, Issue:21 Topics: Amino Acid Sequence; Base Sequence; Carrier Proteins; Child, Preschool; Cloning, Molecular; DNA; Exons; Galactose; Glucose; Humans; Introns; Malabsorption Syndromes; Male; Membrane Glycoproteins; Membrane Proteins; Molecular Sequence Data; Monosaccharide Transport Proteins; Mutation; Protein Structure, Secondary; Restriction Mapping; Sodium; Sodium-Glucose Transporter 1; Transcription, Genetic	1994
[Thirty years of research on congenital glucose and galactose malabsorption: from phenotype to genotype]. Bulletin de l'Academie nationale de medecine, 1993, Volume: 177, Issue:1 Topics: Dietary Carbohydrates; Galactose; Genotype; Glucose; Humans; Infant, Newborn; Malabsorption Syndromes; Phenotype; Research	1993
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption. Nature genetics, 1996, Volume: 12, Issue:2 Topics: Amino Acid Sequence; Animals; Base Sequence; Biological Transport; Cell Membrane; Galactose; Genetic Carrier Screening; Glucose; Homozygote; Humans; Malabsorption Syndromes; Membrane Glycoproteins; Membrane Potentials; Methylglucosides; Molecular Sequence Data; Monosaccharide Transport Proteins; Mutation; Oocytes; Polymorphism, Single-Stranded Conformational; Protein Structure, Secondary; Sodium-Glucose Transporter 1; Xenopus laevis	1996
Congenital fructose-glucose-galactose malabsorption. Journal of pediatric gastroenterology and nutrition, 1995, Volume: 21, Issue:1 Topics: Biopsy; Female; Fructose; Galactose; Glucose; Humans; Hydrocephalus; Infant, Newborn; Intestinal Absorption; Intestinal Mucosa; Malabsorption Syndromes; Male	1995
Prenatal identification of a heterozygous status in two fetuses at risk for glucose-galactose malabsorption. Prenatal diagnosis, 1996, Volume: 16, Issue:5 Topics: Amniocentesis; Breath Tests; Consanguinity; Deoxyribonucleases, Type II Site-Specific; Diarrhea; DNA; DNA Primers; Female; Fetal Diseases; Galactose; Genetic Carrier Screening; Glucose; Humans; Malabsorption Syndromes; Membrane Glycoproteins; Monosaccharide Transport Proteins; Pedigree; Polymerase Chain Reaction; Pregnancy; Reagent Kits, Diagnostic; Restriction Mapping; Risk Factors; Sodium-Glucose Transporter 1	1996
Congenital glucose-galactose malabsorption in Arab children. Journal of pediatric gastroenterology and nutrition, 1996, Volume: 23, Issue:5 Topics: Consanguinity; Diarrhea; Female; Food, Formulated; Fructose; Galactose; Glucose; Humans; Infant; Malabsorption Syndromes; Male; Saudi Arabia	1996
Glucose-galactose malabsorption: is it an indication to bowel transplantation in childhood? Transplantation proceedings, 1997, Volume: 29, Issue:3 Topics: Child; Child, Preschool; Consanguinity; Dietary Carbohydrates; Enteral Nutrition; Failure to Thrive; Female; Follow-Up Studies; Galactose; Glucose; Humans; Infant; Intestines; Malabsorption Syndromes; Male; Nuclear Family; Parenteral Nutrition, Total; Prognosis	1997
Nutrition management of congenital glucose-galactose malabsorption: a case study. Journal of the American Dietetic Association, 1997, Volume: 97, Issue:12 Topics: Absorption; Carbohydrate Metabolism, Inborn Errors; Female; Galactose; Glucose; Humans; Infant Food; Infant, Newborn; Intestinal Mucosa; Jejunum; Malabsorption Syndromes; Nutrition Assessment	1997
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects. Biochimica et biophysica acta, 1999, Feb-24, Volume: 1453, Issue:2 Topics: Cell Membrane; Endoplasmic Reticulum; Female; Galactose; Glucose; Humans; Infant, Newborn; Malabsorption Syndromes; Membrane Glycoproteins; Monosaccharide Transport Proteins; Mutation; Polymorphism, Single-Stranded Conformational; Sodium-Glucose Transporter 1	1999
[Glucose-galactose malabsorption. The first reported case in Denmark]. Ugeskrift for laeger, 1999, Jun-28, Volume: 161, Issue:26 Topics: Diagnosis, Differential; Diarrhea, Infantile; Galactose; Glucose; Humans; Infant; Infant, Newborn; Malabsorption Syndromes	1999
A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant protein. Biochimica et biophysica acta, 2001, May-31, Volume: 1536, Issue:2-3 Topics: Animals; Base Sequence; Carbohydrate Metabolism, Inborn Errors; Exons; Female; Galactose; Glucose; Humans; Infant, Newborn; Malabsorption Syndromes; Membrane Glycoproteins; Monosaccharide Transport Proteins; Mutation, Missense; Oocytes; Pedigree; Sodium-Glucose Transporter 1; Xenopus	2001
Congenital glucose galactose malabsorption. The Ceylon medical journal, 2001, Volume: 46, Issue:1 Topics: Consanguinity; Diarrhea; Fluid Therapy; Galactose; Genes, Recessive; Glucose; Humans; Infant Food; Infant, Newborn; Malabsorption Syndromes; Male	2001
Other carbohydrate intolerances. Current concepts in nutrition, 1979, Volume: 8 Topics: beta-Galactosidase; Carbohydrate Metabolism, Inborn Errors; Dietary Carbohydrates; Galactose; Galactosemias; Glucose; Humans; Lactose; Lactose Intolerance; Malabsorption Syndromes	1979
Errors of carbohydrate metabolism in infants and children: a survey. Clinical pediatrics, 1978, Volume: 17, Issue:11 Topics: Carbohydrate Metabolism, Inborn Errors; Diarrhea; Fructokinases; Fructose Intolerance; Fructose-1,6-Diphosphatase Deficiency; Galactokinase; Galactose; Galactosemias; Glucose; Humans; Lactose Intolerance; Malabsorption Syndromes; Sucrase-Isomaltase Complex; Syndrome; Transferases; Uridine Diphosphate Galactose	1978
[Normal nutrition--malnutrition during malassimilation?]. Infusionstherapie und klinische Ernahrung, 1977, Volume: 4, Issue:1 Topics: Amino Acids; Animals; Carbohydrate Metabolism, Inborn Errors; Celiac Disease; Galactose; Glucose; Glycoside Hydrolases; Humans; Intestinal Absorption; Intestinal Mucosa; Intestines; Lactose Intolerance; Malabsorption Syndromes; Milk; Sucrase	1977
[Galactosemia and cow's milk intolerance (author's transl)]. Anales espanoles de pediatria, 1978, Volume: 11, Issue:2 Topics: Animals; Cattle; Galactose; Galactosemias; Humans; Infant, Newborn; Lactose Intolerance; Malabsorption Syndromes; Male; UDPglucose-Hexose-1-Phosphate Uridylyltransferase	1978
[Disorder of galactose metabolism and damage of the small intestine. Possible causal relationship based on the analysis of 40 pediatric cases]. Orvosi hetilap, 1978, Jul-02, Volume: 119, Issue:27 Topics: Child, Preschool; Diagnosis, Differential; Galactose; Galactosemias; Humans; Infant; Infant, Newborn; Malabsorption Syndromes; Metabolism, Inborn Errors	1978
[Glucose-galactose malabsorption]. Nihon rinsho. Japanese journal of clinical medicine, 1978, Volume: Suppl Topics: Adult; Galactose; Glucose; Humans; Infant, Newborn; Malabsorption Syndromes	1978
Absorption of glucose and maltose in congenital glucose-galactose malabsorption. Pediatric research, 1978, Volume: 12, Issue:12 Topics: Biological Transport; Child; Child, Preschool; Galactose; Glucose; Humans; Infant; Infant, Newborn; Intestinal Absorption; Malabsorption Syndromes; Male; Maltose	1978
[Some hereditary disorders of intestinal resorption with renal dysfunction]. Der Internist, 1976, Volume: 17, Issue:7 Topics: Arginine; Child; Chlorides; Cystine; Cystinuria; Diarrhea; Female; Galactose; Glucose; Hartnup Disease; Humans; Infant, Newborn; Intestinal Absorption; Kidney Diseases; Lysine; Malabsorption Syndromes; Male; Pedigree; Tryptophan	1976
Disorders of carbohydrate metabolism in infancy. Major problems in clinical pediatrics, 1976, Volume: 3 Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Diabetes Mellitus, Type 1; Female; Fructose Intolerance; Galactose; Glucose; Glycogen; Homeostasis; Humans; Hydrocortisone; Hypoglycemia; Infant; Infant, Newborn; Malabsorption Syndromes; Male; Metabolic Diseases; Pregnancy; Pregnancy in Diabetics; Syndrome	1976
The glucose-galactose malabsorption syndrome in a 23-year-old woman. Gastroenterology, 1975, Volume: 68, Issue:1 Topics: Adult; Female; Fructose; Galactose; Glucose; Humans; Intestinal Absorption; Malabsorption Syndromes; Monosaccharides; Perfusion	1975
Glucose-galactose malabsorption with renal stones in a Saudi child. Annals of tropical paediatrics, 1992, Volume: 12, Issue:3 Topics: Carbohydrate Metabolism, Inborn Errors; Chronic Disease; Diarrhea, Infantile; Female; Galactose; Glucose; Humans; Infant; Kidney Calculi; Malabsorption Syndromes; Saudi Arabia	1992
Glucose/galactose malabsorption caused by a defect in the Na+/glucose cotransporter. Nature, 1991, Mar-28, Volume: 350, Issue:6316 Topics: Antisense Elements (Genetics); Base Sequence; Child, Preschool; DNA; Female; Galactose; Glucose; Humans; Malabsorption Syndromes; Male; Models, Molecular; Molecular Sequence Data; Monosaccharide Transport Proteins; Mutation; Oligonucleotide Probes; Polymerase Chain Reaction; Protein Conformation; Reference Values	1991
Development of carbohydrate absorption in the fetus and neonate. Pediatrics, 1985, Volume: 75, Issue:1 Pt 2 Topics: Adaptation, Physiological; alpha-Glucosidases; Amylases; beta-Galactosidase; Biological Transport; Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Dietary Carbohydrates; Female; Fetus; Galactose; Glucan 1,4-alpha-Glucosidase; Glucose; Humans; Infant, Newborn; Intestinal Absorption; Intestinal Mucosa; Lactose Intolerance; Malabsorption Syndromes; Oligo-1,6-Glucosidase; Pancreas; Pregnancy; Sucrase; Sucrase-Isomaltase Complex	1985
Glucose-galactose malabsorption--a report in a Chinese family. The Journal of the Singapore Paediatric Society, 1989, Volume: 31, Issue:3-4 Topics: Carbohydrate Metabolism, Inborn Errors; Galactose; Glucose; Humans; Infant; Infant, Newborn; Malabsorption Syndromes; Male	1989
Glucose-galactose malabsorption: demonstration of specific jejunal brush border membrane defect. Gut, 1988, Volume: 29, Issue:12 Topics: Galactose; Glucose; Humans; Infant, Newborn; Jejunum; Malabsorption Syndromes; Male; Microvilli	1988
Complex carbohydrate intolerance: diagnostic pitfalls and approach to management. The Journal of pediatrics, 1988, Volume: 112, Issue:5 Topics: Carbohydrate Metabolism, Inborn Errors; Diarrhea; Galactose; Glucose; Humans; Infant, Newborn; Intestines; Malabsorption Syndromes; Male; Sucrase-Isomaltase Complex; Sucrose	1988
[Congenital malabsorption of glucose-galactose. Apropos of 2 cases]. Annales de pediatrie, 1987, Volume: 34, Issue:4 Topics: Diarrhea, Infantile; Female; Galactose; Glucose; Humans; Infant, Newborn; Malabsorption Syndromes; Male	1987
[Glucose-galactose malabsorption]. Orvosi hetilap, 1986, Dec-28, Volume: 127, Issue:52 Topics: Diet Therapy; Fructose; Galactose; Glucose; Humans; Hypokalemia; Infant, Newborn; Malabsorption Syndromes; Potassium	1986
[A new case of glucose-galactose malabsorption]. Pediatrie, 1986, Volume: 41, Issue:4 Topics: Diarrhea, Infantile; Female; Galactose; Glucose; Humans; Infant, Newborn; Malabsorption Syndromes	1986
Congenital selective malabsorption of glucose and galactose. Journal of pediatric gastroenterology and nutrition, 1985, Volume: 4, Issue:6 Topics: Biological Transport, Active; Diarrhea, Infantile; Dietary Carbohydrates; Disaccharidases; Female; Galactose; Genes, Recessive; Glucose; Humans; Infant, Newborn; Intestinal Mucosa; Jejunum; Malabsorption Syndromes; Male	1985
Digestion and absorption rates of lactose, glucose, galactose, and fructose in three infants with congenital glucose-galactose malabsorption: perfusion studies. Journal of pediatric gastroenterology and nutrition, 1985, Volume: 4, Issue:6 Topics: Biological Transport, Active; Dietary Carbohydrates; Female; Fructose; Galactose; Glucose; Humans; Infant; Intestinal Absorption; Jejunum; Kinetics; Lactose; Malabsorption Syndromes; Male; Perfusion	1985
[Acid fermentation and hydrogen production by colonic flora in a case of malabsorption of glucose and galactose]. Gastroenterologie clinique et biologique, 1985, Volume: 9, Issue:11 Topics: Colon; Female; Galactose; Glucose; Humans; Hydrogen; Infant, Newborn; Lactates; Malabsorption Syndromes	1985
Glucose absorption kinetics in Zambian African patients with and without systemic bacterial infections. Gut, 1971, Volume: 12, Issue:12 Topics: Adult; Aged; Bacterial Infections; Black People; Female; Galactose; gamma-Globulins; Glucose; Humans; Intestinal Absorption; Jejunum; Kinetics; Kwashiorkor; Malabsorption Syndromes; Male; Middle Aged; Serum Albumin; Tuberculosis; Tuberculosis, Pulmonary; Water; Zambia	1971
Clinical phenotypes in kidney transport disorders. Birth defects original article series, 1974, Volume: 10, Issue:4 Topics: Abnormalities, Multiple; Acidosis, Renal Tubular; Cerebrospinal Fluid Proteins; Chronic Kidney Disease-Mineral and Bone Disorder; Cystinuria; Diabetes Insipidus; Galactose; Glucose; Glycosuria, Renal; Growth Disorders; Hartnup Disease; Humans; Hypophosphatemia, Familial; Kidney Tubules; Malabsorption Syndromes; Methionine; Phenotype; Pseudohypoparathyroidism; Pulmonary Heart Disease; Renal Aminoacidurias; Renal Tubular Transport, Inborn Errors; Seizures; Syndrome	1974
Malabsorption in C57 mice experimentally infected with Johne's disease. Comparative biochemistry and physiology. A, Comparative physiology, 1971, Nov-01, Volume: 40, Issue:3 Topics: Animals; Arginine; Body Weight; Cecum; Female; Galactose; Glucose; Hexoses; Histidine; Intestinal Absorption; Intestine, Large; Intestine, Small; Malabsorption Syndromes; Male; Mice; Mice, Inbred Strains; Mycobacterium Infections; Organ Size; Paratuberculosis; Proteins; Rectum; Water	1971
Congenital glucose-galactose malabsorption. Proceedings of the Royal Society of Medicine, 1974, Volume: 67, Issue:8 Topics: Binding Sites; Child; Diarrhea; Galactose; Glucose; Humans; Infant; Infant, Newborn; Insulin; Intestinal Mucosa; Jejunum; Leucine; Malabsorption Syndromes; Male	1974
[Oral galactose tolerance test for the testing of intestinal absorption?]. Medizinische Klinik, 1972, Oct-27, Volume: 67, Issue:43 Topics: Administration, Oral; Adult; Capillaries; Female; Galactose; Galactosemias; Humans; Intestinal Absorption; Malabsorption Syndromes; Male	1972
Familial glucose-galactose malabsorption: remission of glucose intolerance. The Journal of pediatrics, 1973, Volume: 83, Issue:2 Topics: Bacteroides; Blood Glucose; Carbon Dioxide; Carbon Isotopes; Cells, Cultured; Erythrocytes; Female; Fibroblasts; Fructose; Galactose; Glucose; Glucose Tolerance Test; Humans; Infant, Newborn; Intestinal Absorption; Intestinal Mucosa; Intestine, Small; Jejunum; Malabsorption Syndromes; Remission, Spontaneous; Skin	1973
Glucose-galactose malabsorption in an adult: perfusion studies of sugar, electrolyte, and water transport. The American journal of digestive diseases, 1973, Volume: 18, Issue:12 Topics: Adult; Bicarbonates; Biological Transport; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Chlorides; Diarrhea; Dietary Carbohydrates; Feces; Fructose; Galactose; Glucose; Glycosuria; Humans; Hydrogen-Ion Concentration; Intestinal Absorption; Intestinal Mucosa; Jejunum; Lactates; Malabsorption Syndromes; Male; Perfusion; Potassium; Sodium; Water	1973
Intravenous galactose elimination tests with and without ethanol loading in various clinical conditions. Scandinavian journal of gastroenterology, 1973, Volume: 8, Issue:7 Topics: Adult; Aged; Alcoholism; Chronic Disease; Diabetes Mellitus; Dietary Proteins; Ethanol; Fatty Liver; Female; Galactose; Humans; Hyperthyroidism; Liver Cirrhosis; Liver Function Tests; Malabsorption Syndromes; Male; Middle Aged; Obesity	1973
Carbohydrate malabsorption in kwashiorkor. Ethiopian medical journal, 1973, Volume: 11, Issue:1 Topics: Carbohydrate Metabolism; Child, Preschool; Galactose; Glucose; Glucose Tolerance Test; Humans; Infant; Kwashiorkor; Lactose; Malabsorption Syndromes; Male; Sucrose; Xylose	1973
[Lactose malabsorption in patients with gastroduodenal ulcer and resected stomach]. Medicina interna, 1974, Volume: 26, Issue:5 Topics: Adolescent; Adult; Aged; Blood Glucose; Female; Galactose; Glucose; Humans; Intestines; Lactose; Lactose Intolerance; Malabsorption Syndromes; Male; Middle Aged; Peptic Ulcer; Postgastrectomy Syndromes	1974
[Isotope use in the study of hereditary metabolic diseases]. Monatsschrift fur Kinderheilkunde, 1970, Volume: 118, Issue:6 Topics: Animals; Autoradiography; Blood Glucose; Brain Chemistry; Carbon Isotopes; Chromatography, Paper; Deficiency Diseases; Feces; Galactose; Glucokinase; Glucose; Glycosuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Malabsorption Syndromes; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Radioisotope Dilution Technique; Radioisotopes; Rats; Tritium	1970
Quantitative radioautography of sugar transport in intestinal biopsies from normal humans and a patient with glucose-galactose malabsorption. The Journal of clinical investigation, 1972, Volume: 51, Issue:2 Topics: Adult; Autoradiography; Biopsy; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Galactose; Glucose; Humans; Infant; Intestinal Mucosa; Intestine, Small; Malabsorption Syndromes; Membranes; Methods; Microscopy, Electron; Phlorhizin; Tritium	1972
Use of pulmonary hydrogen (H 2 ) measurements to quantitate carbohydrate absorption. Study of partially gastrectomized patients. The Journal of clinical investigation, 1972, Volume: 51, Issue:5 Topics: Carbohydrate Metabolism; Disaccharides; Fructose; Galactose; Gastrectomy; Humans; Hydrogen; Intestinal Absorption; Lung; Malabsorption Syndromes; Methods; Postgastrectomy Syndromes; Spirometry	1972
Acquired disaccharide intolerance in children with malnutrition. The American journal of clinical nutrition, 1972, Volume: 25, Issue:7 Topics: Blood Glucose; Body Weight; Diarrhea; Diet Therapy; Dietary Proteins; Disaccharides; Feces; Female; Galactose; Glucose Tolerance Test; Humans; Hydrogen-Ion Concentration; Infant; Lactose; Lactose Intolerance; Malabsorption Syndromes; Male; Nutrition Disorders; Urine	1972
Studies on the mechanism of sugar malabsorption in infantile infectious diarrhea. The American journal of clinical nutrition, 1972, Volume: 25, Issue:11 Topics: Bicarbonates; Carbohydrate Metabolism; Carbohydrates; Colon; Diarrhea, Infantile; Fermentation; Galactose; Glucose; Humans; Hydrogen-Ion Concentration; Infant; Intestinal Absorption; Intestine, Small; Intubation, Gastrointestinal; Jejunum; Malabsorption Syndromes; Models, Biological; Perfusion; Permeability	1972
[Congenital enzyme defects]. Wiener medizinische Wochenschrift (1946), 1971, Sep-18, Volume: 121, Issue:38 Topics: Amylases; Biotransformation; Carbohydrate Metabolism, Inborn Errors; Fructose; Galactose; Glucose; Glucosephosphate Dehydrogenase Deficiency; Hemoglobinopathies; Heterozygote; Humans; Malabsorption Syndromes; Metabolism, Inborn Errors; Mixed Function Oxygenases; Pyruvate Kinase	1971
[Milk-free nutrition with Sojaval of infants with lactose malabsorption or galactose intolerance]. Das Deutsche Gesundheitswesen, 1971, Feb-11, Volume: 26, Issue:7 Topics: Diet Therapy; Food; Galactose; Glycine max; Humans; Infant; Infant Food; Infant Nutritional Physiological Phenomena; Infant, Newborn; Lactose; Lactose Intolerance; Malabsorption Syndromes	1971
Glucose-galactose malabsorption. A clinical study of 6 cases. Acta paediatrica Scandinavica, 1969 Topics: Adult; Birth Weight; Blood Glucose; Blood Proteins; Carbohydrate Metabolism, Inborn Errors; Chromatography, Paper; Diarrhea, Infantile; Disaccharides; Electrolytes; Female; Fever; Galactose; Galactosemias; Glucose Tolerance Test; Glycosuria; Hemoglobins; Humans; Infant; Infant, Newborn; Intestinal Absorption; Malabsorption Syndromes; Male	1969
[Intestinal monosaccharide malabsorption]. Monatsschrift fur Kinderheilkunde, 1969, Volume: 117, Issue:1 Topics: Adult; Age Factors; Child, Preschool; Diet Therapy; Feces; Fructose; Galactose; Genes, Recessive; Glucose; Humans; Infant; Infant, Newborn; Intestinal Absorption; Intestinal Mucosa; Malabsorption Syndromes; Monosaccharides	1969
[Carbohydrate metabolism anomalies; galactose metabolism]. Monatsschrift fur Kinderheilkunde, 1969, Volume: 117, Issue:1 Topics: Carbohydrate Metabolism, Inborn Errors; Cataract; Clinical Enzyme Tests; Galactose; Galactosidases; Humans; Liver Cirrhosis; Malabsorption Syndromes	1969
Renal and intestinal hexose transport in familial glucose-galactose malabsorption. The Journal of clinical investigation, 1970, Volume: 49, Issue:3 Topics: Adolescent; Adult; Biological Transport; Biopsy; Carbon Isotopes; Child; Child, Preschool; Cyanides; Dinitrophenols; Female; Fructose; Galactose; Genes, Recessive; Glucose; Glycosuria; Heterozygote; Hexoses; Humans; Infant; Intestinal Mucosa; Jejunum; Kidney; Malabsorption Syndromes; Male; Ouabain; Pedigree; Temperature	1970
Glucose-galactose malabsorption. Studies on renal glucosuria. Helvetica paediatrica acta, 1970, Volume: 25, Issue:1 Topics: Absorption; Adult; Child; Child, Preschool; Diuresis; Female; Galactose; Glucose; Glycosuria; Humans; Infant; Inulin; Kidney Tubules; Malabsorption Syndromes; Male	1970
Diagnostic problems in glucose-galactose malabsorption. A case report. Acta paediatrica Scandinavica, 1970, Volume: 59, Issue:2 Topics: Blood Glucose; Body Weight; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Diarrhea; Diet Therapy; Dietary Carbohydrates; Female; Fructose; Galactose; Glucose; Glucose Tolerance Test; Growth; Humans; Infant; Infant, Newborn; Malabsorption Syndromes	1970
Inhibition of amino-acid absorption by monosaccharides in man. East African medical journal, 1970, Volume: 47, Issue:12 Topics: Galactose; Glucose; Glycine; Humans; Intestinal Absorption; Jejunum; Malabsorption Syndromes; Monosaccharides	1970
[Glucose-galactose malabsorption]. Padiatrie und Grenzgebiete, 1970, Volume: 9, Issue:4 Topics: Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diet Therapy; Galactose; Glucose; Humans; Malabsorption Syndromes	1970
Glucose reabsorption in familial renal glycosuria and glucose-galactose malabsorption. Birth defects original article series, 1970, Volume: 6, Issue:3 Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Female; Galactose; Genes, Recessive; Glucose; Glycosuria, Renal; Humans; Jejunum; Kidney; Kidney Concentrating Ability; Kidney Tubules; Malabsorption Syndromes; Male	1970
Reducing substances in neonatal stools detected by Clinitest. Pediatrics, 1970, Volume: 46, Issue:4 Topics: Animals; Carbohydrate Metabolism; Feces; Galactose; Glucose; Humans; Hydrogen-Ion Concentration; Indicators and Reagents; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Lactose; Malabsorption Syndromes; Milk; Milk, Human; Oligosaccharides	1970
Acquired and congenital disorders of intestinal transport of D. glucose in children. Revue europeenne d'etudes cliniques et biologiques. European journal of clinical and biological research, 1971, Volume: 16, Issue:4 Topics: Alanine; Biological Transport; Biopsy; Celiac Disease; Child, Preschool; Female; Galactose; Glucose; Humans; Infant; Intestinal Mucosa; Malabsorption Syndromes; Male	1971
[Enzymopathies in childhood]. Wiener klinische Wochenschrift, 1971, Apr-30, Volume: 83, Issue:17 Topics: Adolescent; Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Galactose; Glucose; Homozygote; Humans; Hypophosphatasia; Infant; Malabsorption Syndromes; Metabolism, Inborn Errors; Rickets; Vitamin D Deficiency	1971
[Diagnosis of mono-and disaccharide malabsorption. Planimetric evaluation of blood glucose curves]. Das Deutsche Gesundheitswesen, 1971, May-06, Volume: 26, Issue:19 Topics: Blood Glucose; Child; Child, Preschool; Cystic Fibrosis; Diarrhea; Disaccharides; Dyspepsia; Galactose; Glucose Tolerance Test; Humans; Infant; Lactose; Lactose Intolerance; Malabsorption Syndromes; Monosaccharides	1971
Glucose-galactose malabsorption in an Oriental-Iraqui Jewish family. The Journal of pediatrics, 1971, Volume: 78, Issue:5 Topics: Adult; Consanguinity; Dehydration; Female; Follow-Up Studies; Fructose; Galactose; Genes, Recessive; Glucose; Glucose Tolerance Test; Humans; Hypernatremia; Infant; Infant, Newborn; Iraq; Jews; Lactose; Malabsorption Syndromes; Male; Pedigree; Sucrose	1971
[Galactose malabsorption in adulthood]. Klinische Wochenschrift, 1967, Jun-01, Volume: 45, Issue:11 Topics: Adult; Galactose; Galactosemias; Humans; Lactose; Malabsorption Syndromes; Male; Middle Aged	1967
[Absorption studies in hereditary mono- and disaccharide malabsorptions]. Nuclear-Medizin, 1967 Topics: Carbon Isotopes; Child; Disaccharides; Female; Fructose; Galactose; Glucose; Glucose Tolerance Test; Humans; Infant; Intestinal Absorption; Malabsorption Syndromes; Maltose; Monosaccharides	1967
[Malabsorption of lactose and galactose in the adult]. Die Medizinische Welt, 1967, Jun-03, Volume: 22 Topics: Adult; Carbon Isotopes; Female; Fractures, Spontaneous; Galactose; Glucose Tolerance Test; Humans; Hypocalcemia; Intestinal Absorption; Lactose; Malabsorption Syndromes	1967
Digestion and absorption after massive resection of the small intestine. II. Recovery of the absorptive function as shown by intestinal absorption tests in two patients and a consideration of compensatory mechanisms. Gastroenterology, 1968, Volume: 54, Issue:4 Topics: Animals; Celiac Disease; Crohn Disease; Galactose; Glucose; Humans; Hypocalcemia; Intestinal Absorption; Intestine, Small; Malabsorption Syndromes; Methionine; Neomycin; Osteomalacia; Postgastrectomy Syndromes; Rats; Vitamin A	1968
[Carbohydrate composition of plant nutrients as the basis for the diet therapy of hereditary metabolic disorders]. Klinische Wochenschrift, 1968, May-01, Volume: 46, Issue:9 Topics: Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Chromatography, Paper; Diet Therapy; Food Analysis; Fruit; Galactose; Galactosemias; Humans; Lactose Intolerance; Malabsorption Syndromes; Plants, Edible; Sucrose; Vegetables	1968
Glucose-galactose malabsorption. A study with biopsy of the small intestinal mucosa. Acta paediatrica Scandinavica, 1968, Volume: 57, Issue:4 Topics: Adolescent; Adult; Alanine; Biological Transport; Biopsy; Carbohydrate Metabolism, Inborn Errors; Carbon Isotopes; Child; Child, Preschool; Culture Techniques; Female; Galactose; Glucose; Humans; Infant; Intestinal Absorption; Intestinal Mucosa; Intestine, Small; Malabsorption Syndromes; Mannitol; Ouabain; Phlorhizin; Sodium	1968
Temporary monosaccharide intolerance. Acta paediatrica Scandinavica, 1968, Volume: 57, Issue:6 Topics: Diet Therapy; Fructose; Galactose; Glucose; Humans; Infant; Malabsorption Syndromes; Male; Pneumonia; Staphylococcal Infections	1968
Familial monosaccharide malabsorption. Bibliotheca paediatrica, 1968, Volume: 87 Topics: Child, Preschool; Diarrhea, Infantile; Diet Therapy; Dietary Fats; Female; Fructose; Galactose; Glucose; Humans; Infant; Infant, Newborn; Intestinal Absorption; Malabsorption Syndromes; Male; Xylose	1968
Defects of sugar absorption. Sugar malabsorption and sugar intolerance in childhood. Proceedings of the Royal Society of Medicine, 1968, Volume: 61, Issue:11 Part 1 Topics: Blood Glucose; Child; Deficiency Diseases; Diarrhea; Female; Galactose; Glucose; Humans; Infant; Intestinal Mucosa; Lactose Intolerance; Malabsorption Syndromes; Male; Sucrase; Vomiting	1968
[Malabsorption in hereditary disorders of the carbohydrate and amino acid metabolism]. Acta paediatrica Academiae Scientiarum Hungaricae, 1969, Volume: 10, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Galactose; Glucose; Hartnup Disease; Humans; Malabsorption Syndromes; Phenylketonurias; Rats	1969
Glucose-galactose malabsorption complicated by monilial arthritis. Pediatrics, 1969, Volume: 43, Issue:1 Topics: Amphotericin B; Arthritis, Infectious; Candidiasis; Dehydration; Diarrhea; Diet Therapy; Fructose; Galactose; Glucose; Humans; Infant; Malabsorption Syndromes; Mitosporic Fungi	1969
Glucose-galactose malabsorption. Report of a case with autoradiographic studies of a mucosal biopsy. The New England journal of medicine, 1966, Feb-10, Volume: 274, Issue:6 Topics: Autoradiography; Biopsy; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Diet Therapy; Dietary Carbohydrates; Duodenum; Female; Galactose; Glucose; Humans; Infant, Newborn; Intestinal Mucosa; Malabsorption Syndromes; Mucous Membrane	1966
Diets in disaccharidase deficiency and defective monosaccharide absorption. Journal of the American Dietetic Association, 1966, Volume: 48, Issue:4 Topics: Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Dietary Carbohydrates; Disaccharides; Galactose; Glucose; Glycoside Hydrolases; Humans; Lactose; Malabsorption Syndromes; Monosaccharides	1966
Glucose-galactose malabsorption. The New England journal of medicine, 1966, Feb-10, Volume: 274, Issue:6 Topics: Animals; Carbohydrate Metabolism, Inborn Errors; Food Hypersensitivity; Galactose; Glucose; Humans; Infant, Newborn; Lactose; Malabsorption Syndromes; Milk; Renal Tubular Transport, Inborn Errors	1966
[On the residual activity of defective enzymes in hereditary monosaccharide and disaccharide malabsorption]. Schweizerische medizinische Wochenschrift, 1966, Apr-02, Volume: 96, Issue:13 Topics: Carbon Isotopes; Child; Galactose; Glucose; Glucose Tolerance Test; Humans; Infant; Malabsorption Syndromes; Maltose; Molecular Biology; Sucrose	1966
Glucagon-like peptide-2 protects against TPN-induced intestinal hexose malabsorption in enterally refed piglets. American journal of physiology. Gastrointestinal and liver physiology, 2006, Volume: 290, Issue:2 Topics: Algorithms; Animals; Animals, Newborn; Carbon Dioxide; DNA; Glucagon-Like Peptide 2; Glucagon-Like Peptides; Glucose; Glucose Transporter Type 2; Hexoses; Ileum; Infusions, Intravenous; Jejunum; Kinetics; Lactase; Malabsorption Syndromes; Oxygen Consumption; Parenteral Nutrition, Total; Sodium-Glucose Transporter 1; Swine; Tissue Distribution	2006
Letter: Intestinal potential difference during glucose absorption. Lancet (London, England), 1974, Oct-26, Volume: 2, Issue:7887 Topics: Action Potentials; Biological Transport, Active; Glucose; Hexoses; Humans; Intestinal Absorption; Intestine, Small; Jejunum; Malabsorption Syndromes	1974
Alpha-chain disease: a new immunoglobulin abnormality. Science (New York, N.Y.), 1968, Dec-20, Volume: 162, Issue:3860 Topics: Arabia; Blood Protein Disorders; Chromatography, Gel; Female; Fucose; gamma-Globulins; Glycoproteins; Heavy Chain Disease; Hexoses; Humans; Immunodiffusion; Immunoelectrophoresis; Lymphatic Diseases; Lymphoma; Malabsorption Syndromes; Multiple Myeloma; Neoplasm Proteins; Neuraminic Acids; Plasma Cells; Ultracentrifugation; White People	1968
Immunochemical studies in four cases of alpha chain disease. The Journal of clinical investigation, 1969, Volume: 48, Issue:12 Topics: Blood Protein Disorders; Blood Protein Electrophoresis; Chromatography, Gel; Fluorescent Antibody Technique; Fucose; Hexosamines; Hexoses; Humans; Immunochemistry; Immunodiffusion; Immunoelectrophoresis; Intestinal Neoplasms; Intestine, Small; Jejunum; Lymphoma; Malabsorption Syndromes; Neuraminic Acids; Proteinuria; Racial Groups; Saliva	1969
Alpha chain disease. Annals of the New York Academy of Sciences, 1971, Dec-31, Volume: 190 Topics: Africa, Northern; Amino Acid Sequence; Asia, Eastern; Europe; Fucose; Heavy Chain Disease; Hexosamines; Hexoses; Humans; Immunodiffusion; Immunoelectrophoresis; Immunoglobulin A; Iran; Israel; Lymphatic Diseases; Lymphoma; Malabsorption Syndromes; Molecular Weight; Neuraminic Acids; Peptides; South America; Syria	1971