acebutolol and Malabsorption Syndromes

acebutolol has been researched along with Malabsorption Syndromes in 24 studies

Research

Studies (24)

Timeframe	Studies, this research(%)	All Research%
pre-1990	22 (91.67)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (4.17)	24.3611
2020's	1 (4.17)	2.80

Authors

Authors	Studies
Ganz, T; Goodnough, LT; Kalantar-Zadeh, K; Levine, MA; Seid, MH; Trumbo, H	1
Barish, C; Bregman, D; He, A; Malone, M	1
HOLMAN, GH; LIFSHITZ, F	1
AURICCHIO, S; PRADER, A; SEMENZA, G	1
MONCRIEFF, AA	1
AMMANN, R; AURICCHIO, S; HAEMMERLI, UP; KISTLER, H; MARTHALER, T; PRADER, A; SEMENZA, G	1
AURICCHIO, S; DAVIDSON, M; FREZAL, J; JOS, J; PRADER, A; REY, J; RUBINO, A	1
AURICCHIO, S; HADORN, B; PRADER, A; RUBINO, A; SHMERLING, DH	1
Dyduch, A; Karczewska, K	1
Clark, ML; Dawson, AM; Fairclough, PD; Harries, JT; Milla, PJ; Silk, DB	1
Gudmand-Hoyer, E; Krasilnikoff, PA	1
Brügmann, G; Niessen, KH; Schmidt, K	1
Kleinbaum, H	1
Harms, K; Lentze, M; Schaub, J	1
Desjeux, JF; Lestradet, H; Sarrut, S; Sassier, P; Tichet, J	1
Frézal, JF; Lamy, M; Rey, J	1
Bergoz, R	1
Beyreiss, K; Theile, H; Winkler, U	1
Visakorpi, JK	1
Lugo-de-Rivera, C; Rodriguez-de-Curet, H; Torres-Pinedo, R	1
Bergoz, R; Righetti, A	1
Graul, EH; Linneweh, F; Schaumlöffel, E	1
Auricchio, S; Prader, A; Rubino, A; Semenza, G; Welsh, JD	1
Bode, HH; Graul, EH; Linneweh, F; Schaumlöffel, E	1

Reviews

3 review(s) available for acebutolol and Malabsorption Syndromes

Article	Year
Parenteral iron therapy and phosphorus homeostasis: A review. American journal of hematology, 2021, 05-01, Volume: 96, Issue:5 Topics: Anemia, Hypochromic; Calcitriol; Ferric Compounds; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Homeostasis; Humans; Hypophosphatemia; Infusions, Parenteral; Iron; Iron Deficiencies; Kidney; Malabsorption Syndromes; Maltose; Osteomalacia; Parathyroid Hormone; Phosphorus; Phosphorus, Dietary	2021
[Processes of digestion of saccharose, maltose and isomaltose and their disorders in children]. Pediatria polska, 1980, Volume: 55, Issue:9 Topics: Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Digestion; Disaccharides; Humans; Infant; Intestinal Absorption; Isomaltose; Malabsorption Syndromes; Maltose; Models, Biological; Sucrose	1980
Disaccharide malabsorption. Bibliotheca paediatrica, 1968, Volume: 87 Topics: Diarrhea, Infantile; Diet Therapy; Humans; Infant; Intestinal Mucosa; Lactose Intolerance; Malabsorption Syndromes; Maltose; Sucrose	1968

Other Studies

21 other study(ies) available for acebutolol and Malabsorption Syndromes

Article	Year
Comparative review of the safety and efficacy of ferric carboxymaltose versus standard medical care for the treatment of iron deficiency anemia in bariatric and gastric surgery patients. Obesity surgery, 2013, Volume: 23, Issue:9 Topics: Adult; Anemia, Iron-Deficiency; Bariatric Surgery; Biomarkers; Dietary Supplements; Dose-Response Relationship, Drug; Female; Ferric Compounds; Ferritins; Hematinics; Hemoglobins; Humans; Infusions, Intravenous; Iron, Dietary; Malabsorption Syndromes; Male; Maltose; Middle Aged; Obesity, Morbid; Parenteral Nutrition; Postoperative Complications; Randomized Controlled Trials as Topic; Retrospective Studies; Transferrin; Treatment Outcome; United States	2013
DISACCHARIDASE DEFICIENCIES WITH STEATORRHEA. The Journal of pediatrics, 1964, Volume: 64 Topics: Celiac Disease; Chromatography; Deficiency Diseases; Disaccharidases; Genetics, Medical; Glucose; Glycoside Hydrolases; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lactose; Malabsorption Syndromes; Maltose; Metabolism; Metabolism, Inborn Errors; Steatorrhea; Sucrose	1964
[HEREDITARY SACCHAROSE AND ISOMALTOSE MALABSORPTION]. Monatsschrift fur Kinderheilkunde, 1964, Volume: 112 Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Disaccharides; Genetics, Medical; Humans; Isomaltose; Malabsorption Syndromes; Maltose; Sucrose	1964
SUCROSE AND ISOMALTOSE INTOLERANCE IN SIBLINGS. Proceedings of the Royal Society of Medicine, 1964, Volume: 57 Topics: Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Child; Chromatography; Diagnosis; Diarrhea; Diarrhea, Infantile; Feces; Genetics, Medical; Humans; Isomaltose; Lactose; Malabsorption Syndromes; Maltose; Siblings; Starch; Sucrose	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
INTESTINAL GLYCOSIDASE ACTIVITIES IN CONGENITAL MALABSORPTION OF DISACCHARIDES. The Journal of pediatrics, 1965, Volume: 66 Topics: Alcohol Oxidoreductases; Biopsy; Carbohydrate Metabolism; Carbohydrate Metabolism, Inborn Errors; Child; Disaccharides; Glycoside Hydrolases; Histocytochemistry; Histological Techniques; Humans; Infant; Intestinal Absorption; Intestine, Small; Intestines; Lactose; Malabsorption Syndromes; Maltose; Sucrase; Sucrose	1965
[SECONDARY DEFICIENCY INTESTINAL DISACCHARIDASE IN CELIAC DISEASE. QUANTITATIVE DETERMINATION OF THE ENZYMATIC ACTIVITY AND CLINICAL DIAGNOSIS]. Helvetica paediatrica acta, 1964, Volume: 19 Topics: Biopsy; Celiac Disease; Child; Clinical Enzyme Tests; Duodenum; Glucosyltransferases; Humans; Jejunum; Lactose; Malabsorption Syndromes; Maltose; Sucrase	1964
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
[Hereditary sucrose-isomaltose malabsorption]. Ugeskrift for laeger, 1975, Jun-23, Volume: 137, Issue:26 Topics: Humans; Isoenzymes; Malabsorption Syndromes; Maltose; Sucrose	1975
[Hereditary deficiency of isomaltase and saccharase responsible for a malabsorption syndrone (author's transl)]. Klinische Padiatrie, 1975, Volume: 187, Issue:2 Topics: Adolescent; Blood Glucose; Chromosome Aberrations; Chromosome Disorders; Deficiency Diseases; Diarrhea, Infantile; Disaccharides; Duodenum; Dwarfism; Female; Glucosidases; Humans; Infant; Intestinal Mucosa; Lactose Intolerance; Malabsorption Syndromes; Male; Maltose; Sucrase; Sucrose; Trehalase; Xylose	1975
[Malabsorption syndrome caused by a transitory disorder of isomaltose hydrolysis in atrophic infants]. Acta paediatrica Academiae Scientiarum Hungaricae, 1969, Volume: 10, Issue:1 Topics: Adenoviridae Infections; Amylases; Blood Glucose; Feces; Glucose Tolerance Test; Humans; Hydrogen-Ion Concentration; Infant; Influenza, Human; Malabsorption Syndromes; Maltose	1969
A simple and rapid thin-layer chromatographic method for the assay of intestinal disaccharidases. Clinica chimica acta; international journal of clinical chemistry, 1971, Volume: 33, Issue:2 Topics: Adolescent; Celiac Disease; Child; Child, Preschool; Chromatography, Thin Layer; Disaccharides; Female; Glucose-6-Phosphatase; Glycoside Hydrolases; Hexokinase; Humans; Infant; Intestinal Mucosa; Lactose; Malabsorption Syndromes; Male; Maltose; Methods; Sucrase; Sucrose	1971
Sugar absorption by flat jejunal mucosa. Acta paediatrica Scandinavica, 1973, Volume: 62, Issue:5 Topics: Adolescent; Biopsy; Child; Child, Preschool; Disaccharidases; Disaccharides; Female; Galactosidases; Glucose; Glucosidases; Humans; Infant; Intestinal Absorption; Intestinal Mucosa; Jejunum; Malabsorption Syndromes; Male; Maltose; Sucrase	1973
Trehalose malabsorption causing intolerance to mushrooms. Report of a probable case. Gastroenterology, 1971, Volume: 60, Issue:5 Topics: Adult; Aged; Basidiomycota; Carbohydrate Metabolism, Inborn Errors; Celiac Disease; Diabetes Mellitus; Disaccharides; Female; Food Hypersensitivity; Glucose; Glycoside Hydrolases; Humans; Malabsorption Syndromes; Male; Maltose; Middle Aged; Sucrose	1971
[Diagnosis of hereditary saccharose-isomaltose-malabsorption]. Kinderarztliche Praxis, 1971, Volume: 39, Issue:8 Topics: Blood Glucose; Carbazoles; Carbohydrate Metabolism, Inborn Errors; Celiac Disease; Child, Preschool; Female; Fructose; Glucose Tolerance Test; Humans; Infant; Malabsorption Syndromes; Male; Maltose; Sucrose	1971
[Intestinal disaccharide decomposition and its cogenital disturbances]. Monatsschrift fur Kinderheilkunde, 1969, Volume: 117, Issue:1 Topics: Carbohydrate Metabolism, Inborn Errors; Diagnosis, Differential; Disaccharides; Glycoside Hydrolases; Growth Disorders; Humans; Infant, Newborn; Lactose; Malabsorption Syndromes; Maltose	1969
Studies on infant diarrhea. IV. Sugar transit and absorp- tion in small intestine after a feeding. Gastroenterology, 1970, Volume: 59, Issue:3 Topics: Carbohydrate Metabolism; Diarrhea, Infantile; Dietary Carbohydrates; Fructose; Gastrointestinal Motility; Glucose; Humans; Infant; Infant, Newborn; Intestinal Absorption; Intubation, Gastrointestinal; Lactose; Malabsorption Syndromes; Maltose; Osmolar Concentration	1970
[Mushroom intolerance due to selective malabsorption of trehalose: a little known syndrome]. Schweizerische medizinische Wochenschrift, 1970, Jul-11, Volume: 100, Issue:28 Topics: Basidiomycota; Carbohydrate Metabolism, Inborn Errors; Disaccharides; Glucose; Glycoside Hydrolases; Glycosides; Humans; Intestinal Absorption; Malabsorption Syndromes; Maltose	1970
[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
Lack of some intestinal maltases in a human disease transmitted by a single genetic factor. Biochimica et biophysica acta, 1965, Aug-24, Volume: 105, Issue:2 Topics: Carbohydrate Metabolism; Chromatography, Gel; Glycoside Hydrolases; Humans; In Vitro Techniques; Intestinal Mucosa; Intestine, Small; Malabsorption Syndromes; Maltose; Sucrose	1965
[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