galactose has been researched along with Infant, Newborn, Diseases in 66 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 62 (93.94) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (3.03) | 29.6817 |
2010's | 2 (3.03) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Balogh, L; Kiss, E; Reismann, P | 1 |
Alonso-Fernandez, JR; Baleato, J; Carpinteiro, MI; Fidalgo, J | 1 |
CROOKS, R; EDMONDS, AM; HENNIGAR, GR | 1 |
ALLORE, S | 1 |
McAULEY, FD | 1 |
HUDSON, FP; IRELAND, JT; OCKENDEN, BG; WHITE-JONES, RH | 1 |
FOX, EG; FYFE, WM; MOLLISON, AW | 1 |
HOLZEL, A | 1 |
LOCKHART, JD; ROBOZ, E | 1 |
COX, PJ | 1 |
ARTHURTON, MW; MEADE, BW | 1 |
SMITH, FM | 1 |
BERGER, H; FLURY, M | 1 |
CLEMENT, R; COMBES-HAMELLE, A; SAADA, B | 1 |
RODIER, P | 1 |
DALAUT, JC; GILLOT, F; SCHAEFER, JC | 1 |
HOLZEL, A; KOMROWER, GM; SCHWARZ, V | 1 |
JACOBSON, FM | 1 |
MILLIS, SC | 1 |
YBEMA, HJ | 1 |
COTTE, J; LARBRE, F; MONNET, P; TISSOT, A | 1 |
CARRON, R; COTTE, J; DUC, H; JEUNE, M | 1 |
BAGOT, T; CALDERA, R; PRINGUET, G; ROSSIER, A | 1 |
MELIS, R; ROVINSKI, J | 1 |
BERNHEIM, M; FOURNIER, P; FRANCOIS, R; GILLY, R; JOSSERAND, P | 1 |
ADAM, H; FRIEDRICH, E; ROUPERT, G | 1 |
BERRY, HK; GUEST, GM; RUBINSTEIN, J | 1 |
FULD, J; LONDON, M; MARYMONT, JH | 1 |
NATZSCHKA, J; WERNER, E | 1 |
HERVEI, S; KISS, S; SCHULER, D | 1 |
HAAS, L; NEWMAN, C | 1 |
JONES, NL; LEAK, D | 1 |
MOULEDOUS, P | 1 |
MULLIGAN, PB; SCHWARTZ, R | 1 |
Martín, MG; Turk, E; Wright, EM | 1 |
DE HAAS, PK | 1 |
Packman, S; Zlatunich, CO | 1 |
Freese, D | 1 |
Handrick, W; Rieske, K; Scheerschmidt, G; Spencker, FB | 1 |
Kaloud, H; Sitzmann, FC | 1 |
Enzenauer, J; Matz, D; Menne, F | 1 |
Gitzelmann, R | 2 |
Brivet, M; Lemonnier, A; Moatti, N | 1 |
Hammersen, G; Levy, HL | 1 |
Ament, ME | 1 |
Murphy, D; Pennock, CA | 1 |
Sadjimin, T; Surjono, A | 1 |
Woolf, LI | 1 |
Beutler, E; Efron, ML; Houghton, S; Isselbacher, KJ; Karolkewicz, V; Levy, HI; MacCready, RA; Shih, VE | 1 |
Linneweh, F | 1 |
Iseki, S | 1 |
Scheibenreiter, S; Thalhammer, O | 1 |
Beneke, G; Schrader, KE | 1 |
Abraham, JM; Burgess, EA; Levin, B; Wallis, PG | 1 |
Johansson, S; Thalme, B; Werner, B | 1 |
Linneweh, F; Schaumlöffel, E; Vetrella, M | 1 |
Thalhammer, O | 1 |
Davidson, AG; Mullinger, M | 1 |
Coodin, FJ; Haworth, JC | 1 |
Tengström, B; Wranne, L | 1 |
Dahlqvist, A; Svenningsen, NW | 1 |
Chandra, RK; Ghai, OP; Pawa, RR | 1 |
Fordtran, JS; Marks, JF; Norton, JB | 1 |
Eto, Y; Maekawa, K; Mori, T; Ohta, H | 1 |
Girard, J; Herz, G | 1 |
7 review(s) available for galactose and Infant, Newborn, Diseases
Article | Year |
---|---|
[Diet treatment of classical galactosemia].
Topics: Diet, Healthy; Female; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male | 2017 |
Intestinal absorption in health and disease--sugars.
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 |
Intracellular cholestatic syndromes of infancy.
Topics: Bacterial Infections; Bile Acids and Salts; Biopsy, Needle; Cholestasis, Intrahepatic; Fructose; Galactose; Glycogen Storage Disease; Hepatitis; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Liver; Metabolism, Inborn Errors; Prognosis; Syndrome; Tyrosine | 1982 |
[Congenital disorders of galactose metabolism].
Topics: Austria; Black or African American; Black People; Carbohydrate Epimerases; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Galactose; Galactosemias; Genetic Counseling; Germany, West; Heterozygote; Homozygote; Humans; Hungary; Infant; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Nucleotidyltransferases; Phosphotransferases; Pregnancy; Prenatal Diagnosis; Prognosis | 1975 |
[Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].
Topics: Biological Assay; Carbohydrate Epimerases; Carbohydrate Metabolism, Inborn Errors; Chromatography, Paper; Erythrocytes; Escherichia coli; Female; Galactokinase; Galactose; Galactosemias; Heterozygote; Homozygote; Humans; Infant, Newborn; Infant, Newborn, Diseases; Nucleotidyltransferases; Pregnancy; Prenatal Diagnosis; UDPglucose 4-Epimerase; UDPglucose-Hexose-1-Phosphate Uridylyltransferase | 1979 |
Malabsorption syndromes in infancy and childhood. I.
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 |
Recent studies on galactosaemia, phenylketonuria and homocystinuria.
Topics: Adult; Brain Chemistry; Child; Female; Galactose; Galactosemias; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Phenylketonurias; Phosphotransferases | 1968 |
59 other study(ies) available for galactose and Infant, Newborn, Diseases
Article | Year |
---|---|
Vertical sandwich-type continuous/evaporative TLC with fixed mobile phase volume for separating sugars of clinical relevance in paper-borne urine and blood samples in newborn screening.
Topics: Carbohydrates; Chromatography, Thin Layer; Diabetes Mellitus; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Neonatal Screening; Paper | 2010 |
Galactosemia; report of case with autopsy.
Topics: Autopsy; Child; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Pediatrics | 1952 |
Galactosemia.
Topics: Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Metabolic Diseases | 1953 |
Cataracts in galactosaemia.
Topics: Cataract; Child; Galactose; Galactosemias; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases | 1953 |
Diagnosis and treatment of galactosaemia.
Topics: Galactose; Galactosemias; Humans; Infant; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases | 1954 |
Galactose diabetes.
Topics: Diabetes Mellitus; Galactose; Humans; Infant; Infant Nutritional Physiological Phenomena; Infant, Newborn; Infant, Newborn, Diseases; Liver Cirrhosis | 1954 |
Galactosaemia.
Topics: Blood; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1954 |
Case of galactosemia identified in a four day old infant by paper chromatographic technic.
Topics: Chromatography; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Metabolic Diseases | 1954 |
Galactosaemia.
Topics: Blood; Child; Galactose; Galactosemias; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Jaundice; Liver Diseases | 1954 |
Congenital galactosaemia; report of a case.
Topics: Blood; Erythroblastosis, Fetal; Fetus; Galactose; Galactosemias; Hematologic Diseases; Humans; Infant, Newborn; Infant, Newborn, Diseases; Kidney Diseases | 1954 |
Galactosemia in an eight day old infant.
Topics: Blood; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1955 |
The galactosemia.
Topics: Blood; Galactose; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1955 |
[Galactosic diabetes].
Topics: Child; Diabetes Mellitus; Galactose; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases | 1956 |
[A case of galactosemia in a two-month-old infant].
Topics: Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1957 |
[First case of congenital galactosemia in Algeria].
Topics: Algeria; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1957 |
Laboratory diagnosis of congenital galactosaemia at birth.
Topics: Clinical Laboratory Techniques; Female; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Parturition | 1958 |
Galactosemia: a case report.
Topics: Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1958 |
Jaundice associated with galactosemia in the newborn.
Topics: Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Jaundice | 1958 |
[Laboratory diagnosis of congenital galactosemia in newborn].
Topics: Clinical Laboratory Techniques; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1959 |
[Galactosemia; death despite supression of dietary galactose].
Topics: Death; Diet; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1959 |
[Galactosemia; survival].
Topics: Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1959 |
[Galactosemia in infants; a further case].
Topics: Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1959 |
[Anasarca of fatal course in a newborn infant. Possible role of a congenital galactosemia].
Topics: Edema; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1961 |
[Galactosemia-servere neonatal form. Favorable result of a new dietetic product].
Topics: Dietetics; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1959 |
[Galactosemia: early detection of a case].
Topics: Early Diagnosis; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1961 |
Newborn siblings in families known to have hereditary disorders. Diagnostic procedures.
Topics: Galactose; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Metabolic Diseases; Phenylketonurias; Siblings | 1962 |
A MICRODIFFUSION TEST FOR CONGENITAL GALACTOSEMIA UTILIZING GALACTOSE-1-C14.
Topics: Blood Chemical Analysis; Carbon Isotopes; Galactose; Galactosemias; Genetics, Medical; Glucose Oxidase; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases | 1964 |
[GALACTOSE INTOLERANCE IN A NEWBORN].
Topics: Diagnosis; Diet; Diet Therapy; Galactose; Galactosemias; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Jaundice; Jaundice, Neonatal | 1964 |
[INVESTIGATIONS IN GALACTOSAEMIA CASES].
Topics: Chromosomes; Clinical Enzyme Tests; Galactose; Galactosemias; Glucose Tolerance Test; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Liver Function Tests | 1964 |
Galactosaemia presenting with gangrene of the right foot.
Topics: Blood; Foot; Foot Diseases; Galactose; Galactosemias; Gangrene; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Ischemia | 1955 |
The treatment of congenital galactosaemia.
Topics: Diet; Diet Therapy; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1959 |
[Galactosemia in infants. Apropos of a new familial case].
Topics: Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1962 |
Hepatic carbohydrate metabolism in the genesis of neonatal hypoglycemia. Effects of the administration of epinephrine, glucagon, and galactose.
Topics: Carbohydrate Metabolism; Child; Epinephrine; Galactose; Glucagon; Humans; Hypoglycemia; Infant; Infant, Newborn; Infant, Newborn, Diseases; Liver | 1962 |
[Familial fatty degeneration of the liver associated with galactosemia].
Topics: Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Liver Diseases | 1951 |
Galactosaemia: early treatment with an elemental formula.
Topics: Erythrocytes; Female; Food, Formulated; Galactose; Galactosemias; Galactosephosphates; Humans; Infant Formula; Infant, Newborn; Infant, Newborn, Diseases | 2005 |
[Sepsis due to E. coli in newborns with galactose intolerance (author's transl)].
Topics: Anti-Bacterial Agents; Carbohydrate Metabolism, Inborn Errors; Escherichia coli Infections; Galactose; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male | 1981 |
[Diagnosis and therapy of 6 hereditary, to mental-deficiency-leading, metabolic disorders. 2].
Topics: Acute Disease; Diagnosis, Differential; Galactose; Galactosemias; Germany, West; Histidine; Homocystine; Homocystinuria; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Mass Screening; Metabolism, Inborn Errors; Methionine; Phosphotransferases | 1976 |
[Screening of newborns for inborn errors of galactose metabolism. Methods and results].
Topics: Biological Assay; Clinical Enzyme Tests; Erythrocytes; Escherichia coli; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening; Nucleotidyltransferases; Phosphotransferases; Switzerland; UTP-Hexose-1-Phosphate Uridylyltransferase | 1976 |
Newborn screening for galactosemia and other galactose metabolic defects.
Topics: Carbohydrate Metabolism, Inborn Errors; Costs and Cost Analysis; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Screening | 1978 |
Deficiency of uridine diphosphate galactose 4-epimerase in blood cells of an apparently healthy infant. Preliminary communication.
Topics: Carbohydrate Epimerases; Erythrocytes; Female; Galactose; Glucose; Humans; Infant, Newborn; Infant, Newborn, Diseases; Metabolism, Inborn Errors; Uridine Diphosphate Sugars | 1972 |
Gas chromatographic measurement of blood and urine glucose and other monosaccharides.
Topics: Blood Glucose; Chromatography, Gas; Fructose; Galactose; Glucose; Glucose Oxidase; Glycosuria; Humans; Hydroxylamines; Hypoglycemia; Infant, Newborn; Infant, Newborn, Diseases; Methods | 1972 |
Lactose tolerance test on Indonesian newborn infants.
Topics: Galactose; Glucose Tolerance Test; Humans; Indonesia; Infant, Newborn; Infant, Newborn, Diseases; Lactose Intolerance; Lactose Tolerance Test; Sucrose | 1973 |
Galactosemia screening of newborns in Massachusetts.
Topics: Biological Assay; Clinical Enzyme Tests; Erythrocytes; Escherichia coli Infections; Female; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Mass Screening; Massachusetts; Methods; Nucleotidyltransferases | 1971 |
[Isotope use in the study of hereditary metabolic diseases].
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 |
[Blood group substances studied from the aspect of the immune phenomenon].
Topics: ABO Blood-Group System; Antigens; Blood Chemical Analysis; Blood Group Antigens; Erythroblastosis, Fetal; Female; Fucose; Galactose; Humans; Infant, Newborn; Infant, Newborn, Diseases; Lewis Blood Group Antigens; Pregnancy; Rh-Hr Blood-Group System | 1968 |
[Galactosemia, generally with a fulminating course. 10 cases found through an early detection program].
Topics: Austria; Blood Transfusion; Deficiency Diseases; Diagnosis, Differential; Diet Therapy; Dietary Carbohydrates; Female; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Nucleotidyltransferases; Time Factors | 1972 |
[Morphological and histochemical studies of the galactose cataract of the albino rat].
Topics: Animals; Carbohydrate Metabolism, Inborn Errors; Cataract; Galactose; Humans; Infant, Newborn; Infant, Newborn, Diseases; Microscopy; Oxidoreductases; Proteins; Rats | 1965 |
Congenital lactose malabsorption.
Topics: Blood Glucose; Duodenum; Female; Galactose; Glucose; Humans; Infant, Newborn; Infant, Newborn, Diseases; Intestinal Mucosa; Lactose Intolerance; Male | 1970 |
[Galactosemia urine--screening with test paper].
Topics: False Positive Reactions; Female; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Male; Methods; Time Factors | 1970 |
[Galactokinase defect in a newborn infant].
Topics: Carbon Isotopes; Cataract; Chromatography, Paper; Chromatography, Thin Layer; Diet Therapy; Erythrocytes; Ethnicity; Female; Galactose; Glucokinase; Humans; Infant, Newborn; Infant, Newborn, Diseases; Metabolism, Inborn Errors; Oxidation-Reduction; RNA Nucleotidyltransferases | 1970 |
[Secondary results of a Guthrie test programm. Galactose blood level in children of various ages following approximate physiologic galactose administrations].
Topics: Adolescent; Adult; Age Factors; Body Weight; Child; Child, Preschool; Galactose; Galactosemias; Glucokinase; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Male; Transferases | 1970 |
Reducing substances in neonatal stools detected by Clinitest.
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 |
Liver failure in galactosemia successfully treated by exchange blood transfusion.
Topics: Ascites; Cholestasis; Edema; Exchange Transfusion, Whole Blood; Galactose; Galactosemias; Hepatomegaly; Humans; Infant, Newborn; Infant, Newborn, Diseases; Liver; Liver Diseases; Male | 1971 |
Sugars in blood and urine of milk-fed normal young infants.
Topics: Blood Glucose; Female; Galactose; Galactosemias; Glycosuria; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lactose; Male; Mass Screening; Milk, Human | 1968 |
Galactose in the urine of newborn infants.
Topics: Alcohol Oxidoreductases; Female; Galactose; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Infant, Premature; Jaundice, Neonatal; Male; Methods; Urine | 1969 |
Disaccharide intolerance in the aetiology of chronic and-or recurrent diarrhoea in young children.
Topics: Carbohydrate Metabolism, Inborn Errors; Celiac Disease; Child, Preschool; Chronic Disease; Diarrhea, Infantile; Disaccharides; Feces; Female; Galactose; Glucose; Glucose Tolerance Test; Humans; Hydrogen-Ion Concentration; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lactose Intolerance; Male; Maltose; Sucrose; Xylose | 1969 |
Glucose-galactose malabsorption.
Topics: Carbohydrate Metabolism, Inborn Errors; Dehydration; Diarrhea; Female; Fructose; Galactose; Glucose; Glucose Tolerance Test; Humans; Infant, Newborn; Infant, Newborn, Diseases | 1966 |
Neonatal I-cell disease: clinical and biochemical observations.
Topics: Brain; Female; Hexosamines; Hexoses; Humans; Hydrolases; Infant, Newborn; Infant, Newborn, Diseases; Kidney; Liver; Mucolipidoses; Sialic Acids | 1981 |
Some aspects of hypoglycemia in pediatrics.
Topics: Acids; Age Factors; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Glutamine; Glycogen Storage Disease; Hexoses; Humans; Hypoglycemia; Infant, Newborn; Infant, Newborn, Diseases; Injections, Intravenous; Insulin; Mannose | 1972 |