Compounds > leucine

leucine and Galactosemias

leucine has been researched along with Galactosemias in 12 studies

Research

Studies (12)

Timeframe	Studies, this research(%)	All Research%
pre-1990	10 (83.33)	18.7374
1990's	1 (8.33)	18.2507
2000's	1 (8.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Blatny, J; Chukwu, J; Crushell, E; Mayne, P; Treacy, EP	1
Paunier, L	1
Baptista, J; Brivet, M; Gautier, M; Kadhom, N; Wolfrom, C	1
Brown, E; Hughes, RC; Watts, RW	1
Barashnev, IuI; Vel'tishchev, IuE	1
Blum, KU	1
Royer, P	1
Thalhammer, O	1
Steuer, W	1
Raoul, Y	1
Albeaux-Fernet, M	1

Reviews

3 review(s) available for leucine and Galactosemias

Article	Year
[CONGENITAL DISORDERS OF CARBOHYDRATE METABOLISM]. Polskie Archiwum Medycyny Wewnetrznej, 1963, Volume: 33 Topics: Carbohydrate Metabolism; Diabetes Mellitus; Fructose; Galactosemias; Glucosephosphate Dehydrogenase Deficiency; Glucosephosphates; Glycogen Storage Disease; Humans; Hypoglycemia; Leucine; Metabolic Diseases; Pentoses; Urine	1963
[Early detection of hereditary anomalies of metabolism in children (screening programs)]. Voprosy okhrany materinstva i detstva, 1975, Volume: 20, Issue:8 Topics: Age Factors; Cysteine; Galactosemias; Glucosephosphate Dehydrogenase Deficiency; Glutamate Dehydrogenase; Histidine Ammonia-Lyase; Humans; Hyperlipidemias; Infant, Newborn; Leucine; Mass Screening; Metabolism, Inborn Errors; Oxalates; Phenylketonurias; Pyruvate Kinase; Respiratory Distress Syndrome, Newborn; Time Factors; UTP-Hexose-1-Phosphate Uridylyltransferase	1975
[Early detection of congenital metabolic anomalies]. Klinische Padiatrie, 1973, Volume: 185, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Austria; Blood; Chromatography, Paper; Chromatography, Thin Layer; Economics; Fluorometry; Galactosemias; Humans; Infant, Newborn; Leucine; Mass Screening; Metabolism, Inborn Errors; Phenylketonurias; Umbilical Cord	1973

Other Studies

9 other study(ies) available for leucine and Galactosemias

Article	Year
Negative screening tests in classical galactosaemia caused by S135L homozygosity. Journal of inherited metabolic disease, 2009, Volume: 32, Issue:3 Topics: Amino Acid Substitution; False Negative Reactions; Galactosemias; Homozygote; Humans; Infant; Infant, Newborn; Leucine; Male; Neonatal Screening; Serine; UDPglucose-Hexose-1-Phosphate Uridylyltransferase	2009
[Detections tests for newborn infants]. Revue medicale de la Suisse romande, 1981, Volume: 101, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Galactosemias; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Methionine; Phenylalanine	1981
Low efficiency of [14C]galactose incorporation by galactosemic skin fibroblasts: relationship with neurological sequelae. Biochemical medicine and metabolic biology, 1994, Volume: 52, Issue:2 Topics: Adolescent; Cells, Cultured; Child; Fibroblasts; Galactose; Galactosemias; Humans; Infant; Infant, Newborn; Leucine; Nervous System Diseases; Phenotype; Skin; UTP-Hexose-1-Phosphate Uridylyltransferase	1994
Biochemical expression of the galactosemic defect in lymphocytes and the effects on glycoprotein synthesis. Metabolism: clinical and experimental, 1977, Volume: 26, Issue:9 Topics: Adolescent; Adult; Child, Preschool; Female; Fucose; Galactosamine; Galactose; Galactosemias; Glycoproteins; Hexosamines; Hexoses; Humans; Lectins; Leucine; Lymphocyte Activation; Lymphocytes; Male; Mannose; Thymidine	1977
[Blood cells as indicators of metabolic disorders]. Zeitschrift fur klinische Chemie und klinische Biochemie, 1967, Volume: 5, Issue:5 Topics: Acidosis; Adrenal Insufficiency; Alcoholism; Alkalosis; Diabetes Mellitus; Down Syndrome; Electrolytes; Erythrocytes; Galactosemias; Glucosephosphate Dehydrogenase; Glycogen Storage Disease; Humans; Hyperaldosteronism; Hypertension; Hyperthyroidism; Kidney Failure, Chronic; Leucine; Leukocytes; Maple Syrup Urine Disease; Metabolic Diseases; Muscular Dystrophies; Paralyses, Familial Periodic; Potassium; Sodium; Vitamin B Deficiency	1967
[Dietetics in hereditary enzyme deficiencies]. La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris, 1970, Feb-26, Volume: 46, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Diarrhea, Infantile; Diet Therapy; Galactosemias; Homocystinuria; Humans; Infant Nutritional Physiological Phenomena; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Methionine; Phenylalanine; Phenylketonurias; Tyrosine; Valine	1970
[Early diagnosis of congenital metabolic diseases]. Minerva medica, 1971, Nov-03, Volume: 62, Issue:83 Topics: Diet Therapy; Galactosemias; Histidine; Homocystinuria; Humans; Hyperglycemia; Infant, Newborn; Leucine; Lipoproteins; Lysine; Metabolism, Inborn Errors; Phenylketonurias; Time Factors; Valine	1971
[Modern dietetic aspects]. Bollettino chimico farmaceutico, 1971, Volume: 110, Issue:2 Topics: Calorimetry; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Diet, Diabetic; Diet, Reducing; Dietary Proteins; Dietetics; Female; Galactosemias; Gastrointestinal Diseases; Humans; Hypertension; Leucine; Nutrition Disorders; Pregnancy; Urinary Calculi; Vitamins	1971
[Management of functional hypoglycemia in the adult]. Folia clinica internacional, 1967, Volume: 17, Issue:10 Topics: Adult; Fructose; Galactosemias; Glucagon; Glucose Tolerance Test; Humans; Hypoglycemia; Leucine; Tolbutamide	1967