galactose has been researched along with BCKD Deficiency in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (80.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Berry, GT; Gibson, JB; Mazur, AT; Palmieri, MJ; Reynolds, RA; Segal, S | 1 |
| Enzenauer, J; Matz, D; Menne, F | 1 |
| Rüdiger, HW; Wöhler, W | 1 |
| Bickel, H; Schmidt, H; Schürrle, L | 1 |
| Boisse, J | 1 |
2 review(s) available for galactose and BCKD Deficiency
| Article | Year |
|---|---|
Dietary treatment of inborn errors of amino acid and carbohydrate metabolism.
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 |
[New etiologic approach to periodic ketoacidosis in children].
Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Butyrates; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Dehydration; Diabetic Ketoacidosis; Female; Glycogen Storage Disease; Hexoses; Humans; Hydrogen-Ion Concentration; Hypoglycemia; Infant; Infant, Newborn; Ketone Bodies; Lactation Disorders; Lipid Metabolism, Inborn Errors; Maple Syrup Urine Disease; Methionine; Periodicity; Pregnancy; Propionates; Pyruvates; Vomiting | 1971 |
3 other study(ies) available for galactose and BCKD Deficiency
| Article | Year |
|---|---|
Sugar nucleotide concentrations in red blood cells of patients on protein- and lactose-limited diets: effect of galactose supplementation.
Topics: Adolescent; Adult; Analysis of Variance; Child; Child, Preschool; Dietary Carbohydrates; Dietary Proteins; Erythrocytes; Female; Food, Fortified; Galactose; Humans; Infant; Infant, Newborn; Lactose; Male; Maple Syrup Urine Disease; Metabolic Diseases; Nitrogen; Phenylketonurias; Uridine Diphosphate Galactose; Uridine Diphosphate Glucose | 1996 |
[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 |
[Prenatal diagnosis of metabolic abnormalities in cell cultures (author's transl)].
Topics: Amniotic Fluid; Autoradiography; Carbon Dioxide; Carbon Radioisotopes; Cell Line; Cells, Cultured; Culture Media; Cytodiagnosis; Female; Fibroblasts; Galactose; Galactosemias; Humans; Lesch-Nyhan Syndrome; Maple Syrup Urine Disease; Metabolism, Inborn Errors; Mucopolysaccharidoses; Pregnancy; Prenatal Diagnosis; Sulfur | 1975 |