galactose has been researched along with BH4 Deficiency in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 15 (88.24) | 18.7374 |
| 1990's | 1 (5.88) | 18.2507 |
| 2000's | 1 (5.88) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| CARVER, MJ; WITTSON, C | 1 |
| BERRY, HK; GUEST, GM; RUBINSTEIN, J | 1 |
| GOMMI, BW; WOOLLEY, DW | 1 |
| BICKEL, H | 1 |
| HOLLMANN, S | 1 |
| COWIE, VA | 1 |
| Hardy, J; Link, B | 1 |
| Piccardo, MG; Rosa, M; Russo, L | 1 |
| Berry, GT; Gibson, JB; Mazur, AT; Palmieri, MJ; Reynolds, RA; Segal, S | 1 |
| Bickel, H; Schmidt, H; Schürrle, L | 1 |
| McKean, CM; Peterson, NA; Shah, SN | 1 |
| Woolf, LI | 1 |
| Linneweh, F | 2 |
| Oldendorf, WH | 1 |
| Menkes, JH | 1 |
3 review(s) available for galactose and BH4 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 |
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 |
The blood-brain barrier.
Topics: Amino Acids; Animals; Biological Transport, Active; Blood-Brain Barrier; Brain; Capillary Permeability; Hexoses; Humans; Membrane Lipids; Methods; Nucleic Acids; Pharmaceutical Preparations; Phenylketonurias; Rats | 1977 |
14 other study(ies) available for galactose and BH4 Deficiency
| Article | Year |
|---|---|
Metabolic errors and mental retardation.
Topics: Biochemical Phenomena; Galactose; Hepatolenticular Degeneration; Humans; Intellectual Disability; Phenylketonurias | 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 |
[RAPID CLINICO-CHEMICAL TESTS].
Topics: Acetone; Clinical Laboratory Techniques; Diabetes Mellitus; Galactose; Glycosuria; Humans; Indicators and Reagents; Phenylketonurias; Research | 1963 |
SEROTONIN RECEPTORS. IV. SPECIFIC DEFICIENCY OF RECEPTORS IN GALACTOSE POISONING AND ITS POSSIBLE RELATIONSHIP TO THE IDIOCY OF GALACTOSEMIA.
Topics: Acetylcholine; Brain Chemistry; Cerebrosides; Dietary Carbohydrates; Epinephrine; Galactose; Galactosemias; Gangliosides; Glucose; Intellectual Disability; Lipids; Pharmacology; Phenylketonurias; Rats; Receptors, Serotonin; Research; Serotonin; Stomach; Toxicology; Transferases | 1964 |
[Diagnosis and therapy of galactosemia and phenylketonuria].
Topics: Blood; Body Fluids; Galactose; Galactosemias; Humans; Phenylalanine; Phenylketonurias; Urine | 1955 |
[On the biochemistry of essential pentosuria, congenital galactosemia and phenylketonuria].
Topics: Carbohydrate Metabolism, Inborn Errors; Galactose; Galactosemias; Humans; Pentoses; Phenylketonurias; Sugar Alcohol Dehydrogenases; Xylulose | 1959 |
The galactose tolerance test in phenylketonuria.
Topics: Body Fluids; Galactose; Humans; Immune Tolerance; Liver; Phenylketonurias; Phenylpyruvic Acids; Urine | 1950 |
Reuse of filter plates for elution of dried blood spot samples in neonatal assays.
Topics: Blood Specimen Collection; Equipment Reuse; Filtration; Galactose; Humans; Infant, Newborn; Neonatal Screening; Phenylketonurias | 2003 |
Preliminary report on mellituria in phenylketonuric children: modification in the excretion of glucose and pentoses.
Topics: Adolescent; Child; Child, Preschool; Chromatography, Paper; Female; Galactose; Glycosuria; Humans; Pentoses; Phenylketonurias | 1981 |
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 |
Lipid composition of human cerebral white matter and myelin in phenylketonuria.
Topics: Adolescent; Adult; Aged; Autopsy; Brain; Brain Chemistry; Cholesterol; Female; Galactose; Glycolipids; Humans; Intellectual Disability; Lipids; Male; Myelin Sheath; Phenylketonurias | 1972 |
[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 |
[Malabsorption in hereditary disorders of the carbohydrate and amino acid metabolism].
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Galactose; Glucose; Hartnup Disease; Humans; Malabsorption Syndromes; Phenylketonurias; Rats | 1969 |
Cerebral proteolipids in phenylketonuria.
Topics: Amino Acids; Brain Chemistry; Child; Cholesterol; Chromatography; Dialysis; Gangliosides; Hexoses; Humans; Lipids; Lipoproteins; Male; Phenylketonurias; Phosphorus | 1968 |