tryptophan and BCKD Deficiency

tryptophan has been researched along with BCKD Deficiency in 5 studies

Research

Studies (5)

Timeframe	Studies, this research(%)	All Research%
pre-1990	4 (80.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (20.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Barschak, AG; Busanello, EN; Cipriani, F; Coelho, DM; Deon, M; Dutra-Filho, CS; Giugliani, R; Sitta, A; Vargas, CR; Wajner, M	1
SCHULTZE-JENA, BS	1
Lees, GJ; Weiner, N	1
Menne, F	1
Carpenter, DG; Carter, CH	1

Reviews

1 review(s) available for tryptophan and BCKD Deficiency

Article	Year
[Feeble mindedness caused by genetic disorders of amino acid metabolism]. Hippokrates, 1968, May-31, Volume: 39, Issue:10 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Intellectual Disability; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Sarcosine; Succinates; Transferases; Tryptophan; Valine	1968

Article

Year

[Feeble mindedness caused by genetic disorders of amino acid metabolism].

Hippokrates, 1968, May-31, Volume: 39, Issue:10

Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Citrulline; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Hydroxyproline; Intellectual Disability; Lysine; Maple Syrup Urine Disease; Methionine; Phenylketonurias; Proline; Sarcosine; Succinates; Transferases; Tryptophan; Valine

1968

Other Studies

4 other study(ies) available for tryptophan and BCKD Deficiency

Article	Year
Amino acids levels and lipid peroxidation in maple syrup urine disease patients. Clinical biochemistry, 2009, Volume: 42, Issue:6 Topics: Adult; Amino Acids; Antioxidants; Humans; Hydroxy Acids; Isoleucine; Keto Acids; Leucine; Lipid Peroxidation; Maple Syrup Urine Disease; Methionine; Oxidative Stress; Thiobarbituric Acid Reactive Substances; Tryptophan; Valine	2009
[Hereditary enzyme defects of amino acid metabolism]. Ergebnisse der inneren Medizin und Kinderheilkunde, 1962, Volume: 18 Topics: Albinism; Alkaptonuria; Amino Acids; Humans; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proteins; Tryptophan; Tyrosine	1962
Transaminations between amino acids and keto acids elevated in phenylketonuria and maple syrup urine disease. Journal of neurochemistry, 1973, Volume: 20, Issue:2 Topics: Amino Acids; Animals; Brain Stem; Carbon Isotopes; Cerebellum; Dialysis; Dihydroxyphenylalanine; Humans; Hydrogen-Ion Concentration; In Vitro Techniques; Keto Acids; Ketoglutaric Acids; Kinetics; Liver; Maple Syrup Urine Disease; Phenylketonurias; Pyruvates; Rats; Transaminases; Tritium; Tryptophan	1973
Inborn errors of metabolism associated with unusual odors. The Journal of the Florida Medical Association, 1970, Volume: 57, Issue:5 Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Fatty Acids; Female; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Malabsorption Syndromes; Maple Syrup Urine Disease; Methionine; Odorants; Phenylalanine; Tryptophan; Valerates	1970