glutamine and CBS Deficiency

glutamine has been researched along with CBS Deficiency in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Levy, HL	1
Harper, PS	1

Other Studies

2 other study(ies) available for glutamine and CBS Deficiency

Article	Year
Metabolic disorders in the center of genetic medicine. The New England journal of medicine, 2005, Nov-03, Volume: 353, Issue:18 Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic, Inborn; Glutamate-Ammonia Ligase; Glutamic Acid; Glutamine; Homocystinuria; Humans; Hyperhomocysteinemia; Infant, Newborn; Mutation; Phenylketonurias	2005
Inborn errors of metabolism-the relationship of clinical and biochemical abnormalities. Acta Universitatis Carolinae. Medica. Monographia, 1973, Volume: 56 Topics: Cystathionine; Diseases in Twins; Glutamine; Homocystinuria; Humans; Infant, Newborn; Intellectual Disability; Lesch-Nyhan Syndrome; Metabolism, Inborn Errors; NADH, NADPH Oxidoreductases; Phenotype; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias	1973

Article

Year

Metabolic disorders in the center of genetic medicine.

The New England journal of medicine, 2005, Nov-03, Volume: 353, Issue:18

Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic, Inborn; Glutamate-Ammonia Ligase; Glutamic Acid; Glutamine; Homocystinuria; Humans; Hyperhomocysteinemia; Infant, Newborn; Mutation; Phenylketonurias

2005

Inborn errors of metabolism-the relationship of clinical and biochemical abnormalities.

Acta Universitatis Carolinae. Medica. Monographia, 1973, Volume: 56

Topics: Cystathionine; Diseases in Twins; Glutamine; Homocystinuria; Humans; Infant, Newborn; Intellectual Disability; Lesch-Nyhan Syndrome; Metabolism, Inborn Errors; NADH, NADPH Oxidoreductases; Phenotype; Phenylalanine; Phenylalanine Hydroxylase; Phenylketonurias

1973