citrulline and BH4 Deficiency

citrulline has been researched along with BH4 Deficiency in 10 studies

Research

Studies (10)

Timeframe	Studies, this research(%)	All Research%
pre-1990	8 (80.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (10.00)	24.3611
2020's	1 (10.00)	2.80

Authors

Authors	Studies
Cao, Z; Kong, Y; Li, T; Liu, W; Ma, Z; Rosenbaum, ER; Song, B; Wan, Z; Yue, X; Zhai, Y	1
Gioni, V; Kalogerakou, M; Papassotiriou, I; Papastamataki, M; Schulpis, KH	1
COFFEY, VP	1
EFRON, ML; MACCREADY, RA; MOSER, HW; YOUNG, D	1
Stern, J	1
Reavey, PC; Yadav, GC	1
Menne, F	1
O'Reilly, S	1
Berry, HK	1
Gjessing, LR; Seip, M; Vellan, EJ	1

Reviews

1 review(s) available for citrulline and BH4 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

9 other study(ies) available for citrulline and BH4 Deficiency

Article	Year
Benchmark Examination of Blood Amino Acids Patterns in Phenylketonuria Neonates and Young Children on Phenylalanine-Restricted Dietary Treatment. Fetal and pediatric pathology, 2022, Volume: 41, Issue:3 Topics: Arginine; Benchmarking; Child; Child, Preschool; Citrulline; Diet; Humans; Infant, Newborn; Methionine; Phenylalanine; Phenylketonurias; Proline; Tyrosine; Valine	2022
Glutamine, ornithine, citrulline and arginine levels in children with phenylketonuria: The diet effect. Clinical biochemistry, 2011, Volume: 44, Issue:10-11 Topics: Arginine; Case-Control Studies; Child; Citrulline; Diet; Female; Glutamine; Humans; Male; Nutritional Status; Ornithine; Phenylketonurias	2011
MENTAL RETARDATION AND THE INBORN ERRORS OF METABOLISM. Journal of the Irish Medical Association, 1964, Volume: 54 Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Arginine; Citrulline; Fructose; Galactosemias; Histidine; Homocysteine; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Renal Aminoacidurias; Vitamin B 6 Deficiency	1964
A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER. The New England journal of medicine, 1964, Jun-25, Volume: 270 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Blood Chemical Analysis; Chromatography; Citrulline; Glycine; Histidine; Homocysteine; Humans; Hydroxyproline; Intellectual Disability; Maple Syrup Urine Disease; Metabolic Diseases; Phenylketonurias; Proline; Proteins; Renal Aminoacidurias; Urine	1964
Biochemistry of mental retardation. Proceedings of the Royal Society of Medicine, 1975, Volume: 68, Issue:9 Topics: Aged; Citrulline; Female; Glycine; Histidine; Humans; Infant; Infant, Newborn; Intellectual Disability; Metabolism, Inborn Errors; Phenylketonurias	1975
Aminoacidopathies: a review of 3 years experience of investigations in a Kuwait hospital. Journal of inherited metabolic disease, 1988, Volume: 11, Issue:3 Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Child; Child, Preschool; Citrulline; Cystinuria; Female; Glycine; Homocystinuria; Humans; Infant; Infant, Newborn; Kuwait; Male; Maple Syrup Urine Disease; Phenylalanine; Phenylketonurias; Proline; Tyrosine	1988
Neurologic disorders and liver disease. Postgraduate medicine, 1971, Volume: 50, Issue:3 Topics: Adipose Tissue; Ammonia; Brain Diseases; Citrulline; Fatty Liver; Galactosemias; Hepatic Encephalopathy; Hepatitis; Hepatolenticular Degeneration; Humans; Hyperbilirubinemia, Hereditary; Kidney Diseases; Liver; Liver Diseases; Metabolism, Inborn Errors; Mucopolysaccharidoses; Nervous System Diseases; Neurologic Manifestations; Paraplegia; Phenylketonurias; Quadriplegia; Urea	1971
Hereditary disorders of amino acid metabolism associated with mental deficiency. Annals of the New York Academy of Sciences, 1969, Sep-30, Volume: 166, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Child, Preschool; Citrulline; Deficiency Diseases; Hartnup Disease; Homocystinuria; Humans; Intellectual Disability; Maple Syrup Urine Disease; Phenylketonurias; Succinates	1969
Hair amino acids in cystinosis, homocystinuria, Fölling's disease and tyrosinosis. Acta paediatrica Scandinavica, 1969, Volume: 58, Issue:3 Topics: Amino Acids; Autoanalysis; Citrulline; Cystine; Cystinosis; Female; Hair; Homocysteine; Homocystinuria; Humans; In Vitro Techniques; Male; Metabolic Diseases; Methionine; Methods; Phenylalanine; Phenylketonurias; Proline; Tyrosine	1969