citrulline has been researched along with ARG1 Deficiency in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (62.50) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 1 (12.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Burgard, P; Cederbaum, S; Cuthbertson, D; Holbert, A; McCarter, R; Waisbren, SE | 1 |
| Bazer, FW; Jaeger, LA; Rhoads, JM; Wu, G | 1 |
| Batshaw, ML | 1 |
| Nakao, T; Oyanagi, K; Sogawa, H | 1 |
| Shih, VE | 1 |
| Clara, R; Mardens, Y; Strauven, T; Terheggen, H | 1 |
| Shimizu, H | 1 |
| Inoue, I; Kobayashi, K; Saheki, T | 1 |
2 review(s) available for citrulline and ARG1 Deficiency
| Article | Year |
|---|---|
Arginine deficiency in preterm infants: biochemical mechanisms and nutritional implications.
Topics: Animals; Arginine; Argininosuccinate Lyase; Argininosuccinate Synthase; Citrulline; Deficiency Diseases; Female; Glucocorticoids; Humans; Hydrocortisone; Hyperargininemia; Infant, Newborn; Infant, Premature; Intestinal Mucosa; Intestines; Nutritional Requirements; Ornithine-Oxo-Acid Transaminase; Pregnancy | 2004 |
Hereditary disorders of the urea cycle in man: biochemical and molecular approaches.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Carbamoyl-Phosphate Synthase (Ammonia); Citrulline; Female; Humans; Hyperargininemia; Ornithine Carbamoyltransferase Deficiency Disease; Pregnancy; Prenatal Diagnosis; RNA, Messenger; Urea | 1987 |
6 other study(ies) available for citrulline and ARG1 Deficiency
| Article | Year |
|---|---|
Biochemical markers and neuropsychological functioning in distal urea cycle disorders.
Topics: Adolescent; Adult; Ammonia; Arginine; Argininosuccinic Aciduria; Biomarkers; Child; Child, Preschool; Citrulline; Citrullinemia; Female; Glutamine; Humans; Hyperargininemia; Longitudinal Studies; Male; Middle Aged; Neuropsychological Tests; Young Adult | 2018 |
Hyperammonemia.
Topics: Acetyltransferases; Amino Acid Metabolism, Inborn Errors; Amino-Acid N-Acetyltransferase; Ammonia; Arginine; Argininosuccinate Synthase; Argininosuccinic Aciduria; Brain Edema; Carbamoyl-Phosphate Synthase (Ammonia); Child, Preschool; Citrulline; Diagnosis, Differential; Female; Humans; Hyperargininemia; Infant; Infant, Newborn; Leucine; Ornithine Carbamoyltransferase; Respiratory Distress Syndrome, Newborn; Urea | 1984 |
Periodic hyperammonemia, hyperlysinemia, and homocitrullinuria associated with decreased argininosuccinate synthetase and arginase activities.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginase; Arginine; Argininosuccinate Synthase; Citrulline; Humans; Hyperargininemia; Intellectual Disability; Ligases; Liver; Lysine; Male | 1977 |
Congenital hyperammonemic syndromes.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Argininosuccinate Synthase; Argininosuccinic Aciduria; Carbamoyl-Phosphate Synthase (Ammonia); Citrulline; Diagnosis, Differential; Humans; Hyperargininemia; Infant, Newborn; Infant, Newborn, Diseases; Lysine; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease; Syndrome; Urea | 1976 |
Intravenous loading with arginine-hydrochloride and ornithine-aspartate in siblings of two families, presenting a familial neurological syndrome associated with cystinuria.
Topics: Amino Acids; Arginine; Aspartic Acid; Child; Citrulline; Cystinuria; Glutamine; Humans; Hyperargininemia; Lysine; Ornithine | 1976 |
[The dibasic amino acid metabolic disorders].
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Arginine; Blood Transfusion; Citrulline; Humans; Hyperargininemia; Ornithine; Ornithine Carbamoyltransferase Deficiency Disease; Renal Dialysis | 1992 |