Compounds > citrulline

citrulline and Coma

citrulline has been researched along with Coma in 14 studies

Research

Studies (14)

Timeframe	Studies, this research(%)	All Research%
pre-1990	6 (42.86)	18.7374
1990's	2 (14.29)	18.2507
2000's	5 (35.71)	29.6817
2010's	1 (7.14)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bellantuono, R; Bellino, V; De Palo, T; Favia, V; Morrone, A; Papadia, F; Ranieri, A; Tummolo, A	1
Antuzzi, D; Arcangeli, A; Conti, G; Gaspari, R; Mensi, S; Proietti, R; Tartaglione, T; Wismayer, DS	1
Au, WL; Koh, PL; Lim, MS; Lim, TC; Loh, NK; Seow, DC; Tan, IK; Yee, WC	1
Au, WL; Lim, CC; Wong, YC; Xu, M; Ye, J	1
Batshaw, ML; Blom, W; Brubakk, AM; Brusilow, S; Burton, BK; Cann, HM; Kerr, D; Mamunes, P; Matalon, R; Myerberg, D; Schafer, IA; Waber, L	1
Batshaw, ML; Brusilow, S; Painter, MJ; Schafer, IA; Sproul, GT; Thomas, GH	1
Bauer, MF; Bieger, I; Gempel, K; Gerbitz, KD; Hofmann, S; Pontz, BF; Stadler, S	1
Hashikura, Y; Ikeda, S; Ikegami, T; Iwai, M; Kawasaki, S; Kobayashi, K; Saheki, T; Takei, Y; Yazaki, M	1
Ban, S; Ishii, A; Ohkoshi, N; Oka, Y; Takahashi, A	1
Geiger, R; Maurer, H; Murr, C; Sailer, M; Schmoigl, C; Sperl, W; Steichen-Gersdorf, E	1
Coskun, T; Kneer, J; Mönch, S; Ozalp, I	1
Girgis, N; Herrin, J; McGravey, V; Shah, BL; Shih, VE	1
Batshaw, ML	1
Mitsutsuka, K; Miyakoshi, T; Takahashi, T; Wada, T	1

Other Studies

14 other study(ies) available for citrulline and Coma

Article	Year
Successful early management of a female patient with a metabolic stroke due to ornithine transcarbamylase deficiency. Pediatric emergency care, 2013, Volume: 29, Issue:5 Topics: Adolescent; Arginine; Brain; Carnitine; Case Management; Citrulline; Coma; Combined Modality Therapy; Drug Therapy, Combination; Electroencephalography; Female; Glutamates; Hemofiltration; Humans; Hyperammonemia; Lethargy; Ornithine Carbamoyltransferase Deficiency Disease; Phenylbutyrates; Renal Dialysis; Tomography, Emission-Computed, Single-Photon; Vomiting	2013
Late-onset presentation of ornithine transcarbamylase deficiency in a young woman with hyperammonemic coma. Annals of emergency medicine, 2003, Volume: 41, Issue:1 Topics: Adult; Age Factors; Anticonvulsants; Brain; Citrulline; Coma; Diagnosis, Differential; Electroencephalography; Female; Follow-Up Studies; Glasgow Coma Scale; Hemodiafiltration; Humans; Hyperammonemia; Injections, Intravenous; Lorazepam; Magnetic Resonance Imaging; Ornithine Carbamoyltransferase Deficiency Disease; Time Factors; Tomography, X-Ray Computed	2003
Serial diffusion-weighted magnetic resonance imaging in adult-onset citrullinaemia. Journal of the neurological sciences, 2003, May-15, Volume: 209, Issue:1-2 Topics: Adult; Ammonia; Argininosuccinic Acid; Brain; Citrulline; Citrullinemia; Coma; Diagnosis, Differential; Disease Progression; Fatty Liver; Humans; Magnetic Resonance Imaging; Male; Recurrence; Remission, Spontaneous; Substance-Related Disorders; Ultrasonography	2003
Magnetic resonance spectroscopy in adult-onset citrullinemia: elevated glutamine levels in comatose patients. Archives of neurology, 2007, Volume: 64, Issue:7 Topics: Adult; Ammonia; Biomarkers; Brain; Brain Mapping; Cerebral Cortex; Choline; Citrulline; Citrullinemia; Coma; Diffusion Magnetic Resonance Imaging; Disease Progression; Early Diagnosis; Fatal Outcome; Glutamic Acid; Glutamine; Gyrus Cinguli; Humans; Hyperammonemia; Inositol; Magnetic Resonance Spectroscopy; Male; Predictive Value of Tests	2007
Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion. The New England journal of medicine, 1982, Jun-10, Volume: 306, Issue:23 Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Essential; Ammonia; Arginine; Argininosuccinate Synthase; Argininosuccinic Aciduria; Benzoates; Benzoic Acid; Carbamoyl-Phosphate Synthase (Ammonia); Child, Preschool; Citrulline; Coma; Female; Humans; Infant; Infant, Newborn; Infusions, Parenteral; Male; Nitrogen; Ornithine Carbamoyltransferase Deficiency Disease; Urea	1982
Therapy of urea cycle enzymopathies: three case studies. The Johns Hopkins medical journal, 1981, Volume: 148, Issue:1 Topics: Ammonia; Arginine; Argininosuccinic Acid; Argininosuccinic Aciduria; Child, Preschool; Citrulline; Coma; Female; Humans; Infant; Infant, Newborn; Intellectual Disability; Lyases; Male; Ornithine Carbamoyltransferase Deficiency Disease; Urea	1981
Detection of neonatal argininosuccinate lyase deficiency by serum tandem mass spectrometry. Journal of inherited metabolic disease, 2001, Volume: 24, Issue:3 Topics: Amino Acid Sequence; Amino Acids; Ammonia; Arginine; Argininosuccinate Lyase; Argininosuccinic Acid; Argininosuccinic Aciduria; Base Sequence; Citrulline; Coma; Frameshift Mutation; Humans; Hyperammonemia; Infant, Newborn; Mass Spectrometry; Molecular Sequence Data; Neonatal Screening; Ornithine	2001
Type II (adult onset) citrullinaemia: clinical pictures and the therapeutic effect of liver transplantation. Journal of neurology, neurosurgery, and psychiatry, 2001, Volume: 71, Issue:5 Topics: Adolescent; Adult; Ammonia; Brain; Brain Edema; Citrulline; Citrullinemia; Cognition Disorders; Coma; Consciousness Disorders; Electroencephalography; Female; Hepatic Encephalopathy; Humans; Liver Transplantation; Magnetic Resonance Imaging; Male; Middle Aged; Neuropsychological Tests; Severity of Illness Index; Tomography, Emission-Computed, Single-Photon; Tomography, X-Ray Computed; Treatment Outcome	2001
[A case of citrullinemia associated with isolated ACTH deficiency, rapidly developing coma]. Rinsho shinkeigaku = Clinical neurology, 1992, Volume: 32, Issue:8 Topics: Adrenal Cortex; Adrenocorticotropic Hormone; Adult; Ammonia; Argininosuccinate Synthase; Citrulline; Coma; Humans; Hydrocortisone; Liver; Male	1992
Continuous arteriovenous haemofiltration in a neonate with hyperammonaemic coma due to citrullinaemia. Journal of inherited metabolic disease, 1992, Volume: 15, Issue:1 Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Citrulline; Coma; Hemofiltration; Humans; Infant, Newborn; Male	1992
Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten-year-old boy. Journal of inherited metabolic disease, 1987, Volume: 10, Issue:3 Topics: Ammonia; Brain Stem; Child; Citrulline; Coma; Diagnosis, Differential; Encephalitis; Humans; Male; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid	1987
Lethal ornithine transcarbamylase deficiency in a female neonate. Journal of inherited metabolic disease, 1987, Volume: 10, Issue:3 Topics: Ammonia; Arginine; Citrulline; Coma; Female; Humans; Infant, Newborn; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Peritoneal Dialysis; Stevens-Johnson Syndrome	1987
The diagnosis of ornithine transcarbamylase deficiency. Journal of pediatric gastroenterology and nutrition, 1985, Volume: 4, Issue:1 Topics: Animals; Carbamyl Phosphate; Citrulline; Coma; Female; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Metabolism, Inborn Errors; Mitochondria; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid	1985
[Treatment of a consciousness disorder seizure specific to hepato-encephalopathy (Inose type)--trial use of gamma-hydroxy-beta-aminobutyric acid]. No to shinkei = Brain and nerve, 1969, Volume: 21, Issue:8 Topics: Adult; Aminobutyrates; Ammonia; Brain Diseases; Citrulline; Coma; Electroencephalography; Female; Humans; Hydroxybutyrates; Injections, Intravenous; Liver Cirrhosis; Liver Diseases; Liver Function Tests; Unconsciousness	1969