citrulline and Nervous System Disorders

citrulline has been researched along with Nervous System Disorders in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's1 (14.29)18.2507
2000's1 (14.29)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Everett, AD; Fu, Z; Jin, Z; Troncosco, J; Van Eyk, JE; Yang, J1
Barrot, L; Belin, N; Belon, F; Capellier, G; Cypriani, B; Navellou, JC; Piton, G1
Adoue, V; Arnaud, J; Coudane, F; Méchin, MC; Nachat, R; Serre, G; Simon, M1
Kanazawa, N; Miyamoto, T; Tsujino, S1
Arbour, JF; Dubé, J; Flessas, J; Laberge, M; Lafleur, L; Lambert, MA; Lemay, JF; Mitchell, GA; Valle, D; Vanasse, M1
Dennis, JA; Harper, PA; Healy, PJ; O'Brien, JJ; Rayward, DH1
O'Reilly, S1

Reviews

2 review(s) available for citrulline and Nervous System Disorders

ArticleYear
[Deimination or citrullination, a post-translational modification with many physiological and pathophysiological facets].
    Medecine sciences : M/S, 2011, Volume: 27, Issue:1

    Topics: Animals; Arginine; Autoimmune Diseases; Body Water; Calcium; Chromatin; Citrulline; Conserved Sequence; Cornea; Epidermis; Evolution, Molecular; Gene Expression Regulation; Humans; Hydrolases; Isoenzymes; Mice; Myelin Proteins; Neoplasms; Nervous System Diseases; Protein Processing, Post-Translational; Protein-Arginine Deiminase Type 6; Protein-Arginine Deiminases; Skin Diseases

2011
[Molecular genetic studies of mitochondrial ornithine transporter deficiency (HHH syndrome)].
    Nihon rinsho. Japanese journal of clinical medicine, 2001, Volume: 59, Issue:11

    Topics: Amino Acid Transport Systems, Basic; Ammonia; Animals; Base Sequence; Carrier Proteins; Citrulline; Humans; Membrane Transport Proteins; Mitochondria; Molecular Sequence Data; Mutation; Nervous System Diseases; Ornithine; Syndrome

2001

Other Studies

5 other study(ies) available for citrulline and Nervous System Disorders

ArticleYear
Identification and characterization of citrulline-modified brain proteins by combining HCD and CID fragmentation.
    Proteomics, 2013, Volume: 13, Issue:17

    Topics: Alzheimer Disease; Animals; Brain; Cattle; Chromatography, Liquid; Citrulline; Glial Fibrillary Acidic Protein; Humans; Hydrolases; Mass Spectrometry; Myelin Basic Protein; Nervous System Diseases; Neurogranin; Protein-Arginine Deiminases

2013
Enterocyte Damage: A Piece in the Puzzle of Post-Cardiac Arrest Syndrome.
    Shock (Augusta, Ga.), 2015, Volume: 44, Issue:5

    Topics: Aged; Biomarkers; Citrulline; Enterocytes; Fatty Acid-Binding Proteins; Female; Heart Arrest; Humans; Intensive Care Units; Male; Middle Aged; Nervous System Diseases; Prognosis; Prospective Studies

2015
Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients.
    The Journal of pediatrics, 1992, Volume: 121, Issue:5 Pt 1

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Citrulline; Eye Diseases; Female; Humans; Male; Nervous System Diseases; Neuropsychological Tests; Ornithine; Psychomotor Performance

1992
Citrullinaemia as a cause of neurological disease in neonatal Friesian calves.
    Australian veterinary journal, 1986, Volume: 63, Issue:11

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Argininosuccinate Synthase; Cattle; Cattle Diseases; Citrulline; Female; Ligases; Male; Nervous System Diseases

1986
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