glutamine and ARG1 Deficiency

glutamine has been researched along with ARG1 Deficiency in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's0 (0.00)18.2507
2000's2 (33.33)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Allegri, G; Burke, KE; Cederbaum, SD; Häberle, J; Lipshutz, GS; Liu, XB; Martini, PGV; Truong, B; Zhu, X1
Burgard, P; Cederbaum, S; Cuthbertson, D; Holbert, A; McCarter, R; Waisbren, SE1
Eichinger-Öttl, U; Ertl, C; Haberlandt, E; Häberle, J; Heinz-Erian, P; Karall, D; Rostásy, K; Scholl-Bürgi, S; Sigl, SB1
Bhargava, R; Cederbaum, SD; Grody, WW; Hu, C; Lee, EK; Lipshutz, GS; Rozengurt, N; Stout, D1
Cederbaum, SD; Cox, GF; Degirolami, U; Kern, RM; Levy, HL; Ligon, KL; Marsden, D; Picker, JD; Puga, AC; Shih, VE1
Clara, R; Mardens, Y; Strauven, T; Terheggen, H1

Other Studies

6 other study(ies) available for glutamine and ARG1 Deficiency

ArticleYear
Lipid nanoparticle-targeted mRNA therapy as a treatment for the inherited metabolic liver disorder arginase deficiency.
    Proceedings of the National Academy of Sciences of the United States of America, 2019, 10-15, Volume: 116, Issue:42

    Topics: Ammonia; Animals; Arginase; Arginine; Codon; Disease Models, Animal; Glutamine; Hyperammonemia; Hyperargininemia; Lipids; Liver; Liver Diseases; Male; Mice; Mice, Inbred C57BL; Nanoparticles; RNA, Messenger; Urea

2019
Biochemical markers and neuropsychological functioning in distal urea cycle disorders.
    Journal of inherited metabolic disease, 2018, Volume: 41, Issue:4

    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
Amino acids in CSF and plasma in hyperammonaemic coma due to arginase1 deficiency.
    Journal of inherited metabolic disease, 2008, Volume: 31 Suppl 2

    Topics: Adult; Amino Acids; Ammonia; Arginine; Biomarkers; Chromatography, Ion Exchange; Coma; Glutamine; Humans; Hyperammonemia; Hyperargininemia; Lysine; Male; Ornithine

2008
Long-term survival of the juvenile lethal arginase-deficient mouse with AAV gene therapy.
    Molecular therapy : the journal of the American Society of Gene Therapy, 2012, Volume: 20, Issue:10

    Topics: Amino Acids; Ammonia; Animals; Arginase; Blotting, Western; Dependovirus; Female; Fertility; Gene Expression Regulation; Gene Transfer Techniques; Genetic Therapy; Genetic Vectors; Genotype; Glutamine; Hyperargininemia; Immunohistochemistry; Male; Mice; Mice, Knockout

2012
Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edema.
    The Journal of pediatrics, 2003, Volume: 142, Issue:3

    Topics: Amino Acids, Basic; Ammonia; Arginase; Arginine; Brain Edema; Female; Glutamine; Humans; Hyperargininemia; Infant, Newborn; Kidney; Liver; Renal Dialysis

2003
Intravenous loading with arginine-hydrochloride and ornithine-aspartate in siblings of two families, presenting a familial neurological syndrome associated with cystinuria.
    Biomedicine / [publiee pour l'A.A.I.C.I.G.], 1976, Volume: 24, Issue:3

    Topics: Amino Acids; Arginine; Aspartic Acid; Child; Citrulline; Cystinuria; Glutamine; Humans; Hyperargininemia; Lysine; Ornithine

1976