Page last updated: 2024-08-17

lysine and Hyperargininemia

lysine has been researched along with Hyperargininemia in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19904 (80.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Eichinger-Öttl, U; Ertl, C; Haberlandt, E; Häberle, J; Heinz-Erian, P; Karall, D; Rostásy, K; Scholl-Bürgi, S; Sigl, SB1
Beaudet, AL; Michels, VV1
Nakao, T; Oyanagi, K; Sogawa, H1
Shih, VE1
Clara, R; Mardens, Y; Strauven, T; Terheggen, H1

Other Studies

5 other study(ies) available for lysine and Hyperargininemia

ArticleYear
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
Arginase deficiency in multiple tissues in argininemia.
    Clinical genetics, 1978, Volume: 13, Issue:1

    Topics: Abnormalities, Multiple; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginase; Arginine; Blood Transfusion; Child; Erythrocytes; Female; Humans; Hyperargininemia; Lysine

1978
Periodic hyperammonemia, hyperlysinemia, and homocitrullinuria associated with decreased argininosuccinate synthetase and arginase activities.
    Pediatric research, 1977, Volume: 11, Issue:9 Pt 1

    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.
    Clinics in perinatology, 1976, Volume: 3, Issue:1

    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.
    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