arginine and Cystinosis
arginine has been researched along with Cystinosis in 5 studies
Research
Studies (5)
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (80.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors
Authors | Studies |
---|---|
Ben-Omran, T; Blom, HJ; Dewik, AN; Gallego-Villar, L; Häberle, J; Hannibal, L; Kruger, WD; Nasrallah, GK; Thöny, B | 1 |
Kroll, S; Toussaint, W; Zebisch, P | 2 |
Copeland, W; Kelly, S; Leikhim, E | 1 |
Antener, I | 1 |
Reviews
1 review(s) available for arginine and Cystinosis
Article | Year |
---|---|
Cysteamine revisited: repair of arginine to cysteine mutations.
Topics: Animals; Apolipoprotein E3; Arginine; Argininosuccinate Lyase; Cystathionine beta-Synthase; Cysteamine; Cysteine; Cystinosis; Homeostasis; Humans; Hydrogen-Ion Concentration; Molecular Conformation; Mutation; Mutation, Missense; Oxidation-Reduction; Sulfhydryl Compounds; Thromboplastin | 2017 |
Other Studies
4 other study(ies) available for arginine and Cystinosis
Article | Year |
---|---|
[Hereditary amino acid metabolism disorders. Indications for early diagnosis].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Cystathionine; Cystinosis; Diagnosis, Differential; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Infant; Infant, Newborn; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine | 1972 |
[Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods].
Topics: Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Clinical Laboratory Techniques; Cystathionine; Cystinosis; Glycine; Hartnup Disease; Histidine; Homocystinuria; Humans; Maple Syrup Urine Disease; Methods; Methylmalonic Acid; Phenylketonurias; Proline; Propionates; Tyrosine | 1972 |
Amino acid excretion patterns in the offspring of a 'doubly-heterozygous' cystine stone former.
Topics: Alleles; Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Child; Child, Preschool; Chromatography, Paper; Cysteine; Cystinosis; Cystinuria; Female; Ferrocyanides; Heterozygote; Homocysteine; Humans; Lysine; Molecular Biology; Ornithine | 1970 |
[Biochemical studies on inherited disorders of amino acid metabolism in pediatrics].
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Chemistry, Clinical; Child; Child, Preschool; Chromatography, Paper; Cystine; Cystinosis; Cystinuria; Electrophoresis; Fanconi Syndrome; Feces; Histidine; Humans; Keto Acids; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias | 1970 |