lysine has been researched along with Cystinosis in 10 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 9 (90.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (10.00) | 2.80 |
Authors | Studies |
---|---|
Antignac, C; Cairoli, S; Courtoy, GE; Courtoy, PJ; Emma, F; Goffredo, BM; Graversen, JH; Janssens, V; Jouret, F; Moestrup, SK; Nevo, N; Pierreux, CE; Rega, LR | 1 |
Meister, A; Wellner, D | 1 |
Ankăr, V; Ciortoloman, H; Grigorescu, G; Pâtea, P; Petrescu, L; Popescu, M; Tănase-Mogoş, I | 1 |
Becker, K | 1 |
Gahl, WA; Raiford, D; Schulman, JD; Steinherz, R; Tietze, F | 1 |
Greco, GM; Magli, A | 1 |
Christensen, HN; Pisoni, RL; Thoene, JG | 1 |
Ampola, MG | 1 |
Copeland, W; Kelly, S; Leikhim, E | 1 |
Antener, I | 1 |
3 review(s) available for lysine and Cystinosis
Article | Year |
---|---|
A survey of inborn errors of amino acid metabolism and transport in man.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Amino Acids, Branched-Chain; Biological Transport; Cystinosis; Female; Glutathione; Glycine; Homocystinuria; Humans; Hydroxyproline; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Phenylalanine; Proline; Serine; Tyrosine; Urea; Valine | 1981 |
[Eye manifestations of amino acid disorders].
Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria; Eye Diseases; Eye Manifestations; Glycine; Hartnup Disease; Hepatolenticular Degeneration; Homocystinuria; Humans; Lysine; Oculocerebrorenal Syndrome; Oxidoreductases; Phenylketonurias; Proline; Pyruvates | 1978 |
Phenylketonuria and other disorders of amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Child, Preschool; Counseling; Cystathionine; Cystinosis; Cystinuria; Diet Therapy; Dietary Proteins; Family; Female; Hartnup Disease; Histidine; Homocystinuria; Humans; Hyperglycemia; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Ornithine; Phenylketonurias; Pregnancy; Proline; Tyrosine | 1973 |
7 other study(ies) available for lysine and Cystinosis
Article | Year |
---|---|
Dietary supplementation of cystinotic mice by lysine inhibits the megalin pathway and decreases kidney cystine content.
Topics: Adult; Animals; Cystine; Cystinosis; Dietary Supplements; Humans; Kidney; Low Density Lipoprotein Receptor-Related Protein-2; Lysine; Mice | 2023 |
[Metabolic errors of the cystinuria-lysinuria, cystinosis type detected in the newborn infant and child with renal and ocular diseases].
Topics: Adolescent; Child; Child, Preschool; Cystinosis; Cystinuria; Eye Diseases; Female; Humans; Hydroxyproline; Infant; Infant, Newborn; Kidney Diseases; Lysine; Male; Renal Tubular Transport, Inborn Errors | 1981 |
[Phaenotypic aspects of hereditary aminoacidopathies (author's transl)].
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Cystinosis; Germany, West; Homocystinuria; Humans; Infant; Infant, Newborn; Lysine; Maple Syrup Urine Disease; Mass Screening; Phenotype; Phenylketonurias; Time Factors; Tyrosine | 1981 |
Patterns of amino acid efflux from isolated normal and cystinotic human leucocyte lysosomes.
Topics: Alanine; Amino Acids; Cystine; Cystinosis; Esters; Humans; Kinetics; Leucine; Leukocytes; Lysine; Lysosomes; Methionine; Phenylalanine; Tryptophan | 1982 |
Detection and characterization of carrier-mediated cationic amino acid transport in lysosomes of normal and cystinotic human fibroblasts. Role in therapeutic cystine removal?
Topics: Amino Acids; Biological Transport, Active; Cell Line; Chloroquine; Cysteamine; Cystinosis; Electrophoresis; Fibroblasts; Humans; Hydrogen-Ion Concentration; Lysine; Lysosomes | 1985 |
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 |