glutamine has been researched along with Cerebral Pseudosclerosis in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (42.86) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abonyi, M; Folhoffer, A; Lakatos, PL | 1 |
Hsu, CM; Lee, CC; Tsai, CH; Tsai, FJ; Tsai, Y; Wan, L | 1 |
Cherninkova, S; Jelev, H; Kremensky, I; Mihaylova, V; Raycheva, M; Savov, A; Todorov, T; Tournev, I | 1 |
Chang, JG; Jong, YJ; Lee, CC; Lin, SP; Lo, MC; Tsai, CH; Tsai, FJ; Wu, JY; Yang, CF | 1 |
Goldstein, NP; Wilson, DM | 1 |
Goldstein, P; Wilson, DM | 1 |
Neumann, PZ; Silverberg, M | 1 |
1 review(s) available for glutamine and Cerebral Pseudosclerosis
Article | Year |
---|---|
[Wilson disease].
Topics: Adenosine Triphosphatases; Cation Transport Proteins; Copper; Copper-Transporting ATPases; Glutamine; Hepatolenticular Degeneration; Histidine; Humans; Mutation | 2004 |
6 other study(ies) available for glutamine and Cerebral Pseudosclerosis
Article | Year |
---|---|
Mutation analysis of Taiwanese Wilson disease patients.
Topics: Adenosine Triphosphatases; Alleles; Arginine; Base Sequence; DNA Mutational Analysis; Exons; False Positive Reactions; Gene Frequency; Genetic Carrier Screening; Glutamine; Hepatolenticular Degeneration; Humans; Leucine; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Sequence Analysis, DNA; Taiwan | 2006 |
Wilson's disease in two consecutive generations in a Bulgarian Roma family.
Topics: Adult; Aspartate Aminotransferases; Bulgaria; Child; Family Health; Female; Glutamine; Hepatolenticular Degeneration; Histidine; Humans; Male; Mutation | 2007 |
Mutation analysis of Wilson disease in Taiwan and description of six new mutations.
Topics: Alleles; Alternative Splicing; Amino Acid Substitution; Arginine; Aspartic Acid; DNA; DNA Mutational Analysis; Glutamine; Glycine; Hepatolenticular Degeneration; Humans; Leucine; Leukocytes; Mutation; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Proline; Taiwan | 1998 |
Renal urate excretion in patients with Wilson's disease.
Topics: Arginine; Depression, Chemical; Glomerular Filtration Rate; Glutamine; Hepatolenticular Degeneration; Humans; Inulin; Kidney Tubules, Proximal; Penicillamine; Pyrazinamide; Serine; Uric Acid; Valine | 1973 |
Evidence for a urate reabsorptive defect in patients with Wilson's disease.
Topics: Arginine; Follow-Up Studies; Glomerular Filtration Rate; Glutamine; Hepatolenticular Degeneration; Humans; Kidney; Penicillamine; Pyrazinamide; Serine; Time Factors; Uric Acid | 1974 |
Active copper transport in mammalian tissues--a possible role in Wilson's disease.
Topics: Animals; Asparagine; Carcinoma, Ehrlich Tumor; Copper; Glutamine; Hepatolenticular Degeneration; Histidine; In Vitro Techniques; Kidney; Liver; Radioisotopes; Rats; Threonine | 1966 |