glutamine and Cerebral Pseudosclerosis

glutamine has been researched along with Cerebral Pseudosclerosis in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19903 (42.86)18.7374
1990's1 (14.29)18.2507
2000's3 (42.86)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abonyi, M; Folhoffer, A; Lakatos, PL1
Hsu, CM; Lee, CC; Tsai, CH; Tsai, FJ; Tsai, Y; Wan, L1
Cherninkova, S; Jelev, H; Kremensky, I; Mihaylova, V; Raycheva, M; Savov, A; Todorov, T; Tournev, I1
Chang, JG; Jong, YJ; Lee, CC; Lin, SP; Lo, MC; Tsai, CH; Tsai, FJ; Wu, JY; Yang, CF1
Goldstein, NP; Wilson, DM1
Goldstein, P; Wilson, DM1
Neumann, PZ; Silverberg, M1

Reviews

1 review(s) available for glutamine and Cerebral Pseudosclerosis

ArticleYear
[Wilson disease].
    Orvosi hetilap, 2004, Oct-17, Volume: 145, Issue:42

    Topics: Adenosine Triphosphatases; Cation Transport Proteins; Copper; Copper-Transporting ATPases; Glutamine; Hepatolenticular Degeneration; Histidine; Humans; Mutation

2004

Other Studies

6 other study(ies) available for glutamine and Cerebral Pseudosclerosis

ArticleYear
Mutation analysis of Taiwanese Wilson disease patients.
    Biochemical and biophysical research communications, 2006, Jun-30, Volume: 345, Issue:2

    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.
    Journal of neurology, 2007, Volume: 254, Issue:10

    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.
    Human mutation, 1998, Volume: 12, Issue:6

    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.
    Kidney international, 1973, Volume: 4, Issue:5

    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.
    Advances in experimental medicine and biology, 1974, Volume: 41

    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.
    Nature, 1966, Apr-23, Volume: 210, Issue:5034

    Topics: Animals; Asparagine; Carcinoma, Ehrlich Tumor; Copper; Glutamine; Hepatolenticular Degeneration; Histidine; In Vitro Techniques; Kidney; Liver; Radioisotopes; Rats; Threonine

1966