Compounds > arginine

arginine and Cerebral Pseudosclerosis

arginine has been researched along with Cerebral Pseudosclerosis in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's3 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hong, MF; Hu, JY; Yang, B1
Hsu, CM; Lee, CC; Tsai, CH; Tsai, FJ; Tsai, Y; Wan, L1
Chang, JG; Jong, YJ; Lee, CC; Lin, SP; Lo, MC; Tsai, CH; Tsai, FJ; Wu, JY; Yang, CF1
Fang, L; Lin, MT; Murong, SX; Wang, N; Wu, ZY; Yu, L1
Goldstein, NP; Wilson, DM1
Goldstein, P; Wilson, DM1

Other Studies

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

ArticleYear
[Study on relationship between Arg778Leu/Gln gene mutation spot in ATP7B and TCM syndrome type in Chinese patients with Wilson disease].
    Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine, 2002, Volume: 22, Issue:4

    Topics: Adenosine Triphosphatases; Adolescent; Arginine; Asian People; Cation Transport Proteins; Child; Copper-Transporting ATPases; Diagnosis, Differential; Exons; Female; Hepatolenticular Degeneration; Humans; Leucine; Male; Medicine, Chinese Traditional; Phenotype; Point Mutation

2002
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
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
Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in chinese patients with Wilson disease.
    Archives of neurology, 2001, Volume: 58, Issue:6

    Topics: Adolescent; Adult; Arginine; Chi-Square Distribution; Child; China; Exons; Female; Genotype; Hepatolenticular Degeneration; Humans; Leucine; Male; Phenotype; Point Mutation; Polymorphism, Genetic

2001
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