glycine has been researched along with Cerebral Pseudosclerosis in 8 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Mutation screening in Wilson disease has led to the detection of at least 89 disease-specific mutations." | 1.30 | Mutation analysis of Wilson disease in Taiwan and description of six new mutations. ( Chang, JG; Jong, YJ; Lee, CC; Lin, SP; Lo, MC; Tsai, CH; Tsai, FJ; Wu, JY; Yang, CF, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (50.00) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ray, K | 1 |
| Gupta, A | 1 |
| MILNE, MD | 1 |
| Cater, MA | 1 |
| La Fontaine, S | 1 |
| Mercer, JF | 1 |
| Tsai, CH | 1 |
| Tsai, FJ | 1 |
| Wu, JY | 1 |
| Chang, JG | 1 |
| Lee, CC | 1 |
| Lin, SP | 1 |
| Yang, CF | 1 |
| Jong, YJ | 1 |
| Lo, MC | 1 |
| Malhi, H | 1 |
| Bhargava, KK | 1 |
| Afriyie, MO | 1 |
| Volenberg, I | 1 |
| Schilsky, ML | 1 |
| Palestro, CJ | 1 |
| Gupta, S | 1 |
| Greco, GM | 1 |
| Magli, A | 1 |
| Omenn, GS | 1 |
| Cowen, AE | 1 |
| Korman, MG | 1 |
| Hofmann, AF | 1 |
| Goldstein, NP | 1 |
3 reviews available for glycine and Cerebral Pseudosclerosis
| Article | Year |
|---|---|
[RENAL TUBULAR DISEASES, WITH SPECIAL REFERENCE TO AMINOACIDURIA].
Topics: Cystinosis; Cystinuria; Galactosemias; Genetics, Medical; Glycine; Hepatolenticular Degeneration; Hu | 1964 |
[Eye manifestations of amino acid disorders].
Topics: Alanine; Albinism; Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Child; Cystinosis; Cystinuria | 1978 |
Inborn errors of metabolism: clues to understanding human behavioral disorders.
Topics: Adrenal Hyperplasia, Congenital; Brain; Galactosemias; Glycine; Hepatolenticular Degeneration; Heter | 1976 |
5 other studies available for glycine and Cerebral Pseudosclerosis
| Article | Year |
|---|---|
Gene symbol: ATP7B. Disease: Wilson disease.
Topics: Adenosine Triphosphatases; Amino Acid Substitution; Animals; Cation Transport Proteins; Codon; Conse | 2008 |
Copper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B).
Topics: Adenosine Triphosphatases; Amino Acid Sequence; Binding Sites; Cation Transport Proteins; Copper; Co | 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 | 1998 |
99mTc-mebrofenin scintigraphy for evaluating liver disease in a rat model of Wilson's disease.
Topics: Alanine Transaminase; Aniline Compounds; Animals; Bilirubin; Ceruloplasmin; Copper; Glycine; Hepatol | 2002 |
Biliary bile acid composition in Wilson's disease.
Topics: Adolescent; Adult; Bile; Bile Acids and Salts; Carbon Radioisotopes; Cholic Acids; Chromatography, G | 1975 |