سندرم شبه هانتینگتون (Persian Wikipedia)

Analysis of information sources in references of the Wikipedia article "سندرم شبه هانتینگتون" in Persian language version.

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doi.org

  • Wild, Edward J.; Tabrizi, Sarah J. (December 2007). "Huntington's disease phenocopy syndromes". Current Opinion in Neurology. 20 (6): 681–687. doi:10.1097/WCO.0b013e3282f12074. ISSN 1350-7540. PMID 17992089.
  • Hensman Moss, Davina J.; Poulter, Mark; Beck, Jon; Hehir, Jason; Polke, James M.; Campbell, Tracy; Adamson, Garry; Mudanohwo, Ese; McColgan, Peter (2014-01-28). "C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies". Neurology. 82 (4): 292–299. doi:10.1212/WNL.0000000000000061. ISSN 1526-632X. PMC 3929197. PMID 24363131.
  • Cooper-Knock, Johnathan; Shaw, Pamela J.; Kirby, Janine (March 2014). "The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype". Acta Neuropathologica. 127 (3): 333–345. doi:10.1007/s00401-014-1251-9. ISSN 1432-0533. PMC 3925297. PMID 24493408.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Wild, Edward J.; Tabrizi, Sarah J. (December 2007). "Huntington's disease phenocopy syndromes". Current Opinion in Neurology. 20 (6): 681–687. doi:10.1097/WCO.0b013e3282f12074. ISSN 1350-7540. PMID 17992089.
  • Hensman Moss, Davina J.; Poulter, Mark; Beck, Jon; Hehir, Jason; Polke, James M.; Campbell, Tracy; Adamson, Garry; Mudanohwo, Ese; McColgan, Peter (2014-01-28). "C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies". Neurology. 82 (4): 292–299. doi:10.1212/WNL.0000000000000061. ISSN 1526-632X. PMC 3929197. PMID 24363131.
  • Cooper-Knock, Johnathan; Shaw, Pamela J.; Kirby, Janine (March 2014). "The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype". Acta Neuropathologica. 127 (3): 333–345. doi:10.1007/s00401-014-1251-9. ISSN 1432-0533. PMC 3925297. PMID 24493408.

ncbi.nlm.nih.gov

worldcat.org

  • Wild, Edward J.; Tabrizi, Sarah J. (December 2007). "Huntington's disease phenocopy syndromes". Current Opinion in Neurology. 20 (6): 681–687. doi:10.1097/WCO.0b013e3282f12074. ISSN 1350-7540. PMID 17992089.
  • Hensman Moss, Davina J.; Poulter, Mark; Beck, Jon; Hehir, Jason; Polke, James M.; Campbell, Tracy; Adamson, Garry; Mudanohwo, Ese; McColgan, Peter (2014-01-28). "C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies". Neurology. 82 (4): 292–299. doi:10.1212/WNL.0000000000000061. ISSN 1526-632X. PMC 3929197. PMID 24363131.
  • Cooper-Knock, Johnathan; Shaw, Pamela J.; Kirby, Janine (March 2014). "The widening spectrum of C9ORF72-related disease; genotype/phenotype correlations and potential modifiers of clinical phenotype". Acta Neuropathologica. 127 (3): 333–345. doi:10.1007/s00401-014-1251-9. ISSN 1432-0533. PMC 3925297. PMID 24493408.