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Volumn 156, Issue 1, 2010, Pages

Longevity in Rett Syndrome: Analysis of the North American Database

Author keywords

[No Author keywords available]

Indexed keywords

METHYL CPG BINDING PROTEIN 2;

EID: 72049107802     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2009.07.015     Document Type: Article
Times cited : (72)

References (7)
  • 1
    • 0014011176 scopus 로고
    • Uber ein eigenartiges hirnatrophisches Syndrom bei Hyperammonamie im Kindesalter
    • Rett A. Uber ein eigenartiges hirnatrophisches Syndrom bei Hyperammonamie im Kindesalter. Wiener Med Wochenschrift 116 (1966) 723-726
    • (1966) Wiener Med Wochenschrift , vol.116 , pp. 723-726
    • Rett, A.1
  • 2
    • 0037002625 scopus 로고    scopus 로고
    • An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001
    • Hagberg B., Hanefeld F., Percy A., and Skjeldal O. An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001. Eur J Paediatr Neurol 6 (2002) 293-297
    • (2002) Eur J Paediatr Neurol , vol.6 , pp. 293-297
    • Hagberg, B.1    Hanefeld, F.2    Percy, A.3    Skjeldal, O.4
  • 3
    • 0032830639 scopus 로고    scopus 로고
    • Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    • Amir R., Van den Veyver I., Wan M., Tran C., Francke U., and Zoghbi H. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23 (1999) 185-188
    • (1999) Nat Genet , vol.23 , pp. 185-188
    • Amir, R.1    Van den Veyver, I.2    Wan, M.3    Tran, C.4    Francke, U.5    Zoghbi, H.6
  • 4
    • 27144493864 scopus 로고    scopus 로고
    • Rett syndrome: model of neurodevelopmental disorders
    • Percy A.K., and Lane J.B. Rett syndrome: model of neurodevelopmental disorders. J Child Neurol 20 (2005) 718-721
    • (2005) J Child Neurol , vol.20 , pp. 718-721
    • Percy, A.K.1    Lane, J.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.