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Journal Abstract Search

232 related items for PubMed ID: 17562589

  • 1. Rett syndrome.
    Ben Zeev Ghidoni B.
    Child Adolesc Psychiatr Clin N Am; 2007 Jul; 16(3):723-43. PubMed ID: 17562589
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  • 2. MeCP2 dysfunction in Rett syndrome and related disorders.
    Moretti P, Zoghbi HY.
    Curr Opin Genet Dev; 2006 Jun; 16(3):276-81. PubMed ID: 16647848
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  • 4. Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients.
    Santos M, Temudo T, Kay T, Carrilho I, Medeira A, Cabral H, Gomes R, Lourenço MT, Venâncio M, Calado E, Moreira A, Oliveira G, Maciel P.
    J Child Neurol; 2009 Jan; 24(1):49-55. PubMed ID: 19168818
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  • 5. Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders.
    Wong VC, Li SY.
    J Child Neurol; 2007 Dec; 22(12):1397-400. PubMed ID: 18174559
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  • 9. Rett syndrome: of girls and mice--lessons for regression in autism.
    Glaze DG.
    Ment Retard Dev Disabil Res Rev; 2004 Dec; 10(2):154-8. PubMed ID: 15362175
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  • 10. MECP2 mutations in Serbian Rett syndrome patients.
    Djarmati A, Dobricić V, Kecmanović M, Marsh P, Jancić-Stefanović J, Klein C, Djurić M, Romac S.
    Acta Neurol Scand; 2007 Dec; 116(6):413-9. PubMed ID: 17986102
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  • 12. Screening for MECP2 mutations in Spanish patients with an unexplained mental retardation.
    Tejada MI, Peñagarikano O, Rodriguez-Revenga L, Martinez-Bouzas C, García B, Bádenas C, Guitart M, Minguez M, García-Alegría E, Sanz-Parra A, Beristain E, Milá M.
    Clin Genet; 2006 Aug; 70(2):140-4. PubMed ID: 16879196
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  • 13. Another patient with MECP2 mutation without classic Rett syndrome phenotype.
    Milani D, Pantaleoni C, D'Arrigo S, Selicorni A, Riva D.
    Pediatr Neurol; 2005 May; 32(5):355-7. PubMed ID: 15866439
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  • 14. Rett syndrome: from the gene to the disease.
    Matijevic T, Knezevic J, Slavica M, Pavelic J.
    Eur Neurol; 2009 May; 61(1):3-10. PubMed ID: 18948693
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  • 17. The overlapping spectrum of rett and angelman syndromes: a clinical review.
    Jedele KB.
    Semin Pediatr Neurol; 2007 Sep; 14(3):108-17. PubMed ID: 17980307
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  • 20. Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation.
    Parmeggiani A, Tedde MR, Arbizzani A, Posar A, Scaduto MC, Santucci M, Sangiorgi S.
    J Child Neurol; 2009 Jun; 24(6):772-4. PubMed ID: 19189931
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