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Journal Abstract Search

986 related items for PubMed ID: 18174559

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  • 2. 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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  • 3. 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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  • 6. Identification and characterization of novel sequence variations in MECP2 gene in Rett syndrome patients.
    Monnerat LS, Moreira Ados S, Alves MC, Bonvicino CR, Vargas FR.
    Brain Dev; 2010 Nov; 32(10):843-8. PubMed ID: 20031356
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  • 9. Investigating genotype-phenotype relationships in Rett syndrome using an international data set.
    Bebbington A, Anderson A, Ravine D, Fyfe S, Pineda M, de Klerk N, Ben-Zeev B, Yatawara N, Percy A, Kaufmann WE, Leonard H.
    Neurology; 2008 Mar 11; 70(11):868-75. PubMed ID: 18332345
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  • 19. The incidence of Rett syndrome in France.
    Bienvenu T, Philippe C, De Roux N, Raynaud M, Bonnefond JP, Pasquier L, Lesca G, Mancini J, Jonveaux P, Moncla A, Feingold J, Chelly J, Villard L.
    Pediatr Neurol; 2006 May 11; 34(5):372-5. PubMed ID: 16647997
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