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Journal Abstract Search

196 related items for PubMed ID: 16629931

  • 1. People with MECP2 mutation-positive Rett disorder who converse.
    Kerr AM, Archer HL, Evans JC, Prescott RJ, Gibbon F.
    J Intellect Disabil Res; 2006 May; 50(Pt 5):386-94. PubMed ID: 16629931
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  • 3. Preserved speech variant is allelic of classic Rett syndrome.
    De Bona C, Zappella M, Hayek G, Meloni I, Vitelli F, Bruttini M, Cusano R, Loffredo P, Longo I, Renieri A.
    Eur J Hum Genet; 2000 May; 8(5):325-30. PubMed ID: 10854091
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  • 4. 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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  • 5. 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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  • 7. Predictive value of the early clinical signs in Rett disorder.
    Kerr AM, Prescott RJ.
    Brain Dev; 2005 Nov 11; 27 Suppl 1():S20-S24. PubMed ID: 16182500
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  • 8. 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 11; 116(6):413-9. PubMed ID: 17986102
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  • 9. APOE epsilon4: a potential modulation factor in Rett syndrome.
    Zahorakova D, Jachymova M, Kemlink D, Baxova A, Martasek P.
    J Child Neurol; 2010 May 11; 25(5):546-50. PubMed ID: 20139413
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  • 10. Early determinants of fractures in Rett syndrome.
    Downs J, Bebbington A, Woodhead H, Jacoby P, Jian L, Jefferson A, Leonard H.
    Pediatrics; 2008 Mar 11; 121(3):540-6. PubMed ID: 18310203
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  • 11. Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type.
    Temudo T, Ramos E, Dias K, Barbot C, Vieira JP, Moreira A, Calado E, Carrilho I, Oliveira G, Levy A, Fonseca M, Cabral A, Cabral P, Monteiro JP, Borges L, Gomes R, Santos M, Sequeiros J, Maciel P.
    Mov Disord; 2008 Jul 30; 23(10):1384-90. PubMed ID: 18512755
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  • 12. Classic Rett syndrome in a boy with R133C mutation of MECP2.
    Masuyama T, Matsuo M, Jing JJ, Tabara Y, Kitsuki K, Yamagata H, Kan Y, Miki T, Ishii K, Kondo I.
    Brain Dev; 2005 Sep 30; 27(6):439-42. PubMed ID: 16122633
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  • 13. 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 30; 24(1):49-55. PubMed ID: 19168818
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  • 14. Rett syndrome: North American database.
    Percy AK, Lane JB, Childers J, Skinner S, Annese F, Barrish J, Caeg E, Glaze DG, MacLeod P.
    J Child Neurol; 2007 Dec 30; 22(12):1338-41. PubMed ID: 18174548
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  • 15. Genotype and early development in Rett syndrome: the value of international data.
    Leonard H, Moore H, Carey M, Fyfe S, Hall S, Robertson L, Wu XR, Bao X, Pan H, Christodoulou J, Williamson S, Klerk Nd.
    Brain Dev; 2005 Nov 30; 27 Suppl 1():S59-S68. PubMed ID: 16182492
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  • 17. Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutations.
    Temudo T, Oliveira P, Santos M, Dias K, Vieira J, Moreira A, Calado E, Carrilho I, Oliveira G, Levy A, Barbot C, Fonseca M, Cabral A, Dias A, Cabral P, Monteiro J, Borges L, Gomes R, Barbosa C, Mira G, Eusébio F, Santos M, Sequeiros J, Maciel P.
    Neurology; 2007 Apr 10; 68(15):1183-7. PubMed ID: 17420401
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  • 19. Clinical profile of a male with Rett syndrome.
    Budden SS, Dorsey HC, Steiner RD.
    Brain Dev; 2005 Nov 10; 27 Suppl 1():S69-S71. PubMed ID: 16182490
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