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Journal Abstract Search

466 related items for PubMed ID: 18310203

  • 1. Early determinants of fractures in Rett syndrome.
    Downs J, Bebbington A, Woodhead H, Jacoby P, Jian L, Jefferson A, Leonard H.
    Pediatrics; 2008 Mar; 121(3):540-6. PubMed ID: 18310203
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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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  • 6. 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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  • 9. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
    Buoni S, Zannolli R, Felice CD, Saponari S, Strambi M, Dotti MT, Castrucci E, Corbini L, Orsi A, Hayek J.
    Clin Neurophysiol; 2008 Nov 11; 119(11):2455-8. PubMed ID: 18842453
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  • 13. Predictors of seizure onset in Rett syndrome.
    Jian L, Nagarajan L, de Klerk N, Ravine D, Bower C, Anderson A, Williamson S, Christodoulou J, Leonard H.
    J Pediatr; 2006 Oct 11; 149(4):542-7. PubMed ID: 17011329
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  • 14. 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 11; 24(1):49-55. PubMed ID: 19168818
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  • 16. Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndrome.
    Charman T, Neilson TC, Mash V, Archer H, Gardiner MT, Knudsen GP, McDonnell A, Perry J, Whatley SD, Bunyan DJ, Ravn K, Mount RH, Hastings RP, Hulten M, Orstavik KH, Reilly S, Cass H, Clarke A, Kerr AM, Bailey ME.
    Eur J Hum Genet; 2005 Oct 11; 13(10):1121-30. PubMed ID: 16077736
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  • 17. 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 11; 50(Pt 5):386-94. PubMed ID: 16629931
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  • 18. Rett syndrome in Australia: a review of the epidemiology.
    Laurvick CL, de Klerk N, Bower C, Christodoulou J, Ravine D, Ellaway C, Williamson S, Leonard H.
    J Pediatr; 2006 Mar 11; 148(3):347-52. PubMed ID: 16615965
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  • 19. Survival with Rett syndrome: comparing Rett's original sample with data from the Australian Rett Syndrome Database.
    Freilinger M, Bebbington A, Lanator I, De Klerk N, Dunkler D, Seidl R, Leonard H, Ronen GM.
    Dev Med Child Neurol; 2010 Oct 11; 52(10):962-5. PubMed ID: 20573179
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  • 20. X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.
    Xinhua Bao, Shengling Jiang, Fuying Song, Hong Pan, Meirong Li, Wu XR.
    J Child Neurol; 2008 Jan 11; 23(1):22-5. PubMed ID: 18184939
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