These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

791 related items for PubMed ID: 18948693

  • 21. Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.
    Stearns NA, Schaevitz LR, Bowling H, Nag N, Berger UV, Berger-Sweeney J.
    Neuroscience; 2007 May 25; 146(3):907-21. PubMed ID: 17383101
    [Abstract] [Full Text] [Related]

  • 22. [Rett syndrome: a diagnostic, clinical and molecular update].
    Tejada MI.
    Rev Neurol; 2006 Jan 07; 42 Suppl 1():S55-9. PubMed ID: 16506134
    [Abstract] [Full Text] [Related]

  • 23. 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 07; 24(1):49-55. PubMed ID: 19168818
    [Abstract] [Full Text] [Related]

  • 24. Rett syndrome: a prototypical neurodevelopmental disorder.
    Neul JL, Zoghbi HY.
    Neuroscientist; 2004 Apr 07; 10(2):118-28. PubMed ID: 15070486
    [Abstract] [Full Text] [Related]

  • 25. MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients.
    Moog U, Van Roozendaal K, Smeets E, Tserpelis D, Devriendt K, Buggenhout GV, Frijns JP, Schrander-Stumpel C.
    Brain Dev; 2006 Jun 07; 28(5):305-10. PubMed ID: 16376510
    [Abstract] [Full Text] [Related]

  • 26. 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 07; 22(12):1397-400. PubMed ID: 18174559
    [Abstract] [Full Text] [Related]

  • 27. 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 07; 119(11):2455-8. PubMed ID: 18842453
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Mechanisms of disease: neurogenetics of MeCP2 deficiency.
    Francke U.
    Nat Clin Pract Neurol; 2006 Apr 07; 2(4):212-21. PubMed ID: 16932552
    [Abstract] [Full Text] [Related]

  • 31. Somatic mosaicism for Y120X mutation in the MECP2 gene causes atypical Rett syndrome in a male.
    Pieras JI, Muñoz-Cabello B, Borrego S, Marcos I, Sanchez J, Madruga M, Antiñolo G.
    Brain Dev; 2011 Aug 07; 33(7):608-11. PubMed ID: 20970936
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Identification of cis-regulatory elements for MECP2 expression.
    Liu J, Francke U.
    Hum Mol Genet; 2006 Jun 01; 15(11):1769-82. PubMed ID: 16613900
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome.
    Belichenko NP, Belichenko PV, Li HH, Mobley WC, Francke U.
    J Comp Neurol; 2008 May 01; 508(1):184-95. PubMed ID: 18306326
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. The ups and downs of BDNF in Rett syndrome.
    Sun YE, Wu H.
    Neuron; 2006 Feb 02; 49(3):321-3. PubMed ID: 16446133
    [Abstract] [Full Text] [Related]

  • 38. Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis.
    Alvarez-Saavedra M, Sáez MA, Kang D, Zoghbi HY, Young JI.
    Hum Mol Genet; 2007 Oct 01; 16(19):2315-25. PubMed ID: 17635839
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 40.