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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 21624480)

  • 1. Cognitive deficits in Rett syndrome: what we know and what we need to know to treat them.
    Berger-Sweeney J
    Neurobiol Learn Mem; 2011 Nov; 96(4):637-46. PubMed ID: 21624480
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
    Hoffbuhr KC; Moses LM; Jerdonek MA; Naidu S; Hoffman EP
    Ment Retard Dev Disabil Res Rev; 2002; 8(2):99-105. PubMed ID: 12112735
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cognitive and social functions and growth factors in a mouse model of Rett syndrome.
    Schaevitz LR; Moriuchi JM; Nag N; Mellot TJ; Berger-Sweeney J
    Physiol Behav; 2010 Jun; 100(3):255-63. PubMed ID: 20045424
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Correlations between neurophysiological, behavioral, and cognitive function in Rett syndrome.
    Vignoli A; Fabio RA; La Briola F; Giannatiempo S; Antonietti A; Maggiolini S; Canevini MP
    Epilepsy Behav; 2010 Apr; 17(4):489-96. PubMed ID: 20236870
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Rett syndrome (RS) and profound intellectual disability: cognitive and communicative similarities and differences.
    Woodyatt G; Ozanne A
    Eur Child Adolesc Psychiatry; 1997; 6 Suppl 1():31-2. PubMed ID: 9452917
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Spectrum of MECP2 mutations in New Zealand Rett syndrome patients.
    Raizis AM; Saleem M; MacKay R; George PM
    N Z Med J; 2009 Jun; 122(1296):21-8. PubMed ID: 19652677
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Glatiramer acetate (GA, Copolymer-1) an hypothetical treatment option for Rett syndrome.
    Ben-Zeev B; Aharoni R; Nissenkorn A; Arnon R
    Med Hypotheses; 2011 Feb; 76(2):190-3. PubMed ID: 20951500
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 146(3):907-21. PubMed ID: 17383101
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.
    Moretti P; Bouwknecht JA; Teague R; Paylor R; Zoghbi HY
    Hum Mol Genet; 2005 Jan; 14(2):205-20. PubMed ID: 15548546
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial dysfunction as a central actor in intellectual disability-related diseases: an overview of Down syndrome, autism, Fragile X and Rett syndrome.
    Valenti D; de Bari L; De Filippis B; Henrion-Caude A; Vacca RA
    Neurosci Biobehav Rev; 2014 Oct; 46 Pt 2():202-17. PubMed ID: 24548784
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 18. [Rett syndrome: clinical and molecular aspects].
    Záhoráková D; Zeman J; Martásek P
    Cas Lek Cesk; 2007; 146(8):647-52. PubMed ID: 17874730
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rett syndrome: of girls and mice--lessons for regression in autism.
    Glaze DG
    Ment Retard Dev Disabil Res Rev; 2004; 10(2):154-8. PubMed ID: 15362175
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Towards a behavioral phenotype for Rett syndrome.
    Mount RH; Hastings RP; Reilly S; Cass H; Charman T
    Am J Ment Retard; 2003 Jan; 108(1):1-12. PubMed ID: 12475362
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.