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 *

236 related articles for article (PubMed ID: 17562589)

  • 1. Rett syndrome.
    Ben Zeev Ghidoni B
    Child Adolesc Psychiatr Clin N Am; 2007 Jul; 16(3):723-43. PubMed ID: 17562589
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. [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]  

  • 7. [Rett's syndrome. Clinical features and advances in genetics].
    Temudo T; Maciel P
    Rev Neurol; 2002 Feb; 34 Suppl 1():S54-8. PubMed ID: 12447790
    [TBL] [Abstract][Full Text] [Related]  

  • 8. MECP2 analysis in mentally retarded patients: implications for routine DNA diagnostics.
    Kleefstra T; Yntema HG; Nillesen WM; Oudakker AR; Mullaart RA; Geerdink N; van Bokhoven H; de Vries BB; Sistermans EA; Hamel BC
    Eur J Hum Genet; 2004 Jan; 12(1):24-8. PubMed ID: 14560307
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. [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]  

  • 12. Screening for MECP2 mutations in Spanish patients with an unexplained mental retardation.
    Tejada MI; Peñagarikano O; Rodriguez-Revenga L; Martinez-Bouzas C; García B; Bádenas C; Guitart M; Minguez M; García-Alegría E; Sanz-Parra A; Beristain E; Milá M
    Clin Genet; 2006 Aug; 70(2):140-4. PubMed ID: 16879196
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Another patient with MECP2 mutation without classic Rett syndrome phenotype.
    Milani D; Pantaleoni C; D'Arrigo S; Selicorni A; Riva D
    Pediatr Neurol; 2005 May; 32(5):355-7. PubMed ID: 15866439
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rett syndrome: from the gene to the disease.
    Matijevic T; Knezevic J; Slavica M; Pavelic J
    Eur Neurol; 2009; 61(1):3-10. PubMed ID: 18948693
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 13(10):1121-30. PubMed ID: 16077736
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Systemic oxidative stress in classic Rett syndrome.
    De Felice C; Ciccoli L; Leoncini S; Signorini C; Rossi M; Vannuccini L; Guazzi G; Latini G; Comporti M; Valacchi G; Hayek J
    Free Radic Biol Med; 2009 Aug; 47(4):440-8. PubMed ID: 19464363
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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; 70(11):868-75. PubMed ID: 18332345
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MeCP2 involvement in the regulation of neuronal alpha-tubulin production.
    Abuhatzira L; Shemer R; Razin A
    Hum Mol Genet; 2009 Apr; 18(8):1415-23. PubMed ID: 19174478
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation.
    Parmeggiani A; Tedde MR; Arbizzani A; Posar A; Scaduto MC; Santucci M; Sangiorgi S
    J Child Neurol; 2009 Jun; 24(6):772-4. PubMed ID: 19189931
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.