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 *

276 related articles for article (PubMed ID: 23859859)

  • 1. Atypical features in MECP2 P152R-associated Rett syndrome.
    Sheen V; Valencia IM; Torres AR
    Pediatr Neurol; 2013 Aug; 49(2):124-6. PubMed ID: 23859859
    [TBL] [Abstract][Full Text] [Related]  

  • 2. MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders.
    Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H
    Brain Dev; 2012 Jun; 34(6):487-95. PubMed ID: 21982064
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Novel mutations in the C-terminal region of the MECP2 gene in Tunisian Rett syndrome patients.
    Fendri-Kriaa N; Rouissi A; Ghorbel R; Mkaouar-Rebai E; Belguith N; Gouider-Khouja N; Fakhfakh F
    J Child Neurol; 2012 May; 27(5):564-8. PubMed ID: 21940684
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Rett syndrome. Classical form and preserved speech variant as a different phenotype effect of deletion with the same starting point in MeCP2 gene - report of 2 cases].
    Stembalska A; Gil J; Pesz KA
    Med Wieku Rozwoj; 2011; 15(4):445-50. PubMed ID: 22516699
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes.
    Temudo T; Santos M; Ramos E; Dias K; Vieira JP; Moreira A; Calado E; Carrilho I; Oliveira G; Levy A; Barbot C; Fonseca M; Cabral A; Cabral P; Monteiro J; Borges L; Gomes R; Mira G; Pereira SA; Santos M; Fernandes A; Epplen JT; Sequeiros J; Maciel P
    Brain Dev; 2011 Jan; 33(1):69-76. PubMed ID: 20116947
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical profile of a male with Rett syndrome.
    Budden SS; Dorsey HC; Steiner RD
    Brain Dev; 2005 Nov; 27 Suppl 1():S69-S71. PubMed ID: 16182490
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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; 33(7):608-11. PubMed ID: 20970936
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation.
    Corbani S; Chouery E; Fayyad J; Fawaz A; El Tourjuman O; Badens C; Lacoste C; Delague V; Megarbane A
    J Intellect Disabil Res; 2012 Apr; 56(4):415-20. PubMed ID: 21954873
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Epilepsy in Rett syndrome--lessons from the Rett networked database.
    Nissenkorn A; Levy-Drummer RS; Bondi O; Renieri A; Villard L; Mari F; Mencarelli MA; Lo Rizzo C; Meloni I; Pineda M; Armstrong J; Clarke A; Bahi-Buisson N; Mejaski BV; Djuric M; Craiu D; Djukic A; Pini G; Bisgaard AM; Melegh B; Vignoli A; Russo S; Anghelescu C; Veneselli E; Hayek J; Ben-Zeev B
    Epilepsia; 2015 Apr; 56(4):569-76. PubMed ID: 25789914
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
    Kaufmann WE; Tierney E; Rohde CA; Suarez-Pedraza MC; Clarke MA; Salorio CF; Bibat G; Bukelis I; Naram D; Lanham DC; Naidu S
    J Intellect Disabil Res; 2012 Mar; 56(3):233-47. PubMed ID: 21385260
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Identification and characterization of novel sequence variations in MECP2 gene in Rett syndrome patients.
    Monnerat LS; Moreira Ados S; Alves MC; Bonvicino CR; Vargas FR
    Brain Dev; 2010 Nov; 32(10):843-8. PubMed ID: 20031356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel mutation in forkhead box G1 (FOXG1) gene in an Indian patient with Rett syndrome.
    Das DK; Jadhav V; Ghattargi VC; Udani V
    Gene; 2014 Mar; 538(1):109-12. PubMed ID: 24412290
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.