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 *

136 related articles for article (PubMed ID: 21626673)

  • 1. Rett syndrome: a study of the face.
    Allanson JE; Hennekam RC; Moog U; Smeets EE
    Am J Med Genet A; 2011 Jul; 155A(7):1563-7. PubMed ID: 21626673
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rett syndrome: significant clinical overlap with Angelman syndrome but not with methylation status.
    Ellaway C; Buchholz T; Smith A; Leonard H; Christodoulou J
    J Child Neurol; 1998 Sep; 13(9):448-51. PubMed ID: 9733292
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Early infantile onset ''congenital'' Rett syndrome variants: Swedish experience through four decades and mutation analysis.
    Rajaei S; Erlandson A; Kyllerman M; Albage M; Lundstrom I; Karrstedt EL; Hagberg B
    J Child Neurol; 2011 Jan; 26(1):65-71. PubMed ID: 21212452
    [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 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]  

  • 6. Molecular Testing of MECP2 Gene in Rett Syndrome Phenotypes in Indian Girls.
    Lallar M; Rai A; Srivastava P; Mandal K; Gupta N; Kabra M; Phadke SR
    Indian Pediatr; 2018 Jun; 55(6):474-477. PubMed ID: 29428920
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Aspects of speech-language abilities are influenced by MECP2 mutation type in girls with Rett syndrome.
    Urbanowicz A; Downs J; Girdler S; Ciccone N; Leonard H
    Am J Med Genet A; 2015 Feb; 167A(2):354-62. PubMed ID: 25428820
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. The diagnosis of autism in a female: could it be Rett syndrome?
    Young DJ; Bebbington A; Anderson A; Ravine D; Ellaway C; Kulkarni A; de Klerk N; Kaufmann WE; Leonard H
    Eur J Pediatr; 2008 Jun; 167(6):661-9. PubMed ID: 17684768
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.
    Zahorakova D; Lelkova P; Gregor V; Magner M; Zeman J; Martasek P
    J Hum Genet; 2016 Jul; 61(7):617-25. PubMed ID: 26984561
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome.
    Caffarelli C; Gonnelli S; Pitinca MDT; Camarri S; Al Refaie A; Hayek J; Nuti R
    BMC Med Genet; 2020 Jan; 21(1):21. PubMed ID: 32005172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Determinants of sleep disturbances in Rett syndrome: Novel findings in relation to genotype.
    Boban S; Wong K; Epstein A; Anderson B; Murphy N; Downs J; Leonard H
    Am J Med Genet A; 2016 Sep; 170(9):2292-300. PubMed ID: 27255190
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Rett syndrome].
    van Urk PR; van den Berg MP; van Royen BJ; Smeets EE; Curfs LM
    Ned Tijdschr Geneeskd; 2014; 158(3):A6686. PubMed ID: 24423488
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MECP2 abnormality phenotypes: clinicopathologic area with broad variability.
    Erlandson A; Hagberg B
    J Child Neurol; 2005 Sep; 20(9):727-32. PubMed ID: 16225826
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genotype-phenotype relationships as prognosticators in Rett syndrome should be handled with care in clinical practice.
    Halbach NS; Smeets EE; van den Braak N; van Roozendaal KE; Blok RM; Schrander-Stumpel CT; Frijns JP; Maaskant MA; Curfs LM
    Am J Med Genet A; 2012 Feb; 158A(2):340-50. PubMed ID: 22190343
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.
    Hammer S; Dorrani N; Dragich J; Kudo S; Schanen C
    Ment Retard Dev Disabil Res Rev; 2002; 8(2):94-8. PubMed ID: 12112734
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Another Rett patient with a typical Angelman EEG.
    Valente KD
    Epilepsia; 2003 Jun; 44(6):873-4; author reply 874. PubMed ID: 12790908
    [No Abstract]   [Full Text] [Related]  

  • 20. Molecular diagnosis of Rett syndrome.
    Huppke P; Gärtner J
    J Child Neurol; 2005 Sep; 20(9):732-6. PubMed ID: 16225827
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.