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 *

167 related articles for article (PubMed ID: 31838863)

  • 1. [
    Düh A; Till Á; Bánfai Z; Hegyi M; Melegh B; Hadzsiev K
    Orv Hetil; 2019 Dec; 160(51):2036-2039. PubMed ID: 31838863
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A rare MeCP2_e1 mutation first described in a male patient with severe neonatal encephalopathy.
    Soffer OD; Sidlow R
    Am J Med Genet A; 2016 Jul; 170(7):1881-3. PubMed ID: 27090848
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.
    Jentarra GM; Olfers SL; Rice SG; Srivastava N; Homanics GE; Blue M; Naidu S; Narayanan V
    BMC Neurosci; 2010 Feb; 11():19. PubMed ID: 20163734
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expanding phenotype of p.Ala140Val mutation in MECP2 in a 4 generation family with X-linked intellectual disability and spasticity.
    Lambert S; Maystadt I; Boulanger S; Vrielynck P; Destrée A; Lederer D; Moortgat S
    Eur J Med Genet; 2016 Oct; 59(10):522-5. PubMed ID: 27465203
    [TBL] [Abstract][Full Text] [Related]  

  • 5. First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation.
    Ghorbel R; Ghorbel R; Rouissi A; Fendri-Kriaa N; Ben Salah G; Belguith N; Ammar-Keskes L; Gouider-Khouja N; Fakhfakh F
    Biochem Biophys Res Commun; 2018 Feb; 497(1):93-101. PubMed ID: 29421650
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test results.
    Gerald B; Ramsey K; Belnap N; Szelinger S; Siniard AL; Balak C; Russell M; Richholt R; De Both M; Claasen AM; Schrauwen I; Huentelman MJ; Craig DW; Rangasamy S; Narayanan V
    Semin Pediatr Neurol; 2018 Jul; 26():28-32. PubMed ID: 29961512
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An insertion mutation of the MECP2 gene in severe neonatal encephalopathy and ocular and oropharyngeal dyskinesia: a case report.
    Liang J; Xin C; Xin M; Wang G; Wu X
    BMC Med Genomics; 2023 Aug; 16(1):181. PubMed ID: 37537631
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).
    Moog U; Smeets EE; van Roozendaal KE; Schoenmakers S; Herbergs J; Schoonbrood-Lenssen AM; Schrander-Stumpel CT
    Eur J Paediatr Neurol; 2003; 7(1):5-12. PubMed ID: 12615169
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Advances in understanding of Rett syndrome and MECP2 duplication syndrome: prospects for future therapies.
    Sandweiss AJ; Brandt VL; Zoghbi HY
    Lancet Neurol; 2020 Aug; 19(8):689-698. PubMed ID: 32702338
    [TBL] [Abstract][Full Text] [Related]  

  • 14.
    Pascual-Alonso A; Martínez-Monseny AF; Xiol C; Armstrong J
    Int J Mol Sci; 2021 Sep; 22(17):. PubMed ID: 34502518
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Homozygous c.1160C>T (P38L) in the MECP2 gene in a female Rett syndrome patient.
    Bhanushali AA; Mandsaurwala A; Das BR
    J Clin Neurosci; 2016 Mar; 25():127-9. PubMed ID: 26755454
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations.
    Shahbazian MD; Zoghbi HY
    Curr Opin Neurol; 2001 Apr; 14(2):171-6. PubMed ID: 11262731
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MECP2 and beyond: phenotype-genotype correlations in Rett syndrome.
    Christodoulou J; Weaving LS
    J Child Neurol; 2003 Oct; 18(10):669-74. PubMed ID: 14649547
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.