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.
228 related articles for article (PubMed ID: 24423488)
1. [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]
2. 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]
3. [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]
4. 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]
5. Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets. Jordan C; Li HH; Kwan HC; Francke U BMC Med Genet; 2007 Jun; 8():36. PubMed ID: 17584923 [TBL] [Abstract][Full Text] [Related]
6. Rett syndrome: clinical and molecular characterization of two Brazilian patients. Stachon A; Assumpção FB; Raskin S Arq Neuropsiquiatr; 2007 Mar; 65(1):36-40. PubMed ID: 17420824 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Trisomy 21 and Rett syndrome: a double burden. Leonard H; Weaving L; Eastaugh P; Smith L; Delatycki M; Witt Engerström I; Christodoulou J J Paediatr Child Health; 2004 Jul; 40(7):406-9. PubMed ID: 15228575 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. [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]
14. [Clinical features and MECP2 mutations in children with Rett syndrome]. Zhao PW; He XL; Lin J; Wu GF; Yue X; Bi B; Hu JS; Liu ZS Zhongguo Dang Dai Er Ke Za Zhi; 2014 Apr; 16(4):393-6. PubMed ID: 24750837 [TBL] [Abstract][Full Text] [Related]
15. MECP2 mutations in Malaysian Rett syndrome patients. Fong CB; Thong MK; Sam CK; Mohamed Noor MN; Ariffin R Singapore Med J; 2009 May; 50(5):529-33. PubMed ID: 19495527 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. 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]
18. [Application of long range polymerase chain reaction and DNA direct sequencing in diagnosis of Rett syndrome]. Li MR; Pan H; Bao XH; Cao GN; Wu XR Zhonghua Er Ke Za Zhi; 2007 Aug; 45(8):579-82. PubMed ID: 18021529 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]