919 related articles for article (PubMed ID: 21385260)
1. 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]
2. 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]
3. Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.
Moretti P; Bouwknecht JA; Teague R; Paylor R; Zoghbi HY
Hum Mol Genet; 2005 Jan; 14(2):205-20. PubMed ID: 15548546
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Epilepsy in Rett syndrome---the experience of a National Rett Center.
Nissenkorn A; Gak E; Vecsler M; Reznik H; Menascu S; Ben Zeev B
Epilepsia; 2010 Jul; 51(7):1252-8. PubMed ID: 20491871
[TBL] [Abstract][Full Text] [Related]
6. Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome.
Buoni S; Zannolli R; Felice CD; Saponari S; Strambi M; Dotti MT; Castrucci E; Corbini L; Orsi A; Hayek J
Clin Neurophysiol; 2008 Nov; 119(11):2455-8. PubMed ID: 18842453
[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. Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
Cuddapah VA; Pillai RB; Shekar KV; Lane JB; Motil KJ; Skinner SA; Tarquinio DC; Glaze DG; McGwin G; Kaufmann WE; Percy AK; Neul JL; Olsen ML
J Med Genet; 2014 Mar; 51(3):152-8. PubMed ID: 24399845
[TBL] [Abstract][Full Text] [Related]
9. Genotype-phenotype relationship among Egyptian children with Rett syndrome.
Mansour L; El Sobky E; Mohamed SM; Marzouk H; Tarek LA
J Egypt Public Health Assoc; 2015 Sep; 90(3):133-7. PubMed ID: 26544843
[TBL] [Abstract][Full Text] [Related]
10. Genotype and early development in Rett syndrome: the value of international data.
Leonard H; Moore H; Carey M; Fyfe S; Hall S; Robertson L; Wu XR; Bao X; Pan H; Christodoulou J; Williamson S; Klerk Nd
Brain Dev; 2005 Nov; 27 Suppl 1():S59-S68. PubMed ID: 16182492
[TBL] [Abstract][Full Text] [Related]
11. The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome.
Nectoux J; Bahi-Buisson N; Guellec I; Coste J; De Roux N; Rosas H; Tardieu M; Chelly J; Bienvenu T
Neurology; 2008 May; 70(22 Pt 2):2145-51. PubMed ID: 18434641
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Improvement in motor and exploratory behavior in Rett syndrome mice with restricted ketogenic and standard diets.
Mantis JG; Fritz CL; Marsh J; Heinrichs SC; Seyfried TN
Epilepsy Behav; 2009 Jun; 15(2):133-41. PubMed ID: 19249385
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations.
Hadzsiev K; Polgar N; Bene J; Komlosi K; Karteszi J; Hollody K; Kosztolanyi G; Renieri A; Melegh B
J Hum Genet; 2011 Mar; 56(3):183-7. PubMed ID: 21160487
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.
Schaevitz LR; Gómez NB; Zhen DP; Berger-Sweeney JE
Genes Brain Behav; 2013 Oct; 12(7):732-40. PubMed ID: 24283265
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]