662 related articles for article (PubMed ID: 18842453)
1. 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]
2. 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]
3. 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]
4. Epilepsy in Rett syndrome: clinical and genetic features.
Pintaudi M; Calevo MG; Vignoli A; Parodi E; Aiello F; Baglietto MG; Hayek Y; Buoni S; Renieri A; Russo S; Cogliati F; Giordano L; Canevini M; Veneselli E
Epilepsy Behav; 2010 Nov; 19(3):296-300. PubMed ID: 20728410
[TBL] [Abstract][Full Text] [Related]
5. EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome.
Buoni S; Zannolli R; De Felice C; De Nicola A; Guerri V; Guerra B; Casali S; Pucci B; Corbini L; Mari F; Renieri A; Zappella M; Hayek J
Clin Neurophysiol; 2010 May; 121(5):652-7. PubMed ID: 20153689
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutations.
Temudo T; Oliveira P; Santos M; Dias K; Vieira J; Moreira A; Calado E; Carrilho I; Oliveira G; Levy A; Barbot C; Fonseca M; Cabral A; Dias A; Cabral P; Monteiro J; Borges L; Gomes R; Barbosa C; Mira G; Eusébio F; Santos M; Sequeiros J; Maciel P
Neurology; 2007 Apr; 68(15):1183-7. PubMed ID: 17420401
[TBL] [Abstract][Full Text] [Related]
8. X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.
Xinhua Bao ; Shengling Jiang ; Fuying Song ; Hong Pan ; Meirong Li ; Wu XR
J Child Neurol; 2008 Jan; 23(1):22-5. PubMed ID: 18184939
[TBL] [Abstract][Full Text] [Related]
9. Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms.
Fukuda T; Yamashita Y; Nagamitsu S; Miyamoto K; Jin JJ; Ohmori I; Ohtsuka Y; Kuwajima K; Endo S; Iwai T; Yamagata H; Tabara Y; Miki T; Matsuishi T; Kondo I
Brain Dev; 2005 Apr; 27(3):211-7. PubMed ID: 15737703
[TBL] [Abstract][Full Text] [Related]
10. People with MECP2 mutation-positive Rett disorder who converse.
Kerr AM; Archer HL; Evans JC; Prescott RJ; Gibbon F
J Intellect Disabil Res; 2006 May; 50(Pt 5):386-94. PubMed ID: 16629931
[TBL] [Abstract][Full Text] [Related]
11. Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband.
Hardwick SA; Reuter K; Williamson SL; Vasudevan V; Donald J; Slater K; Bennetts B; Bebbington A; Leonard H; Williams SR; Smith RL; Cloosterman D; Christodoulou J
Eur J Hum Genet; 2007 Dec; 15(12):1218-29. PubMed ID: 17712354
[TBL] [Abstract][Full Text] [Related]
12. 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]
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. 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]
15. 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]
16. Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update.
Philippe C; Villard L; De Roux N; Raynaud M; Bonnefond JP; Pasquier L; Lesca G; Mancini J; Jonveaux P; Moncla A; Chelly J; Bienvenu T
Eur J Med Genet; 2006; 49(1):9-18. PubMed ID: 16473305
[TBL] [Abstract][Full Text] [Related]
17. Large genomic rearrangements in MECP2.
Ravn K; Nielsen JB; Skjeldal OH; Kerr A; Hulten M; Schwartz M
Hum Mutat; 2005 Mar; 25(3):324. PubMed ID: 15712379
[TBL] [Abstract][Full Text] [Related]
18. Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndrome.
Charman T; Neilson TC; Mash V; Archer H; Gardiner MT; Knudsen GP; McDonnell A; Perry J; Whatley SD; Bunyan DJ; Ravn K; Mount RH; Hastings RP; Hulten M; Orstavik KH; Reilly S; Cass H; Clarke A; Kerr AM; Bailey ME
Eur J Hum Genet; 2005 Oct; 13(10):1121-30. PubMed ID: 16077736
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type.
Temudo T; Ramos E; Dias K; Barbot C; Vieira JP; Moreira A; Calado E; Carrilho I; Oliveira G; Levy A; Fonseca M; Cabral A; Cabral P; Monteiro JP; Borges L; Gomes R; Santos M; Sequeiros J; Maciel P
Mov Disord; 2008 Jul; 23(10):1384-90. PubMed ID: 18512755
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
