216 related articles for article (PubMed ID: 23421866)
1. Using a large international sample to investigate epilepsy in Rett syndrome.
Bao X; Downs J; Wong K; Williams S; Leonard H
Dev Med Child Neurol; 2013 Jun; 55(6):553-8. PubMed ID: 23421866
[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. 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]
4. 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]
5. 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]
6. Epilepsy and the natural history of Rett syndrome.
Glaze DG; Percy AK; Skinner S; Motil KJ; Neul JL; Barrish JO; Lane JB; Geerts SP; Annese F; Graham J; McNair L; Lee HS
Neurology; 2010 Mar; 74(11):909-12. PubMed ID: 20231667
[TBL] [Abstract][Full Text] [Related]
7. Treatment of epilepsy in Rett syndrome.
Huppke P; Köhler K; Brockmann K; Stettner GM; Gärtner J
Eur J Paediatr Neurol; 2007 Jan; 11(1):10-6. PubMed ID: 17178248
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Epilepsy treatment in Rett syndrome.
Krajnc N; Župančič N; Oražem J
J Child Neurol; 2011 Nov; 26(11):1429-33. PubMed ID: 21636780
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Epilepsy in classic Rett syndrome: Course and characteristics in adult age.
Henriksen MW; Breck H; von Tetzchner S; Paus B; Skjeldal OH; Brodtkorb E
Epilepsy Res; 2018 Sep; 145():134-139. PubMed ID: 29966812
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. Early determinants of fractures in Rett syndrome.
Downs J; Bebbington A; Woodhead H; Jacoby P; Jian L; Jefferson A; Leonard H
Pediatrics; 2008 Mar; 121(3):540-6. PubMed ID: 18310203
[TBL] [Abstract][Full Text] [Related]
19. Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome.
Henriksen MW; Breck H; Sejersted Y; Diseth T; von Tetzchner S; Paus B; Skjeldal OH
Brain Dev; 2020 Aug; 42(7):484-495. PubMed ID: 32336485
[TBL] [Abstract][Full Text] [Related]
20. Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients.
Archer HL; Whatley SD; Evans JC; Ravine D; Huppke P; Kerr A; Bunyan D; Kerr B; Sweeney E; Davies SJ; Reardon W; Horn J; MacDermot KD; Smith RA; Magee A; Donaldson A; Crow Y; Hermon G; Miedzybrodzka Z; Cooper DN; Lazarou L; Butler R; Sampson J; Pilz DT; Laccone F; Clarke AJ
J Med Genet; 2006 May; 43(5):451-6. PubMed ID: 16183801
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]