302 related articles for article (PubMed ID: 16615965)
1. Rett syndrome in Australia: a review of the epidemiology.
Laurvick CL; de Klerk N; Bower C; Christodoulou J; Ravine D; Ellaway C; Williamson S; Leonard H
J Pediatr; 2006 Mar; 148(3):347-52. PubMed ID: 16615965
[TBL] [Abstract][Full Text] [Related]
2. The prevalence and incidence of Rett syndrome in Australia.
Leonard H; Bower C; English D
Eur Child Adolesc Psychiatry; 1997; 6 Suppl 1():8-10. PubMed ID: 9452912
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. The incidence of Rett syndrome in France.
Bienvenu T; Philippe C; De Roux N; Raynaud M; Bonnefond JP; Pasquier L; Lesca G; Mancini J; Jonveaux P; Moncla A; Feingold J; Chelly J; Villard L
Pediatr Neurol; 2006 May; 34(5):372-5. PubMed ID: 16647997
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Survival with Rett syndrome: comparing Rett's original sample with data from the Australian Rett Syndrome Database.
Freilinger M; Bebbington A; Lanator I; De Klerk N; Dunkler D; Seidl R; Leonard H; Ronen GM
Dev Med Child Neurol; 2010 Oct; 52(10):962-5. PubMed ID: 20573179
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Epidemiology of Rett syndrome: a population-based registry.
Kozinetz CA; Skender ML; MacNaughton N; Almes MJ; Schultz RJ; Percy AK; Glaze DG
Pediatrics; 1993 Feb; 91(2):445-50. PubMed ID: 8424025
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Epidemiology of Rett syndrome in Serbia: prevalence, incidence and survival.
Sarajlija A; Kisic-Tepavcevic D; Nikolic Z; Savic Pavicevic D; Obradovic S; Djuric M; Pekmezovic T
Neuroepidemiology; 2015; 44(1):1-5. PubMed ID: 25571926
[TBL] [Abstract][Full Text] [Related]
13. Is the girl with Rett syndrome normal at birth?
Leonard H; Bower C
Dev Med Child Neurol; 1998 Feb; 40(2):115-21. PubMed ID: 9489500
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Feeding experiences and growth status in a Rett syndrome population.
Oddy WH; Webb KG; Baikie G; Thompson SM; Reilly S; Fyfe SD; Young D; Anderson AM; Leonard H
J Pediatr Gastroenterol Nutr; 2007 Nov; 45(5):582-90. PubMed ID: 18030237
[TBL] [Abstract][Full Text] [Related]
16. Prevalence, clinical investigation, and management of gallbladder disease in Rett syndrome.
Freilinger M; Böhm M; Lanator I; Vergesslich-Rothschild K; Huber WD; Anderson A; Wong K; Baikie G; Ravikumara M; Downs J; Leonard H
Dev Med Child Neurol; 2014 Aug; 56(8):756-62. PubMed ID: 24528171
[TBL] [Abstract][Full Text] [Related]
17. Rett syndrome: North American database.
Percy AK; Lane JB; Childers J; Skinner S; Annese F; Barrish J; Caeg E; Glaze DG; MacLeod P
J Child Neurol; 2007 Dec; 22(12):1338-41. PubMed ID: 18174548
[TBL] [Abstract][Full Text] [Related]
18. An explanation for another familial case of Rett syndrome: maternal germline mosaicism.
Venâncio M; Santos M; Pereira SA; Maciel P; Saraiva JM
Eur J Hum Genet; 2007 Aug; 15(8):902-4. PubMed ID: 17440498
[TBL] [Abstract][Full Text] [Related]
19. Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene.
Bartholdi D; Klein A; Weissert M; Koenig N; Baumer A; Boltshauser E; Schinzel A; Berger W; Mátyás G
Clin Genet; 2006 Apr; 69(4):319-26. PubMed ID: 16630165
[TBL] [Abstract][Full Text] [Related]
20. Sleep problems in Rett syndrome.
Young D; Nagarajan L; de Klerk N; Jacoby P; Ellaway C; Leonard H
Brain Dev; 2007 Nov; 29(10):609-16. PubMed ID: 17531413
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
