364 related articles for article (PubMed ID: 16182501)
1. Abnormal general movements in girls with Rett disorder: the first four months of life.
Einspieler C; Kerr AM; Prechtl HF
Brain Dev; 2005 Nov; 27 Suppl 1():S8-S13. PubMed ID: 16182501
[TBL] [Abstract][Full Text] [Related]
2. Is the early development of girls with Rett disorder really normal?
Einspieler C; Kerr AM; Prechtl HF
Pediatr Res; 2005 May; 57(5 Pt 1):696-700. PubMed ID: 15718369
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Perturbations in the development of infants with Rett disorder and the implications for early diagnosis.
Burford B
Brain Dev; 2005 Nov; 27 Suppl 1():S3-S7. PubMed ID: 16182489
[TBL] [Abstract][Full Text] [Related]
5. Disorganized rhythm and synchrony: early signs of autism and Rett syndrome.
Trevarthen C; Daniel S
Brain Dev; 2005 Nov; 27 Suppl 1():S25-S34. PubMed ID: 16182487
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Developmental disorder in girls due to Rett syndrome].
Pruissen DM; Sinke RJ; Terhal PA; Beemer FA; Peters AC
Ned Tijdschr Geneeskd; 2003 Aug; 147(32):1560-3. PubMed ID: 12942847
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. 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]
10. General movements in infants with autism spectrum disorders.
Phagava H; Muratori F; Einspieler C; Maestro S; Apicella F; Guzzetta A; Prechtl HF; Cioni G
Georgian Med News; 2008 Mar; (156):100-5. PubMed ID: 18403821
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Eating difficulties in girls with Rett syndrome compared with other developmental disabilities.
Isaacs JS; Murdock M; Lane J; Percy AK
J Am Diet Assoc; 2003 Feb; 103(2):224-30. PubMed ID: 12589330
[TBL] [Abstract][Full Text] [Related]
14. Predictive value of the early clinical signs in Rett disorder.
Kerr AM; Prescott RJ
Brain Dev; 2005 Nov; 27 Suppl 1():S20-S24. PubMed ID: 16182500
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [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]
17. Abnormal movements in Rett syndrome are present before the regression period: a case study.
Temudo T; Maciel P; Sequeiros J
Mov Disord; 2007 Nov; 22(15):2284-7. PubMed ID: 17914728
[TBL] [Abstract][Full Text] [Related]
18. Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation.
Parmeggiani A; Tedde MR; Arbizzani A; Posar A; Scaduto MC; Santucci M; Sangiorgi S
J Child Neurol; 2009 Jun; 24(6):772-4. PubMed ID: 19189931
[TBL] [Abstract][Full Text] [Related]
19. Early progressive encephalopathy in boys and MECP2 mutations.
Kankirawatana P; Leonard H; Ellaway C; Scurlock J; Mansour A; Makris CM; Dure LS; Friez M; Lane J; Kiraly-Borri C; Fabian V; Davis M; Jackson J; Christodoulou J; Kaufmann WE; Ravine D; Percy AK
Neurology; 2006 Jul; 67(1):164-6. PubMed ID: 16832102
[TBL] [Abstract][Full Text] [Related]
20. Rett syndrome in Sweden. Neurodevelopment--disability--pathophysiology.
Engerström IW
Acta Paediatr Scand Suppl; 1990; 369():1-60. PubMed ID: 1701067
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
