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Literature DB >> 9452911

Rett syndrome: epidemiology and geographical variability.

B Hagberg¹, G Hagberg.

Abstract

Entities: Disease

Mesh：

Year: 1997 PMID： 9452911

Source DB: PubMed Journal: Eur Child Adolesc Psychiatry ISSN： 1018-8827 Impact factor: 4.785

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Cited

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20 in total

1. Describing the phenotype in Rett syndrome using a population database.

Authors: L Colvin; S Fyfe; S Leonard; T Schiavello; C Ellaway; N De Klerk; J Christodoulou; M Msall; H Leonard
Journal: Arch Dis Child Date: 2003-01 Impact factor: 3.791

Review 2. Rett syndrome: clinical review and genetic update.

Authors: L S Weaving; C J Ellaway; J Gécz; J Christodoulou
Journal: J Med Genet Date: 2005-01 Impact factor: 6.318

3. Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2-/y knockout mice.

Authors: Georg M Stettner; Peter Huppke; Cornelia Brendel; Diethelm W Richter; Jutta Gärtner; Mathias Dutschmann
Journal: J Physiol Date: 2007-01-04 Impact factor: 5.182

4. Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients.

Authors: H L Archer; S D Whatley; J C Evans; D Ravine; P Huppke; A Kerr; D Bunyan; B Kerr; E Sweeney; S J Davies; W Reardon; J Horn; K D MacDermot; R A Smith; A Magee; A Donaldson; Y Crow; G Hermon; Z Miedzybrodzka; D N Cooper; L Lazarou; R Butler; J Sampson; D T Pilz; F Laccone; A J Clarke
Journal: J Med Genet Date: 2005-09-23 Impact factor: 6.318

5. Comprehensive diagnosis of Rett's syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients.

Authors: Y Petel-Galil; B Benteer; Y P Galil; B B Zeev; I Greenbaum; M Vecsler; B Goldman; H Lohi; B A Minassian; E Gak
Journal: J Med Genet Date: 2006-12 Impact factor: 6.318

Rett syndrome: epidemiology and geographical variability.

1. Describing the phenotype in Rett syndrome using a population database.

Review 2. Rett syndrome: clinical review and genetic update.

3. Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2-/y knockout mice.

4. Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients.

5. Comprehensive diagnosis of Rett's syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients.

Review 6. A review of Rett syndrome (RTT) with induced pluripotent stem cells.

7. 7,8-dihydroxyflavone exhibits therapeutic efficacy in a mouse model of Rett syndrome.

8. Prevalence of autism in Iceland.

9. Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder.

10. Methyl-CpG-binding protein 2 polymorphisms and vulnerability to autism.