Polysomnographic findings in Rett syndrome-Reference-Cited by-同舟云学术

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Polysomnographic findings in Rett syndrome

Published:2019-01 Issue:1 Volume:23 Page:214-221
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Amaddeo Alessandro,De Sanctis Livio,Arroyo Jorge Olmo,Khirani Sonia,Bahi-Buisson Nadia,Fauroux Brigitte

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference47 articles.

1. Rett syndrome in Australia: a review of the epidemiology;Laurvick;J Pediatr,2006

2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999

3. RettBASE: Rett syndrome database update: Krishnaraj et al;Krishnaraj;Hum Mutat,2017

4. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases;Hagberg;Ann Neurol,1983

5. The clinical predictors that facilitate a clinician's decision to order genetic testing for Rett syndrome;Knight;Pediatr Neurol,2016

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2. The Efficacy of Noninvasive Ventilation in Patients Affected by Rett Syndrome With Hypoventilation;Pediatric Neurology;2024-09

3. Characterisation of sleep apneas and respiratory circuitry in mice lacking CDKL5;Journal of Sleep Research;2024-07-24

4. A clinical-translational review of sleep problems in neurodevelopmental disabilities;Journal of Neurodevelopmental Disorders;2024-07-20

5. Rett syndrome: a review of clinical manifestations and therapeutic approaches;Frontiers in Sleep;2024-05-21

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