Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancy-Reference-Cited by-同舟云学术

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Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancy

Published:2022-07 Issue:7 Volume:6 Page:495-508
ISSN:2352-4642
Container-title:The Lancet Child & Adolescent Health
language:en
Short-container-title:The Lancet Child & Adolescent Health

Author:

Silksmith Bryony,Munot Pinki,Starling Luke,Pujar Suresh,Matthews Emma

Funder

National Institute for Health and Care Research

Medical Research Council

Publisher

Elsevier BV

Subject

Developmental and Educational Psychology,Pediatrics, Perinatology and Child Health

Reference75 articles.

1. Brief resolved unexplained events (formerly apparent life-threatening events) and evaluation of lower-risk infants;Tieder;Pediatrics,2016

2. Congenital central hypoventilation syndrome: diagnosis and management;Maloney;Expert Rev Respir Med,2018

3. Congenital central hypoventilation syndrome associated with Hirschsprung's Disease: case report and literature review;Sandoval;Rev Paul Pediatr,2016

4. Life-threatening cardiac arrhythmias in congenital central hypoventilation syndrome;Laifman;Eur J Pediatr,2020

5. Congenital heart disease and aortic arch variants associated with mutation in PHOX2B;Lombardo;Genet Med,2018

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1. Care Recommendations for the Investigation and Management of Children With Skeletal Muscle Channelopathies;Pediatric Neurology;2023-08

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