Communication about spinal muscular atrophy and genetic risk within families: An Australian pilot study-Reference-Cited by-同舟云学术

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Communication about spinal muscular atrophy and genetic risk within families: An Australian pilot study

Published:2020-05-29 Issue:8 Volume:56 Page:1263-1269
ISSN:1034-4810
Container-title:Journal of Paediatrics and Child Health
language:en
Short-container-title:J Paediatr Child Health

Author:

Pieper Ellen¹^ORCID,Sexton Adrienne¹²,Ryan Monique M³⁴⁵,Forbes Robin³⁴⁶

Affiliation:

1. Department of Paediatrics The University of Melbourne Melbourne Victoria Australia

2. Genomic Medicine and Parkville Familial Cancer Centre The Royal Melbourne Hospital Melbourne Victoria Australia

3. Genetics Education and Health Research Murdoch Children's Research Institute Melbourne Victoria Australia

4. Department of Neurology The Royal Children's Hospital Melbourne Victoria Australia

5. Medicine, Dentistry and Health science The University of Melbourne Melbourne Victoria Australia

6. Victorian Clinical Genetics Services, The Royal Children's Hospital Melbourne Victoria Australia

Publisher

Wiley

Subject

Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jpc.14915

Reference24 articles.

1. Spinal muscular atrophy

2. Population screening and cascade testing for carriers of SMA

3. Pathophysiological Insights Derived by Natural History and Motor Function of Spinal Muscular Atrophy

4. Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care

5. Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethics

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The diagnosis communication process in spinal muscular atrophy: A cross-cutting view of the new challenges facing the therapeutic era;Genetics in Medicine Open;2023

2. Spinal muscular atrophy: health related quality of life and burden to parents;REVISTA CIÊNCIAS EM SAÚDE;2022-12-10

3. The experiences of adolescent siblings of children with rare genetic conditions: “It's made me who I am”;Journal of Genetic Counseling;2022-09-19

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