Understanding the experiences and needs of individuals with Spinal Muscular Atrophy and their parents: a qualitative study-Reference-Cited by-同舟云学术

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Understanding the experiences and needs of individuals with Spinal Muscular Atrophy and their parents: a qualitative study

Published:2015-10-24 Issue:1 Volume:15 Page:
ISSN:1471-2377
Container-title:BMC Neurology
language:en
Short-container-title:BMC Neurol

Author:

Qian Ying,McGraw Sarah,Henne Jeff,Jarecki Jill,Hobby Kenneth,Yeh Wei-Shi

Funder

Biogen

Cure SMA

Spinal Muscular Atrophy Foundation

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s12883-015-0473-3

Reference40 articles.

1. Lefebvre S, Reboullet S, Clermont O, Phillippe B. Identification and characterization of a spinal muscular atrophy-determining gene. Cell. 1995;80:155–65.

2. Prior TW. Spinal muscular atrophy: a time for screening. Curr Opin Pediatr. 2010;22:696–702. doi: 10.1097/MOP.0b013e32833f3046 .

3. Ogino S, Leonard DGB, Rennert H, Ewens WJ, Wilson RB. Genetic risk assessment in carrier testing for spinal muscular atrophy. Am J Med Genet. 2002;110:301–7. doi: 10.1002/ajmg.10425 .

4. Wang CH, Bonnemann CG, Rutkowski A, et al. Consensus statement on standard of care for congenital muscular dystrophies. J Child Neurol. 2010;25:1559–81. doi: 10.1177/0883073810381924 .

5. Arnold WD, Kassar D, Kissel JT. Spinal muscular atrophy: diagnosis and management in a new therapeutic era. Muscle Nerve. 2015;51(2):157–67. doi: 10.1002/mus.24497 .

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