Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry-Reference-Cited by-同舟云学术

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Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry

Published:2012-01-16 Issue:3 Volume:83 Page:322-328
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

Lucia Alejandro,Ruiz Jonatan R,Santalla Alfredo,Nogales-Gadea Gisela,Rubio Juan C,García-Consuegra Inés,Cabello Ana,Pérez Margarita,Teijeira Susana,Vieitez Irene,Navarro Carmen,Arenas Joaquín,Martin Miguel A,Andreu Antoni L

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Cited by 110 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. Glycogen myophosphorylase loss causes increased dependence on glucose in iPSC-derived retinal pigment epithelium;Journal of Biological Chemistry;2024-08

2. Glycogen storage disease type V: a still under-recognized condition lacking definitive genotype-phenotype correlates;Pediatric Research;2024-03-21

3. McArdle’s, a Rare Disease That Every Family Doctor Can Manage: A Case Report;Cureus;2023-12-21

4. Diagnostic accuracy and the first genotype–phenotype correlation in glycogen storage disease type V;Pediatric Research;2023-12-05

5. Rhabdomyolysis in McArdle disease caused by scuba diving;BMJ Case Reports;2023-10

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