2.9(top 18%)
Impact Factor
3.3(top 18%)
extended IF
106(top 3%)
H-Index
2.7K
authors
3.8K
papers
82.4K
citations
4.1K
citing journals
28K
citing authors

Most Cited Articles of Neuromuscular Disorders

TitleYearCitations
Population frequencies of inherited neuromuscular diseases--a world survey19911K
Survival in Duchenne muscular dystrophy: improvements in life expectancy since 1967 and the impact of home nocturnal ventilation2002640
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research Group1991483
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care2018319
Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse2004263
Long-term benefits of deflazacort treatment for boys with Duchenne muscular dystrophy in their second decade2006249
Melas: an original case and clinical criteria for diagnosis1992249
A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy2014248
A motor function measure for neuromuscular diseases. Construction and validation study2005245
Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethics2018236
The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein2007234
Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle1991221
Diagnostic approach to the congenital muscular dystrophies2014217
Managing Duchenne muscular dystrophy--the additive effect of spinal surgery and home nocturnal ventilation in improving survival2007215
Evolution of the mdx mouse cardiomyopathy: physiological and morphological findings2004215
Reference values of maximum isometric muscle force obtained in 270 children aged 4-16 years by hand-held dynamometry2001201
188th ENMC International Workshop: Inclusion Body Myositis, 2-4 December 2011, Naarden, The Netherlands2013199
The congenital muscular dystrophies in 2004: a century of exciting progress2004191
Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study2019188
Rhabdomyolysis: review of the literature2014188
Centronuclear myopathies: a widening concept2010184
Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy2002182
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA1993181
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia2003179
Approach to the diagnosis of congenital myopathies2014178