Pages that link to "Q73455541"
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The following pages link to Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden (Q73455541):
Displaying 31 items.
- Central core disease (Q21202972) (← links)
- Congenital muscular dystrophies: a brief review (Q28255519) (← links)
- Prevalence of congenital muscular dystrophy in Italy: a population study (Q28256516) (← links)
- Neb: a zebrafish model of nemaline myopathy due to nebulin mutation (Q30513866) (← links)
- Diagnostic approach to the congenital muscular dystrophies (Q30767612) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - a literature review. (Q33869164) (← links)
- Idiopathic inflammatory myopathies: epidemiology, classification, and diagnostic criteria (Q35037912) (← links)
- Congenital myopathies: Natural history of a large pediatric cohort (Q35106557) (← links)
- Evidence-based guideline summary: evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Asso (Q35304917) (← links)
- Prevalence of Duchenne and Becker muscular dystrophies in the United States (Q35770545) (← links)
- Laminin-211 in skeletal muscle function (Q36531788) (← links)
- The muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): surveillance methodology (Q36621524) (← links)
- Multi-minicore Disease (Q36881612) (← links)
- Centronuclear (myotubular) myopathy (Q36948074) (← links)
- Psychiatric and cognitive phenotype in children and adolescents with myotonic dystrophy (Q37526565) (← links)
- Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark (Q37716090) (← links)
- A Systematic Review and Meta-analysis on the Epidemiology of the Muscular Dystrophies (Q38703274) (← links)
- The Duchenne muscular dystrophy population in Denmark, 1977-2001: prevalence, incidence and survival in relation to the introduction of ventilator use. (Q47316352) (← links)
- A descriptive epidemiological study of Duchenne muscular dystrophy in childhood in Estonia (Q47603674) (← links)
- [Diagnosis and natural history of Duchenne muscular dystrophy]. (Q55032040) (← links)
- Prevalence of muscular dystrophy in patients with muscular disorders in Tehran, Iran. (Q55512151) (← links)
- Hitherto unknown detailed muscle anatomy in an 8-week-old embryo. (Q55556919) (← links)
- Ryanodine Receptor 1-Related Myopathies: Diagnostic and Therapeutic Approaches (Q58600210) (← links)
- Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis (Q60050796) (← links)
- A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report (Q60908834) (← links)
- Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report (Q64065905) (← links)
- Prevalence of Neuromuscular Diseases in Chinese Children: A Study in Southern China (Q73353464) (← links)
- The muscular dystrophies (Q77731754) (← links)
- Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases (Q78705444) (← links)
- Epidemiological study and genetic characterization of inherited muscle diseases in a northern Spanish region (Q91612244) (← links)