Pages that link to "Q71624835"
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The following pages link to The prevalence of inherited neuromuscular disease in Northern Ireland (Q71624835):
Displaying 24 items.
- Central core disease (Q21202972) (← links)
- Fixation of winged scapula in facioscapulohumeral muscular dystrophy (Q24681649) (← 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)
- Changes in pain-related beliefs, coping, and catastrophizing predict changes in pain intensity, pain interference, and psychological functioning in individuals with myotonic muscular dystrophy and facioscapulohumeral dystrophy (Q35207403) (← links)
- Prevalence of Duchenne and Becker muscular dystrophies in the United States (Q35770545) (← links)
- The role of the neuromuscular medicine and physiatry specialists in the multidisciplinary management of neuromuscular disease (Q36351131) (← links)
- Multi-minicore Disease (Q36881612) (← links)
- Centronuclear (myotubular) myopathy (Q36948074) (← 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 CNDR: collaborating to translate new therapies for Canadians (Q44309012) (← links)
- Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase (Q48006442) (← links)
- Core Clinical Phenotypes in Myotonic Dystrophies. (Q55189250) (← links)
- Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis (Q60050796) (← links)
- Prevalence of Neuromuscular Diseases in Chinese Children: A Study in Southern China (Q73353464) (← links)
- Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden (Q73455541) (← links)
- Scapulothoracic arthrodesis for patients with facioscapulohumeral muscular dystrophy (Q74639384) (← links)
- Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation (Q78190267) (← 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)
- Emery-Dreifuss muscular dystrophy (Q91997396) (← links)
- A multistage sequencing strategy pinpoints novel candidate alleles for Emery-Dreifuss muscular dystrophy and supports gene misregulation as its pathomechanism (Q92159992) (← links)