Pages that link to "Q37008948"
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The following pages link to EFNS guideline on diagnosis and management of limb girdle muscular dystrophies (Q37008948):
Displaying 28 items.
- Adenosine A(3) receptor stimulation induces protection of skeletal muscle from eccentric exercise-mediated injury (Q28397072) (← links)
- Cardiac involvement in patients with muscular dystrophies: magnetic resonance imaging phenotype and genotypic considerations (Q30498672) (← links)
- Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing. (Q33558590) (← links)
- Cardiopulmonary dysfunction in patients with limb-girdle muscular dystrophy 2A (Q33578177) (← links)
- Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review). (Q33608787) (← links)
- Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies (Q33645910) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis (Q34779932) (← links)
- SNP-array based whole genome homozygosity mapping: a quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients (Q34902464) (← links)
- Distinct pathophysiological mechanisms of cardiomyopathy in hearts lacking dystrophin or the sarcoglycan complex (Q35169510) (← links)
- Phenotypic and immunohistochemical characterization of sarcoglycanopathies. (Q35232488) (← links)
- Molecular Genetic Diagnosis of a Bethlem Myopathy Family with an Autosomal-Dominant COL6A1 Mutation, as Evidenced by Exome Sequencing (Q35291260) (← links)
- An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia (Q35896989) (← links)
- Epidemiological and Molecular Characterization of a Mexican Population Isolate with High Prevalence of Limb-Girdle Muscular Dystrophy Type 2A Due to a Novel Calpain-3 Mutation. (Q36254120) (← links)
- Finding the sweet spot: assembly and glycosylation of the dystrophin-associated glycoprotein complex (Q38240078) (← links)
- Common recessive limb girdle muscular dystrophies differential diagnosis: why and how? (Q38253968) (← links)
- Nocturnal hypoventilation in neuromuscular disease: prevalence according to different definitions issued from the literature. (Q38580541) (← links)
- An overview of muscle diseases presenting in adulthood (Q38604929) (← links)
- Young adults' experiences of living with recessive limb-girdle muscular dystrophy from a salutogenic orientation: an interview study (Q39061103) (← links)
- The italian limb girdle muscular dystrophy registry: Relative frequency, clinical features, and differential diagnosis (Q39762444) (← links)
- The Need for a Consensus on the Locution "Central Nuclei" in Striated Muscle Myopathies. (Q42237226) (← links)
- Atypical manifestation of late onset limb girdle muscular dystrophy presenting with recurrent falling and shoulder dysfunction: a case report (Q43203490) (← links)
- Ancestral founder mutations in calpain-3 in the Indian Agarwal community: historical, clinical, and molecular perspective (Q44289544) (← links)
- Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers. (Q44991770) (← links)
- Association of Limb-Girdle muscular dystrophy with multiple sclerosis: A case report (Q47547615) (← links)
- Serum CK as a guide to the diagnosis of muscle disease. (Q55068787) (← links)
- Displaced Myonuclei in Cancer Cachexia Suggest Altered Innervation (Q89634359) (← links)
- Cross-sectional study into age-related pathology of mouse models for limb girdle muscular dystrophy types 2D and 2F (Q92727048) (← links)