Pages that link to "Q51344449"
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The following pages link to On the classification, natural history and treatment of the myopathies (Q51344449):
Displaying 50 items.
- β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12 (Q24312878) (← links)
- Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A (Q24314667) (← links)
- Unusual type of benign x-linked muscular dystrophy (Q24519418) (← links)
- Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins (Q24680877) (← links)
- Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate (Q28269213) (← links)
- Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy (Q28298383) (← links)
- Paraffin wax embedded muscle is suitable for the diagnosis of muscular dystrophy (Q28367914) (← links)
- Myopathy in sheep; its relationship to scrapie and to dermatomyositis and muscular dystrophy (Q33189308) (← links)
- Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing. (Q33558590) (← links)
- Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy. (Q33585341) (← links)
- Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene? (Q33863097) (← links)
- Control of breathing in patients with limb girdle dystrophy: a controlled study (Q33605136) (← links)
- Limb-girdle muscular dystrophies: where next after six decades from the first proposal (Review). (Q33608787) (← links)
- A population study of adult onset limb-girdle muscular dystrophy (Q33672061) (← links)
- Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population (Q33685609) (← links)
- Making sense of the limb-girdle muscular dystrophies (Q33701932) (← links)
- Neurogenic muscle involvement in myasthenia gravis: A clinical and histopathological study (Q33756734) (← links)
- Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma Developed in a Patient with Progressive Muscular Dystrophy: A Case Report and Review of the Literature (Q33786885) (← links)
- The muscular dystrophies (Q33792223) (← links)
- Limb-girdle Muscular Dystrophies in India: A Review (Q33795491) (← links)
- What's in a name? Muscular dystrophy revisited (Q33869182) (← links)
- Myotonic dystrophy: hazards of pregnancy and infancy (Q34079057) (← links)
- Scapular instability. The scapulothoracic joint. (Q34089826) (← links)
- The muscle cell (Q34302653) (← links)
- Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association o (Q34386584) (← links)
- X-chromosome mosaicism in females with muscular dystrophy (Q34427092) (← links)
- A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey (Q34436405) (← links)
- From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy (Q34463119) (← links)
- Clinical and genetic aspects of distal myopathies (Q34464423) (← links)
- Myotonic dystrophy and polycystic disease of the kidneys (Q34632558) (← links)
- Distinct pathophysiological mechanisms of cardiomyopathy in hearts lacking dystrophin or the sarcoglycan complex (Q35169510) (← links)
- SOME DISEASES OF MUSCLE (Q35418962) (← links)
- A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families (Q35434715) (← links)
- THE CLINICAL BIOCHEMISTRY OF THE MUSCULAR DYSTROPHIES. (Q35490561) (← links)
- Genetic factors in neurological disease. Clinical aspects (Q35667347) (← links)
- Discrimination of genetic entities in muscular dystrophy (Q35911785) (← links)
- Progressive Muscular Dystrophy. V. The Identification of the Carrier State in the Duchenne Type by Serum Creatine Kinase Determination (Q35912145) (← links)
- Significance of Extensor Plantar Responses in Muscular Dystrophy (Q36060272) (← links)
- Intellectual Impairment in Muscular Dystrophy (Q36060777) (← links)
- Intelligence and the gene for Duchenne muscular dystrophy (Q36062050) (← links)
- New data on the genetics and classification of muscular dystrophies (Q36519722) (← links)
- Lung and respiratory muscle function in limb girdle muscular dystrophy (Q36542681) (← links)
- Myotonia congenita and myotonic dystrophy: descriptive epidemiological investigation in Turin, Italy (1955-1979). (Q36650960) (← links)
- Muscular Dystrophy and Related Disorders (Q36789408) (← links)
- Calpain 3, the "gatekeeper" of proper sarcomere assembly, turnover and maintenance (Q37039715) (← links)
- Sources of error in the biochemical diagnosis of muscular dystrophy (Q37111908) (← links)
- Enzymes of the glycogen cycle and glycolysis in various human neuromuscular disorders (Q37128700) (← links)
- Benign congenital myopathy with myasthenic features (Q37149372) (← links)
- The limp child (Q37149876) (← links)
- Occult left ventricular dysfunction diagnosed by myocardial performance index in patients with limb girdle muscle dystrophy: A case control study (Q37321661) (← links)