14 results on '"Sewry, C"'
Search Results
2. 096 Inclusion body myositis: a diagnostic challenge
3. Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease
4. McArdle disease: a clinical review
5. Multiple mitochondrial DNA deletions in monozygotic twins with OPMD
6. Paraffin wax embedded muscle is suitable for the diagnosis of muscular dystrophy
7. Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression.
8. Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).
9. Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.
10. Deletions in the 5' region of dystrophin and resulting phenotypes.
11. Rhabdomyolysis after intramuscular iron-dextran in malabsorption.
12. Increased calcium in dystrophic muscle.
13. Diagnostic needle muscle biopsy. A practical and reliable alternative to open biopsy.
14. Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of disease.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.