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178 results on '"Sewry C"'

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1. CONGENITAL MYOPATHIES – NEMALINE MYOPATHIES

2. CONGENITAL MUSCULAR DYSTROPHIES

3. Results of an open label feasibility study of sodium valproate in people with McArdle disease

5. P.254The clinical and genetic spectrum of a UK cohort of paediatric and adult patients with MYH7 gene related skeletal myopathies

6. P.166Retrospective longitudinal study of patients with NEB-related nemaline myopathy in the United Kingdom

8. P.241Congenital titinopathy as a cause of severe to profound congenital weakness and early death

13. P.236Myofibres with subsarcolemmal rims and/or central aggregates of mitochondria (SRCAM) are prevalent in congenital titinopathies

14. P.108Recessive MYH7-related myopathy in two families

15. P.387A novel in situ hybridisation (ISH) assay mapping the in-frame pseudoexon 11 (pE11) expression in cultured dermal fibroblasts (CDF) and skeletal muscle in patients with severe collagen VI disease due to a deep intronic mutation in COL6A1

17. P.143Correlation between dystrophin espression and clinical phenotype using high-throughput digital immunoanalysis in Duchenne and Becker muscular dystrophy patients

18. P.145Optimisation of a high–throughput digital script for multiplexed immunofluorescent analysis of sarcolemmal dystrophin - associated protein complex (DPC) and myofibre regeneration in entire transverse sections of muscle biopsies in Duchenne muscular dystrophy

19. The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

20. CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES

21. NEXT GENERATION SEQUENCING AND EXPERIMENTAL MYOLOGY

22. MITOCHONDRIAL DISEASES (Posters)

23. CONGENITAL MYOPATHIES: GENERAL AND RYR1

27. Dystrophin quantification in Duchenne and Becker muscular dystrophy: correlation between dystrophin protein and clinical phenotype

28. Recessive mutations in novel gene MST01 cause early onset neuromuscular condition

29. Optimization and implementation of best practices for collection and preparation of muscle biopsies for analysis during clinical trials of neuromuscular disease therapeutics

38. Mobility shift of beta-dystroglycan combined with reduced laminin alpha2 expression is a marker of genetic defects in the GMPPB gene

42. Eight novel UK families further expand current knowledge on GMPPB-gene related dystroglycanopathies

44. Congenital muscular dystrophies in the UK population: Update of clinical and molecular spectrum of patients diagnosed over a 12-year period

46. Sodium valproate for McArdle disease (glycogen storage disease type V – GSDV)

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