C. Sewry - Concepedia

Author

C. Sewry

Hammersmith Hospital

Also Known As

C A Sewry, C Sewry, C. A. Sewry, C. Sewry, C.A Sewry, C.A. Sewry, CA Sewry

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Hammersmith Hospital Robert Jones and Agnes Hunt Orthopaedic Hospital Imperial College London University of Helsinki University College London

About

C. Sewry is an author at Hammersmith Hospital specializing in medicine, pathology, and neuromuscular pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	13	559
2	Health Sciences	3	3	131
3	Public Health	1	1	36
4	Anatomy	1	1	72
5	Cell Biology	1	1	20

C. Sewry

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan C. Godfrey, Emma Clement, R. Mein, Brain	2007	433
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies Haiyan Zhou, Heinz Jungbluth, C. Sewry, Brain Mendelian DisorderRyr1-related Congenital MyopathiesSkeletal MuscleMalignant Hyperthermia SusceptibilityGenetics	2007	173
Collagen VI involvement in Ullrich syndrome Eugenio Mercuri, Yeliz Yuva, S. Brown, Neurology	2002	102
Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype Eugenio Mercuri, C. Cini, Anna Pichiecchio, Neuromuscular Disorders Imaging AnatomyHealth SciencesMedical ImagingResonanceDegenerative Disease	2003	86
Myopathy with unique ultrastructural feature in marchinesco‐sjögren syndrome C. Sewry, T. Voit, Victor Dubowitz Annals of Neurology PathologyUnique Ultrastructural FeatureAnatomyOrthopaedic SurgeryFiber Size	1988	72
X-inactivation patterns in carriers of X-linked myotubular myopathy Marianne Kristiansen, Gun Peggy Knudsen, Scott Tanner, Neuromuscular Disorders MechanobiologyX-inactivation PatternsHistopathologyPathologyDegenerative Disease	2003	43
Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression. Rossella Tupler, Laura Barbierato, Mirella Memmi, Journal of Medical Genetics GeneticsImmunologyGenetic EpidemiologyPathologyMolecular Genetics	1998	36
The role of Coxsackie B viruses in the pathogenesis of myocarditis, dilated cardiomyopathy and inflammatory muscle disease. L. C. Archard, Peter J. Richardson, E. G. J. Olsen, PubMed Diagnostic VirologyCardiomyopathyBiopsy SpecimenMolecular VirologyMedicine	1987	34
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2. A. Leclerc, Haluk Topaloğlu, Tomé Fm, PubMed Developmental BiologyRadiation Hybrid MappingMendelian DisorderGenetic DisorderMedicine	1995	33
Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy Guglielmina Pepe, Enrico Bertini, Paolo Bonaldo, Mitochondrial MyopathyNeuromusculoskeletal DisorderMusculoskeletal DisordersBethlem MyopathyDegenerative Disease	2002	30

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