C. Pollitt
Newcastle University(GB)
Publications by Year
Research Areas
Muscle Physiology and Disorders, Calpain Protease Function and Regulation, Genetic Neurodegenerative Diseases, Tuberculosis Research and Epidemiology, RNA Research and Splicing
Most-Cited Works
- → Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene(2000)486 cited
- → Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B(2000)232 cited
- → Calpainopathy—A Survey of Mutations and Polymorphisms(1999)206 cited
- → Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)(2000)164 cited
- → The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach(2001)95 cited
- → Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports(1998)78 cited
- → Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies(2001)51 cited
- → Clinical and molecular genetic spectrum of autosomal dominant Emery‐Dreifuss muscular dystrophy due to mutations of the lamin A/C gene(2000)32 cited
- → Multicore myopathy: respiratory failure and paraspinal muscle contractures are important complications(2000)23 cited
- → Non-tuberculous mycobacterial infection in children with cancer(1998)13 cited