Items where Author is "Sewry, C"

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Number of items: 7.

Article

Walmsley, G L and Blott, S and Venner, K and Sewry, C and Laport, J and Blondelle, J and Barthelemy, I and Maurer, M and Blanchard-Gutton, N and Pilot-Storck, F and Tiret, L and Piercy, R J (2016) Progressive Structural Defects in Canine Centronuclear Myopathy Indicate a Role for HACD1 in Maintaining Skeletal Muscle Membrane Systems. AMERICAN JOURNAL OF PATHOLOGY, 187 (2). pp. 441-456.

Cirak, S and Arechavala-Gomeza, V and Guglieri, M and Feng, L and Torelli, S and Anthony, K and Abbs, S and Garralda, M E and Wells, DJ and Dickson, G and Wood, M J A and Wilton, S D and Straub, V and Shrewsbury, S and Sewry, C and Morgan, J E and Bushby, K and Muntoni, F (2011) Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-esclation study. Lancet, 378 (9791). pp. 595-605.

Arechavala-Gomeza, V and Kinali, M and Feng, L and Brown, S C and Sewry, C and Morgan, J E and Muntoni, F (2010) Immunohistological intensity measurements as a tool to assess sarcolemma-associated protein expression. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 36 (4). pp. 265-74.

Kinali, M and Arechavala-Gomeza, V and Feng, L and Cirak, S and Hunt, D and Adkin, C and Guglieri, M and Ashton, E and Abbs, S and Nihoyannopoulos, P and Garralda, M E and Rutherford, M and McCulley, C and Popplewell, L and Graham, I R and Dickson, G and Wood, M J and Wells, D J and Wilton, S D and Kole, R and Staub, V and Bushby, K and Sewry, C and Morgan, J E and Muntoni, F (2009) Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-esclation, proof-of-concept study. Lancet Neurology, 8 (10). pp. 918-28.

Mercuri, E and Brown, S C and Nihoyannopoulos, P and Poulton, J and Kinali, M and Richard, P and Piercy, R J and Messina, S and Sewry, C and Burke, M M and McKenna, W and Bonne, G and Muntoni, F (2005) Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene. MUSCLE & NERVE, 31 (5). pp. 602-609.

Conference or Workshop Item

Cirak, S and Arechavala-Gomeza, V and Guglieri, M and Feng, L and Torelli, S and Anthony, K and Garralda, M E and Wells, D J and Dickson, G and Wood, M J A and Wilton, S D and Straub, V and Shrewsbury, S B and Sewry, C and Morgan, J E and Bushby, K and Muntoni, F (2011) EXON SKIPPING AND DYSTROPHIN RESTORATION IN DUCHENNE MUSCULAR DYSTROPHY PATIENTS AFTER SYSTEMIC PHOSPHORODIAMIDATE MORPHOLINO OLIGOMER TREATMENT. In: UNSPECIFIED.

Muntoni, F and Brown, S and Sewry, C and Patel, K (2002) Muscle development genes: their relevance in neuromuscular disorders. In: UNSPECIFIED.

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