Items where Author is "Sewry, C A"

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Number of items: 8.

Article

Humphrey, E L and Lacey, E and Le, L T and Feng, L and Sciandra, F and Morris, C R and Hewitt, J E and Holt, I and Brancaccio, A and Barresi, R and Sewry, C A and Brown, S C and Morris, G E (2015) A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patients. Neuromuscular Disorders, 25 (1). pp. 32-42.

Humphrey, E L and Lacey, E and Le, L T and Sciandra, F and Morris, C and Hewitt, J E and Holt, I and Brancaccio, A and Barresi, R and Sewry, C A and Brown, S C and Morris, G E (2014) A NEW MONOCLONAL ANTIBODY AGAINST HUMAN ALPHA-DYSTROGLYCAN HAS POTENTIAL DIAGNOSTIC APPLICATIONS. Neuromuscular Disorders, 24 (9-10). p. 918.

Kim, J and Jimenez-Mallebrera, C and Foley, A R and Fernandez-Fuente, M and Brown, S C and Torelli, S and Feng, L and Sewry, C A and Muntoni, F (2012) Flow cytometry analysis: a quantitative method for collagen VI deficiency screening. Neuromuscular Disorders, 22 (2). pp. 139-48.

Jimenez-Mallebrera, C and Torelli, S and Feng, L and Kim, J and Godfrey, C and Clement, E and Mein, R and Abbs, S and Brown, S C and Campbell, K P and Kröger, S and Talim, B and Topaloglu, H and Quinlivan, R and Roper, H and Childs, A M and Kinali, M and Sewry, C A and Muntoni, F (2009) A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity. Brain Pathology, 19 (4). pp. 596-611.

Brown, S C and Piercy, R J and Muntoni, F and Sewry, C A (2008) Investigating the pathology of Emery-Dreifuss muscular dystrophy. BIOCHEMICAL SOCIETY TRANSACTIONS, 36 (Pt 6). pp. 1335-1338.

Clement, E M and Godfrey, C and Tan, J and Brockington, M A and Torelli, S and Feng, L and Brown, S C and Jimenez-Mallebrera, C and Sewry, C A and Longman, C and Mein, R and Abbs, S and Vajsar, J and Schachter, H and Muntoni, F (2008) Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variant. Archives of Neurology, 65 (1). pp. 137-4.

Muntoni, F and Bonne, G and Goldfarb, L G and Mercuri, E and Piercy, R J and Burke, M and Ben Yaou, R and Richard, P and Recan, D and Shatunov, A and Sewry, C A and Brown, S C (2006) Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins. BRAIN, 129. pp. 1260-1268.

Conference or Workshop Item

Wilson, E and Lacey, E and Holt, I and Sciandra, F and Brancaccio, A and Hewitt, J E and Kobayashi, K and Toda, T and Sewry, C A and Brown, S C and Morris, G E (2013) IMMUNOSTAINING OF THE SARCOLEMMA WITH A NEW MONOCLONAL ANTIBODY AGAINST ALPHA-DYSTROGLYCAN CORE AND ITS RELEVANCE TO DIAGNOSIS. In: UNSPECIFIED.

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