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P Sabatelli

Showing results (51-60 of 56) with videos related to

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Biochimica Et Biophysica Acta|June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesF Tagliavini, C Pellegrini, F Sardone, et al.
Acta Neuropathologica|January 28, 1998
Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural studyM Villanova, A Malandrini, P Sabatelli, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.
Gene Therapy|November 13, 2009
Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexesA Ferlini, P Sabatelli, M Fabris, et al.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
Neuromuscular Disorders : NMD|August 19, 2003
114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE)F Muntoni, B Valero de Bernabe, R Bittner, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
Biochimica Et Biophysica Acta|June 8, 2014
Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesF Tagliavini, C Pellegrini, F Sardone, et al.
Acta Neuropathologica|January 28, 1998
Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural studyM Villanova, A Malandrini, P Sabatelli, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.
Gene Therapy|November 13, 2009
Dystrophin restoration in skeletal, heart and skin arrector pili smooth muscle of mdx mice by ZM2 NP-AON complexesA Ferlini, P Sabatelli, M Fabris, et al.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
Neuromuscular Disorders : NMD|August 19, 2003
114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE)F Muntoni, B Valero de Bernabe, R Bittner, et al.
Pageof 6