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Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report.
Martoni E, Petrini S, Trabanelli C, Sabatelli P, Urciuolo A, Selvatici R, D'Amico A, Falzarano S, Bertini E, Bonaldo P, Ferlini A, Gualandi F. Martoni E, et al. Among authors: sabatelli p. BMC Med Genet. 2013 Jun 5;14:59. doi: 10.1186/1471-2350-14-59. BMC Med Genet. 2013. PMID: 23738969 Free PMC article.
Immunocytochemical detection of emerin within the nuclear matrix.
Squarzoni S, Sabatelli P, Ognibene A, Toniolo D, Cartegni L, Cobianchi F, Petrini S, Merlini L, Maraldi NM. Squarzoni S, et al. Among authors: sabatelli p. Neuromuscul Disord. 1998 Jun;8(5):338-44. doi: 10.1016/s0960-8966(98)00031-5. Neuromuscul Disord. 1998. PMID: 9673989
Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy.
Ognibene A, Sabatelli P, Petrini S, Squarzoni S, Riccio M, Santi S, Villanova M, Palmeri S, Merlini L, Maraldi NM. Ognibene A, et al. Among authors: sabatelli p. Muscle Nerve. 1999 Jul;22(7):864-9. doi: 10.1002/(sici)1097-4598(199907)22:7<864::aid-mus8>3.0.co;2-g. Muscle Nerve. 1999. PMID: 10398203
Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC international workshop, 23-24 November 2001, Naarden, The Netherlands.
Pepe G, Bertini E, Bonaldo P, Bushby K, Giusti B, de Visser M, Guicheney P, Lattanzi G, Merlini L, Muntoni F, Nishino I, Nonaka I, Yaou RB, Sabatelli P, Sewry C, Topaloglu H, van der Kooi A. Pepe G, et al. Among authors: sabatelli p. Neuromuscul Disord. 2002 Dec;12(10):984-93. doi: 10.1016/s0960-8966(02)00139-6. Neuromuscul Disord. 2002. PMID: 12467756 No abstract available.
148 results