Talim B - Search Results

1

Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-year follow-up.

Merlini L, Gennari M, Malaspina E, Cecconi I, Armaroli A, Gnudi S, Talim B, Ferlini A, Cicognani A, Franzoni E. Merlini L, et al. Among authors: talim b. Muscle Nerve. 2012 Jun;45(6):796-802. doi: 10.1002/mus.23272. Muscle Nerve. 2012. PMID: 22581531

2

Early prednisone treatment in Duchenne muscular dystrophy.

Merlini L, Cicognani A, Malaspina E, Gennari M, Gnudi S, Talim B, Franzoni E. Merlini L, et al. Among authors: talim b. Muscle Nerve. 2003 Feb;27(2):222-7. doi: 10.1002/mus.10319. Muscle Nerve. 2003. PMID: 12548530 Clinical Trial.

3

Vertebral compression in Duchenne muscular dystrophy following deflazacort.

Talim B, Malaguti C, Gnudi S, Politano L, Merlini L. Talim B, et al. Neuromuscul Disord. 2002 Mar;12(3):294-5. doi: 10.1016/s0960-8966(01)00307-8. Neuromuscul Disord. 2002. PMID: 11801403 No abstract available.

4

Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A.

Talim B, Ognibene A, Mattioli E, Richard I, Anderson LV, Merlini L. Talim B, et al. Neurology. 2001 Mar 13;56(5):692-3. doi: 10.1212/wnl.56.5.692-a. Neurology. 2001. PMID: 11245732 No abstract available.

5

Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy.

Giusti B, Lucarini L, Pietroni V, Lucioli S, Bandinelli B, Sabatelli P, Squarzoni S, Petrini S, Gartioux C, Talim B, Roelens F, Merlini L, Topaloglu H, Bertini E, Guicheney P, Pepe G. Giusti B, et al. Among authors: talim b. Ann Neurol. 2005 Sep;58(3):400-10. doi: 10.1002/ana.20586. Ann Neurol. 2005. PMID: 16130093

6

Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromes.

Merlini L, Gooding R, Lochmüller H, Müller-Felber W, Walter MC, Angelicheva D, Talim B, Hallmayer J, Kalaydjieva L. Merlini L, et al. Among authors: talim b. Neurology. 2002 Jan 22;58(2):231-6. doi: 10.1212/wnl.58.2.231. Neurology. 2002. PMID: 11805249

7

Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p (RSMD1).

Mercuri E, Talim B, Moghadaszadeh B, Petit N, Brockington M, Counsell S, Guicheney P, Muntoni F, Merlini L. Mercuri E, et al. Among authors: talim b. Neuromuscul Disord. 2002 Oct;12(7-8):631-8. doi: 10.1016/s0960-8966(02)00023-8. Neuromuscul Disord. 2002. PMID: 12207930

8

Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy.

van der Kooi AJ, Bonne G, Eymard B, Duboc D, Talim B, Van der Valk M, Reiss P, Richard P, Demay L, Merlini L, Schwartz K, Busch HF, de Visser M. van der Kooi AJ, et al. Among authors: talim b. Neurology. 2002 Aug 27;59(4):620-3. doi: 10.1212/wnl.59.4.620. Neurology. 2002. PMID: 12196663

9

Coexistence of two distinct intragenic dystrophin deletions in two maternal cousins with Duchenne Muscular Dystrophy.

Balci-Hayta B, Talim B, Dinçer P, Topaloğlu H. Balci-Hayta B, et al. Among authors: talim b. Neuromuscul Disord. 2013 Jan;23(1):15-8. doi: 10.1016/j.nmd.2012.07.001. Epub 2012 Sep 15. Neuromuscul Disord. 2013. PMID: 22985905

10

82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands.

Bonne G, Capeau J, De Visser M, Duboc D, Merlini L, Morris GE, Muntoni F, Recan D, Sewry C, Squarzoni S, Stewart C, Talim B, van der Kooi A, Worman H, Schwartz K. Bonne G, et al. Among authors: talim b. Neuromuscul Disord. 2002 Feb;12(2):187-94. doi: 10.1016/s0960-8966(01)00243-7. Neuromuscul Disord. 2002. PMID: 11738362 No abstract available.

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