Meola G - Search Results

1

SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype.

Bugiardini E, Rivolta I, Binda A, Soriano Caminero A, Cirillo F, Cinti A, Giovannoni R, Botta A, Cardani R, Wicklund MP, Meola G. Bugiardini E, et al. Among authors: meola g. Neuromuscul Disord. 2015 Apr;25(4):301-7. doi: 10.1016/j.nmd.2015.01.006. Epub 2015 Jan 21. Neuromuscul Disord. 2015. PMID: 25660391

2

A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies.

Meola G, Sansone V, Radice S, Skradski S, Ptacek L. Meola G, et al. Neuromuscul Disord. 1996 May;6(3):143-50. doi: 10.1016/0960-8966(95)00040-2. Neuromuscul Disord. 1996. PMID: 8784800 Free article.

3

Oculopharyngeal muscular dystrophy in Italy.

Meola G, Sansone V, Rotondo G, Tomé FM, Bouchard JP. Meola G, et al. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S53-6. doi: 10.1016/s0960-8966(97)00083-7. Neuromuscul Disord. 1997. PMID: 9392017 Free article.

4

Myotonic dystrophies.

Meola G. Meola G. Curr Opin Neurol. 2000 Oct;13(5):519-25. doi: 10.1097/00019052-200010000-00003. Curr Opin Neurol. 2000. PMID: 11073357 Review.

5

Clinical and genetic heterogeneity in myotonic dystrophies.

Meola G. Meola G. Muscle Nerve. 2000 Dec;23(12):1789-99. doi: 10.1002/1097-4598(200012)23:12<1789::aid-mus2>3.0.co;2-4. Muscle Nerve. 2000. PMID: 11102902 Review.

6

Report of the 84th ENMC workshop: PROMM (proximal myotonic myopathy) and other myotonic dystrophy-like syndromes: 2nd workshop. 13-15th October, 2000, Loosdrecht, The Netherlands.

Moxley RT 3rd, Meola G, Udd B, Ricker K. Moxley RT 3rd, et al. Among authors: meola g. Neuromuscul Disord. 2002 Mar;12(3):306-17. doi: 10.1016/s0960-8966(01)00284-x. Neuromuscul Disord. 2002. PMID: 11801405 No abstract available.

7

Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2).

Meola G, Sansone V, Perani D, Scarone S, Cappa S, Dragoni C, Cattaneo E, Cotelli M, Gobbo C, Fazio F, Siciliano G, Mancuso M, Vitelli E, Zhang S, Krahe R, Moxley RT. Meola G, et al. Neuromuscul Disord. 2003 Dec;13(10):813-21. doi: 10.1016/s0960-8966(03)00137-8. Neuromuscul Disord. 2003. PMID: 14678804

8

New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).

Sallinen R, Vihola A, Bachinski LL, Huoponen K, Haapasalo H, Hackman P, Zhang S, Sirito M, Kalimo H, Meola G, Horelli-Kuitunen N, Wessman M, Krahe R, Udd B. Sallinen R, et al. Among authors: meola g. Neuromuscul Disord. 2004 Apr;14(4):274-83. doi: 10.1016/j.nmd.2004.01.002. Neuromuscul Disord. 2004. PMID: 15019706

9

Myotonic dystrophy type 2 and related myotonic disorders.

Meola G, Moxley RT 3rd. Meola G, et al. J Neurol. 2004 Oct;251(10):1173-82. doi: 10.1007/s00415-004-0590-1. J Neurol. 2004. PMID: 15503094 Review.

10

Proximal myotonic dystrophy mimicking progressive muscular atrophy.

Rotondo G, Sansone V, Cardani R, Mancinelli E, Krahe R, Stangalini D, Meola G. Rotondo G, et al. Among authors: meola g. Eur J Neurol. 2005 Feb;12(2):160-1. doi: 10.1111/j.1468-1331.2004.01032.x. Eur J Neurol. 2005. PMID: 15679706 No abstract available.

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