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Ribonuclear inclusions as biomarker of myotonic dystrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies.
Cardani R, Mancinelli E, Giagnacovo M, Sansone V, Meola G. Cardani R, et al. Among authors: meola g. Eur J Histochem. 2009 Apr-Jun;53(2):107-11. doi: 10.4081/ejh.2009.107. Eur J Histochem. 2009. PMID: 19683984
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease.
Wood L, Bassez G, Bleyenheuft C, Campbell C, Cossette L, Jimenez-Moreno AC, Dai Y, Dawkins H, Manera JAD, Dogan C, El Sherif R, Fossati B, Graham C, Hilbert J, Kastreva K, Kimura E, Korngut L, Kostera-Pruszczyk A, Lindberg C, Lindvall B, Luebbe E, Lusakowska A, Mazanec R, Meola G, Orlando L, Takahashi MP, Peric S, Puymirat J, Rakocevic-Stojanovic V, Rodrigues M, Roxburgh R, Schoser B, Segovia S, Shatillo A, Thiele S, Tournev I, van Engelen B, Vohanka S, Lochm├╝ller H. Wood L, et al. Among authors: meola g. Orphanet J Rare Dis. 2018 Sep 5;13(1):155. doi: 10.1186/s13023-018-0889-0. Orphanet J Rare Dis. 2018. PMID: 30185236 Free PMC article.
Diagnosis and new treatment in muscle channelopathies.
Meola G, Hanna MG, Fontaine B. Meola G, et al. J Neurol Neurosurg Psychiatry. 2009 Apr;80(4):360-5. doi: 10.1136/jnnp.2008.164046. J Neurol Neurosurg Psychiatry. 2009. PMID: 19289476 Review.
Muscle biopsy and cell cultures: potential diagnostic tools in hereditary skeletal muscle channelopathies.
Meola G, Sansone V, Rotondo G, Mancinelli E. Meola G, et al. Eur J Histochem. 2003;47(1):17-28. doi: 10.4081/803. Eur J Histochem. 2003. PMID: 12685554
Treatment in myotonia and periodic paralysis.
Meola G, Sansone V. Meola G, et al. Rev Neurol (Paris). 2004 May;160(5 Pt 2):S55-69. doi: 10.1016/s0035-3787(04)71007-3. Rev Neurol (Paris). 2004. PMID: 15269662 Review.
Therapy in myotonic disorders and in muscle channelopathies.
Meola G, Sansone V. Meola G, et al. Neurol Sci. 2000;21(5 Suppl):S953-61. doi: 10.1007/s100720070009. Neurol Sci. 2000. PMID: 11382195 Review.
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
Cardiac involvement in patients with myotonic dystrophy: characteristic features of magnetic resonance imaging.
De Ambroggi L, Raisaro A, Marchian├│ V, Radice S, Meola G. De Ambroggi L, et al. Among authors: meola g. Eur Heart J. 1995 Jul;16(7):1007-10. doi: 10.1093/oxfordjournals.eurheartj.a061011. Eur Heart J. 1995. PMID: 7498193
Enzymatic activity and morphological differentiation in de novo innervated human muscle cultures.
Meola G, Sansone V, Radice S, Rotondo G, Tremblay JP. Meola G, et al. Eur J Histochem. 1994;38(2):125-36. Eur J Histochem. 1994. PMID: 7524809
Advanced microscopic and histochemical techniques: diagnostic tools in the molecular era of myology.
Meola G. Meola G. Eur J Histochem. 2005 Jan-Mar;49(1):93-6. Eur J Histochem. 2005. PMID: 15823800 Review.
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