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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: sansone v. Eur J Histochem. 2009 Apr-Jun;53(2):107-11. doi: 10.4081/ejh.2009.107. Eur J Histochem. 2009. PMID: 19683984
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. Among authors: sansone v. Eur J Histochem. 1994;38(2):125-36. Eur J Histochem. 1994. PMID: 7524809
Cytoplasmic restoration and persistence of glucose-6-phosphate dehydrogenase activity in stable hybrid myotubes.
Sansone V, Rotondo G, Bottiroli G, Tremblay JP, Meola G. Sansone V, et al. Eur J Histochem. 1993;37(3):241-8. Eur J Histochem. 1993. PMID: 7693062
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. Among authors: sansone v. Neuromuscul Disord. 1996 May;6(3):143-50. doi: 10.1016/0960-8966(95)00040-2. Neuromuscul Disord. 1996. PMID: 8784800
Muscle surface mechanical and electrical activities in myotonic dystrophy.
Orizio C, Esposito F, Sansone V, Parrinello G, Meola G, Veicsteinas A. Orizio C, et al. Among authors: sansone v. Electromyogr Clin Neurophysiol. 1997 Jun-Jul;37(4):231-9. Electromyogr Clin Neurophysiol. 1997. PMID: 9208218
Oculopharyngeal muscular dystrophy in Italy.
Meola G, Sansone V, Rotondo G, Tomé FM, Bouchard JP. Meola G, et al. Among authors: sansone v. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S53-6. doi: 10.1016/s0960-8966(97)00083-7. Neuromuscul Disord. 1997. PMID: 9392017
Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathy.
Meola G, Sansone V, Perani D, Colleluori A, Cappa S, Cotelli M, Fazio F, Thornton CA, Moxley RT. Meola G, et al. Among authors: sansone v. Neurology. 1999 Sep 22;53(5):1042-50. doi: 10.1212/wnl.53.5.1042. Neurology. 1999. PMID: 10496264
Hypothyroidism unmasking proximal myotonic myopathy.
Sansone V, Griggs RC, Moxley RT 3rd. Sansone V, et al. Neuromuscul Disord. 2000 Mar;10(3):165-72. doi: 10.1016/s0960-8966(99)00097-8. Neuromuscul Disord. 2000. PMID: 10734262
Therapy in myotonic disorders and in muscle channelopathies.
Meola G, Sansone V. Meola G, et al. Among authors: sansone v. Neurol Sci. 2000;21(5 Suppl):S953-61. doi: 10.1007/s100720070009. Neurol Sci. 2000. PMID: 11382195 Review.
Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.
Mankodi A, Urbinati CR, Yuan QP, Moxley RT, Sansone V, Krym M, Henderson D, Schalling M, Swanson MS, Thornton CA. Mankodi A, et al. Among authors: sansone v. Hum Mol Genet. 2001 Sep 15;10(19):2165-70. doi: 10.1093/hmg/10.19.2165. Hum Mol Genet. 2001. PMID: 11590133
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