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G Meola

Showing results (131-140 of 142) with videos related to

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Brain Research|February 9, 1988
Cultures of human Schwann cells isolated from fetal nervesE Scarpini, B Q Kreider, R P Lisak, et al.
Neuromuscular Disorders : NMD|February 10, 2015
SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotypeE Bugiardini, I Rivolta, A Binda, et al.
Neurology|August 1, 1994
Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysisL J Ptáĉek, R Tawil, R C Griggs, et al.
Neuromuscular Disorders : NMD|May 3, 2016
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathyV Guglielmi, A Oosterhof, N C Voermans, et al.
Annals of Neurology|October 23, 1997
Andersen's syndrome: a distinct periodic paralysisV Sansone, R C Griggs, G Meola, et al.
Neurology|January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisE Matthews, R Labrum, M G Sweeney, et al.
Neuromuscular Disorders : NMD|March 17, 2004
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)R Sallinen, A Vihola, L L Bachinski, et al.
Neurology|June 11, 2003
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2A Vihola, G Bassez, G Meola, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)G Meola, V Sansone, D Perani, et al.
Scientific Reports|December 2, 2016
Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1A Perfetti, S Greco, R Cardani, et al.
Pageof 15

Showing results (131-140 of 142) with videos related to

Sort By:
Pageof 15
Brain Research|February 9, 1988
Cultures of human Schwann cells isolated from fetal nervesE Scarpini, B Q Kreider, R P Lisak, et al.
Neuromuscular Disorders : NMD|February 10, 2015
SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotypeE Bugiardini, I Rivolta, A Binda, et al.
Neurology|August 1, 1994
Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysisL J Ptáĉek, R Tawil, R C Griggs, et al.
Neuromuscular Disorders : NMD|May 3, 2016
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathyV Guglielmi, A Oosterhof, N C Voermans, et al.
Annals of Neurology|October 23, 1997
Andersen's syndrome: a distinct periodic paralysisV Sansone, R C Griggs, G Meola, et al.
Neurology|January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysisE Matthews, R Labrum, M G Sweeney, et al.
Neuromuscular Disorders : NMD|March 17, 2004
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)R Sallinen, A Vihola, L L Bachinski, et al.
Neurology|June 11, 2003
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2A Vihola, G Bassez, G Meola, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)G Meola, V Sansone, D Perani, et al.
Scientific Reports|December 2, 2016
Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1A Perfetti, S Greco, R Cardani, et al.
Pageof 15