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Luisa Politano

Showing results (81-90 of 176) with videos related to

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Neuromuscular Disorders : NMD|January 17, 2012
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesGiulia Ricci, Isabella Scionti, Greta Alì, et al.
Neuromuscular Disorders : NMD|May 24, 2016
TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvementGuja Astrea, Ilaria Pezzini, Ester Picillo, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|November 1, 2012
Increased dispersion of ventricular repolarization in Emery Dreifuss muscular dystrophy patientsVincenzo Russo, Anna Rago, Luisa Politano, et al.
Genes|November 14, 2019
X-Linked Emery-Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female CarriersEmanuela Viggiano, Agnieszka Madej-Pilarczyk, Nicola Carboni, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 16, 2015
The effect of atrial preference pacing on atrial fibrillation electrophysiological substrate in Myotonic Dystrophy type 1 populationVincenzo Russo, Gerardo Nigro, Federica DI Meo, et al.
Plos One|August 20, 2020
The position of nonsense mutations can predict the phenotype severity: A survey on the DMD geneAnnalaura Torella, Mariateresa Zanobio, Roberta Zeuli, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 21, 2016
Novel mutations in LMNA A/C gene and associated phenotypesRoberta Petillo, Paola D'Ambrosio, Annalaura Torella, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 8, 2014
Atrial fibrillation burden in Myotonic Dystrophy type 1 patients implanted with dual chamber pacemaker: the efficacy of the overdrive atrial algorithm at 2 year follow-upVincenzo Russo, Gerardo Nigro, Anna Rago, et al.
European Journal of Human Genetics : EJHG|April 28, 2011
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutationsMafalda Cacciottolo, Gelsomina Numitone, Stefania Aurino, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 25, 2015
Far field R-wave sensing in Myotonic Dystrophy type 1: right atrial appendage versus Bachmann's bundle region lead placementVincenzo Russo, Gerardo Nigro, Andrea Antonio Papa, et al.
Pageof 18

Showing results (81-90 of 176) with videos related to

Sort By:
Pageof 18
Neuromuscular Disorders : NMD|January 17, 2012
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying a heterozygous CAV3 T78M mutation and a D4Z4 partial deletion: Further evidence for "double trouble" overlapping syndromesGiulia Ricci, Isabella Scionti, Greta Alì, et al.
Neuromuscular Disorders : NMD|May 24, 2016
TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvementGuja Astrea, Ilaria Pezzini, Ester Picillo, et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|November 1, 2012
Increased dispersion of ventricular repolarization in Emery Dreifuss muscular dystrophy patientsVincenzo Russo, Anna Rago, Luisa Politano, et al.
Genes|November 14, 2019
X-Linked Emery-Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female CarriersEmanuela Viggiano, Agnieszka Madej-Pilarczyk, Nicola Carboni, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 16, 2015
The effect of atrial preference pacing on atrial fibrillation electrophysiological substrate in Myotonic Dystrophy type 1 populationVincenzo Russo, Gerardo Nigro, Federica DI Meo, et al.
Plos One|August 20, 2020
The position of nonsense mutations can predict the phenotype severity: A survey on the DMD geneAnnalaura Torella, Mariateresa Zanobio, Roberta Zeuli, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 21, 2016
Novel mutations in LMNA A/C gene and associated phenotypesRoberta Petillo, Paola D'Ambrosio, Annalaura Torella, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 8, 2014
Atrial fibrillation burden in Myotonic Dystrophy type 1 patients implanted with dual chamber pacemaker: the efficacy of the overdrive atrial algorithm at 2 year follow-upVincenzo Russo, Gerardo Nigro, Anna Rago, et al.
European Journal of Human Genetics : EJHG|April 28, 2011
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutationsMafalda Cacciottolo, Gelsomina Numitone, Stefania Aurino, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 25, 2015
Far field R-wave sensing in Myotonic Dystrophy type 1: right atrial appendage versus Bachmann's bundle region lead placementVincenzo Russo, Gerardo Nigro, Andrea Antonio Papa, et al.
Pageof 18