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Giulio Piluso

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Biochimica Et Biophysica Acta|August 3, 2014
Spectrum of muscular dystrophies associated with sarcolemmal-protein genetic defectsVincenzo Nigro, Giulio Piluso
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 27, 2013
Next generation sequencing (NGS) strategies for the genetic testing of myopathiesVincenzo Nigro, Giulio Piluso
Current Opinion in Neurology|August 10, 2011
Limb girdle muscular dystrophies: update on genetic diagnosis and therapeutic approachesVincenzo Nigro, Stefania Aurino, Giulio Piluso
Frontiers in Genetics|April 10, 2024
The complex landscape of DMD mutations: moving towards personalized medicineFrancesca Gatto, Silvia Benemei, Giulio Piluso, et al.
American Journal of Medical Genetics. Part A|October 8, 2022
Are SHROOM4 loss-of-function variants pathogenic?Cristina Peduto, Giulio Piluso, Vincenzo Nigro, et al.
Cancers|February 25, 2023
Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype-Phenotype CorrelationsCristina Peduto, Mariateresa Zanobio, Vincenzo Nigro, et al.
European Journal of Human Genetics : EJHG|November 20, 2022
Patients carrying Arg1809 substitution with no choroidal abnormalities: a further proof of a "Quasi-Incomplete" NF1 phenotypeClaudia Santoro, Rosa Boccia, Claudio Iovino, et al.
Neuromuscular Disorders : NMD|April 25, 2016
Identification of an intragenic deletion in the SGCB gene through a re-evaluation of negative next generation sequencing resultsTeresa Giugliano, Marina Fanin, Marco Savarese, et al.
Clinical Chemistry|April 12, 2008
Log-PCR: a new tool for immediate and cost-effective diagnosis of up to 85% of dystrophin gene mutationsAmelia Trimarco, Annalaura Torella, Giulio Piluso, et al.
European Journal of Haematology|January 4, 2013
Identification and molecular characterization of a novel 55-kb deletion recurrent in southern Italy: the Italian (G) γ((A) γδβ)°-thalassemiaGiuseppina Lacerra, Romeo Prezioso, Gennaro Musollino, et al.
Pageof 9

Showing results (1-10 of 90) with videos related to

Sort By:
Pageof 9
Biochimica Et Biophysica Acta|August 3, 2014
Spectrum of muscular dystrophies associated with sarcolemmal-protein genetic defectsVincenzo Nigro, Giulio Piluso
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 27, 2013
Next generation sequencing (NGS) strategies for the genetic testing of myopathiesVincenzo Nigro, Giulio Piluso
Current Opinion in Neurology|August 10, 2011
Limb girdle muscular dystrophies: update on genetic diagnosis and therapeutic approachesVincenzo Nigro, Stefania Aurino, Giulio Piluso
Frontiers in Genetics|April 10, 2024
The complex landscape of DMD mutations: moving towards personalized medicineFrancesca Gatto, Silvia Benemei, Giulio Piluso, et al.
American Journal of Medical Genetics. Part A|October 8, 2022
Are SHROOM4 loss-of-function variants pathogenic?Cristina Peduto, Giulio Piluso, Vincenzo Nigro, et al.
Cancers|February 25, 2023
Neurofibromatosis Type 1: Pediatric Aspects and Review of Genotype-Phenotype CorrelationsCristina Peduto, Mariateresa Zanobio, Vincenzo Nigro, et al.
European Journal of Human Genetics : EJHG|November 20, 2022
Patients carrying Arg1809 substitution with no choroidal abnormalities: a further proof of a "Quasi-Incomplete" NF1 phenotypeClaudia Santoro, Rosa Boccia, Claudio Iovino, et al.
Neuromuscular Disorders : NMD|April 25, 2016
Identification of an intragenic deletion in the SGCB gene through a re-evaluation of negative next generation sequencing resultsTeresa Giugliano, Marina Fanin, Marco Savarese, et al.
Clinical Chemistry|April 12, 2008
Log-PCR: a new tool for immediate and cost-effective diagnosis of up to 85% of dystrophin gene mutationsAmelia Trimarco, Annalaura Torella, Giulio Piluso, et al.
European Journal of Haematology|January 4, 2013
Identification and molecular characterization of a novel 55-kb deletion recurrent in southern Italy: the Italian (G) γ((A) γδβ)°-thalassemiaGiuseppina Lacerra, Romeo Prezioso, Gennaro Musollino, et al.
Pageof 9