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Massimo Carella

Showing results (31-40 of 207) with videos related to

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Cells|August 12, 2022
The Role of Cardiac Resynchronization Therapy for the Management of Functional Mitral RegurgitationEleonora Russo, Giulio Russo, Mauro Cassese, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|November 5, 2020
Electrocardiogram in Friedreich's ataxia: A short-term surrogate endpoint for treatment efficacySandra Mastroianno, Michele Germano, Angela Maggio, et al.
Gigascience|October 21, 2020
Pyntacle: a parallel computing-enabled framework for large-scale network biology analysisLuca Parca, Mauro Truglio, Tommaso Biagini, et al.
Briefings in Bioinformatics|August 5, 2021
A comparative benchmark of classic DNA motif discovery tools on synthetic dataStefano Castellana, Tommaso Biagini, Luca Parca, et al.
International Journal of Audiology|January 29, 2009
Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohortElona Cama, Salvatore Melchionda, Teresa Palladino, et al.
Blood Transfusion = Trasfusione Del Sangue|October 29, 2019
Pulmonary embolism associated with transfusion after severe post-partum haemorrhage: is less more?Elvira Grandone, Donatella Colaizzo, Mario Mastroianno, et al.
Human Genetics|February 22, 2003
A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian familyPio D'Adamo, Maura Pinna, Saverio Capobianco, et al.
American Journal of Medical Genetics. Part A|September 22, 2025
The De Novo p.(Ser802Phe) Variant Causes Helsmoortel-Van der Aa/ ADNP Syndrome in a 24-Year-Old Woman and Is Predicted to Perturb ADNP-DNA AffinityMario Benvenuto, Marilena Carmela Di Giacomo, Ada Piepoli, et al.
Genes|April 30, 2021
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell SyndromeLaura Pignata, Angela Sparago, Orazio Palumbo, et al.
European Journal of Medical Genetics|October 4, 2012
Interstitial 16p13.3 microduplication: case report and critical review of genotype-phenotype correlationTeresa Mattina, Orazio Palumbo, Raffaella Stallone, et al.
Pageof 21

Showing results (31-40 of 207) with videos related to

Sort By:
Pageof 21
Cells|August 12, 2022
The Role of Cardiac Resynchronization Therapy for the Management of Functional Mitral RegurgitationEleonora Russo, Giulio Russo, Mauro Cassese, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|November 5, 2020
Electrocardiogram in Friedreich's ataxia: A short-term surrogate endpoint for treatment efficacySandra Mastroianno, Michele Germano, Angela Maggio, et al.
Gigascience|October 21, 2020
Pyntacle: a parallel computing-enabled framework for large-scale network biology analysisLuca Parca, Mauro Truglio, Tommaso Biagini, et al.
Briefings in Bioinformatics|August 5, 2021
A comparative benchmark of classic DNA motif discovery tools on synthetic dataStefano Castellana, Tommaso Biagini, Luca Parca, et al.
International Journal of Audiology|January 29, 2009
Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohortElona Cama, Salvatore Melchionda, Teresa Palladino, et al.
Blood Transfusion = Trasfusione Del Sangue|October 29, 2019
Pulmonary embolism associated with transfusion after severe post-partum haemorrhage: is less more?Elvira Grandone, Donatella Colaizzo, Mario Mastroianno, et al.
Human Genetics|February 22, 2003
A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian familyPio D'Adamo, Maura Pinna, Saverio Capobianco, et al.
American Journal of Medical Genetics. Part A|September 22, 2025
The De Novo p.(Ser802Phe) Variant Causes Helsmoortel-Van der Aa/ ADNP Syndrome in a 24-Year-Old Woman and Is Predicted to Perturb ADNP-DNA AffinityMario Benvenuto, Marilena Carmela Di Giacomo, Ada Piepoli, et al.
Genes|April 30, 2021
Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell SyndromeLaura Pignata, Angela Sparago, Orazio Palumbo, et al.
European Journal of Medical Genetics|October 4, 2012
Interstitial 16p13.3 microduplication: case report and critical review of genotype-phenotype correlationTeresa Mattina, Orazio Palumbo, Raffaella Stallone, et al.
Pageof 21