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Massimo Carella

Showing results (81-90 of 207) with videos related to

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International Journal of Pediatric Otorhinolaryngology|July 21, 2009
Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing lossElona Cama, Maria Stella Alemanno, Emanuele Bellacchio, et al.
Molecular Genetics & Genomic Medicine|July 27, 2019
Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescriptionGiuseppe Di Stolfo, Maria Accadia, Sandra Mastroianno, et al.
Journal of Clinical Medicine|February 5, 2020
Comparison of the Genomic Profile of Cancer Stem Cells and Their Non-Stem Counterpart: The Case of Ovarian CancerElena Laura Mazzoldi, Anna Pastò, Giorgia Pilotto, et al.
In Silico Biology|March 21, 2012
Overlapping genes may control reprogramming of mouse somatic cells into induced pluripotent stem cells (iPSCs) and breast cancer stem cellsEttore Mosca, Cinzia Cocola, Davood Sabour, et al.
Frontiers in Genetics|December 23, 2017
Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter DeletionMarianna De Cinque, Orazio Palumbo, Ermelinda Mazzucco, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|September 17, 2019
Double missense mutations in cardiac myosin-binding protein C and myopalladin genes: A case report with diffuse coronary disease, complete atrioventricular block, and progression to dilated cardiomyopathySandra Mastroianno, Pietro Palumbo, Stefano Castellana, et al.
Orphanet Journal of Rare Diseases|August 22, 2025
Clinical course and management challenges in Lafora disease: a narrative analysis in an Apulian cohortGiuseppe d'Orsi, Maria Teresa Di Claudio, Antonella Liantonio, et al.
Journal of Human Genetics|March 27, 2015
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotypeAgostina De Crescenzo, Valentina Citro, Andrea Freschi, et al.
Frontiers in Genetics|August 29, 2025
Case Report: Unmasking the role of rem sleep in modulating non-convulsive status epilepticus in ring chromosome 20 syndrome: a genetic disorder of sleep architecture?Filippo Mandato, Maria Teresa Di Claudio, Umberto Costantino, et al.
Human Mutation|May 18, 2022
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variantsAgnese Giovannetti, Salvatore Daniele Bianco, Alice Traversa, et al.
Pageof 21

Showing results (81-90 of 207) with videos related to

Sort By:
Pageof 21
International Journal of Pediatric Otorhinolaryngology|July 21, 2009
Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing lossElona Cama, Maria Stella Alemanno, Emanuele Bellacchio, et al.
Molecular Genetics & Genomic Medicine|July 27, 2019
Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescriptionGiuseppe Di Stolfo, Maria Accadia, Sandra Mastroianno, et al.
Journal of Clinical Medicine|February 5, 2020
Comparison of the Genomic Profile of Cancer Stem Cells and Their Non-Stem Counterpart: The Case of Ovarian CancerElena Laura Mazzoldi, Anna Pastò, Giorgia Pilotto, et al.
In Silico Biology|March 21, 2012
Overlapping genes may control reprogramming of mouse somatic cells into induced pluripotent stem cells (iPSCs) and breast cancer stem cellsEttore Mosca, Cinzia Cocola, Davood Sabour, et al.
Frontiers in Genetics|December 23, 2017
Developmental Coordination Disorder in a Patient with Mental Disability and a Mild Phenotype Carrying Terminal 6q26-qter DeletionMarianna De Cinque, Orazio Palumbo, Ermelinda Mazzucco, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|September 17, 2019
Double missense mutations in cardiac myosin-binding protein C and myopalladin genes: A case report with diffuse coronary disease, complete atrioventricular block, and progression to dilated cardiomyopathySandra Mastroianno, Pietro Palumbo, Stefano Castellana, et al.
Orphanet Journal of Rare Diseases|August 22, 2025
Clinical course and management challenges in Lafora disease: a narrative analysis in an Apulian cohortGiuseppe d'Orsi, Maria Teresa Di Claudio, Antonella Liantonio, et al.
Journal of Human Genetics|March 27, 2015
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotypeAgostina De Crescenzo, Valentina Citro, Andrea Freschi, et al.
Frontiers in Genetics|August 29, 2025
Case Report: Unmasking the role of rem sleep in modulating non-convulsive status epilepticus in ring chromosome 20 syndrome: a genetic disorder of sleep architecture?Filippo Mandato, Maria Teresa Di Claudio, Umberto Costantino, et al.
Human Mutation|May 18, 2022
MiRLog and dbmiR: Prioritization and functional annotation tools to study human microRNA sequence variantsAgnese Giovannetti, Salvatore Daniele Bianco, Alice Traversa, et al.
Pageof 21