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Massimo Carella

Showing results (201-210 of 207) with videos related to

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Journal of Medical Genetics|November 29, 2024
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in ItalyDavide Mei, Simona Balestrini, Elena Parrini, et al.
European Journal of Human Genetics : EJHG|October 30, 2014
Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1Laïla El Khattabi, Fabien Guimiot, Eva Pipiras, et al.
Frontiers in Medicine|June 1, 2023
Thoracic ultrasound combined with low-dose computed tomography may represent useful screening strategy in highly exposed population in the industrial city of Taranto (Italy)Carla Maria Irene Quarato, Elisa Dama, Michele Maggi, et al.
Cell Stem Cell|November 28, 2023
Phase I clinical trial of intracerebroventricular transplantation of allogeneic neural stem cells in people with progressive multiple sclerosisMaurizio A Leone, Maurizio Gelati, Daniela C Profico, et al.
Seizure|April 8, 2021
Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European studyFederico Raviglione, Sofia Douzgou, Marcello Scala, et al.
Human Molecular Genetics|January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.
Nature Genetics|June 23, 2014
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationDan E Arking, Sara L Pulit, Lia Crotti, et al.
Pageof 21

Showing results (201-210 of 207) with videos related to

Sort By:
Pageof 21
You have reached the last page of results.This site can display upto 207 results.
Journal of Medical Genetics|November 29, 2024
National survey on the prevalence of single-gene aetiologies for genetic developmental and epileptic encephalopathies in ItalyDavide Mei, Simona Balestrini, Elena Parrini, et al.
European Journal of Human Genetics : EJHG|October 30, 2014
Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1Laïla El Khattabi, Fabien Guimiot, Eva Pipiras, et al.
Frontiers in Medicine|June 1, 2023
Thoracic ultrasound combined with low-dose computed tomography may represent useful screening strategy in highly exposed population in the industrial city of Taranto (Italy)Carla Maria Irene Quarato, Elisa Dama, Michele Maggi, et al.
Cell Stem Cell|November 28, 2023
Phase I clinical trial of intracerebroventricular transplantation of allogeneic neural stem cells in people with progressive multiple sclerosisMaurizio A Leone, Maurizio Gelati, Daniela C Profico, et al.
Seizure|April 8, 2021
Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European studyFederico Raviglione, Sofia Douzgou, Marcello Scala, et al.
Human Molecular Genetics|January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.
Nature Genetics|June 23, 2014
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationDan E Arking, Sara L Pulit, Lia Crotti, et al.
Pageof 21