Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Carlo Minetti

Showing results (131-140 of 190) with videos related to

Pageof 19
Sort By:
Italian Journal of Pediatrics|July 8, 2020
Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the 'beyond epilepsy' projectElisabetta Amadori, Marcello Scala, Giulia Sofia Cereda, et al.
Nature Cell Biology|November 17, 2015
The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membraneJeremy M Baskin, Xudong Wu, Romain Christiano, et al.
Neuromuscular Disorders : NMD|March 28, 2016
Novel findings associated with MTM1 suggest a higher number of female symptomatic carriersMarco Savarese, Olimpia Musumeci, Teresa Giugliano, et al.
Frontiers in Neuroscience|June 26, 2020
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical DevelopmentMichele Iacomino, Simona Baldassari, Yuki Tochigi, et al.
Nature Genetics|September 5, 2006
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataractFederico Zara, Roberta Biancheri, Claudio Bruno, et al.
Expert Review of Neurotherapeutics|January 17, 2024
A proposal for a shared therapeutic algorithm in children with prolonged convulsive seizures and status epilepticusRoberta Roberti, Antonella Riva, Gianluca D'Onofrio, et al.
Muscle & Nerve|October 23, 2021
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemiaChiara Gemelli, Monica Traverso, Lucia Trevisan, et al.
Arthritis and Rheumatism|June 8, 2011
Therapeutic approaches in the treatment of juvenile dermatomyositis in patients with recent-onset disease and in those experiencing disease flare: an international multicenter PRINTO studyRachana Hasija, Angela Pistorio, Angelo Ravelli, et al.
Vaccine|September 17, 2014
Vaccination recommendations for patients with neuromuscular diseaseSusanna Esposito, Claudio Bruno, Angela Berardinelli, et al.
The American Journal of Pathology|April 28, 2009
Caveolin-1 (P132L), a common breast cancer mutation, confers mammary cell invasiveness and defines a novel stem cell/metastasis-associated gene signatureGloria Bonuccelli, Mathew C Casimiro, Federica Sotgia, et al.
Pageof 19

Showing results (131-140 of 190) with videos related to

Sort By:
Pageof 19
Italian Journal of Pediatrics|July 8, 2020
Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the 'beyond epilepsy' projectElisabetta Amadori, Marcello Scala, Giulia Sofia Cereda, et al.
Nature Cell Biology|November 17, 2015
The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membraneJeremy M Baskin, Xudong Wu, Romain Christiano, et al.
Neuromuscular Disorders : NMD|March 28, 2016
Novel findings associated with MTM1 suggest a higher number of female symptomatic carriersMarco Savarese, Olimpia Musumeci, Teresa Giugliano, et al.
Frontiers in Neuroscience|June 26, 2020
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical DevelopmentMichele Iacomino, Simona Baldassari, Yuki Tochigi, et al.
Nature Genetics|September 5, 2006
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataractFederico Zara, Roberta Biancheri, Claudio Bruno, et al.
Expert Review of Neurotherapeutics|January 17, 2024
A proposal for a shared therapeutic algorithm in children with prolonged convulsive seizures and status epilepticusRoberta Roberti, Antonella Riva, Gianluca D'Onofrio, et al.
Muscle & Nerve|October 23, 2021
An integrated approach to the evaluation of patients with asymptomatic or minimally symptomatic hyperCKemiaChiara Gemelli, Monica Traverso, Lucia Trevisan, et al.
Arthritis and Rheumatism|June 8, 2011
Therapeutic approaches in the treatment of juvenile dermatomyositis in patients with recent-onset disease and in those experiencing disease flare: an international multicenter PRINTO studyRachana Hasija, Angela Pistorio, Angelo Ravelli, et al.
Vaccine|September 17, 2014
Vaccination recommendations for patients with neuromuscular diseaseSusanna Esposito, Claudio Bruno, Angela Berardinelli, et al.
The American Journal of Pathology|April 28, 2009
Caveolin-1 (P132L), a common breast cancer mutation, confers mammary cell invasiveness and defines a novel stem cell/metastasis-associated gene signatureGloria Bonuccelli, Mathew C Casimiro, Federica Sotgia, et al.
Pageof 19