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

Maria Iascone

Showing results (61-70 of 178) with videos related to

Pageof 18
Sort By:
European Heart Journal|April 24, 2012
A contemporary European experience with surgical septal myectomy in hypertrophic cardiomyopathyAttilio Iacovoni, Paolo Spirito, Caterina Simon, et al.
Giornale Italiano Di Cardiologia (2006)|June 30, 2022
[Clinical pathway on pediatric cardiomyopathies: a genetic testing strategy proposed by the Italian Society of Pediatric Cardiology]Francesca Girolami, Maria Iascone, Laura Pezzoli, et al.
American Journal of Medical Genetics. Part A|February 11, 2023
Rock around DYRK1A: Ethnic diversity, clinical challengesAlice Moroni, Lidia Pezzani, Enrico Alfei, et al.
American Journal of Medical Genetics. Part A|February 27, 2023
Chung-Jansen syndrome can mimic Cornelia de Lange syndrome: Another player among chromatinopathies?Beatrice Conti, Berardo Rinaldi, Martina Rimoldi, et al.
JPGN Reports|May 19, 2023
Infantile <i>ATP7B</i>-Related End-Stage Liver Disease: An Exceptional Wilson Disease Phenotype From Consecutive GenerationsEmanuele Nicastro, Maria Iascone, Angelo Di Giorgio, et al.
Annali Dell'Istituto Superiore Di Sanita|June 17, 2026
External quality assessment programs in cytogenomics in the Lombardy Region, Italy (2018-2024): performance and trendsFabio Pasotti, Valentina Achille, Simona Da Molin, et al.
Clinical Case Reports|August 26, 2022
Prenatal overgrowth and polydramnios: Would you think about Noonan syndrome?Benedetta Beltrami, Jacopo Cerasani, Alessandra Consales, et al.
American Journal of Medical Genetics. Part A|September 30, 2016
First evidence of Smith-Magenis syndrome in mother and daughter due to a novel RAI mutationFabio Acquaviva, Maria Elena Sana, Matteo Della Monica, et al.
Clinical Case Reports|December 28, 2020
A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysisValentina Spinelli, Francesca Girolami, Chiara Marrone, et al.
Genes|July 27, 2022
Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed PatientsErica Rosina, Lidia Pezzani, Laura Pezzoli, et al.
Pageof 18

Showing results (61-70 of 178) with videos related to

Sort By:
Pageof 18
European Heart Journal|April 24, 2012
A contemporary European experience with surgical septal myectomy in hypertrophic cardiomyopathyAttilio Iacovoni, Paolo Spirito, Caterina Simon, et al.
Giornale Italiano Di Cardiologia (2006)|June 30, 2022
[Clinical pathway on pediatric cardiomyopathies: a genetic testing strategy proposed by the Italian Society of Pediatric Cardiology]Francesca Girolami, Maria Iascone, Laura Pezzoli, et al.
American Journal of Medical Genetics. Part A|February 11, 2023
Rock around DYRK1A: Ethnic diversity, clinical challengesAlice Moroni, Lidia Pezzani, Enrico Alfei, et al.
American Journal of Medical Genetics. Part A|February 27, 2023
Chung-Jansen syndrome can mimic Cornelia de Lange syndrome: Another player among chromatinopathies?Beatrice Conti, Berardo Rinaldi, Martina Rimoldi, et al.
JPGN Reports|May 19, 2023
Infantile <i>ATP7B</i>-Related End-Stage Liver Disease: An Exceptional Wilson Disease Phenotype From Consecutive GenerationsEmanuele Nicastro, Maria Iascone, Angelo Di Giorgio, et al.
Annali Dell'Istituto Superiore Di Sanita|June 17, 2026
External quality assessment programs in cytogenomics in the Lombardy Region, Italy (2018-2024): performance and trendsFabio Pasotti, Valentina Achille, Simona Da Molin, et al.
Clinical Case Reports|August 26, 2022
Prenatal overgrowth and polydramnios: Would you think about Noonan syndrome?Benedetta Beltrami, Jacopo Cerasani, Alessandra Consales, et al.
American Journal of Medical Genetics. Part A|September 30, 2016
First evidence of Smith-Magenis syndrome in mother and daughter due to a novel RAI mutationFabio Acquaviva, Maria Elena Sana, Matteo Della Monica, et al.
Clinical Case Reports|December 28, 2020
A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysisValentina Spinelli, Francesca Girolami, Chiara Marrone, et al.
Genes|July 27, 2022
Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed PatientsErica Rosina, Lidia Pezzani, Laura Pezzoli, et al.
Pageof 18