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Angela Peron

Showing results (1-10 of 79) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 17, 2018
Tuberous sclerosis complexAngela Peron, Hope Northrup
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 27, 2018
Genetics, genomics, and genotype-phenotype correlations of TSC: Insights for clinical practiceAngela Peron, Kit Sing Au, Hope Northrup
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 26, 2018
Healthcare transition from childhood to adulthood in Tuberous Sclerosis ComplexAngela Peron, Maria Paola Canevini, Filippo Ghelma, et al.
American Journal of Medical Genetics. Part A|April 6, 2021
SLC35F1 as a candidate gene for neurodevelopmental disorders resembling Rett syndromeElisabetta Di Fede, Angela Peron, Elisa Adele Colombo, et al.
Epilepsia|November 4, 2018
Hot water epilepsy and SYN1 variantsAngela Peron, Nissan V Baratang, Maria Paola Canevini, et al.
Pediatric Allergy, Immunology, and Pulmonology|August 5, 2022
Negative Atopy Patch Test and Negative Skin Prick Test Reduce the Need for Oral Food Challenge in Children with Atopic DermatitisAngela Peron, Rossana Tenconi, Maddalena Leone, et al.
American Journal of Medical Genetics. Part A|June 25, 2013
Interstitial 6q microdeletion syndrome and epilepsy: a new patient and review of the literatureAglaia Vignoli, Giulia Federica Scornavacca, Angela Peron, et al.
Neurocase|May 21, 2024
Continuous spike-wave of slow sleep in a patient with <i>KCNB1</i>-related epilepsy responsive to highly purified cannabidiol: a case report and comparison with literatureGiulia Ferrera, Emilia Ricci, Angela Peron, et al.
American Journal of Medical Genetics. Part A|March 22, 2020
PIGW-related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literatureAngela Peron, Maria Iascone, Elisabetta Salvatici, et al.
Journal of Medical Genetics|October 27, 2020
Phenotypes in adult patients with Rett syndrome: results of a 13-year experience and insights into healthcare transitionAngela Peron, Maria Paola Canevini, Filippo Ghelma, et al.
Pageof 8

Showing results (1-10 of 79) with videos related to

Sort By:
Pageof 8
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 17, 2018
Tuberous sclerosis complexAngela Peron, Hope Northrup
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 27, 2018
Genetics, genomics, and genotype-phenotype correlations of TSC: Insights for clinical practiceAngela Peron, Kit Sing Au, Hope Northrup
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 26, 2018
Healthcare transition from childhood to adulthood in Tuberous Sclerosis ComplexAngela Peron, Maria Paola Canevini, Filippo Ghelma, et al.
American Journal of Medical Genetics. Part A|April 6, 2021
SLC35F1 as a candidate gene for neurodevelopmental disorders resembling Rett syndromeElisabetta Di Fede, Angela Peron, Elisa Adele Colombo, et al.
Epilepsia|November 4, 2018
Hot water epilepsy and SYN1 variantsAngela Peron, Nissan V Baratang, Maria Paola Canevini, et al.
Pediatric Allergy, Immunology, and Pulmonology|August 5, 2022
Negative Atopy Patch Test and Negative Skin Prick Test Reduce the Need for Oral Food Challenge in Children with Atopic DermatitisAngela Peron, Rossana Tenconi, Maddalena Leone, et al.
American Journal of Medical Genetics. Part A|June 25, 2013
Interstitial 6q microdeletion syndrome and epilepsy: a new patient and review of the literatureAglaia Vignoli, Giulia Federica Scornavacca, Angela Peron, et al.
Neurocase|May 21, 2024
Continuous spike-wave of slow sleep in a patient with <i>KCNB1</i>-related epilepsy responsive to highly purified cannabidiol: a case report and comparison with literatureGiulia Ferrera, Emilia Ricci, Angela Peron, et al.
American Journal of Medical Genetics. Part A|March 22, 2020
PIGW-related glycosylphosphatidylinositol deficiency: Description of a new patient and review of the literatureAngela Peron, Maria Iascone, Elisabetta Salvatici, et al.
Journal of Medical Genetics|October 27, 2020
Phenotypes in adult patients with Rett syndrome: results of a 13-year experience and insights into healthcare transitionAngela Peron, Maria Paola Canevini, Filippo Ghelma, et al.
Pageof 8