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

Angela Peron

Showing results (31-40 of 79) with videos related to

Pageof 8
Sort By:
Frontiers in Cell and Developmental Biology|May 7, 2021
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and ChromatinopathiesChiara Parodi, Elisabetta Di Fede, Angela Peron, et al.
American Journal of Medical Genetics. Part A|April 11, 2016
Do patients with tuberous sclerosis complex have an increased risk for malignancies?Angela Peron, Aglaia Vignoli, Francesca La Briola, et al.
American Journal of Medical Genetics. Part A|January 17, 2020
Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotypeAngela Peron, Francesca Novara, Francesca La Briola, et al.
BMC Pulmonary Medicine|July 30, 2017
Lymphangioleiomyomatosis, multifocal micronodular pneumocyte hyperplasia, and sarcoidosis: more pathological findings in the same chest CT, or a single pathological pathway?Fabiano Di Marco, Giuseppina Palumbo, Silvia Terraneo, et al.
Scientific Reports|December 1, 2025
Long-read genome sequencing resolves the breakpoints of a chromosome 8;22 balanced translocation in NF2-related schwannomatosisMarco Montini, Lorenzo Bonacchi, Diletta Sidoti, et al.
Epilepsy & Behavior : E&B|November 11, 2017
Lennox-Gastaut syndrome in adulthood: Long-term clinical follow-up of 38 patients and analysis of their recorded seizuresAglaia Vignoli, Gaia Oggioni, Giovanni De Maria, et al.
American Journal of Medical Genetics. Part A|April 15, 2020
Aortic dilation in Sotos syndrome: An underestimated feature?Lidia Pezzani, Lucia Mauri, Angelo Selicorni, et al.
American Journal of Medical Genetics. Part A|August 18, 2020
Tuberous sclerosis complex (TSC), lymphangioleiomyomatosis, and COVID-19: The experience of a TSC clinic in ItalyAngela Peron, Francesca La Briola, Fabio Bruschi, et al.
Frontiers in Medicine|May 13, 2021
Exploring the Role of Matrix Metalloproteinases as Biomarkers in Sporadic Lymphangioleiomyomatosis and Tuberous Sclerosis Complex. A Pilot StudySilvia Terraneo, Elena Lesma, Silvia Ancona, et al.
Orphanet Journal of Rare Diseases|January 31, 2018
Early diagnosis of tuberous sclerosis complex: a race against time. How to make the diagnosis before seizures?Monika Słowińska, Sergiusz Jóźwiak, Angela Peron, et al.
Pageof 8

Showing results (31-40 of 79) with videos related to

Sort By:
Pageof 8
Frontiers in Cell and Developmental Biology|May 7, 2021
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and ChromatinopathiesChiara Parodi, Elisabetta Di Fede, Angela Peron, et al.
American Journal of Medical Genetics. Part A|April 11, 2016
Do patients with tuberous sclerosis complex have an increased risk for malignancies?Angela Peron, Aglaia Vignoli, Francesca La Briola, et al.
American Journal of Medical Genetics. Part A|January 17, 2020
Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotypeAngela Peron, Francesca Novara, Francesca La Briola, et al.
BMC Pulmonary Medicine|July 30, 2017
Lymphangioleiomyomatosis, multifocal micronodular pneumocyte hyperplasia, and sarcoidosis: more pathological findings in the same chest CT, or a single pathological pathway?Fabiano Di Marco, Giuseppina Palumbo, Silvia Terraneo, et al.
Scientific Reports|December 1, 2025
Long-read genome sequencing resolves the breakpoints of a chromosome 8;22 balanced translocation in NF2-related schwannomatosisMarco Montini, Lorenzo Bonacchi, Diletta Sidoti, et al.
Epilepsy & Behavior : E&B|November 11, 2017
Lennox-Gastaut syndrome in adulthood: Long-term clinical follow-up of 38 patients and analysis of their recorded seizuresAglaia Vignoli, Gaia Oggioni, Giovanni De Maria, et al.
American Journal of Medical Genetics. Part A|April 15, 2020
Aortic dilation in Sotos syndrome: An underestimated feature?Lidia Pezzani, Lucia Mauri, Angelo Selicorni, et al.
American Journal of Medical Genetics. Part A|August 18, 2020
Tuberous sclerosis complex (TSC), lymphangioleiomyomatosis, and COVID-19: The experience of a TSC clinic in ItalyAngela Peron, Francesca La Briola, Fabio Bruschi, et al.
Frontiers in Medicine|May 13, 2021
Exploring the Role of Matrix Metalloproteinases as Biomarkers in Sporadic Lymphangioleiomyomatosis and Tuberous Sclerosis Complex. A Pilot StudySilvia Terraneo, Elena Lesma, Silvia Ancona, et al.
Orphanet Journal of Rare Diseases|January 31, 2018
Early diagnosis of tuberous sclerosis complex: a race against time. How to make the diagnosis before seizures?Monika Słowińska, Sergiusz Jóźwiak, Angela Peron, et al.
Pageof 8