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

Giovanni Neri

Showing results (151-160 of 273) with videos related to

Pageof 28
Sort By:
Investigative Ophthalmology & Visual Science|July 21, 2025
Deep Learning Model for Automated Classification of Macular Neovascularization Subtypes in AMDGiovanni Neri, Chiara Rebecchi, Jonathan D Oakley, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|December 3, 2009
Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitaliaGian Franco Zannoni, Valerio Gaetano Vellone, Emanuela Lucci Cordisco, et al.
ACS Omega|August 29, 2019
Hybrid Noble-Metals/Metal-Oxide Bifunctional Nano-Heterostructure Displaying Outperforming Gas-Sensing and Photochromic PerformancesDavid Maria Tobaldi, Salvatore Gianluca Leonardi, Kaveh Movlaee, et al.
American Journal of Medical Genetics. Part A|April 2, 2004
Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndromeFiorella Gurrieri, Gioacchino Scarano, Livia Garavelli, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
The intellectual disabilities evaluation and advice system (IDEAS): outcome of the first 55 casesAlasdair G W Hunter, John M Graham, Giovanni Neri, et al.
Human Molecular Genetics|November 26, 2004
Molecular dissection of the events leading to inactivation of the FMR1 geneRoberta Pietrobono, Elisabetta Tabolacci, Francesca Zalfa, et al.
Nature Genetics|May 1, 2012
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotypeMarcella Zollino, Daniela Orteschi, Marina Murdolo, et al.
Ophthalmology Science|July 9, 2026
Baseline Optical Coherence Tomography Biomarkers Associated with the 2-Year Development of Macular Atrophy or Fibrosis in Neovascular Age-related Macular DegenerationChiara Olivieri, Giacomo Perin, Xuenan Zhuang, et al.
Biosensors|October 27, 2022
Emotion Recognition: Photoplethysmography and Electrocardiography in ComparisonSergio Rinella, Simona Massimino, Piero Giorgio Fallica, et al.
Plos Genetics|July 23, 2013
Role of CTCF protein in regulating FMR1 locus transcriptionStella Lanni, Martina Goracci, Loredana Borrelli, et al.
Pageof 28

Showing results (151-160 of 273) with videos related to

Sort By:
Pageof 28
Investigative Ophthalmology & Visual Science|July 21, 2025
Deep Learning Model for Automated Classification of Macular Neovascularization Subtypes in AMDGiovanni Neri, Chiara Rebecchi, Jonathan D Oakley, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|December 3, 2009
Morphology and immunophenotyping of a monolateral ovotestis in a 46,XderY/45,X mosaic individual with ambiguous genitaliaGian Franco Zannoni, Valerio Gaetano Vellone, Emanuela Lucci Cordisco, et al.
ACS Omega|August 29, 2019
Hybrid Noble-Metals/Metal-Oxide Bifunctional Nano-Heterostructure Displaying Outperforming Gas-Sensing and Photochromic PerformancesDavid Maria Tobaldi, Salvatore Gianluca Leonardi, Kaveh Movlaee, et al.
American Journal of Medical Genetics. Part A|April 2, 2004
Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndromeFiorella Gurrieri, Gioacchino Scarano, Livia Garavelli, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
The intellectual disabilities evaluation and advice system (IDEAS): outcome of the first 55 casesAlasdair G W Hunter, John M Graham, Giovanni Neri, et al.
Human Molecular Genetics|November 26, 2004
Molecular dissection of the events leading to inactivation of the FMR1 geneRoberta Pietrobono, Elisabetta Tabolacci, Francesca Zalfa, et al.
Nature Genetics|May 1, 2012
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotypeMarcella Zollino, Daniela Orteschi, Marina Murdolo, et al.
Ophthalmology Science|July 9, 2026
Baseline Optical Coherence Tomography Biomarkers Associated with the 2-Year Development of Macular Atrophy or Fibrosis in Neovascular Age-related Macular DegenerationChiara Olivieri, Giacomo Perin, Xuenan Zhuang, et al.
Biosensors|October 27, 2022
Emotion Recognition: Photoplethysmography and Electrocardiography in ComparisonSergio Rinella, Simona Massimino, Piero Giorgio Fallica, et al.
Plos Genetics|July 23, 2013
Role of CTCF protein in regulating FMR1 locus transcriptionStella Lanni, Martina Goracci, Loredana Borrelli, et al.
Pageof 28