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 (141-150 of 273) with videos related to

Pageof 28
Sort By:
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 14, 2026
OCTA in age-related macular degeneration: consensus on practical guidelines for optimal imaging strategies across different clinical scenariosGiovanni Neri, Daniela Bacherini, Rodolfo Mastropasqua, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
A premature infant with Costello syndrome due to a rare G13C HRAS mutationMaria Piccione, Ettore Piro, Maria Grazia Pomponi, et al.
Small (Weinheim an Der Bergstrasse, Germany)|November 24, 2024
Interplay Between Calcination Temperature and Alkaline Oxygen Evolution of Electrospun High-Entropy (Cr<sub>1/5</sub>Mn<sub>1/5</sub>Fe<sub>1/5</sub>Co<sub>1/5</sub>Ni<sub>1/5</sub>)<sub>3</sub>O<sub>4</sub> NanofibersKeti Vezzù, Claudia Triolo, Kaveh Moulaee, et al.
Investigative Ophthalmology & Visual Science|August 28, 2025
Retinal Vessel Changes in Geographic Atrophy in AMD: Insights From Imaging and HistologyChiara Olivieri, Antonio Fai, Imran A Bhutto, et al.
Nanotechnology|May 5, 2018
CO<sub>2</sub> sensing properties of electro-spun Ca-doped ZnO fibresFabiola Pantò, Salvatore Gianluca Leonardi, Enza Fazio, et al.
ACS Omega|January 8, 2026
Enhanced Electrochemical Detection of Lead Ions Using Schiff Base/MoS<sub>2</sub> Modified Screen-Printed ElectrodesDaniela Iannazzo, Zahra Akbari, Consuelo Celesti, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndromeJohn M Graham, Nancy Kramer, Bassem A Bejjani, et al.
European Journal of Medical Genetics|July 21, 2015
NFIX mutations affecting the DNA-binding domain cause a peculiar overgrowth syndrome (Malan syndrome): a new patients seriesFiorella Gurrieri, Maria Luigia Cavaliere, Anita Wischmeijer, et al.
American Journal of Human Genetics|February 4, 2003
Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2Marcella Zollino, Rosetta Lecce, Rita Fischetto, et al.
American Journal of Human Genetics|December 9, 2004
A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genesLuisa Russo, Paolo Mariotti, Eugenio Sangiorgi, et al.
Pageof 28

Showing results (141-150 of 273) with videos related to

Sort By:
Pageof 28
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|March 14, 2026
OCTA in age-related macular degeneration: consensus on practical guidelines for optimal imaging strategies across different clinical scenariosGiovanni Neri, Daniela Bacherini, Rodolfo Mastropasqua, et al.
American Journal of Medical Genetics. Part A|February 13, 2009
A premature infant with Costello syndrome due to a rare G13C HRAS mutationMaria Piccione, Ettore Piro, Maria Grazia Pomponi, et al.
Small (Weinheim an Der Bergstrasse, Germany)|November 24, 2024
Interplay Between Calcination Temperature and Alkaline Oxygen Evolution of Electrospun High-Entropy (Cr<sub>1/5</sub>Mn<sub>1/5</sub>Fe<sub>1/5</sub>Co<sub>1/5</sub>Ni<sub>1/5</sub>)<sub>3</sub>O<sub>4</sub> NanofibersKeti Vezzù, Claudia Triolo, Kaveh Moulaee, et al.
Investigative Ophthalmology & Visual Science|August 28, 2025
Retinal Vessel Changes in Geographic Atrophy in AMD: Insights From Imaging and HistologyChiara Olivieri, Antonio Fai, Imran A Bhutto, et al.
Nanotechnology|May 5, 2018
CO<sub>2</sub> sensing properties of electro-spun Ca-doped ZnO fibresFabiola Pantò, Salvatore Gianluca Leonardi, Enza Fazio, et al.
ACS Omega|January 8, 2026
Enhanced Electrochemical Detection of Lead Ions Using Schiff Base/MoS<sub>2</sub> Modified Screen-Printed ElectrodesDaniela Iannazzo, Zahra Akbari, Consuelo Celesti, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndromeJohn M Graham, Nancy Kramer, Bassem A Bejjani, et al.
European Journal of Medical Genetics|July 21, 2015
NFIX mutations affecting the DNA-binding domain cause a peculiar overgrowth syndrome (Malan syndrome): a new patients seriesFiorella Gurrieri, Maria Luigia Cavaliere, Anita Wischmeijer, et al.
American Journal of Human Genetics|February 4, 2003
Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2Marcella Zollino, Rosetta Lecce, Rita Fischetto, et al.
American Journal of Human Genetics|December 9, 2004
A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genesLuisa Russo, Paolo Mariotti, Eugenio Sangiorgi, et al.
Pageof 28