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

Alvaro Mesoraca

Showing results (11-20 of 43) with videos related to

Pageof 5
Sort By:
Current Issues in Molecular Biology|April 26, 2024
Prenatal Diagnosis by Trio Clinical Exome Sequencing: Single Center ExperienceKatia Margiotti, Marco Fabiani, Antonella Cima, et al.
Virology Journal|July 2, 2020
Evaluation of SARS-CoV-2 viral RNA in fecal samplesAlvaro Mesoraca, Katia Margiotti, Antonella Viola, et al.
Vaccines|March 26, 2022
A Rapid and Consistent Method to Identify Four SARS-CoV-2 Variants during the First Half of 2021 by RT-PCRMarco Fabiani, Katia Margiotti, Manuela Sabatino, et al.
Viral Immunology|May 4, 2023
Dynamics of SARS-CoV-2-Specific B Cell Memory Responses in Infected and Vaccinated IndividualsMarco Fabiani, Katia Margiotti, Francesca Monaco, et al.
Genes|December 30, 2025
Neurodevelopmental Phenotype Associated with <i>TRIP12</i>: Report of a Family Carrying the p.Asp1135Val VariantKatia Margiotti, Marco Fabiani, Antonella Cima, et al.
Fetal and Pediatric Pathology|December 11, 2024
A Case Report of 10q24.32 Microduplication Associated with Split Hand/Foot Malformation (SHFM) in Prenatal DiagnosisMarco Fabiani, Katia Margiotti, Francesco Libotte, et al.
Experimental and Therapeutic Medicine|February 10, 2023
<i>De novo</i> 3q13.13q21.2 interstitial deletion and paternal 12p13.3 microdeletion in a fetus with dysplasia of the corpus callosum and ventriculomegaly: A case reportFrancesco Libotte, Marco Fabiani, Katia Margiotti, et al.
Archives of Gynecology and Obstetrics|November 13, 2015
Predictive value of pregnancy-associated plasma protein-A (PAPP-A) and free beta-hCG on fetal growth restriction: results of a prospective studyPietro Cignini, Laura Maggio Savasta, Ferdinando Antonio Gulino, et al.
Journal of Prenatal Medicine|October 22, 2014
Next generation sequencing in the identification of a rare genetic disease from preconceptional couple screening to preimplantation genetic diagnosisClaudio Dello Russo, Gianluca Di Giacomo, Alvaro Mesoraca, et al.
Journal of Prenatal Medicine|March 11, 2014
Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluidManuela Coco, Fabrizio Salvinelli, Fabio Greco, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Current Issues in Molecular Biology|April 26, 2024
Prenatal Diagnosis by Trio Clinical Exome Sequencing: Single Center ExperienceKatia Margiotti, Marco Fabiani, Antonella Cima, et al.
Virology Journal|July 2, 2020
Evaluation of SARS-CoV-2 viral RNA in fecal samplesAlvaro Mesoraca, Katia Margiotti, Antonella Viola, et al.
Vaccines|March 26, 2022
A Rapid and Consistent Method to Identify Four SARS-CoV-2 Variants during the First Half of 2021 by RT-PCRMarco Fabiani, Katia Margiotti, Manuela Sabatino, et al.
Viral Immunology|May 4, 2023
Dynamics of SARS-CoV-2-Specific B Cell Memory Responses in Infected and Vaccinated IndividualsMarco Fabiani, Katia Margiotti, Francesca Monaco, et al.
Genes|December 30, 2025
Neurodevelopmental Phenotype Associated with <i>TRIP12</i>: Report of a Family Carrying the p.Asp1135Val VariantKatia Margiotti, Marco Fabiani, Antonella Cima, et al.
Fetal and Pediatric Pathology|December 11, 2024
A Case Report of 10q24.32 Microduplication Associated with Split Hand/Foot Malformation (SHFM) in Prenatal DiagnosisMarco Fabiani, Katia Margiotti, Francesco Libotte, et al.
Experimental and Therapeutic Medicine|February 10, 2023
<i>De novo</i> 3q13.13q21.2 interstitial deletion and paternal 12p13.3 microdeletion in a fetus with dysplasia of the corpus callosum and ventriculomegaly: A case reportFrancesco Libotte, Marco Fabiani, Katia Margiotti, et al.
Archives of Gynecology and Obstetrics|November 13, 2015
Predictive value of pregnancy-associated plasma protein-A (PAPP-A) and free beta-hCG on fetal growth restriction: results of a prospective studyPietro Cignini, Laura Maggio Savasta, Ferdinando Antonio Gulino, et al.
Journal of Prenatal Medicine|October 22, 2014
Next generation sequencing in the identification of a rare genetic disease from preconceptional couple screening to preimplantation genetic diagnosisClaudio Dello Russo, Gianluca Di Giacomo, Alvaro Mesoraca, et al.
Journal of Prenatal Medicine|March 11, 2014
Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluidManuela Coco, Fabrizio Salvinelli, Fabio Greco, et al.
Pageof 5