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Massimo Carella

Showing results (11-20 of 207) with videos related to

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Genes|May 4, 2026
A 350 kb <i>NEXMIF</i> Microdeletion Identified by Chromosomal Microarray in an Adult Patient with Jeavons SyndromeMario Benvenuto, Umberto Costantino, Pietro Palumbo, et al.
Molecular Cytogenetics|May 31, 2016
Clinical and molecular characterization of a de novo 19p13.3 microdeletionPietro Palumbo, Orazio Palumbo, Maria Pia Leone, et al.
American Journal of Medical Genetics. Part A|December 2, 2017
Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndromePietro Palumbo, Maria Accadia, Maria P Leone, et al.
Genes|July 2, 2020
A Private 16q24.2q24.3 Microduplication in a Boy with Intellectual Disability, Speech Delay and Mild Dysmorphic FeaturesOrazio Palumbo, Pietro Palumbo, Ester Di Muro, et al.
Methods and Protocols|May 23, 2025
Empagliflozin Repurposing for Lafora Disease: A Pilot Clinical Trial and Preclinical Investigation of Novel Therapeutic TargetsGiuseppe d'Orsi, Antonella Liantonio, Paola Imbrici, et al.
American Journal of Medical Genetics. Part A|November 28, 2014
Microdeletion of 12q24.31: report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphismsOrazio Palumbo, Pietro Palumbo, Maurizio Delvecchio, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 23, 2012
Altered expression of the clock gene machinery in kidney cancer patientsGianluigi Mazzoccoli, Ada Piepoli, Massimo Carella, et al.
Gene|February 4, 2014
Variable phenotype in 17q12 microdeletions: clinical and molecular characterization of a new casePietro Palumbo, Vincenzo Antona, Orazio Palumbo, et al.
Frontiers in Oncology|October 19, 2020
Early-Onset Diabetes as Risk Factor for Pancreatic Cancer: miRNA Expression Profiling in Plasma Uncovers a Role for miR-20b-5p, miR-29a, and miR-18a-5p in Diabetes of Recent DiagnosisFrancesca Tavano, Andrea Fontana, Tommaso Mazza, et al.
Gene|December 24, 2013
Patient affected by neurofibromatosis type 1 and thyroid C-cell hyperplasia harboring pathogenic germ-line mutations in both NF1 and RET genesTonino Ercolino, Roberta Lai, Valentino Giachè, et al.
Pageof 21

Showing results (11-20 of 207) with videos related to

Sort By:
Pageof 21
Genes|May 4, 2026
A 350 kb <i>NEXMIF</i> Microdeletion Identified by Chromosomal Microarray in an Adult Patient with Jeavons SyndromeMario Benvenuto, Umberto Costantino, Pietro Palumbo, et al.
Molecular Cytogenetics|May 31, 2016
Clinical and molecular characterization of a de novo 19p13.3 microdeletionPietro Palumbo, Orazio Palumbo, Maria Pia Leone, et al.
American Journal of Medical Genetics. Part A|December 2, 2017
Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndromePietro Palumbo, Maria Accadia, Maria P Leone, et al.
Genes|July 2, 2020
A Private 16q24.2q24.3 Microduplication in a Boy with Intellectual Disability, Speech Delay and Mild Dysmorphic FeaturesOrazio Palumbo, Pietro Palumbo, Ester Di Muro, et al.
Methods and Protocols|May 23, 2025
Empagliflozin Repurposing for Lafora Disease: A Pilot Clinical Trial and Preclinical Investigation of Novel Therapeutic TargetsGiuseppe d'Orsi, Antonella Liantonio, Paola Imbrici, et al.
American Journal of Medical Genetics. Part A|November 28, 2014
Microdeletion of 12q24.31: report of a girl with intellectual disability, stereotypies, seizures and facial dysmorphismsOrazio Palumbo, Pietro Palumbo, Maurizio Delvecchio, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 23, 2012
Altered expression of the clock gene machinery in kidney cancer patientsGianluigi Mazzoccoli, Ada Piepoli, Massimo Carella, et al.
Gene|February 4, 2014
Variable phenotype in 17q12 microdeletions: clinical and molecular characterization of a new casePietro Palumbo, Vincenzo Antona, Orazio Palumbo, et al.
Frontiers in Oncology|October 19, 2020
Early-Onset Diabetes as Risk Factor for Pancreatic Cancer: miRNA Expression Profiling in Plasma Uncovers a Role for miR-20b-5p, miR-29a, and miR-18a-5p in Diabetes of Recent DiagnosisFrancesca Tavano, Andrea Fontana, Tommaso Mazza, et al.
Gene|December 24, 2013
Patient affected by neurofibromatosis type 1 and thyroid C-cell hyperplasia harboring pathogenic germ-line mutations in both NF1 and RET genesTonino Ercolino, Roberta Lai, Valentino Giachè, et al.
Pageof 21