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Vitello

Showing results (311-320 of 360) with videos related to

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Epilepsia|April 21, 2011
Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsyCarlo Di Bonaventura, Francesca F Operto, Giorgia Busolin, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|March 18, 2026
Practical management of glucagon-like peptide-1 receptor agonists in gastroenterology: a position paper by the Italian Society of Gastroenterology (SIGE)Antonio Facciorusso, Edoardo G Giannini, Matteo Tacelli, et al.
Genes|August 29, 2024
<i>PLEKHG1</i>: New Potential Candidate Gene for Periventricular White Matter AbnormalitiesFrancesco Calì, Mirella Vinci, Simone Treccarichi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 10, 2014
Increased risk of impulse control symptoms in Parkinson's disease with REM sleep behaviour disorderM L Fantini, L Macedo, M Zibetti, et al.
Heliyon|March 14, 2023
Medical emergencies in dental practice: A nationwide web-based survey of Italian dentistsElena M Varoni, Marta Rigoni, Giovanni Lodi, et al.
Frontiers in Public Health|July 10, 2023
Knowledge and adherence to the Mediterranean diet in individuals practicing regular amatorial physical activity: a cross-sectional study conducted in the Metropolitan Area of Palermo, ItalyClaudio Costantino, Alessandra Casuccio, Miriam Belluzzo, et al.
Mitochondrion|May 4, 2010
Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortexCarmela Scuderi, Eugenia Borgione, Filippa Castello, et al.
Journal of Endocrinological Investigation|June 1, 2026
Differential associations of traditional and shape-based adiposity indices with steatosis and fibrosis risk in metabolic dysfunction-associated steatotic liver diseaseGiulio Geraci, Valentina Paternò, Alessandro Vitello, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 20, 2020
Impact of the COVID-19 pandemic on Gastroenterology Divisions in Italy: A national surveyM Maida, S Sferrazza, E Savarino, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypesCharlotte Snijders Blok, Nicole Corsten-Janssen, David R FitzPatrick, et al.
Pageof 36

Showing results (311-320 of 360) with videos related to

Sort By:
Pageof 36
Epilepsia|April 21, 2011
Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsyCarlo Di Bonaventura, Francesca F Operto, Giorgia Busolin, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|March 18, 2026
Practical management of glucagon-like peptide-1 receptor agonists in gastroenterology: a position paper by the Italian Society of Gastroenterology (SIGE)Antonio Facciorusso, Edoardo G Giannini, Matteo Tacelli, et al.
Genes|August 29, 2024
<i>PLEKHG1</i>: New Potential Candidate Gene for Periventricular White Matter AbnormalitiesFrancesco Calì, Mirella Vinci, Simone Treccarichi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 10, 2014
Increased risk of impulse control symptoms in Parkinson's disease with REM sleep behaviour disorderM L Fantini, L Macedo, M Zibetti, et al.
Heliyon|March 14, 2023
Medical emergencies in dental practice: A nationwide web-based survey of Italian dentistsElena M Varoni, Marta Rigoni, Giovanni Lodi, et al.
Frontiers in Public Health|July 10, 2023
Knowledge and adherence to the Mediterranean diet in individuals practicing regular amatorial physical activity: a cross-sectional study conducted in the Metropolitan Area of Palermo, ItalyClaudio Costantino, Alessandra Casuccio, Miriam Belluzzo, et al.
Mitochondrion|May 4, 2010
Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortexCarmela Scuderi, Eugenia Borgione, Filippa Castello, et al.
Journal of Endocrinological Investigation|June 1, 2026
Differential associations of traditional and shape-based adiposity indices with steatosis and fibrosis risk in metabolic dysfunction-associated steatotic liver diseaseGiulio Geraci, Valentina Paternò, Alessandro Vitello, et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|May 20, 2020
Impact of the COVID-19 pandemic on Gastroenterology Divisions in Italy: A national surveyM Maida, S Sferrazza, E Savarino, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
Definition of 5q11.2 microdeletion syndrome reveals overlap with CHARGE syndrome and 22q11 deletion syndrome phenotypesCharlotte Snijders Blok, Nicole Corsten-Janssen, David R FitzPatrick, et al.
Pageof 36