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Capovilla

Showing results (251-260 of 359) with videos related to

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Nature Plants|April 19, 2017
A circRNA from SEPALLATA3 regulates splicing of its cognate mRNA through R-loop formationVanessa M Conn, Véronique Hugouvieux, Aditya Nayak, et al.
Epilepsia|June 4, 2009
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: a homogeneous epileptic condition among the patients presenting with eyelid myocloniaGiuseppe Capovilla, Pasquale Striano, Antonio Gambardella, et al.
Epilepsia|February 6, 2010
Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in ItalyVeriano Alexandre, Giuseppe Capovilla, Cinzia Fattore, et al.
Circulation. Genomic and Precision Medicine|April 1, 2026
Twenty-Five-Year Follow-Up of the MDDC1 Family: A <i>LMNA</i> Gene Variant Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle InvolvementTeresa Maria Capovilla, Manuela Iseppi, Salvatore Distaso, et al.
Global Spine Journal|April 23, 2021
Pharyngo-Esophageal Perforation Following Anterior Cervical Spine Surgery: A Single Center Experience and a Systematic Review of the LiteratureLucia Moletta, Elisa Sefora Pierobon, Renato Salvador, et al.
Epilepsia|June 21, 2020
Relationship between saliva and plasma rufinamide concentrations in patients with epilepsyValentina Franco, Giuliana Gatti, Iolanda Mazzucchelli, et al.
Surgical Endoscopy|October 10, 2022
Laparoscopic Heller-Dor is an effective long-term treatment for end-stage achalasiaRenato Salvador, Giulia Nezi, Francesca Forattini, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|June 27, 2025
Genetic testing in cardiomyopathies: updates and future perspectivesFederico Garoia, Teresa Maria Capovilla, Anna Reginato, et al.
American Journal of Medical Genetics. Part A|October 7, 2015
Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical regionFrancesco Nicita, Giacomo Garone, Alberto Spalice, et al.
Histopathology|March 15, 2018
High rate of PIK3CA mutations but no TP53 mutations in low-grade adenosquamous carcinoma of the breastGuillaume Bataillon, Laetitia Fuhrmann, Elodie Girard, et al.
Pageof 36

Showing results (251-260 of 359) with videos related to

Sort By:
Pageof 36
Nature Plants|April 19, 2017
A circRNA from SEPALLATA3 regulates splicing of its cognate mRNA through R-loop formationVanessa M Conn, Véronique Hugouvieux, Aditya Nayak, et al.
Epilepsia|June 4, 2009
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: a homogeneous epileptic condition among the patients presenting with eyelid myocloniaGiuseppe Capovilla, Pasquale Striano, Antonio Gambardella, et al.
Epilepsia|February 6, 2010
Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in ItalyVeriano Alexandre, Giuseppe Capovilla, Cinzia Fattore, et al.
Circulation. Genomic and Precision Medicine|April 1, 2026
Twenty-Five-Year Follow-Up of the MDDC1 Family: A <i>LMNA</i> Gene Variant Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle InvolvementTeresa Maria Capovilla, Manuela Iseppi, Salvatore Distaso, et al.
Global Spine Journal|April 23, 2021
Pharyngo-Esophageal Perforation Following Anterior Cervical Spine Surgery: A Single Center Experience and a Systematic Review of the LiteratureLucia Moletta, Elisa Sefora Pierobon, Renato Salvador, et al.
Epilepsia|June 21, 2020
Relationship between saliva and plasma rufinamide concentrations in patients with epilepsyValentina Franco, Giuliana Gatti, Iolanda Mazzucchelli, et al.
Surgical Endoscopy|October 10, 2022
Laparoscopic Heller-Dor is an effective long-term treatment for end-stage achalasiaRenato Salvador, Giulia Nezi, Francesca Forattini, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|June 27, 2025
Genetic testing in cardiomyopathies: updates and future perspectivesFederico Garoia, Teresa Maria Capovilla, Anna Reginato, et al.
American Journal of Medical Genetics. Part A|October 7, 2015
Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical regionFrancesco Nicita, Giacomo Garone, Alberto Spalice, et al.
Histopathology|March 15, 2018
High rate of PIK3CA mutations but no TP53 mutations in low-grade adenosquamous carcinoma of the breastGuillaume Bataillon, Laetitia Fuhrmann, Elodie Girard, et al.
Pageof 36