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Nature Plants
|
April 19, 2017
A circRNA from SEPALLATA3 regulates splicing of its cognate mRNA through R-loop formation
Vanessa 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 myoclonia
Giuseppe 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 Italy
Veriano 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 Involvement
Teresa 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 Literature
Lucia Moletta, Elisa Sefora Pierobon, Renato Salvador, et al.
Epilepsia
|
June 21, 2020
Relationship between saliva and plasma rufinamide concentrations in patients with epilepsy
Valentina Franco, Giuliana Gatti, Iolanda Mazzucchelli, et al.
Surgical Endoscopy
|
October 10, 2022
Laparoscopic Heller-Dor is an effective long-term treatment for end-stage achalasia
Renato Salvador, Giulia Nezi, Francesca Forattini, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
June 27, 2025
Genetic testing in cardiomyopathies: updates and future perspectives
Federico 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 region
Francesco 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 breast
Guillaume Bataillon, Laetitia Fuhrmann, Elodie Girard, et al.
Page
of 36
Search research articles
Search
Showing results (251-260 of 359) with videos related to
Sort By:
Page
of 36
Nature Plants
|
April 19, 2017
A circRNA from SEPALLATA3 regulates splicing of its cognate mRNA through R-loop formation
Vanessa 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 myoclonia
Giuseppe 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 Italy
Veriano 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 Involvement
Teresa 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 Literature
Lucia Moletta, Elisa Sefora Pierobon, Renato Salvador, et al.
Epilepsia
|
June 21, 2020
Relationship between saliva and plasma rufinamide concentrations in patients with epilepsy
Valentina Franco, Giuliana Gatti, Iolanda Mazzucchelli, et al.
Surgical Endoscopy
|
October 10, 2022
Laparoscopic Heller-Dor is an effective long-term treatment for end-stage achalasia
Renato Salvador, Giulia Nezi, Francesca Forattini, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)
|
June 27, 2025
Genetic testing in cardiomyopathies: updates and future perspectives
Federico 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 region
Francesco 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 breast
Guillaume Bataillon, Laetitia Fuhrmann, Elodie Girard, et al.
Page
of 36