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European Journal of Haematology
|
November 15, 2020
Histology of the spleen in immune thrombocytopenia: clinical-pathological characterization and prognostic implications
Marco Pizzi, Alberto Friziero, Fabrizio Vianello, et al.
European Journal of Preventive Cardiology
|
August 12, 2025
Cardiopulmonary exercise testing in hypertrophic cardiomyopathy: the role of reduced O2 pulse and chronotropic incompetence in myocardial adaptation
Robin Willixhofer, Massimo Mapelli, Nikita Baracchini, et al.
Epilepsy Research
|
April 16, 2003
No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy
Francesca Madia, Elena Gennaro, Massimiliano Cecconi, et al.
Epilepsia Open
|
August 23, 2024
Italian report on RARE epilepsies (i-RARE): A consensus on multidisciplinarity
Antonella Riva, Antonietta Coppola, Francesca Bisulli, et al.
European Journal of Neurology
|
October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution
S Agostinelli, M Traverso, P Accorsi, et al.
Epilepsy Research
|
May 7, 2011
A clinical and genetic study of 33 new cases with early-onset absence epilepsy
Lucio Giordano, Aglaia Vignoli, Patrizia Accorsi, et al.
Epilepsy & Behavior : E&B
|
December 16, 2014
An educational campaign about epilepsy among Italian primary school teachers. 2. The results of a focused training program
Oriano Mecarelli, Paolo Messina, Giuseppe Capovilla, et al.
Journal of the American Heart Association
|
April 9, 2026
RoMa: A Cardiopulmonary Exercise Testing Based Risk Tool in Hypertrophic Cardiomyopathy
Robin Willixhofer, Massimo Mapelli, Nikita Baracchini, et al.
Epilepsia
|
October 24, 2006
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations
Maria Margherita Mancardi, Pasquale Striano, Elena Gennaro, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 21, 2015
Paediatric anti-N-methyl-D-aspartate receptor encephalitis: The first Italian multicenter case series
Stefano Sartori, Margherita Nosadini, Elisabetta Cesaroni, et al.
Page
of 36
Search research articles
Search
Showing results (321-330 of 359) with videos related to
Sort By:
Page
of 36
European Journal of Haematology
|
November 15, 2020
Histology of the spleen in immune thrombocytopenia: clinical-pathological characterization and prognostic implications
Marco Pizzi, Alberto Friziero, Fabrizio Vianello, et al.
European Journal of Preventive Cardiology
|
August 12, 2025
Cardiopulmonary exercise testing in hypertrophic cardiomyopathy: the role of reduced O2 pulse and chronotropic incompetence in myocardial adaptation
Robin Willixhofer, Massimo Mapelli, Nikita Baracchini, et al.
Epilepsy Research
|
April 16, 2003
No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy
Francesca Madia, Elena Gennaro, Massimiliano Cecconi, et al.
Epilepsia Open
|
August 23, 2024
Italian report on RARE epilepsies (i-RARE): A consensus on multidisciplinarity
Antonella Riva, Antonietta Coppola, Francesca Bisulli, et al.
European Journal of Neurology
|
October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution
S Agostinelli, M Traverso, P Accorsi, et al.
Epilepsy Research
|
May 7, 2011
A clinical and genetic study of 33 new cases with early-onset absence epilepsy
Lucio Giordano, Aglaia Vignoli, Patrizia Accorsi, et al.
Epilepsy & Behavior : E&B
|
December 16, 2014
An educational campaign about epilepsy among Italian primary school teachers. 2. The results of a focused training program
Oriano Mecarelli, Paolo Messina, Giuseppe Capovilla, et al.
Journal of the American Heart Association
|
April 9, 2026
RoMa: A Cardiopulmonary Exercise Testing Based Risk Tool in Hypertrophic Cardiomyopathy
Robin Willixhofer, Massimo Mapelli, Nikita Baracchini, et al.
Epilepsia
|
October 24, 2006
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations
Maria Margherita Mancardi, Pasquale Striano, Elena Gennaro, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 21, 2015
Paediatric anti-N-methyl-D-aspartate receptor encephalitis: The first Italian multicenter case series
Stefano Sartori, Margherita Nosadini, Elisabetta Cesaroni, et al.
Page
of 36