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American Journal of Medical Genetics. Part A
|
January 17, 2025
Mitochondrial Complex I Deficiency: Unraveling the Relevance of NDUFAF1 in Pediatric Hypertrophic Cardiomyopathy
Silvia Kalantari, Daniele Veraldi, Davide Politano, et al.
Acta Bio-Medica : Atenei Parmensis
|
November 29, 2021
Tailored therapies for primary immunodeficiencies
Bianca Cinicola, Federica Pulvirenti, Giulia Brindisi, et al.
Seizure
|
March 12, 2013
Epilepsy in patients with Cornelia de Lange syndrome: a clinical series
Alberto Verrotti, Sergio Agostinelli, Giovanni Prezioso, et al.
Cephalalgia : an International Journal of Headache
|
July 23, 2024
Headache in Sturge-Weber syndrome: A systematic review
Alessandro Ferretti, Marta Muscianese, Claudia Fanfoni, et al.
Neurology. Clinical Practice
|
April 25, 2024
Early Developmental Intervention and Enriched Environment in CDKL5 Developmental and Epileptic Encephalopathy: A Case Report
Martina Giorgia Perinelli, Cecilia Naboni, Ganna Balagura, et al.
Acta Bio-Medica : Atenei Parmensis
|
April 20, 2022
PRES-like leukoencephalopathy presenting with status epilepticus associated with Brentuximab Vedotin treatment
Alessandro Orsini, Sayla Bernasconi, Maria Cristina Bianchi, et al.
Acta Bio-Medica : Atenei Parmensis
|
October 2, 2020
SARS-CoV-2 infection in pediatric population
Sara Manti, Amelia Licari, Lorenza Montagna, et al.
Epilepsia
|
June 27, 2014
Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy
Alberto Verrotti, Maria Valentina Spartà, Debora Monacelli, et al.
Molecular Genetics and Metabolism
|
December 6, 2021
Alexander disease evolution over time: data from an Italian cohort of pediatric-onset patients
Eleonora Mura, Francesco Nicita, Silvia Masnada, et al.
Seizure
|
October 15, 2021
Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-up
Vincenzo Belcastro, Susanna Casellato, Pasquale Striano, et al.
Page
of 9
Search research articles
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Showing results (51-60 of 85) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics. Part A
|
January 17, 2025
Mitochondrial Complex I Deficiency: Unraveling the Relevance of NDUFAF1 in Pediatric Hypertrophic Cardiomyopathy
Silvia Kalantari, Daniele Veraldi, Davide Politano, et al.
Acta Bio-Medica : Atenei Parmensis
|
November 29, 2021
Tailored therapies for primary immunodeficiencies
Bianca Cinicola, Federica Pulvirenti, Giulia Brindisi, et al.
Seizure
|
March 12, 2013
Epilepsy in patients with Cornelia de Lange syndrome: a clinical series
Alberto Verrotti, Sergio Agostinelli, Giovanni Prezioso, et al.
Cephalalgia : an International Journal of Headache
|
July 23, 2024
Headache in Sturge-Weber syndrome: A systematic review
Alessandro Ferretti, Marta Muscianese, Claudia Fanfoni, et al.
Neurology. Clinical Practice
|
April 25, 2024
Early Developmental Intervention and Enriched Environment in CDKL5 Developmental and Epileptic Encephalopathy: A Case Report
Martina Giorgia Perinelli, Cecilia Naboni, Ganna Balagura, et al.
Acta Bio-Medica : Atenei Parmensis
|
April 20, 2022
PRES-like leukoencephalopathy presenting with status epilepticus associated with Brentuximab Vedotin treatment
Alessandro Orsini, Sayla Bernasconi, Maria Cristina Bianchi, et al.
Acta Bio-Medica : Atenei Parmensis
|
October 2, 2020
SARS-CoV-2 infection in pediatric population
Sara Manti, Amelia Licari, Lorenza Montagna, et al.
Epilepsia
|
June 27, 2014
Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy
Alberto Verrotti, Maria Valentina Spartà, Debora Monacelli, et al.
Molecular Genetics and Metabolism
|
December 6, 2021
Alexander disease evolution over time: data from an Italian cohort of pediatric-onset patients
Eleonora Mura, Francesco Nicita, Silvia Masnada, et al.
Seizure
|
October 15, 2021
Epilepsy in "Sunflower syndrome": electroclinical features, therapeutic response, and long-term follow-up
Vincenzo Belcastro, Susanna Casellato, Pasquale Striano, et al.
Page
of 9