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Author/Creator Partemi, Sara

1. Corrigendum to "Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant" [Seizure 25 (2015) 65–67]. (August 2015)

Authors:
Tiron, Coloma; Campuzano, Oscar; Pérez-Serra, Alexandra; Mademont, Irene; Coll, Monica; Allegue, Catarina; Iglesias, Anna; Partemi, Sara; Striano, Pasquale; Oliva, Antonio; Brugada, Ramon
Journal:
Seizure
Issue:
Volume 30(2015)
Page Start:
136
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant. (February 2015)

Authors:
Tiron, Coloma; Campuzano, Oscar; Pérez-Serra, Alexandra; Mademont, Irene; Coll, Monica; Allegue, Catarina; Iglesias, Anna; Partemi, Sara; Striano, Pasquale; Oliva, Antonio; Brugada, Ramon
Journal:
Seizure
Issue:
Volume 25(2015)
Page Start:
65
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant. (February 2015)

Authors:
de Llano, Coloma Tiron; Campuzano, Oscar; Pérez-Serra, Alexandra; Mademont, Irene; Coll, Monica; Allegue, Catarina; Iglesias, Anna; Partemi, Sara; Striano, Pasquale; Oliva, Antonio; Brugada, Ramon
Journal:
Seizure
Issue:
Volume 25(2015)
Page Start:
65
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Genetics of arrhythmogenic right ventricular cardiomyopathy. Issue 5 (6th March 2013)

Authors:
Campuzano, Oscar; Alcalde, Mireia; Allegue, Catarina; Iglesias, Anna; García-Pavía, Pablo; Partemi, Sara; Oliva, Antonio; Pascali, Vincenzo L; Berne, Paola; Sarquella-Brugada, Georgia; Brugada, Josep; Brugada, Pedro; Brugada, Ramon
Journal:
Journal of medical genetics
Issue:
Volume 50:Issue 5(2013)
Page Start:
280
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Loss‐of‐function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death. Issue 8 (30th July 2013)

Authors:
Partemi, Sara; Cestèle, Sandrine; Pezzella, Marianna; Campuzano, Oscar; Paravidino, Roberta; Pascali, Vincenzo L.; Zara, Federico; Tassinari, Carlo Alberto; Striano, Salvatore; Oliva, Antonio; Brugada, Ramon; Mantegazza, Massimo; Striano, Pasquale
Journal:
Epilepsia
Issue:
Volume 54:Issue 8(2013:Aug.)
Page Start:
e112
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗