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Repository
37
(4)
65
(1)
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Author
Ellenrieder, Nicolás von
(2)
Gotman, Jean
(2)
Abba, Martín Carlos
(1)
Aldaz, C. Marcelo
(1)
Avoli, Massimo
(1)
Bertoli Avella, Aida M.
(1)
Dubeau, François
(1)
Ferguson, B.W.
(1)
Ferrari-Marinho, Taissa
(1)
Frauscher, Birgit
(1)
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Subject
Epilepsy
(5)
Ciencias Médicas
(3)
ARX
(1)
Automatic detection
(1)
Bioquímica
(1)
FRA16D
(1)
High frequency activity
(1)
High frequency oscillations
(1)
Human
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Infantile Diabetes
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2019
(5)
930
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2011
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Subject:
Epilepsy
Year:
2019
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Title:
WWOX at the crossroads of cancer, metabolic syndrome related traits and CNS pathologies
Author:
Aldaz, C. Marcelo
/
Ferguson, B.W.
/
Abba, Martín Carlos
Language:
Inglés
Repository:
37
Subject:
Bioquímica
/
Epilepsy
/
FRA16D
/
Lipid metabolism
/
TGFβ
/
WNT
/
WWOX
Acceder
Title:
Facilitation of epileptic activity during sleep is mediated by high amplitude slow waves
Author:
Frauscher, Birgit
/
Ellenrieder, Nicolás von
/
Ferrari-Marinho, Taissa
/
Avoli, Massimo
/
Dubeau, François
/
Gotman, Jean
Language:
Inglés
Repository:
37
Subject:
Ciencias Médicas
/
Epilepsy
/
High frequency oscillations
/
Intracerebral electroencephalography
/
Sleep
/
Slow wave
Acceder
Title:
Detection and Magnetic Source Imaging of Fast Oscillations (40–160 Hz) Recorded with Magnetoencephalography in Focal Epilepsy Patients
Author:
Ellenrieder, Nicolás von
/
Pellegrino, Giovanni
/
Hedrich, Tanguy
/
Gotman, Jean
/
Lina, Jean Marc
/
Grova, Christophe
/
Kobayashi, Eliane
Language:
Inglés
Repository:
37
Subject:
Ingeniería
/
Ciencias Médicas
/
Automatic detection
/
Epilepsy
/
High frequency activity
/
Human
/
Source localization
Acceder
Title:
Microcephaly with simplified gyration, epilepsy, and infantile diabetes linked to inappropriate apoptosis of neural progenitors
Author:
Poulton, Cathryn J.
/
Schot, Rachel
/
Kia, Sima Kheradmand
/
Jones Bernal, Marta Celina
/
Verheijen, Frans W.
/
Venselaar, Hanka
/
Y. de Wit, Marie Claire
/
Graaff, Esther de
/
Bertoli Avella, Aida M.
/
Mancini, Grazia M. S.
Language:
Inglés
Repository:
37
Subject:
Ciencias Médicas
/
microcephaly
/
Epilepsy
/
Infantile Diabetes
Acceder
Title:
A novel mutation in the OAR domain of the ARX gene
Language:
Inglés
Repository:
65
Subject:
ARX
/
Epilepsy
/
Mental retardation
/
Ohtahara syndrome
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