Co-occurring malformations of cortical development and SCN1A gene mutations.

Carmen Barba; Elena Parrini; Roland Coras; Anna Galuppi; Dana Craiu; Gerhard Kluger; Antonia Parmeggiani; Tom Pieper; Thomas Schmitt-Mechelke; Pasquale Striano; Flavio Giordano; Ingmar Blumcke; Renzo Guerrini

doi:10.1111/epi.12658

Co-occurring malformations of cortical development and SCN1A gene mutations.

Carmen Barba, Elena Parrini, Roland Coras, Anna Galuppi, Dana Craiu, Gerhard Kluger (Co-Autor/-in), Antonia Parmeggiani, Tom Pieper, Thomas Schmitt-Mechelke, Pasquale Striano, Flavio Giordano, Ingmar Blumcke, Renzo Guerrini

Publikation: Beitrag in Fachzeitschrift › Originalarbeit › Begutachtung

79 Quellenangaben (Web of Science)

Originalsprache	Englisch
Seiten (von - bis)	1009-1019
Fachzeitschrift	EPILEPSIA
Jahrgang	55
Ausgabenummer	7
DOIs	https://doi.org/10.1111/epi.12658
Publikationsstatus	Veröffentlicht - 2014

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10.1111/epi.12658

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title = "Co-occurring malformations of cortical development and SCN1A gene mutations.",

keywords = "SEVERE MYOCLONIC EPILEPSY, PERIVENTRICULAR NODULAR HETEROTOPIA, REDUCED SODIUM CURRENT, DRAVET SYNDROME, HIPPOCAMPAL SCLEROSIS, NEURONAL MIGRATION, CEREBRAL-CORTEX, MOUSE MODEL, INFANCY, DYSPLASIA",

author = "Carmen Barba and Elena Parrini and Roland Coras and Anna Galuppi and Dana Craiu and Gerhard Kluger and Antonia Parmeggiani and Tom Pieper and Thomas Schmitt-Mechelke and Pasquale Striano and Flavio Giordano and Ingmar Blumcke and Renzo Guerrini",

note = "Paracelsus Medical University Salzburg, Salzburg, Austria",

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AU - Barba, Carmen

AU - Parrini, Elena

AU - Coras, Roland

AU - Galuppi, Anna

AU - Craiu, Dana

AU - Kluger, Gerhard

AU - Parmeggiani, Antonia

AU - Pieper, Tom

AU - Schmitt-Mechelke, Thomas

AU - Striano, Pasquale

AU - Giordano, Flavio

AU - Blumcke, Ingmar

AU - Guerrini, Renzo

N1 - Paracelsus Medical University Salzburg, Salzburg, Austria

PY - 2014

Y1 - 2014

KW - SEVERE MYOCLONIC EPILEPSY

KW - PERIVENTRICULAR NODULAR HETEROTOPIA

KW - REDUCED SODIUM CURRENT

KW - DRAVET SYNDROME

KW - HIPPOCAMPAL SCLEROSIS

KW - NEURONAL MIGRATION

KW - CEREBRAL-CORTEX

KW - MOUSE MODEL

KW - INFANCY

KW - DYSPLASIA

U2 - 10.1111/epi.12658

DO - 10.1111/epi.12658

M3 - Original Article

C2 - 24902755

SN - 0013-9580

VL - 55

SP - 1009

EP - 1019

JO - EPILEPSIA

JF - EPILEPSIA

IS - 7

ER -