Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation

M Cataldi; L Nobili; F Zara; R Combi; G Prato; T Giacomini; V Capra; P De Marco; L Ferini-Strambi; MM Mancardi

doi:10.1016/j.seizure.2019.02.019

Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation

M Cataldi, L Nobili, F Zara, R Combi, G Prato, T Giacomini, V Capra, P De Marco, L Ferini-Strambi, MM Mancardi

IRCCS Ospedale San Raffaele

Research output: Contribution to journal › Article › peer-review

Abstract

No abstract available

Original language	English
Pages (from-to)	57-60
Number of pages	4
Journal	Seizure
Volume	67
DOIs	https://doi.org/10.1016/j.seizure.2019.02.019
Publication status	Published - 2019

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@article{07004a0ae8c748fdb38204579f5df430,

title = "Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation",

abstract = "No abstract available",

author = "M Cataldi and L Nobili and F Zara and R Combi and G Prato and T Giacomini and V Capra and {De Marco}, P and L Ferini-Strambi and MM Mancardi",

year = "2019",

doi = "10.1016/j.seizure.2019.02.019",

language = "English",

volume = "67",

pages = "57--60",

journal = "Seizure : the journal of the British Epilepsy Association",

issn = "1059-1311",

publisher = "W.B. Saunders Ltd",

}

TY - JOUR

T1 - Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation

AU - Cataldi, M

AU - Nobili, L

AU - Zara, F

AU - Combi, R

AU - Prato, G

AU - Giacomini, T

AU - Capra, V

AU - De Marco, P

AU - Ferini-Strambi, L

AU - Mancardi, MM

PY - 2019

Y1 - 2019

N2 - No abstract available

AB - No abstract available

U2 - 10.1016/j.seizure.2019.02.019

DO - 10.1016/j.seizure.2019.02.019

M3 - Article

VL - 67

SP - 57

EP - 60

JO - Seizure : the journal of the British Epilepsy Association

JF - Seizure : the journal of the British Epilepsy Association

SN - 1059-1311

ER -

Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation

Abstract

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