Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.

C von Stülpnagel; M Ensslen; R S Møller; D K Pal; S Masnada; P Veggiotti; E Piazza; M Dreesmann; Till Hartlieb; Thomas Herberhold; E Hughes; M Koch; C Kutzer; K Hoertnagel; J Nitanda; M Pohl; K Rostásy; T B Haack; K Stöhr; Gerhard Kluger; I Borggraefe

doi:10.1016/j.ejpn.2017.01.001

Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.

C von Stülpnagel^* (First author), M Ensslen, R S Møller, D K Pal, S Masnada, P Veggiotti, E Piazza, M Dreesmann, Till Hartlieb, Thomas Herberhold (Co-author), E Hughes, M Koch, C Kutzer, K Hoertnagel, J Nitanda, M Pohl, K Rostásy, T B Haack, K Stöhr, Gerhard Kluger (Co-author)I Borggraefe

^*Corresponding author for this work

Research output: Contribution to journal › Original Article (Journal) › peer-review

34 Citations (Web of Science)

Original language	English
Pages (from-to)	530-541
Journal	EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
Volume	21
Issue number	3
DOIs	https://doi.org/10.1016/j.ejpn.2017.01.001
Publication status	Published - 2017

Keywords

BENIGN CHILDHOOD EPILEPSY
CENTROTEMPORAL SPIKES
COGNITIVE FUNCTION
ROLANDIC EPILEPSY
FOCAL EPILEPSY
CHILDREN
MUTATIONS
SULTHIAME
ENCEPHALOPATHIES
SPEECH

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10.1016/j.ejpn.2017.01.001

Cite this

von Stülpnagel, C., Ensslen, M., Møller, R. S., Pal, D. K., Masnada, S., Veggiotti, P., Piazza, E., Dreesmann, M., Hartlieb, T., Herberhold, T., Hughes, E., Koch, M., Kutzer, C., Hoertnagel, K., Nitanda, J., Pohl, M., Rostásy, K., Haack, T. B., Stöhr, K., ... Borggraefe, I. (2017). Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 21(3), 530-541. https://doi.org/10.1016/j.ejpn.2017.01.001

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title = "Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.",

keywords = "BENIGN CHILDHOOD EPILEPSY, CENTROTEMPORAL SPIKES, COGNITIVE FUNCTION, ROLANDIC EPILEPSY, FOCAL EPILEPSY, CHILDREN, MUTATIONS, SULTHIAME, ENCEPHALOPATHIES, SPEECH",

author = "{von St{\"u}lpnagel}, C and M Ensslen and M{\o}ller, {R S} and Pal, {D K} and S Masnada and P Veggiotti and E Piazza and M Dreesmann and Till Hartlieb and Thomas Herberhold and E Hughes and M Koch and C Kutzer and K Hoertnagel and J Nitanda and M Pohl and K Rost{\'a}sy and Haack, {T B} and K St{\"o}hr and Gerhard Kluger and I Borggraefe",

note = "von St{\"u}lpnagel, Kluger: Paracelsus Medical University Salzburg, Salzburg, Austria",

year = "2017",

doi = "10.1016/j.ejpn.2017.01.001",

language = "English",

volume = "21",

pages = "530--541",

journal = "EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY",

issn = "1090-3798",

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number = "3",

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von Stülpnagel, C, Ensslen, M, Møller, RS, Pal, DK, Masnada, S, Veggiotti, P, Piazza, E, Dreesmann, M, Hartlieb, T , Herberhold, T, Hughes, E, Koch, M, Kutzer, C, Hoertnagel, K, Nitanda, J, Pohl, M, Rostásy, K, Haack, TB, Stöhr, K, Kluger, G & Borggraefe, I 2017, 'Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.', EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, vol. 21, no. 3, pp. 530-541. https://doi.org/10.1016/j.ejpn.2017.01.001

TY - JOUR

T1 - Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.

AU - von Stülpnagel, C

AU - Ensslen, M

AU - Møller, R S

AU - Pal, D K

AU - Masnada, S

AU - Veggiotti, P

AU - Piazza, E

AU - Dreesmann, M

AU - Hartlieb, Till

AU - Herberhold, Thomas

AU - Hughes, E

AU - Koch, M

AU - Kutzer, C

AU - Hoertnagel, K

AU - Nitanda, J

AU - Pohl, M

AU - Rostásy, K

AU - Haack, T B

AU - Stöhr, K

AU - Kluger, Gerhard

AU - Borggraefe, I

N1 - von Stülpnagel, Kluger: Paracelsus Medical University Salzburg, Salzburg, Austria

PY - 2017

Y1 - 2017

KW - BENIGN CHILDHOOD EPILEPSY

KW - CENTROTEMPORAL SPIKES

KW - COGNITIVE FUNCTION

KW - ROLANDIC EPILEPSY

KW - FOCAL EPILEPSY

KW - CHILDREN

KW - MUTATIONS

KW - SULTHIAME

KW - ENCEPHALOPATHIES

KW - SPEECH

U2 - 10.1016/j.ejpn.2017.01.001

DO - 10.1016/j.ejpn.2017.01.001

M3 - Original Article (Journal)

C2 - 28109652

SN - 1090-3798

VL - 21

SP - 530

EP - 541

JO - EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

JF - EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

IS - 3

ER -