NOVEL HCN ION CHANNELS MUTATIONS IN IDIOPATHIC GENERALIZED EPILEPSY

被引：0

作者：

Di Francesco, J. C. ^{[1
,2
]}

Castellotti, B. ^{[1
]}

Milanesi, R. ^{[3
]}

Riva, I. ^{[2
]}

Bonzanni, M. ^{[3
]}

Barbuti, A. ^{[3
]}

Castucci, A. ^{[1
]}

Magri, S. ^{[1
]}

Gellera, C. ^{[1
]}

Granata, T. ^{[1
]}

Freri, E. ^{[1
]}

Ragona, F. ^{[1
]}

Canafoglia, L. ^{[1
]}

Casazza, M. ^{[1
]}

Binelli, S. ^{[1
]}

Franceschetti, S. ^{[1
]}

机构：

[1] Fdn Carlo Besta, Neurol Inst, Milan, Italy

[2] Univ Milano Bicocca, San Gerardo Hosp, Monza, Italy

[3] Univ Milan, Milan, Italy

来源：

EPILEPSIA | 2015年 / 56卷

关键词：

D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

p0265

引用

页码：73 / 73

页数：1

共 50 条

[21] Ion channels and epilepsy
Armijo, JA
Shushtarian, M
Valdizan, EM
Cuadrado, A
de las Cuevas, I
Adín, J
CURRENT PHARMACEUTICAL DESIGN, 2005, 11 (15) : 1975 - 2003
[22] Ion channels and epilepsy
Graves, TD
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2006, 99 (04) : 201 - 217
[23] Ion channels and epilepsy
Mazzuca, Michel
Lesage, Florian
Lazdunski, Michel
EPILEPTIC DISORDERS, 2006, 8 : S1 - S16
[24] HCN CHANNELS -A NOVEL TARGET IN PSYCHIATRY
Dua, Sunny
Nagendran, Subramaiah
Makkar, Muskaan
INDIAN JOURNAL OF PSYCHIATRY, 2019, 61 (09) : S567 - S568
[25] MOTOR EVOKED POTENTIAL POLYPHASIA: A NOVEL ENDOPHENOTYPE OF IDIOPATHIC GENERALIZED EPILEPSY
Valls-Sole, Josep
Ziemann, Ulf
NEUROLOGY, 2015, 85 (14) : 1262 - 1262
[26] Motor evoked potential polyphasia A novel endophenotype of idiopathic generalized epilepsy
Chowdhury, Fahmida A.
Pawley, Adam D.
Ceronie, Bryan
Nashef, Lina
Elwes, Robert D. C.
Richardson, Mark P.
NEUROLOGY, 2015, 84 (13) : 1301 - 1307
[27] Generalized epilepsy with febrile seizures plus and classical idiopathic generalized epilepsy
Zhang, Yue-Hua
Scheffer, Ingrid
NEUROLOGY ASIA, 2010, 15 : 3 - 4
[28] The hyperpolarization-activated HCN channels in human and experimental hippocampal epilepsy: A novel, acquired channelopathy?
Bender, RA
Mathern, GW
Brewster, AL
Baram, TZ
ANNALS OF NEUROLOGY, 2003, 54 : S54 - S55
[29] FUNCTIONAL IMPACT OF GABRG2 MUTATIONS ASSOCIATED WITH IDIOPATHIC GENERALIZED EPILEPSY SYNDROMES
Poncer, J. C.
EPILEPSIA, 2009, 50 : 1 - 1
[30] Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes
E. Stogmann
P. Lichtner
C. Baumgartner
M. Schmied
C. Hotzy
F. Asmus
F. Leutmezer
S. Bonelli
E. Assem-Hilger
K. Vass
K. Hatala
T. M. Strom
T. Meitinger
F. Zimprich
A. Zimprich
Neurogenetics, 2006, 7 : 265 - 268

← 1 2 3 4 5 →