首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
Absence of LGI1 mutations in familial mesial temporal lobe epilepsy with or without auditory features and in sporadic temporal lobe epilepsy with auditory features
被引:0
|
作者
:
Badhwar, A
论文数:
0
引用数:
0
h-index:
0
Badhwar, A
Racacho, L
论文数:
0
引用数:
0
h-index:
0
Racacho, L
D'Agostino, D
论文数:
0
引用数:
0
h-index:
0
D'Agostino, D
Dubeau, F
论文数:
0
引用数:
0
h-index:
0
Dubeau, F
Andermann, F
论文数:
0
引用数:
0
h-index:
0
Andermann, F
Bulman, D
论文数:
0
引用数:
0
h-index:
0
Bulman, D
Andermann, E
论文数:
0
引用数:
0
h-index:
0
Andermann, E
机构
:
来源
:
NEUROLOGY
|
2004年
/ 62卷
/ 07期
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
:
引用
收藏
页码:A252 / A252
页数:1
相关论文
共 50 条
[1]
Absence of LGI1 mutations in familial mesial temporal lobe epilepsy patients with or without auditory hallucinations
Badhwar, AP
论文数:
0
引用数:
0
h-index:
0
Badhwar, AP
Racacho, L
论文数:
0
引用数:
0
h-index:
0
Racacho, L
Kobayashi, E
论文数:
0
引用数:
0
h-index:
0
Kobayashi, E
D'Agostino, D
论文数:
0
引用数:
0
h-index:
0
D'Agostino, D
Dubeau, F
论文数:
0
引用数:
0
h-index:
0
Dubeau, F
Andermann, F
论文数:
0
引用数:
0
h-index:
0
Andermann, F
Bulman, D
论文数:
0
引用数:
0
h-index:
0
Bulman, D
Andermann, E
论文数:
0
引用数:
0
h-index:
0
Andermann, E
[J].
ANNALS OF NEUROLOGY,
2004,
56
: S23
-
S23
[2]
Mutations in LGI1 in an Australian family with familial temporal lobe epilepsy with auditory features.
Mulley, JC
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tennessee, Dept Anat & Neurobiol, Memphis, TN USA
Mulley, JC
Wallace, RH
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tennessee, Dept Anat & Neurobiol, Memphis, TN USA
Wallace, RH
Izzillo, P
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tennessee, Dept Anat & Neurobiol, Memphis, TN USA
Izzillo, P
MacIntosh, AM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tennessee, Dept Anat & Neurobiol, Memphis, TN USA
MacIntosh, AM
Berkovic, SF
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Tennessee, Dept Anat & Neurobiol, Memphis, TN USA
Berkovic, SF
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
2002,
71
(04)
: 472
-
472
[3]
Absence of mutations in LGI1 in patients with familial mesial temporal lobe epilepsy
Badhwar, A
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Montreal Neurol Hosp & Inst, Montreal, PQ H3A 2T5, Canada
Badhwar, A
Racacho, L
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Montreal Neurol Hosp & Inst, Montreal, PQ H3A 2T5, Canada
Racacho, L
D'Agostino, D
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Montreal Neurol Hosp & Inst, Montreal, PQ H3A 2T5, Canada
D'Agostino, D
Dubeau, F
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Montreal Neurol Hosp & Inst, Montreal, PQ H3A 2T5, Canada
Dubeau, F
Andermann, F
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Montreal Neurol Hosp & Inst, Montreal, PQ H3A 2T5, Canada
Andermann, F
Bulman, D
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Montreal Neurol Hosp & Inst, Montreal, PQ H3A 2T5, Canada
Bulman, D
Andermann, E
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Montreal Neurol Hosp & Inst, Montreal, PQ H3A 2T5, Canada
Andermann, E
[J].
EPILEPSIA,
2003,
44
: 170
-
170
[4]
Familial temporal lobe epilepsy with auditory features
Cendes, F
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Estadual Campinas, Dept Neurol, FCM, BR-13083970 Campinas, SP, Brazil
Cendes, F
Kobayashi, E
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Estadual Campinas, Dept Neurol, FCM, BR-13083970 Campinas, SP, Brazil
Kobayashi, E
Lopes-Cendes, I
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Estadual Campinas, Dept Neurol, FCM, BR-13083970 Campinas, SP, Brazil
Lopes-Cendes, I
[J].
CNS SPECTRUMS,
2006,
11
(02)
: 60
-
61
[5]
Familial temporal lobe epilepsy with auditory features
Cendes, F
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Estadual Campinas, FCM, Dept Neurol, BR-13083970 Campinas, SP, Brazil
Cendes, F
Kobayashi, E
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Estadual Campinas, FCM, Dept Neurol, BR-13083970 Campinas, SP, Brazil
Kobayashi, E
Lopes-Cendes, I
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Estadual Campinas, FCM, Dept Neurol, BR-13083970 Campinas, SP, Brazil
Lopes-Cendes, I
[J].
EPILEPSIA,
2005,
46
: 59
-
60
[6]
Now-allelic genetic heterogeneity in autosomal dominant lateral temporal lobe epilepsy and absence of LGI1 mutations in familial mesial temporal lobe epilepsy
Badhwar, A
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Dept Neurol & Neurosurg, Montreal Neurol Hosp & Inst, Montreal, PQ, Canada
Badhwar, A
Racacho, L
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Dept Neurol & Neurosurg, Montreal Neurol Hosp & Inst, Montreal, PQ, Canada
Racacho, L
D'Agostino, D
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Dept Neurol & Neurosurg, Montreal Neurol Hosp & Inst, Montreal, PQ, Canada
D'Agostino, D
Dubeau, F
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Dept Neurol & Neurosurg, Montreal Neurol Hosp & Inst, Montreal, PQ, Canada
Dubeau, F
Andermann, F
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Dept Neurol & Neurosurg, Montreal Neurol Hosp & Inst, Montreal, PQ, Canada
Andermann, F
Bulman, D
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Dept Neurol & Neurosurg, Montreal Neurol Hosp & Inst, Montreal, PQ, Canada
Bulman, D
Andermann, E
论文数:
0
引用数:
0
h-index:
0
机构:
McGill Univ, Dept Neurol & Neurosurg, Montreal Neurol Hosp & Inst, Montreal, PQ, Canada
Andermann, E
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
2003,
73
(05)
: 510
-
510
[7]
A new LGI1 mutation in familial temporal lobe epilepsy with auditory auras.
Santos, NF
论文数:
0
引用数:
0
h-index:
0
机构:
UNICAMP, Dept Med Genet, Campinas, SP, Brazil
Santos, NF
Secolin, R
论文数:
0
引用数:
0
h-index:
0
机构:
UNICAMP, Dept Med Genet, Campinas, SP, Brazil
Secolin, R
Torres, FR
论文数:
0
引用数:
0
h-index:
0
机构:
UNICAMP, Dept Med Genet, Campinas, SP, Brazil
Torres, FR
Kobayashi, E
论文数:
0
引用数:
0
h-index:
0
机构:
UNICAMP, Dept Med Genet, Campinas, SP, Brazil
Kobayashi, E
Sardinha, LAC
论文数:
0
引用数:
0
h-index:
0
机构:
UNICAMP, Dept Med Genet, Campinas, SP, Brazil
Sardinha, LAC
Cendes, F
论文数:
0
引用数:
0
h-index:
0
机构:
UNICAMP, Dept Med Genet, Campinas, SP, Brazil
Cendes, F
Lopes-Cendes, I
论文数:
0
引用数:
0
h-index:
0
机构:
UNICAMP, Dept Med Genet, Campinas, SP, Brazil
Lopes-Cendes, I
[J].
AMERICAN JOURNAL OF HUMAN GENETICS,
2003,
73
(05)
: 471
-
471
[8]
Autosomal dominant lateral temporal lobe epilepsy and the sporadic form with auditory features
Michelucci, R.
论文数:
0
引用数:
0
h-index:
0
机构:
Bellaria Hosp, Dept Neurosci, Bologna, Italy
Bellaria Hosp, Dept Neurosci, Bologna, Italy
Michelucci, R.
[J].
EPILEPSIA,
2006,
47
: 267
-
267
[9]
LGI1 mutations in autosomal dominant partial epilepsy with auditory features
Ottman, R
论文数:
0
引用数:
0
h-index:
0
机构:
Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10032 USA
Ottman, R
Winawer, MR
论文数:
0
引用数:
0
h-index:
0
机构:
Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10032 USA
Winawer, MR
Kalachikov, S
论文数:
0
引用数:
0
h-index:
0
机构:
Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10032 USA
Kalachikov, S
Barker-Cummings, C
论文数:
0
引用数:
0
h-index:
0
机构:
Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10032 USA
Barker-Cummings, C
Gilliam, TC
论文数:
0
引用数:
0
h-index:
0
机构:
Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10032 USA
Gilliam, TC
Pedley, TA
论文数:
0
引用数:
0
h-index:
0
机构:
Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10032 USA
Pedley, TA
Hauser, WA
论文数:
0
引用数:
0
h-index:
0
机构:
Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10032 USA
Hauser, WA
[J].
NEUROLOGY,
2004,
62
(07)
: 1120
-
1126
[10]
LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures
Gu, WL
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hosp Bonn, Inst Human Genet, D-53111 Bonn, Germany
Gu, WL
Brodtkorb, E
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hosp Bonn, Inst Human Genet, D-53111 Bonn, Germany
Brodtkorb, E
Steinlein, OK
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hosp Bonn, Inst Human Genet, D-53111 Bonn, Germany
Steinlein, OK
[J].
ANNALS OF NEUROLOGY,
2002,
52
(03)
: 364
-
367
←
1
2
3
4
5
→