首页
学术期刊
论文检测
AIGC检测
热点
更多
数据
Childhood epilepsy associated with SCN1A gene mutation: Clinical, EEG and FDG PET correlations
被引:0
|
作者
:
Luat, A. F.
论文数:
0
引用数:
0
h-index:
0
Luat, A. F.
Juhasz, C.
论文数:
0
引用数:
0
h-index:
0
Juhasz, C.
Asano, E.
论文数:
0
引用数:
0
h-index:
0
Asano, E.
Huq, M.
论文数:
0
引用数:
0
h-index:
0
Huq, M.
Chugani, H. T.
论文数:
0
引用数:
0
h-index:
0
Chugani, H. T.
机构
:
来源
:
ANNALS OF NEUROLOGY
|
2007年
/ 62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
:
引用
收藏
页码:S134 / S134
页数:1
相关论文
共 50 条
[21]
CLINICAL VARIABILITY IN THE EXPRESSION OF SCN1A GENE
Morillo, P.
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ Ramon & Cajal, Madrid, Spain
Hosp Univ Ramon & Cajal, Madrid, Spain
Morillo, P.
Toledano, M.
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ Ramon & Cajal, Madrid, Spain
Hosp Univ Ramon & Cajal, Madrid, Spain
Toledano, M.
Buenache, R.
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ Ramon & Cajal, Madrid, Spain
Hosp Univ Ramon & Cajal, Madrid, Spain
Buenache, R.
Alvarez, J. A.
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ Ramon & Cajal, Madrid, Spain
Hosp Univ Ramon & Cajal, Madrid, Spain
Alvarez, J. A.
Pedrera, A.
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ Ramon & Cajal, Madrid, Spain
Hosp Univ Ramon & Cajal, Madrid, Spain
Pedrera, A.
Lorenzo, G.
论文数:
0
引用数:
0
h-index:
0
机构:
Hosp Univ Ramon & Cajal, Madrid, Spain
Hosp Univ Ramon & Cajal, Madrid, Spain
Lorenzo, G.
EPILEPSIA,
2011,
52
: 217
-
217
[22]
First report on the association of SCN1A mutation, childhood schizophrenia and autism spectrum disorder without epilepsy
Papp-Hertelendi, Renata
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Papp-Hertelendi, Renata
Csabi, Gyorgyi
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Csabi, Gyorgyi
Hau, Lidia
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Hau, Lidia
Tenyi, Tamas
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pecs, Sch Med, Dept Psychiat & Psychotherapy, Pecs, Hungary
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Tenyi, Tamas
Hadzsiev, Kinga
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pecs, Sch Med, Dept Med Genet, Pecs, Hungary
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Hadzsiev, Kinga
Benyus, Zsuzsanna
论文数:
0
引用数:
0
h-index:
0
机构:
Outpatient Child Psychiat Ctr, Pecs, Hungary
Univ Pecs, Sch Med, Dept Pediat, Pecs, Hungary
Benyus, Zsuzsanna
PSYCHIATRY RESEARCH,
2018,
270
: 1175
-
1176
[23]
A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus -: and prevalence of variants in patients with epilepsy
Escayg, A
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
Escayg, A
Heils, A
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
Heils, A
MacDonald, BT
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
MacDonald, BT
Haug, K
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
Haug, K
Sander, T
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
Sander, T
Meisler, MH
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Michigan, Dept Human Genet, Ann Arbor, MI 48109 USA
Meisler, MH
AMERICAN JOURNAL OF HUMAN GENETICS,
2001,
68
(04)
: 866
-
873
[24]
Nodular heterotopia: a rare finding in patients with epilepsy and SCN1A mutation
Pereira Klettenberg, Matheus Rocha
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Pereira Klettenberg, Matheus Rocha
Rodrigues, Victor Alves
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Rodrigues, Victor Alves
de Carvalho Bispo, Diogenes Diego
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
de Carvalho Bispo, Diogenes Diego
Lobao Cunha, Paulo Emidio
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Lobao Cunha, Paulo Emidio
Ferreira, Lisiane Seguti
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Univ Brasilia, Fac Med, Brasilia, DF, Brazil
Ferreira, Lisiane Seguti
ARQUIVOS DE NEURO-PSIQUIATRIA,
2021,
79
(10)
: 936
-
937
[25]
A functional polymorphism in the SCN1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy
Zimprich, Fritz
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Zimprich, Fritz
Stogmann, Elisabeth
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Stogmann, Elisabeth
论文数:
引用数:
h-index:
机构:
Bonelli, Silvia
Baumgartner, Christoph
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Baumgartner, Christoph
Mueller, Jakob C.
论文数:
0
引用数:
0
h-index:
0
机构:
Max Planck Inst Ornithol, Dept Behav Ecol & Evolutionary Genet, D-82305 Seewiesen, Germany
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Mueller, Jakob C.
Meitinger, Thomas
论文数:
0
引用数:
0
h-index:
0
机构:
GSF Natl Res Ctr Environm & Hlth, Inst Human Genet, Munich, Germany
Tech Univ Munich, Inst Human Genet, Munich, Germany
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Meitinger, Thomas
Zimprich, Alexander
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Zimprich, Alexander
Strom, Tim M.
论文数:
0
引用数:
0
h-index:
0
机构:
GSF Natl Res Ctr Environm & Hlth, Inst Human Genet, Munich, Germany
Tech Univ Munich, Inst Human Genet, Munich, Germany
Med Univ Vienna, Dept Clin Neurol, Vienna, Austria
Strom, Tim M.
EPILEPSIA,
2008,
49
(06)
: 1108
-
1109
[26]
SCN1A mutation mosaicism in a family with severe myoclonic epilepsy in infancy
Morimoto, Masafumi
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Morimoto, Masafumi
Mazaki, Emi
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Mazaki, Emi
Nishimura, Akira
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Nishimura, Akira
论文数:
引用数:
h-index:
机构:
Chiyonobu, Tomohiro
Sawai, Yasuko
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Sawai, Yasuko
Murakami, Aki
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Murakami, Aki
Nakamura, Keiko
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Nakamura, Keiko
Inoue, Ikuyo
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Inoue, Ikuyo
Ogiwara, Ikuo
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Ogiwara, Ikuo
Sugimoto, Tohru
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Sugimoto, Tohru
Yamakawa, Kazuhiro
论文数:
0
引用数:
0
h-index:
0
机构:
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Kyoto Prefectural Univ Med, Dept Pediat, Kamigyo Ku, Kyoto 6028566, Japan
Yamakawa, Kazuhiro
EPILEPSIA,
2006,
47
(10)
: 1732
-
1736
[27]
Functional polymorphism in the SCN1A gene and treatment of refractory epilepsy
Zimprich, F.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Zimprich, F.
Stogmann, E.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Stogmann, E.
Bonelli, S.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Bonelli, S.
Baumgartner, C.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Baumgartner, C.
Mueller, J.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Mueller, J.
Lichtner, P.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Lichtner, P.
Meitinger, T.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Meitinger, T.
Zimprich, A.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Zimprich, A.
Strom, T.
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Vienna, Dept Neurol, Vienna, Austria
Strom, T.
EPILEPSIA,
2006,
47
: 85
-
86
[28]
Mosaic SCN1A mutation in familial severe myoclonic epilepsy of infancy
Marini, Carla
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pisa, Dept Child Neurol & Psychiat, IRCCS Stella Maris Fdn, Epilepsy Neurophysiol & Neurogenet Unit, I-56018 Pisa, Italy
Marini, Carla
Mei, Davide
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pisa, Dept Child Neurol & Psychiat, IRCCS Stella Maris Fdn, Epilepsy Neurophysiol & Neurogenet Unit, I-56018 Pisa, Italy
Mei, Davide
Cross, J. Helen
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pisa, Dept Child Neurol & Psychiat, IRCCS Stella Maris Fdn, Epilepsy Neurophysiol & Neurogenet Unit, I-56018 Pisa, Italy
Cross, J. Helen
Guerrini, Renzo
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Pisa, Dept Child Neurol & Psychiat, IRCCS Stella Maris Fdn, Epilepsy Neurophysiol & Neurogenet Unit, I-56018 Pisa, Italy
Guerrini, Renzo
EPILEPSIA,
2006,
47
(10)
: 1737
-
1740
[29]
An epilepsy mutation in the sodium channel SCN1A that decreases channel excitability
Barela, AJ
论文数:
0
引用数:
0
h-index:
0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Barela, AJ
Waddy, SP
论文数:
0
引用数:
0
h-index:
0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Waddy, SP
Lickfett, JG
论文数:
0
引用数:
0
h-index:
0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Lickfett, JG
Hunter, J
论文数:
0
引用数:
0
h-index:
0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Hunter, J
Anido, A
论文数:
0
引用数:
0
h-index:
0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Anido, A
Helmers, SL
论文数:
0
引用数:
0
h-index:
0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Helmers, SL
Goldin, AL
论文数:
0
引用数:
0
h-index:
0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Goldin, AL
Escayg, A
论文数:
0
引用数:
0
h-index:
0
机构:
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
Escayg, A
JOURNAL OF NEUROSCIENCE,
2006,
26
(10):
: 2714
-
2723
[30]
Generalized Epilepsy With Febrile Seizures plus: Novel SCN1A Mutation
Dimova, Petia S.
论文数:
0
引用数:
0
h-index:
0
机构:
St Naum Univ Hosp Neurol & Psychiat, Clin Child Neurol, Sofia 1113, Bulgaria
St Naum Univ Hosp Neurol & Psychiat, Clin Child Neurol, Sofia 1113, Bulgaria
Dimova, Petia S.
Yordanova, Iglika
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Sofia, Natl Genet Lab, Sofia, Bulgaria
Med Univ Sofia, Mol Med Ctr, Sofia, Bulgaria
St Naum Univ Hosp Neurol & Psychiat, Clin Child Neurol, Sofia 1113, Bulgaria
Yordanova, Iglika
Bojinova, Veneta
论文数:
0
引用数:
0
h-index:
0
机构:
St Naum Univ Hosp Neurol & Psychiat, Clin Child Neurol, Sofia 1113, Bulgaria
St Naum Univ Hosp Neurol & Psychiat, Clin Child Neurol, Sofia 1113, Bulgaria
Bojinova, Veneta
论文数:
引用数:
h-index:
机构:
Jordanova, Albena
Kremenski, Ivo
论文数:
0
引用数:
0
h-index:
0
机构:
Med Univ Sofia, Natl Genet Lab, Sofia, Bulgaria
St Naum Univ Hosp Neurol & Psychiat, Clin Child Neurol, Sofia 1113, Bulgaria
Kremenski, Ivo
PEDIATRIC NEUROLOGY,
2010,
42
(02)
: 137
-
140
←
1
2
3
4
5
→