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Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations.

机译：在SCN1A突变的婴儿（SMEI）严重肌阵挛性癫痫中，高热惊厥和癫痫的家族性发生。

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作者
M. M. Mancardi; P. Striano; E. Gennaro; F. Madia; R. Paravidino; S. Scapolan; B. D. Bernardina; E. Bertini; A. Bianchi; G. Capovilla; F. Darra; M. Elia; E. Freri; G. Gobbi; T. Granata; R. Guerrini; C. Pantaleoni; A. Parmeggiani; A. Romeo; M. Santucci; M. Vecchi; P. Veggiotti; F. Vigevano; A. Pistorio; R. Gaggero; F. Zara;
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年度 2006
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正文语种 eng
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1. Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations. [J] . Margherita-Mancardi M, Striano P, Gennaro E, Epilepsia: Journal of the International League against Epilepsy . 2006,第10期

机译：严重的肌阵挛性癫痫（SMEI）患者中，SCN1A突变的患者出现高热惊厥和癫痫的家族性发作。
2. A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures. [J] . Kimura K, Sugawara T, Mazaki Miyazaki E, Brain & Development . 2005,第6期

机译：婴儿严重肌阵挛性癫痫（SMEI）兄弟的SCN1A错义突变是由父亲的高热惊厥遗传而来。
3. Familial SCN1A missense mutation over three generations, from febrile seizures to severe myoclonic epilepsy in infancy [J] . Anonymous Journal of pediatric neurology : . 2011,第1期

机译：家族性SCN1A错义突变超过3代，从高热惊厥到婴儿期严重的肌阵挛性癫痫
4. Risk of Febrile Seizures and Epilepsy After Vaccination With Diphtheria, Tetanus,Acellular Pertussis, Inactivated Poliovirus,and Haemophilus Influenzae Type b [C] . Yuelian Sun, Jakob Christensen, Anders Hviid, Second joint biostatistics symposium (2012) . 2012

机译：接种白喉，破伤风，无细胞百日咳，脊髓灰质炎灭活病毒和b型流感嗜血杆菌疫苗后出现高热惊厥和癫痫的风险
5. Role of the human voltage-gated sodium channel, SCN1A, in familial epilepsy. [D] . Lossin, Christoph. 2003

机译：人类电压门控钠通道SCN1A在家族性癫痫中的作用。
6. Nontruncating SCN1A Mutations Associated with Severe Myoclonic Epilepsy of Infancy Impair Cell Surface Expression [O] . Christopher H. Thompson, J. Christopher Porter, Kristopher M. Kahlig, 2012

机译：与婴儿期严重肌阵挛性癫痫相关的非截断SCN1A突变损害细胞表面表达。
7. SCN1A mutation analysis in Myoclonic Astatic Epilepsy and Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic Clonic Seizures [O] . Ebach Katharina 2005

机译：肌阵挛性静止性癫痫和重度特发性婴儿广泛性阵挛性阵挛性癫痫的SCN1A突变分析

Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations.

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