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Literature DB >> 15508920

Myoclonic-astatic epilepsy of early childhood--definition, course, nosography, and genetics.

B A Neubauer¹, A Hahn, H Doose, I Tuxhorn.

Abstract

Entities: Disease

Mesh：

Substances：
Anticonvulsants

Year: 2005 PMID： 15508920

Source DB: PubMed Journal: Adv Neurol ISSN： 0091-3952

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4 in total

1. Clinical and genetic characteristics of patients with Doose syndrome.

Authors: Nodoka Hinokuma; Mitsuko Nakashima; Hideyuki Asai; Kazuyuki Nakamura; Shinjiro Akaboshi; Masataka Fukuoka; Masami Togawa; Shingo Oana; Koyo Ohno; Mariko Kasai; Chikako Ogawa; Kazuna Yamamoto; Kiyohito Okumiya; Pin Fee Chong; Ryutaro Kira; Shumpei Uchino; Tetsuhiro Fukuyama; Tomoe Shinagawa; Yohane Miyata; Yuichi Abe; Akira Hojo; Kozue Kobayashi; Yoshihiro Maegaki; Nobutsune Ishikawa; Hiroko Ikeda; Masano Amamoto; Takeshi Mizuguchi; Kazuhiro Iwama; Toshiyuki Itai; Satoko Miyatake; Hirotomo Saitsu; Naomichi Matsumoto; Mitsuhiro Kato
Journal: Epilepsia Open Date: 2020-07-23

Myoclonic-astatic epilepsy of early childhood--definition, course, nosography, and genetics.

1. Clinical and genetic characteristics of patients with Doose syndrome.

2. Diagnosis switching and outcomes in a cohort of patients with potential epilepsy with myoclonic-atonic seizures.

3. Epilepsy in childhood and adolescence.

4. Paradoxical exacerbation of myoclonic-astatic seizures by levetiracetam in myoclonic astatic epilepsy.