Literature DB >> 8839737

Severe myoclonic epilepsy in infancy and carbamazepine.

S Wakai, N Ito, H Sueoka, Y Kawamoto, H Hayasaka, S Chiba.   

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Year:  1996        PMID： 8839737     DOI： 10.1007/bf01957165

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  2 in total

1.  Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy.

Authors: 
Journal:  Epilepsia       Date:  1989 Jul-Aug       Impact factor: 5.864

2.  Severe myoclonic epilepsy of infancy.

Authors:  D L Hurst
Journal:  Pediatr Neurol       Date:  1987 Sep-Oct       Impact factor: 3.372
  2 in total
  2 in total

1.  Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.

Authors:  J J T van Harssel; S Weckhuysen; M J A van Kempen; K Hardies; N E Verbeek; C G F de Kovel; W B Gunning; E van Daalen; M V de Jonge; A C Jansen; R J Vermeulen; W F M Arts; H Verhelst; A Fogarasi; J F de Rijk-van Andel; A Kelemen; D Lindhout; P De Jonghe; B P C Koeleman; A Suls; E H Brilstra
Journal:  Neurogenetics       Date:  2013-01-20       Impact factor: 2.660

2.  The L1624Q Variant in SCN1A Causes Familial Epilepsy Through a Mixed Gain and Loss of Channel Function.

Authors:  Laura B Jones; Colin H Peters; Richard E Rosch; Maxine Owers; Elaine Hughes; Deb K Pal; Peter C Ruben
Journal:  Front Pharmacol       Date:  2021-12-02       Impact factor: 5.810
  2 in total

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