Literature DB >> 13819848

A familial convulsive disorder with an unusual onset during intrauterine life: a case report.

M K EL-DIN.   

Abstract

Entities:  

Keywords:  CONVULSIONS/genetics; INFANT, NEWBORN/diseases; MENTAL DEFICIENCY/case reports; MYOCLONUS/in infancy and childhood

Mesh：

Year:  1960        PMID： 13819848     DOI： 10.1016/s0022-3476(60)80340-x

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  4 in total

1.  Familial intrauterine convulsions in pyridoxine dependency.

Authors:  M Bejsovec; Z Kulenda; E Ponca
Journal:  Arch Dis Child       Date:  1967-04       Impact factor: 3.791

2.  Prenatal diagnosis of fetal seizure: a case report.

Authors:  Eui Jung; Bo Yon Lee; Chu Yeop Huh
Journal:  J Korean Med Sci       Date:  2008-10       Impact factor: 2.153

3.  The glycinergic system in human startle disease: a genetic screening approach.

Authors:  Jeff S Davies; Seo-Kyung Chung; Rhys H Thomas; Angela Robinson; Carrie L Hammond; Jonathan G L Mullins; Eloisa Carta; Brian R Pearce; Kirsten Harvey; Robert J Harvey; Mark I Rees
Journal:  Front Mol Neurosci       Date:  2010-03-23       Impact factor: 5.639

Review 4.  Pyridoxine-dependent seizures, clinical and therapeutic aspects.

Authors:  C A Haenggeli; E Girardin; L Paunier
Journal:  Eur J Pediatr       Date:  1991-05       Impact factor: 3.183
  4 in total

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