Literature DB >> 10648364

Genetics of childhood epilepsy.

R Robinson1, M Gardiner.   

Abstract

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Year:  2000        PMID： 10648364      PMCID： PMC1718214          DOI： 10.1136/adc.82.2.121

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  45 in total

Review 1.  Genetics of inherited epilepsies.

Authors:  L Bate; M Gardiner
Journal:  Epileptic Disord       Date:  1999-03       Impact factor: 1.819

2.  Genetics of convulsive disorders. II. Genetic and electroencephalographic studies in centrencephalic epilepsy.

Authors:  K METRAKOS; J D METRAKOS
Journal:  Neurology       Date:  1961-06       Impact factor: 9.910

3.  Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this region.

Authors:  F V Elmslie; M P Williamson; M Rees; M Kerr; M J Kjeldsen; K A Pang; A Sundqvist; M L Friis; A Richens; D Chadwick; W P Whitehouse; R M Gardiner
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

4.  Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

Authors:  M Leppert; V E Anderson; T Quattlebaum; D Stauffer; P O'Connell; Y Nakamura; J M Lalouel; R White
Journal:  Nature       Date:  1989-02-16       Impact factor: 49.962

5.  Absence epilepsy in tottering mutant mice is associated with calcium channel defects.

Authors:  C F Fletcher; C M Lutz; T N O'Sullivan; J D Shaughnessy; R Hawkes; W N Frankel; N G Copeland; N A Jenkins
Journal:  Cell       Date:  1996-11-15       Impact factor: 41.582

6.  Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis.

Authors:  D E Sleat; R J Donnelly; H Lackland; C G Liu; I Sohar; R K Pullarkat; P Lobel
Journal:  Science       Date:  1997-09-19       Impact factor: 47.728

7.  Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Authors:  J M Shoffner; M T Lott; A M Lezza; P Seibel; S W Ballinger; D C Wallace
Journal:  Cell       Date:  1990-06-15       Impact factor: 41.582

8.  Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22.

Authors:  A E Lehesjoki; M Koskiniemi; P Sistonen; J Miao; J Hästbacka; R Norio; A de la Chapelle
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-01       Impact factor: 11.205

9.  A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.

Authors:  S Baulac; I Gourfinkel-An; F Picard; M Rosenberg-Bourgin; J F Prud'homme; M Baulac; A Brice; E LeGuern
Journal:  Am J Hum Genet       Date:  1999-10       Impact factor: 11.025

10.  Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6.

Authors:  D A Greenberg; A V Delgado-Escueta; H Widelitz; R S Sparkes; L Treiman; H M Maldonado; M S Park; P I Terasaki
Journal:  Am J Med Genet       Date:  1988-09
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  3 in total

Review 1.  Genetics of epilepsy.

Authors:  Dimitri M Kullmann
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-12       Impact factor: 10.154

2.  Management of epilepsy.

Authors:  T Deonna
Journal:  Arch Dis Child       Date:  2005-01       Impact factor: 3.791

3.  Differential Coassembly of α1-GABAARs Associated with Epileptic Encephalopathy.

Authors:  Saad Hannan; Aida H B Affandi; Marielle Minere; Charlotte Jones; Pollyanna Goh; Gary Warnes; Bernt Popp; Regina Trollmann; Dean Nizetic; Trevor G Smart
Journal:  J Neurosci       Date:  2020-06-08       Impact factor: 6.167
  3 in total

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