Literature DB >> 2231646

Genes and epilepsy.

R M Gardiner1.   

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Year:  1990        PMID： 2231646      PMCID： PMC1017214          DOI： 10.1136/jmg.27.9.537

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  30 in total

1.  Progressive myoclonus epilepsy: genetic and nosological aspects with special reference to 107 Finnish patients.

Authors:  R Norio; M Koskiniemi
Journal:  Clin Genet       Date:  1979-05       Impact factor: 4.438

2.  Hereditary aspects of epilepsy.

Authors:  V EISNER; L L PAULI; S LIVINGSTON
Journal:  Bull Johns Hopkins Hosp       Date:  1959-11

3.  Benign epilepsy of childhood with centrotemporal EEG foci: a genetic study.

Authors:  J Heijbel; S Blom; M Rasmuson
Journal:  Epilepsia       Date:  1975-06       Impact factor: 5.864

4.  On the genetics of the primary generalized epilepsy with sporadic myoclonias of impulsive petit mal type. A clinical and electroencephalographic study of 399 probands.

Authors:  T Tsuboi; W Christian
Journal:  Humangenetik       Date:  1973-07-20

5.  Genetic aspects of epilepsy.

Authors:  T Tsuboi
Journal:  Folia Psychiatr Neurol Jpn       Date:  1980

6.  Febrile convulsions in families: findings in an epidemiologic survey.

Authors:  S H Schuman; L J Miller
Journal:  Clin Pediatr (Phila)       Date:  1966-10       Impact factor: 1.168

7.  Juvenile myoclonic epilepsy of Janz.

Authors:  A V Delgado-Escueta; F Enrile-Bacsal
Journal:  Neurology       Date:  1984-03       Impact factor: 9.910

8.  Looking for epilepsy genes.

Authors:  R White
Journal:  Ann Neurol       Date:  1984       Impact factor: 10.422

9.  Incidence of seizures and EEG abnormalities among offspring of epileptic patients.

Authors:  T Tsuboi; S Endo
Journal:  Hum Genet       Date:  1977-04-15       Impact factor: 4.132

10.  A genetic study of febrile convulsions.

Authors:  Y Fukuyama; K Kagawa; K Tanaka
Journal:  Eur Neurol       Date:  1979       Impact factor: 1.710
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  7 in total

1.  Confirmation of linkage of benign familial neonatal convulsions to D20S19 and D20S20.

Authors:  A Malafosse; M Leboyer; O Dulac; Y Navelet; P Plouin; C Beck; H Laklou; G Mouchnino; P Grandscene; L Vallee
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

2.  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

3.  Genetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8q.

Authors:  T B Lewis; R J Leach; K Ward; P O'Connell; S G Ryan
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

4.  Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8p.

Authors:  S Ranta; A E Lehesjoki; A Hirvasniemi; J Weissenbach; B Ross; S M Leal; A de la Chapelle; T C Gilliam
Journal:  Genome Res       Date:  1996-05       Impact factor: 9.043

5.  The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.

Authors:  E Tahvanainen; S Ranta; A Hirvasniemi; E Karila; J Leisti; P Sistonen; J Weissenbach; A E Lehesjoki; A de la Chapelle
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-19       Impact factor: 11.205

6.  Genetic analysis of kifafa, a complex familial seizure disorder.

Authors:  R J Neuman; J M Kwon; L Jilek-Aall; H T Rwiza; J P Rice; P J Goodfellow
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

7.  Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.

Authors:  R H Wallace; S F Berkovic; R A Howell; G R Sutherland; J C Mulley
Journal:  J Med Genet       Date:  1996-04       Impact factor: 6.318
  7 in total

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