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Genes and epilepsy (Q33598113)

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scientific article

Language	Label	Description	Also known as
default for all languages	No label defined
English	Genes and epilepsy	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Genes and epilepsy (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Gardiner RM

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

publication date

1 September 1990

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

27

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

537-544

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

publication type of scholarly work

1 reference

Europe PubMed Central

Febrile convulsions in families: findings in an epidemiologic survey

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Genetic factors in spike-wave absences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Genetic and maternal influences on susceptibility to seizures. An analytic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Existence of distinct sodium channel messenger RNAs in rat brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Complex segregation analysis of febrile convulsions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

The affected-pedigree-member method of linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Higher risk of seizures in offspring of mothers than of fathers with epilepsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Concepts of absence epilepsies: discrete syndromes or biological continuum?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Sequence and functional expression of the GABA A receptor shows a ligand-gated receptor super-family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Expression of neurotransmitter transport from rat brain mRNA in Xenopus laevis oocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Report of the committee on human mitochondrial DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

The GABAA receptor: molecular biology reveals a complex picture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Cloning by functional expression of a member of the glutamate receptor family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Cloning of a probable potassium channel gene from mouse brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

The role of receptor subtype diversity in the CNS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

Incidence of seizures and EEG abnormalities among offspring of epileptic patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

21 June 2018

HEREDITARY CHARACTERISTICS OF FAMILIAL TEMPORAL-CENTRAL FOCAL EPILEPSY

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

30 October 2018

Juvenile myoclonic epilepsy of Janz

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

30 October 2018

Role of the ?-Aminobytyric acid receptor?Ionophore complex in seizure disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017214

30 October 2018

Hereditary aspects of epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2231646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2231646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Genetic Study of Febrile Convulsions

1 reference

https://pubmed.ncbi.nlm.nih.gov/2231646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic aspects of epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2231646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Looking for epilepsy genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2231646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping complex genetic traits in humans: new methods using a complete RFLP linkage map

1 reference

https://pubmed.ncbi.nlm.nih.gov/2231646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2231646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2231646

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.27.9.537

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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