(Q33673484)

28 July 2017

Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration (English)

1 reference

28 July 2017

1 reference

Hirvasniemi A

1

1 reference

28 July 2017

Lang H

series ordinal

2

1 reference

28 July 2017

Lehesjoki AE

series ordinal

3

1 reference

28 July 2017

Leisti J

series ordinal

4

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 March 1994

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

31

1 reference

28 July 2017

3

1 reference

28 July 2017

177-182

1 reference

Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049737

Hereditary diseases in Finland; rare flora in rare soul

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049737

Genetic counseling in the epilepsies. I. Genetic risks

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049737

Genetic considerations in childhood epilepsy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049737

Childhood epileptic syndromes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049737

Interictal cognitive changes in epilepsy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049737

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049737

Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8014963

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Linkage studies in progressive myoclonus epilepsy: Unverricht-Lundborg and Lafora's diseases

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8014963

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Epileptic seizures and syndromes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8014963

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.31.3.177

1 reference

28 July 2017

1 reference

28 July 2017

1 reference