(Q40807685)

23 September 2017

1 reference

title

Progress in mapping human epilepsy genes (English)

1 reference

23 September 2017

7

Treiman LJ

1 reference

23 September 2017

Delgado-Escueta AV

1

1 reference

23 September 2017

Serratosa JM

2

1 reference

23 September 2017

Liu A

3

1 reference

23 September 2017

Weissbecker K

4

1 reference

23 September 2017

Medina MT

5

1 reference

23 September 2017

Gee M

6

1 reference

23 September 2017

Sparkes RS

8

1 reference

23 September 2017

1 January 1994

1 reference

23 September 2017

1 reference

23 September 2017

35 Suppl 1

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23 September 2017

S29-40

1 reference

Myoclonus epilepsy and ragged-red fibres (MERRF). 1. A clinical, pathological, biochemical, magnetic resonance spectrographic and positron emission tomographic study

23 September 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

ONSET AND CESSATION OF FITS FOLLOWING CRANIOCEREBRAL TRAUMA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

21 January 2018

Post-traumatic epilepsy.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Batten disease (Spielmeyer-Vogt disease, juvenile onset neuronal ceroid-lipofuscinosis) gene (CLN3) maps to human chromosome 16.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Benign familial neonatal convulsions: Evidence for clinical and genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Mapping of a gene determining tuberous sclerosis to human chromosome 11q14-11q23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

Infantile form of neuronal ceroid lipofuscinosis (CLN1) maps to the short arm of chromosome 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1157.1994.TB05926.X

10.1111/J.1528-1157.1994.TB05926.X

21 January 2018

Identifiers

DOI

1 reference

23 September 2017

1 reference