(Q35206649)

7 August 2017

1 reference

title

Familial trigeminal neuralgia: case reports and review of the literature (English)

1 reference

7 August 2017

Paul Smyth

1

1 reference

7 August 2017

Glen Greenough

series ordinal

2

1 reference

7 August 2017

Elijah Stommel

series ordinal

3

1 reference

7 August 2017

publication date

1 September 2003

1 reference

7 August 2017

1 reference

7 August 2017

volume

43

1 reference

7 August 2017

issue

8

1 reference

7 August 2017

page(s)

910-915

1 reference

Vascular contact with the fifth cranial nerve at the pons in patients with trigeminal neuralgia: detection with 3D FISP imaging

7 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

Trigeminal neuralgia after pontine infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

Trigeminal neuralgia triggered by auditory stimuli in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

The long-term outcome of microvascular decompression for trigeminal neuralgia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

Hereditary vestibulo-cochlear dysfunction and vascular disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

A locus for cerebral cavernous malformations maps to chromosome 7q in two families

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

Familial trigeminal neuralgia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

Familial trigeminal neuralgia and contralateral hemifacial spasm

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

CCM1 gene mutations in families segregating cerebral cavernous malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

Craniometric measures in cluster headache patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1526-4610.2003.03172.X

10.1046/J.1526-4610.2003.03172.X

21 January 2018

Identifiers

DOI

1 reference

7 August 2017

1 reference