(Q33735023)

29 July 2017

title

Progressive ataxia, focal seizures, and malabsorption syndrome in a 41 year old woman (English)

1 reference

29 July 2017

Mumford CJ

1

1 reference

29 July 2017

Fletcher NA

series ordinal

2

1 reference

29 July 2017

Ironside JW

series ordinal

3

1 reference

29 July 2017

Warlow CP

series ordinal

4

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 February 1996

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

29 July 2017

published in

1 reference

29 July 2017

volume

60

1 reference

29 July 2017

issue

2

1 reference

29 July 2017

page(s)

225-230

1 reference

Degeneration of the central nervous system associated with celiac disease.

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073814

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073814

Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073814

Isolated vasculitis of the central nervous system in a patient with celiac disease.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073814

Ramsay Hunt syndrome and coeliac disease: a new association?

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073814

The Ramsay Hunt syndrome is a useful clinical entity

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073814

Sialidosis type 1: cherry red spot-myoclonus syndrome with sialidase deficiency and altered electrophoretic mobilities of some enzymes known to be glycoproteins. 1. Clinical findings

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073814

Adult celiac disease presenting as cerebellar syndrome

14 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8708663

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Oculomasticatory myorhythmia: a unique movement disorder occurring in Whipple's disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8708663

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.60.2.225

1 reference

29 July 2017

1 reference

29 July 2017

1 reference