(Q34181237)

31 July 2017

title

Ramsay Hunt syndrome and coeliac disease: a new association? (English)

1 reference

31 July 2017

1 reference

5

Marsden CD

1 reference

31 July 2017

Lu CS

1

1 reference

31 July 2017

Thompson PD

series ordinal

2

1 reference

31 July 2017

Quinn NP

series ordinal

3

1 reference

31 July 2017

Parkes JD

series ordinal

4

1 reference

31 July 2017

language of work or name

English

0 references

publication date

1 January 1986

1 reference

31 July 2017

1 reference

31 July 2017

volume

1

1 reference

31 July 2017

issue

3

1 reference

31 July 2017

page(s)

209-219

1 reference

Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870010306

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870010306

LAFORA'S DISEASE. DISTINCT CLINICO-PATHOLOGIC FORM OF UNVERRICHT'S SYNDROME.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870010306

Atypical neuronal ceroid-lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870010306

Familial juvenile neuronal storage disease. New disease or variant of juvenile lipidosis?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FMDS.870010306

21 January 2018

Identifiers

DOI

10.1002/MDS.870010306

1 reference

31 July 2017

1 reference