Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia (Q57970902)

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Language	Label	Description	Also known as
English	Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia	No description defined

Statements

instance of

scholarly article

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title

Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia (English)

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main subject

generalized dystonia

1 reference

based on heuristic

inferred from title

phenotype

1 reference

based on heuristic

inferred from title

author

Laurent Vercueil

object named as

L. Vercueil

series ordinal

3

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Giovanni Stevanin

object named as

G. Stevanin

series ordinal

10

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author name string

I. Le Ber

series ordinal

1

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F. Clot

series ordinal

2

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A. Camuzat

series ordinal

4

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M. Viemont

series ordinal

5

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N. Benamar

series ordinal

6

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P. De Liege

series ordinal

7

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A. M. Ouvrard-Hernandez

series ordinal

8

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P. Pollak

series ordinal

9

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A. Brice

series ordinal

11

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A. Durr

series ordinal

12

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language of work or name

English

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publication date

27 November 2006

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published in

Neurology

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volume

67

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issue

10

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page(s)

1769-1773

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Identifiers

DOI

10.1212/01.WNL.0000244484.60489.50

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PubMed publication ID

17130408

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