Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia [3]

J. Hagenah; K. Reetz; C. Zühlke; A. Rolfs; F. Binkofski; C. Klein

doi:10.1212/01.wnl.0000269478.69285.7e

Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia [3]

J. Hagenah^*, K. Reetz, C. Zühlke, A. Rolfs, F. Binkofski, C. Klein

^*Corresponding author for this work

Original language	English
Journal	Neurology
Volume	68
Issue number	24
ISSN	0028-3878
DOIs	https://doi.org/10.1212/01.wnl.0000269478.69285.7e
Publication status	Published - 01.06.2007

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This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being
SDG 10 Reduced Inequalities

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10.1212/01.wnl.0000269478.69285.7e

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title = "Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia [3]",

author = "J. Hagenah and K. Reetz and C. Z{\"u}hlke and A. Rolfs and F. Binkofski and C. Klein",

year = "2007",

month = jun,

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doi = "10.1212/01.wnl.0000269478.69285.7e",

language = "English",

volume = "68",

journal = "Neurology",

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TY - JOUR

T1 - Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia [3]

AU - Hagenah, J.

AU - Reetz, K.

AU - Zühlke, C.

AU - Rolfs, A.

AU - Binkofski, F.

AU - Klein, C.

PY - 2007/6/1

Y1 - 2007/6/1

UR - https://www.scopus.com/pages/publications/34250363020

U2 - 10.1212/01.wnl.0000269478.69285.7e

DO - 10.1212/01.wnl.0000269478.69285.7e

M3 - Letters

C2 - 17562842

AN - SCOPUS:34250363020

SN - 0028-3878

VL - 68

JO - Neurology

JF - Neurology

IS - 24

ER -

Predominant dystonia with marked cerebellar atrophy: A rare phenotype in familial dystonia [3]

UN SDGs

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