(Q57316221)

English

Spectrum of movement disorders in neuroferritinopathy

article published in 2004

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title

Spectrum of movement disorders in neuroferritinopathy (English)

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John Burn

7

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Patrick F. Chinnery

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2

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Patrick F. Chinnery

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author name string

Douglas E. Crompton

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1

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David Bates

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3

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Timothy J. Walls

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4

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Margaret J. Jackson

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5

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Andrew J. Curtis

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6

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language of work or name

English

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publication date

18 August 2004

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published in

Movement Disorders

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volume

20

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issue

1

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page(s)

95-99

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cites work

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease

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reference URL

https://api.crossref.org/works/10.1002%2FMDS.20284

retrieved

21 January 2018

Neuroferritinopathy in a French family with late onset dominant dystonia

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reference URL

https://api.crossref.org/works/10.1002%2FMDS.20284

retrieved

21 January 2018

Palatal tremor and cognitive decline in neuroferritinopathy

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reference URL

https://api.crossref.org/works/10.1002%2FMDS.20284

retrieved

21 January 2018

Association between early-onset Parkinson's disease and mutations in the parkin gene

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reference URL

https://api.crossref.org/works/10.1002%2FMDS.20284

retrieved

21 January 2018

State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis

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reference URL

https://api.crossref.org/works/10.1002%2FMDS.20284

retrieved

21 January 2018

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome

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reference URL

https://api.crossref.org/works/10.1002%2FMDS.20284

retrieved

21 January 2018

A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome

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Crossref

reference URL

https://api.crossref.org/works/10.1002%2FMDS.20284

retrieved

21 January 2018

Identifiers

DOI

10.1002/MDS.20284

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PubMed publication ID

15390132

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(Q57316221)

Spectrum of movement disorders in neuroferritinopathy

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