(Q37382475)

20 August 2017

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title

Complicated recessive dystonia parkinsonism syndromes (English)

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20 August 2017

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parkinsonian syndrome

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3

John Hardy

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Kailash Phatechand Bhatia

20 August 2017

series ordinal

2

object named as

Kailash P Bhatia

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20 August 2017

Susanne A Schneider

1

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20 August 2017

language of work or name

English

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publication date

1 March 2009

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20 August 2017

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20 August 2017

volume

24

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20 August 2017

issue

4

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20 August 2017

page(s)

490-499

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[123I]FP-CIT SPECT findings in two patients with Hallervorden-Spatz disease with homozygous mutation in PANK2 gene.

20 August 2017

cites work

1 reference

Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease

21 January 2018

1 reference

Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.

21 January 2018

1 reference

Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.

21 January 2018

1 reference

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation

21 January 2018

1 reference

PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations

21 January 2018

1 reference

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.

21 January 2018

1 reference

Phenotypic expression of X-linked dystonia-parkinsonism (lubag) in two women

21 January 2018

1 reference

Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases.

21 January 2018

1 reference

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

4 November 2023

https://opencitations.net/index/coci/api/v1/citations/10.1038/33416

Identifiers

DOI

10.1002/MDS.22314

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20 August 2017

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