Young-Onset Parkinsonism in a Hong Kong Chinese Man With Adult-Onset Hallervorden–Spatz Syndrome (Q57643620)

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19 January 2020

title

Young-onset parkinsonism in a Hong Kong Chinese man with adult-onset Hallervorden-Spatz syndrome (English)

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19 January 2020

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parkinsonian syndrome

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3

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19 January 2020

author name string

Chloe Miu Mak

1

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19 January 2020

Bun Sheng

2

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19 January 2020

Kwok-kwong Lau

4

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19 January 2020

Wing-tak Chan

5

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19 January 2020

Ching-wan Lam

6

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19 January 2020

Yan-wo Chan

7

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publication date

4 January 2011

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International Journal of Neuroscience

19 January 2020

published in

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volume

121

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issue

4

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page(s)

224-227

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Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms

19 January 2020

cites work

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The eye-of-the-tiger sign is not a reliable disease marker for Hallervorden-Spatz syndrome

21 January 2018

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Clinical and genetic delineation of neurodegeneration with brain iron accumulation

21 January 2018

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Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation

21 January 2018

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

21 January 2018

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Pattern recognition in magnetic resonance imaging of white matter disorders in children and young adults.

21 January 2018

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A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect

21 January 2018

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A Novel PANK2 Mutation in a Patient with Atypical Pantothenate-Kinase-Associated Neurodegeneration Presenting with Adult-Onset Parkinsonism

21 January 2018

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Hallervorden-Spatz Syndrome and Brain Iron Metabolism

21 January 2018

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Hallervorden-Spatz syndrome

21 January 2018

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Genetic heterogeneity in patients with pantothenate kinase-associated neurodegeneration and classic magnetic resonance imaging eye-of-the-tiger pattern.

21 January 2018

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Adult Hallervorden-Spatz syndrome simulating amyotrophic lateral sclerosis

21 January 2018

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Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.3109%2F00207454.2010.542843

10.3109/00207454.2010.542843

21 January 2018

Identifiers

DOI

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19 January 2020

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