(Q24562778)

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Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome

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Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome (English)

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2 references

parkinsonian syndrome

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J E Nielsen

1

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L N Jensen

series ordinal

2

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K Krabbe

series ordinal

3

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language of work or name

English

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publication date

September 1995

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published in

Journal of Neurology, Neurosurgery and Psychiatry

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volume

59

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issue

3

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page(s)

318-21

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cites work

Late-onset Hallervorden-Spatz disease presenting as familial parkinsonism

1 reference

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PubMed Central

reference URL

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Pathogenesis of genetic haemochromatosis.

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PubMed Central

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retrieved

27 September 2017

Hereditary haemochromatosis.

1 reference

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PubMed Central

reference URL

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27 September 2017

Idiopathic hemochromatosis, an interim report.

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27 September 2017

Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs

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PubMed Central

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27 September 2017

Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration

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PubMed Central

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27 September 2017

A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA as

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PubMed Central

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27 September 2017

Adult onset Hallervorden-Spatz disease with neurofibrillary pathology. A discrete clinicopathological entity

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27 September 2017

Identification of patients with hereditary haemochromatosis by magnetic resonance imaging and spectroscopic relaxation time measurements

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PubMed Central

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27 September 2017

An HLA study in 74 Danish haemochromatosis patients and in 21 of their families

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30 May 2018

MR of human postmortem brain tissue: correlative study between T2 and assays of iron and ferritin in Parkinson and Huntington disease

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PubMed Central

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28 November 2018

Hallervorden-Spatz disease: MR and pathologic findings.

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PubMed Central

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28 November 2018

Magnetic resonance imaging and extrapyramidal movement disorders

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7673967

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is Parkinson's disease a progressive siderosis of substantia nigra resulting in iron and melanin induced neurodegeneration?

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7673967

retrieved

12 December 2020

based on heuristic

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Identifiers

DOI

10.1136/JNNP.59.3.318

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stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1574675

OpenCitations bibliographic resource ID

1574675

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1574675

PubMed publication ID

7673967

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1574675

ResearchGate publication ID

15525125

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(Q24562778)

Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome

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