(Q35838939)

English

Hereditary haemochromatosis is unlikely to cause movement disorders--a critical review

scientific article published in July 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

1 reference

Europe PubMed Central

Hereditary haemochromatosis is unlikely to cause movement disorders--a critical review (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

object named as

Mark Edwards

2

0 references

Kailash Phatechand Bhatia

5

object named as

Kailash P Bhatia

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

1

object named as

Noemi Russo

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

author name string

Thomasin Andrews

3

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Michael O'Brien

4

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

publication date

1 July 2004

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Journal of Neurology

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

251

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

849-852

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

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

1 reference

https://api.crossref.org/works/10.1007%2FS00415-004-0445-9

21 January 2018

Systemic iron metabolism: a review and implications for brain iron metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The basal ganglia in haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brain iron homeostasis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deposition of iron in paraventricular areas of the human brain in hemochromatosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical report of three patients with hereditary hemochromatosis and movement disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cellular distribution of ferric iron, ferritin, transferrin and divalent metal transporter 1 (DMT1) in substantia nigra and basal ganglia of normal and beta2-microglobulin deficient mouse brain.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extrapyramidal syndrome in idiopathic hemochromatosis. Significance of laboratory chemical, neurophysiologic and imaging procedures (CCT, MRT)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 17-1979

1 reference

https://pubmed.ncbi.nlm.nih.gov/15258788

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00415-004-0445-9

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

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