(Q58000673)

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Movement disorder due to aceruloplasminemia and incorrect diagnosis of hereditary hemochromatosis

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Movement disorder due to aceruloplasminemia and incorrect diagnosis of hereditary hemochromatosis (English)

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Cesare Colosimo

3

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Anna Rita Bentivoglio

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Anna Rita Bentivoglio

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2

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Alfonso Fasano

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Alfonso Fasano

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1

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publication date

January 2007

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published in

Journal of Neurology

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volume

254

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issue

1

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page(s)

113-114

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exact match

https://scigraph.springernature.com/pub.10.1007/s00415-006-0289-6

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Brain iron deposition in Parkinson's disease imaged using the PRIME magnetic resonance sequence.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17508145

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12 December 2020

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Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum

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https://pubmed.ncbi.nlm.nih.gov/17508145

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12 December 2020

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https://pubmed.ncbi.nlm.nih.gov/17508145

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12 December 2020

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A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans

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https://pubmed.ncbi.nlm.nih.gov/17508145

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12 December 2020

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The basal ganglia in haemochromatosis

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12 December 2020

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

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12 December 2020

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Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series

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https://pubmed.ncbi.nlm.nih.gov/17508145

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12 December 2020

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Restless legs syndrome and low brain iron levels in patients with haemochromatosis.

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https://pubmed.ncbi.nlm.nih.gov/17508145

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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Unraveling the Hallervorden-Spatz syndrome: pantothenate kinase-associated neurodegeneration is the name

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/17508145

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12 December 2020

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Identifiers

DOI

10.1007/S00415-006-0289-6

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PubMed publication ID

17508145

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(Q58000673)

Movement disorder due to aceruloplasminemia and incorrect diagnosis of hereditary hemochromatosis

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