Iron metabolism in Parkinsonian syndromes (Q33248678)

24 July 2017

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title

Iron metabolism in Parkinsonian syndromes (English)

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24 July 2017

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Daniela Berg

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24 July 2017

ORCID Public Data File 2021

author name string

Helmine Hochstrasser

series ordinal

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24 July 2017

language of work or name

English

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publication date

1 September 2006

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24 July 2017

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24 July 2017

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24 July 2017

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24 July 2017

page(s)

1299-1310

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The molecular mechanisms of the metabolism and transport of iron in normal and neoplastic cells

24 July 2017

cites work

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Nonselenium glutathione peroxidase in human brain : elevated levels in Parkinson's disease and dementia with lewy bodies

21 January 2018

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Parkinson's disease risks associated with dietary iron, manganese, and other nutrient intakes

21 January 2018

1 reference

Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease.

21 January 2018

1 reference

A neurological syndrome associated with orthostatic hypotension: a clinical-pathologic study

21 January 2018

1 reference

Widespread nitration of pathological inclusions in neurodegenerative synucleinopathies

21 January 2018

1 reference

T1 and T2 in the brain of healthy subjects, patients with Parkinson disease, and patients with multiple system atrophy: relation to iron content

21 January 2018

1 reference

Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.

21 January 2018

1 reference

Sonographic discrimination of corticobasal degeneration vs progressive supranuclear palsy.

21 January 2018

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Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration

21 January 2018

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Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation

21 January 2018

1 reference

Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights

21 January 2018

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Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene

21 January 2018

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Neurodegeneration caused by proteins with an aberrant carboxyl-terminus

21 January 2018

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Hallervorden-Spatz Syndrome and Brain Iron Metabolism

21 January 2018

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Sea-blue histiocytes, lymphocytic cytosomes, movement disorder and 59Fe-uptake in basal ganglia: Hallervorden-Spatz disease or ceroid storage disease with abnormal isotope scan?

21 January 2018

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Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathology

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.21020

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24 July 2017

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