About: Association study between iron-related genes polymorphisms and Parkinson's disease

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scientific article published on 01 July 2002

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в липні 2002 (uk) im Juli 2002 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunetu de 2002 (ast) scientific article published on 01 July 2002 (en)
publication date	wds:Q74519525-2D29133C-4071-4482-B6BD-CC6DA7A53E66
publication date	2002-07-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q74519525-C6CE4D0D-D26A-4FEC-88A5-29E652AACE14
exact match	https://scigraph.springernature.com/pub.10.1007/s00415-002-0704-6
author name string	wds:Q74519525-02F65637-130B-4370-A6F7-E2AC2882EE4C wds:Q74519525-0EA107E3-BEDF-488E-BA36-F137B2135AD7 wds:Q74519525-47D3472A-94E4-4FAC-AE0D-34557C15C4F9 wds:Q74519525-583C478D-E870-445C-A8C0-5A02F48343D3 wds:Q74519525-7DB057AE-F482-4214-82B1-1C91821CA196 wds:Q74519525-A1B6BB3B-594E-4B87-83BB-AC27124EEEEC wds:Q74519525-ABA72082-64BF-41D3-BBBD-0C421B13F5B9 wds:Q74519525-B97D2FE2-4E09-46EF-B343-BB14E67942E9 wds:Q74519525-DC67E85B-25AD-43BD-B49A-B4DE0B7FB828 wds:Q74519525-E2886A31-A956-482C-A543-D53EB7793E4D
author name string	Bernard Grandchamp Alexandra Dürr Alexis Brice Patrice Verpillat Claire Borie Yves Agid Anne-Marie Bonnet Francesca Gasparini Gilles Hetet French Parkinson's disease genetic study group
rdfs:label	Association study between iron-related genes polymorphisms and Parkinson's disease (en) Association study between iron-related genes polymorphisms and Parkinson's disease (nl)
skos:prefLabel	Association study between iron-related genes polymorphisms and Parkinson's disease (en) Association study between iron-related genes polymorphisms and Parkinson's disease (nl)
name	Association study between iron-related genes polymorphisms and Parkinson's disease (en) Association study between iron-related genes polymorphisms and Parkinson's disease (nl)
title	wds:Q74519525-C82A4128-A4A3-4614-B662-81AFC1C3BFCE
title	Association study between iron-related genes polymorphisms and Parkinson's disease (en)
page(s)	wds:Q74519525-39291CFD-2FDA-48D0-927C-A8AA1CCAD22B
page(s)	801-804
instance of	wds:Q74519525-816633B6-0519-4F9D-8CF6-66F956C5058B
instance of	scholarly article
main subject	wds:Q74519525-621E8142-180D-4E41-8E4A-3409FC36E76E
main subject	Parkinson's disease
PubMed ID	wds:Q74519525-20F61E7E-C454-4A6B-AC09-B1AB5EC5F1F2
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12140659
PubMed ID	12140659
published in	wds:Q74519525-8C2A8FCF-FC92-40BD-B45D-B8C7BCF15194
published in	Journal of Neurology
issue	wds:Q74519525-689D4251-247D-440D-A86A-A7FA4332C837
volume	wds:Q74519525-7952D8CF-D58E-4999-827B-94042909567A
issue	7
volume	249
DOI	wds:Q74519525-33865839-77E9-4C35-BE2C-E9C03AC9340E
DOI	http://dx.doi.org/10.1007/S00415-002-0704-6
DOI	10.1007/S00415-002-0704-6
Dimensions Publication ID	wds:Q74519525-DDA77DF1-1AEA-454D-8E50-A9527D7FEDD7
Dimensions Publication ID	1035782943
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74519525
is cites work of	Disturbance of iron metabolism in Parkinson's disease -- ultrasonography as a biomarker Genetics of iron regulation and the possible role of iron in Parkinson's disease Iron, brain ageing and neurodegenerative disorders Analysis of nucleotide variations in genes of iron management in patients of Parkinson's disease and other movement disorders. Brain iron homeostasis: from molecular mechanisms to clinical significance and therapeutic opportunities Effects of hemochromatosis and transferrin gene mutations on peripheral iron dyshomeostasis in mild cognitive impairment and Alzheimer's and Parkinson's diseases. Interactions of iron, dopamine and neuromelanin pathways in brain aging and Parkinson's disease The role of iron in brain ageing and neurodegenerative disorders. A novel transferrin/TfR2-mediated mitochondrial iron transport system is disrupted in Parkinson's disease Iron-dependent functions of mitochondria--relation to neurodegeneration Brain iron toxicity: differential responses of astrocytes, neurons, and endothelial cells The role of environmental exposures in neurodegeneration and neurodegenerative diseases Neuroimaging, nutrition, and iron-related genes Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study Genetic analysis of coding SNPs in blood-brain barrier transporter MDR1 in European Parkinson's disease patients. A delicate balance: Iron metabolism and diseases of the brain. Analysis of the association between lactotransferrin (LTF) gene polymorphism and dental caries. Prevalence of haemochromatosis gene mutations in Parkinson's disease Dietary factors in the etiology of Parkinson's disease Physiological and pathological role of alpha-synuclein in Parkinson's disease through iron mediated oxidative stress; the role of a putative iron-responsive element Transferrin protects against Parkinsonian neurotoxicity and is deficient in Parkinson's substantia nigra Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort Association study of the G258S transferrin gene polymorphism and Parkinson's disease in the Spanish population Molecular mechanisms of pathogenesis of Parkinson's disease. Iron metabolism and its detection through MRI in parkinsonian disorders: a systematic review. Excessive early-life dietary exposure: a potential source of elevated brain iron and a risk factor for Parkinson's disease A Network-Based Bioinformatics Approach to Identify Molecular Biomarkers for Type 2 Diabetes that Are Linked to the Progression of Neurological Diseases Disturbance of iron metabolism as a contributing factor to SN hyperechogenicity in Parkinson's disease: implications for idiopathic and monogenetic forms Sleep disorders in Parkinson's disease: clinical features, iron metabolism and related mechanism Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease. Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson’s disease in Southern Italy A case of hereditary haemochromatosis in a patient with extrapyramidal syndrome Movement Disorders Associated With Hemochromatosis. Serotonergic dysfunctions and abnormal iron metabolism: Relevant to mental fatigue of Parkinson disease Cardiometabolic risk factors and lactoferrin: polymorphisms and plasma levels in French-Canadian children.
is cites work of	wds:Q35551001-FCF27E27-45D4-4377-863C-A1BAAE831C7C wds:Q60546002-64BE432A-C677-468C-B500-A9497EE8CAFE wds:Q38118617-0D69D84B-DFA7-4AEE-A7F8-A8620BA8FCB8 wds:Q28537911-0183742B-BD07-4FD4-B6EC-F441F566194F wds:Q28085390-60F9767E-CDEF-4772-8CBD-8685B1CA93C9 wds:Q36226909-B4D71AD5-5250-4301-8C55-98B1CAB9E5AD

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