About: Western Nebraska family (family D) with autosomal dominant parkinsonism

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scientific article published on 01 March 1995

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1995 (uk) article scientifique publié en 1995 (fr) im März 1995 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en marzu de 1995 (ast) scientific article published on 01 March 1995 (en)
publication date	wds:Q72649944-EB92C7F7-8C77-4D93-8065-B900439CE189
publication date	1995-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q72649944-BFACD3A5-3E5F-48C6-BB68-4FBF57834785
language of work or name	English
author name string	wds:Q72649944-1783F233-1C3B-4CCD-A906-D6D2A744F43A wds:Q72649944-2766FE12-A8E5-4020-BB50-199660EBAAFF wds:Q72649944-53044F6F-E42E-4470-947F-23E09AB6F9E3 wds:Q72649944-5423EA4C-D216-4F09-82C5-4440E67A07F3 wds:Q72649944-86FAF5FB-0D9F-4579-8FE2-A963A513B1C6 wds:Q72649944-CAC5FF9D-9988-4089-8039-63D1030F72DE wds:Q72649944-DD1960A3-D74A-4A6D-B593-CE0A1A4FFB94
author name string	D B Calne R J Uitti J R Fulgham J E Parisi R F Pfeiffer B Pfeiffer B M Thompson
rdfs:label	Western Nebraska family (nl) Western Nebraska family (family D) with autosomal dominant parkinsonism (en)
skos:prefLabel	Western Nebraska family (nl) Western Nebraska family (family D) with autosomal dominant parkinsonism (en)
name	Western Nebraska family (nl) Western Nebraska family (family D) with autosomal dominant parkinsonism (en)
author	wds:Q72649944-0CFD8ED6-4A7E-4498-BCEC-8F75C5027538
author	Zbigniew K Wszolek
title	wds:Q72649944-66FB3341-DF1D-4413-9100-A258D73A16CB
title	Western Nebraska family (family D) with autosomal dominant parkinsonism (en)
page(s)	wds:Q72649944-546CC8F7-63D3-49A2-A7B6-43458501E2D9
page(s)	502-505
instance of	wds:Q72649944-16E6DBD7-0E59-401A-908E-518F469AE1A4
instance of	scholarly article
main subject	wds:Q72649944-9547603D-E3C6-48E2-A84D-29A927BF6E61
main subject	parkinsonian syndrome
PubMed ID	wds:Q72649944-3B362AE7-0CA3-4C0D-B931-CB555AFB2FB7
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7898705
PubMed ID	7898705
published in	wds:Q72649944-62A3F1CA-B5A2-4640-809A-6FE417074A10
published in	Neurology
issue	wds:Q72649944-FEBC6086-CD49-473A-899B-69A5DF02CE1E
volume	wds:Q72649944-C2317C1B-76C1-4261-B5A8-8417CEC94214
issue	3 Pt 1
volume	45
DOI	wds:Q72649944-7C854FF8-FD12-48DF-93BE-47507F676D8A
DOI	http://dx.doi.org/10.1212/WNL.45.3.502
DOI	10.1212/WNL.45.3.502
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q72649944
is cites work of	A susceptibility locus for Parkinson's disease maps to chromosome 2p13. Multisystem Lewy body disease and the other parkinsonian disorders Synaptic dysfunction in genetic models of Parkinson's disease: a role for autophagy? Creation of an open-access, mutation-defined fibroblast resource for neurological disease research Leucine-rich repeat kinase 2 for beginners: six key questions. Clinical features of LRRK2 parkinsonism Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls Clinical and pathologic features of families with LRRK2-associated Parkinson's disease The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations Positron emission tomography of dopamine pathways in familial Parkinsonian syndromes Molecular genetics of familial parkinsonism Occupational risk factors in Parkinson's disease Familial parkinsonism: study of original Sagamihara PARK8 (I2020T) kindred with variable clinicopathologic outcomes Genes and parkinsonism. Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7). Genetically engineered mouse models of Parkinson's disease Epidemiology of Parkinson's disease Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study Clinical neurophysiologic findings in patients with rapidly progressive familial parkinsonism and dementia with pallido-ponto-nigral degeneration. Ten years and counting: moving leucine-rich repeat kinase 2 inhibitors to the clinic Genetics of Parkinson's disease Two large Polish kindreds with levodopa-responsive Parkinsonism not linked to known Parkinsonian genes and loci. Physiological and pathological functions of LRRK2: implications from substrate proteins Epigenetics in Parkinson's Disease. The Identification of Alpha-Synuclein as the First Parkinson Disease Gene Parkinsonism associated with autosomal dominant bilateral striopallidodentate calcinosis Parkinson Disease from Mendelian Forms to Genetic Susceptibility: New Molecular Insights into the Neurodegeneration Process. Genetics of Parkinson's disease Genetic aspects of Parkinson's disease Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study Cancer in Parkinson's disease
is cites work of	wds:Q30485675-91108FA5-A4B3-4E61-B26B-A516D583C1C9 wds:Q30440991-4466685E-64C2-4806-9367-B428E3D8CE29 wds:Q28266674-E193C20A-8D07-4933-AA0F-4DE6BD1D3E4E wds:Q48373895-83243C61-0F02-4646-8260-E48DC2071B78 wds:Q59099056-E0368A3E-4445-4BE6-B479-D7D624C5B01F wds:Q81554186-D45F82A8-C16B-4D46-964B-E9FFD2F4EE00 wds:Q81554370-BE3684B1-2930-4DC7-8230-5FEEA069CB43 wds:Q64860870-0B0522EC-A273-4D12-B542-DF8AF9A818F8 wds:Q34093433-051511BA-9EF6-45D2-9D43-70A639BC1383 wds:Q42642426-8BA078BF-8F64-4409-930F-B3048A6B5235 wds:Q47320399-F6958DA1-EBB2-4BCD-85F3-A80A35470595 wds:Q73853102-12A9346C-F696-493B-B93B-11F21EAA4747

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