(Q46399448)

21 December 2017

title

Clinical and genetic evaluation of 8 Polish families with levodopa-responsive parkinsonism (English)

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21 December 2017

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4

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21 December 2017

Zbigniew K Wszolek

9

object named as

Z K Wszolek

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21 December 2017

Anna Krygowska-Wajs

1

object named as

A Krygowska-Wajs

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21 December 2017

author name string

J M Kachergus

2

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21 December 2017

M M Hulihan

3

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21 December 2017

J A Searcy

5

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21 December 2017

J Booij

6

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21 December 2017

H W Berendse

7

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21 December 2017

E Ch Wolters

8

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21 December 2017

publication date

23 March 2005

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21 December 2017

Journal of Neural Transmission

published in

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21 December 2017

volume

112

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21 December 2017

page(s)

1487-1502

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21 December 2017

issue

11

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21 December 2017

https://scigraph.springernature.com/pub.10.1007/s00702-005-0290-8

exact match

0 references

cites work

Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers.

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A kindred with Parkinson's disease not showing genetic linkage to established loci

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Longitudinal fluorodopa positron emission tomographic studies of the evolution of idiopathic parkinsonism

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12 December 2020

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12 December 2020

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

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12 December 2020

Dementia associated with Parkinson's disease

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Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27

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12 December 2020

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Age at onset in two common neurodegenerative diseases is genetically controlled

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Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.

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Subclinical dopaminergic dysfunction in asymptomatic Parkinson's disease patients' relatives with a decreased sense of smell

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alpha-Synuclein locus triplication causes Parkinson's disease

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12 December 2020

Two large Polish kindreds with levodopa-responsive Parkinsonism not linked to known Parkinsonian genes and loci.

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[Hereditary Parkinson disease: report of 3 families with dominant autosomal inheritance]

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12 December 2020

[123I]FP-CIT SPECT shows a pronounced decline of striatal dopamine transporter labelling in early and advanced Parkinson's disease

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12 December 2020

Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism

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12 December 2020

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The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia

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12 December 2020

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

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Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family

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A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

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12 December 2020

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Significant linkage of Parkinson disease to chromosome 2q36-37

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12 December 2020

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12 December 2020

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Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

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12 December 2020

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

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12 December 2020

Large French-Canadian family with Lewy body parkinsonism: exclusion of known loci.

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12 December 2020

Kufor-Rakeb syndrome, pallido-pyramidal degeneration with supranuclear upgaze paresis and dementia, maps to 1p36

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12 December 2020

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

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12 December 2020

10.1007/S00702-005-0290-8

Identifiers

DOI

1 reference

21 December 2017

release_iyjlb3rshzch3ni2mw3tvmm4eu

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/iyjlb3rshzch3ni2mw3tvmm4eu

24 November 2022

mapped directly with Wikidata item

PubMed ID

15785861

1 reference

21 December 2017