(Q51727066)

10 April 2018

title

Involvement of spinal motor neurons in parkin-positive autosomal recessive juvenile parkinsonism. (English)

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10 April 2018

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Shoichi Sasaki

1

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10 April 2018

Akiko Shirata

series ordinal

2

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10 April 2018

Kiyomi Yamane

series ordinal

3

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10 April 2018

Makoto Iwata

series ordinal

4

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publication date

20 November 2007

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10 April 2018

published in

Neuropathology

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volume

28

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issue

1

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page(s)

74-80

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Lewy bodies and parkinsonism in families with parkin mutations

cites work

1 reference

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Steele-Richardson-Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein.

21 January 2018

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Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q.

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Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations.

21 January 2018

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Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.

21 January 2018

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Association between early-onset Parkinson's disease and mutations in the parkin gene

21 January 2018

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Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2007.00829.X

How much phenotypic variation can be attributed to parkin genotype?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2007.00829.X

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

21 January 2018

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Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism

21 January 2018

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Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification.

21 January 2018

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A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

21 January 2018

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Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

21 January 2018

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Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers

21 January 2018

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Neuropathology of autonomic nervous system in Parkinson's disease

21 January 2018

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Alpha-synuclein pathology in the spinal cords of neurologically asymptomatic aged individuals

21 January 2018

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Familial amyotrophic lateral sclerosis. A subgroup characterized by posterior and spinocerebellar tract involvement and hyaline inclusions in the anterior horn cells

21 January 2018

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Immunocytochemical and ultrastructural studies of hyaline inclusions in sporadic motor neuron disease

21 January 2018

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Pael-R is accumulated in Lewy bodies of Parkinson's disease.

21 January 2018

1 reference

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An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin

21 January 2018

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Neuroscience. Parkin and its substrates.

21 January 2018

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Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2007.00829.X

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1440-1789.2007.00829.X

Aggregation of ?-synuclein in the pathogenesis of Parkinson?s disease

21 January 2018

1 reference

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10.1111/J.1440-1789.2007.00829.X

21 January 2018

Identifiers

DOI

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10 April 2018

PubMed ID

18031467

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10 April 2018