(Q37186857)

18 August 2017

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title

Recent advances in the genetics of dementia with lewy bodies (English)

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18 August 2017

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1

Vincenzo Bonifati

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18 August 2017

publication date

1 May 2008

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Current Neurology and Neuroscience Reports

18 August 2017

published in

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18 August 2017

volume

8

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18 August 2017

issue

3

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18 August 2017

page(s)

187-189

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https://scigraph.springernature.com/pub.10.1007/s11910-008-0030-1

18 August 2017

exact match

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cites work

Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-008-0030-1

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-008-0030-1

Beta-synuclein gene alterations in dementia with Lewy bodies

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-008-0030-1

How to diagnose dementia with Lewy bodies: state of the art.

21 January 2018

1 reference

12 December 2020

Glucocerebrosidase mutations are an important risk factor for Lewy body disorders.

1 reference

12 December 2020

Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): report of the Consortium on DLB International Workshop.

1 reference

12 December 2020

Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication

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12 December 2020

Lrrk2 and Lewy body disease

1 reference

12 December 2020

Clinical genetic analysis of Parkinson's disease in the Contursi kindred

1 reference

12 December 2020

Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease

1 reference

12 December 2020

Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease

1 reference

12 December 2020

beta-Synuclein inhibits alpha-synuclein aggregation: a possible role as an anti-parkinsonian factor

1 reference

12 December 2020

Familial occurrence of dementia with Lewy bodies

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12 December 2020

alpha-Synuclein locus triplication causes Parkinson's disease

1 reference

12 December 2020

Identification of families with cortical Lewy body disease.

1 reference

12 December 2020

Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the alpha-synuclein gene.

1 reference

12 December 2020

A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder

1 reference

12 December 2020

LRRK2 low-penetrance mutations (Gly2019Ser) and risk alleles (Gly2385Arg)-linking familial and sporadic Parkinson's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews

1 reference

12 December 2020

A novelLRRK2 mutation in an Austrian cohort of patients with Parkinson's disease

1 reference

12 December 2020

Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype

1 reference

12 December 2020

Alpha-synuclein locus duplication as a cause of familial Parkinson's disease

1 reference

12 December 2020

Enhanced lysosomal pathology caused by beta-synuclein mutants linked to dementia with Lewy bodies

1 reference

12 December 2020

Significant linkage of Parkinson disease to chromosome 2q36-37

1 reference

12 December 2020

Dementia with Lewy bodies in an elderly Greek male due to alpha-synuclein gene mutation

1 reference

12 December 2020

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

12 December 2020

DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkers

1 reference

12 December 2020

A mutant PSEN1 causes dementia with Lewy bodies and variant Alzheimer's disease.

1 reference

12 December 2020

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

1 reference

12 December 2020

10.1007/S11910-008-0030-1

Identifiers

DOI

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18 August 2017

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