Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations. - Wikidata - awgldk - TriplyDB

Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.

Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.

http://www.wikidata.org/entity/Q36748778

about

Parkinson's disease: from monogenic forms to genetic susceptibility factors Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease.Primary progressive aphasias and their contribution to the contemporary knowledge about the brain-language relationship Benign tremulous Parkinsonism: a unique entity or another facet of Parkinson's disease?Genetics Underlying Atypical Parkinsonism and Related Neurodegenerative Disorders The role of the LRRK2 gene in Parkinsonism Atypical parkinsonism and cerebrotendinous xanthomatosis: report of a family with corticobasal syndrome and a literature review.Exome sequencing in familial corticobasal degeneration Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation Parkinson's disease: Exit toxins, enter genetics A familial form of parkinsonism, dementia, and motor neuron disease: a longitudinal study.123I-MIBG cardiac uptake and smell identification in parkinsonian patients with LRRK2 mutations Evaluating LRRK2 genetic variants with unclear pathogenicity.Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations.Clinical and pathological characteristics of patients with leucine-rich repeat kinase-2 mutations.Zeroing in on LRRK2-linked pathogenic mechanisms in Parkinson's disease.Primary progressive aphasia.LRRK2 at the Crossroad Between Autophagy and Microtubule Trafficking: Insights into Parkinson's Disease.Leucine-Rich Repeat Kinase (LRRK2) Genetics and Parkinson's Disease.LRRK2 variation and dementia with Lewy bodies.Parkin and PINK1 parkinsonism may represent nigral mitochondrial cytopathies distinct from Lewy body Parkinson's disease.Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.Neurodegenerative disease: can synucleinopathy and tauopathy be identified during life?A case of restless leg syndrome in a family with LRRK2 gene mutation.

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Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.

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B L Miller

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C Anderson

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C M Clark

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E McCarty Wood

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V M Van Deerlin

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V M-Y Lee

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P2860

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

A common LRRK2 mutation in idiopathic Parkinson's disease

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

Primary progressive aphasia--a language-based dementia.

Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.

Analysis of the LRRK2 G2019S mutation in Alzheimer Disease.

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease.

Corticodentatonigral degeneration with neuronal achromasia.

The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases.

What's in a name: voxel-based morphometric analyses of MRI and naming difficulty in Alzheimer's disease, frontotemporal dementia and corticobasal degeneration.

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