(Q37778568)

23 August 2017

1 reference

title

TCS in monogenic forms of Parkinson's disease (English)

1 reference

23 August 2017

TCS in Monogenic Forms of Parkinson’s Disease (English)

1 reference

10.1016/S0074-7742(10)90011-1

DOI

https://api.crossref.org/works/10.1016/S0074-7742(10)90011-1

18 June 2024

1 reference

Kathrin Brockmann

1

1 reference

23 August 2017

Johann Hagenah

series ordinal

2

1 reference

23 August 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20692500

18 June 2024

publication date

1 January 2010

1 reference

International Review of Neurobiology

23 August 2017

published in

1 reference

23 August 2017

volume

90

1 reference

23 August 2017

page(s)

157-164

1 reference

Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: a TMS study

23 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Re: Alpha-synuclein gene duplication is present in sporadic Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Motor reorganization in asymptomatic carriers of a single mutant Parkin allele: a human model for presymptomatic parkinsonism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Parkinson's disease in twins studied with 18F-dopa and positron emission tomography

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Risk of Parkinson's disease among first-degree relatives: A community-based study

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7 January 2021

Familial Parkinson's disease: clinical and genetic analysis of four Basque families.

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7 January 2021

Mitochondrial dysfunction and Parkinson's disease genes: insights from Drosophila

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7 January 2021

The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins.

1 reference

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7 January 2021

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Echogenicity of the substantia nigra in relatives of patients with sporadic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Cross-sectional study discloses a positive family history for Parkinson's disease and male gender as epidemiological risk factors for substantia nigra hyperechogenicity

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Parkinson's disease: a test of the multifactorial etiologic hypothesis

1 reference

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7 January 2021

Brain parenchyma sonography detects preclinical parkinsonism.

1 reference

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7 January 2021

Kufor Rakeb disease: autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

Parkin, PINK1, and DJ-1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7742%2810%2990011-1

7 January 2021

10.1016/S0074-7742(10)90011-1

Identifiers

DOI

1 reference

23 August 2017

1 reference