Substantia nigra hyperechogenicity with LRRK2 G2019S mutations (Q34861140)

4 August 2017

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations (English)

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4 August 2017

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Rachel Saunders-Pullman

series ordinal

9

object named as

Rachel Saunders-Pullman

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4 August 2017

4

Christine Klein

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4 August 2017

6

Deborah Raymond

1 reference

4 August 2017

7

Laurie Ozelius

1 reference

4 August 2017

8

Susan Bressman

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4 August 2017

5

Cuiling Wang

1 reference

4 August 2017

Norbert Brüggemann

1

1 reference

4 August 2017

Johann Hagenah

series ordinal

2

1 reference

4 August 2017

Kaili Stanley

series ordinal

3

1 reference

4 August 2017

language of work or name

English

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publication date

10 February 2011

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4 August 2017

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4 August 2017

26

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4 August 2017

885-888

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4 August 2017

5

1 reference

Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype

4 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

Gaucher disease ascertained through a Parkinson's center: imaging and clinical characterization

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

Transcranial brain parenchyma sonography in movement disorders: state of the art.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

Detection of presymptomatic Parkinson's disease: combining smell tests, transcranial sonography, and SPECT.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

Echogenicity of the substantia nigra: association with increased iron content and marker for susceptibility to nigrostriatal injury

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

Vulnerability of the nigrostriatal system as detected by transcranial ultrasound.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

Random-effects models for longitudinal data

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3082617

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

8 July 2018

1 reference

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

21 January 2018

1 reference

Brain parenchyma sonography detects preclinical parkinsonism.

21 January 2018

1 reference

Substantia nigra echomorphology in the healthy very old: Correlation with motor slowing.

21 January 2018

1 reference

Clinical expression of LRRK2 G2019S mutations in the elderly

21 January 2018

1 reference

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

21 January 2018

1 reference

Transcranial brain sonography findings in clinical subgroups of idiopathic Parkinson's disease.

21 January 2018

1 reference

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

21 January 2018

1 reference

Evaluation of LRRK2 G2019S penetrance: Relevance for genetic counseling in Parkinson disease

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Brain parenchyma sonography discriminates Parkinson's disease and atypical parkinsonian syndromes

1 reference

12 December 2020

Identifiers

DOI

10.1002/MDS.23644

1 reference

4 August 2017

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4 August 2017

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