Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles. (Q53459145)

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8 January 2020

title

Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles (English)

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2

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author name string

J M Hagenah

1

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8 January 2020

B Becker

3

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R Hilker

4

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M Kasten

5

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K Hedrich

6

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P P Pramstaller

7

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C Klein

8

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G Seidel

9

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publication date

15 October 2007

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8 January 2020

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volume

254

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issue

10

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page(s)

1407-1413

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https://scigraph.springernature.com/pub.10.1007/s00415-007-0567-y

8 January 2020

exact match

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cites work

Vulnerability of the nigrostriatal system as detected by transcranial ultrasound.

1 reference

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https://api.crossref.org/works/10.1007%2FS00415-007-0567-Y

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation

21 January 2018

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

21 January 2018

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12 December 2020

Brain parenchyma sonography detects preclinical parkinsonism.

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Does ultrasound disclose a vulnerability factor for Parkinson's disease?

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12 December 2020

Blink amplitude but not saccadic hypometria indicates carriers of Parkin mutations

1 reference

12 December 2020

Phenotype-genotype correlation in Dutch patients with myoclonus-dystonia

1 reference

12 December 2020

In vivo detection of iron and neuromelanin by transcranial sonography: a new approach for early detection of substantia nigra damage.

1 reference

12 December 2020

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

1 reference

12 December 2020

Neuroimaging in basal ganglia disorders: perspectives for transcranial ultrasound

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12 December 2020

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

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12 December 2020

Stages in the development of Parkinson's disease-related pathology

1 reference

12 December 2020

Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.

1 reference

12 December 2020

Transcranial sonography and [123I]FP-CIT SPECT disclose complementary aspects of Parkinson's disease.

1 reference

12 December 2020

The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism

1 reference

12 December 2020

Five-year follow-up study of hyperechogenicity of the substantia nigra in Parkinson's disease

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00415-007-0567-Y

Identifiers

DOI

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