Book/Journal Article (Review Article)

DZNE-2020-02424

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png TCS in monogenic forms of Parkinson's disease.

Brockmann, K. (First author)DZNE* ; Hagenah, J.

2010
Elsevier New York, NY [u.a.]

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Please use a persistent id in citations: doi:10.1016/S0074-7742(10)90011-1

Abstract: During the last decade, mutations in a growing number of genes have been found to cause monogenic forms of Parkinson's disease (PD). Moreover, many studies shed light on their contribution to sporadic variants of PD. Since hyperechogenicity of the substantia nigra (SN) represents a characteristic hallmark of sporadic PD questions arise concerning the echo pattern of monogenic forms of this disorder on TCS.

Keyword(s): Genetic Predisposition to Disease: genetics (MeSH) ; Humans (MeSH) ; Mutation: genetics (MeSH) ; Parkinson Disease: diagnostic imaging (MeSH) ; Parkinson Disease: genetics (MeSH) ; Parkinson Disease: pathology (MeSH) ; Ultrasonography, Doppler, Transcranial: methods (MeSH) ; Ultrasonography, Doppler, Transcranial: standards (MeSH)

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Contributing Institute(s):

1. Parkinson Genetics (AG Gasser)

Research Program(s):

1. 345 - Population Studies and Genetics (POF3-345) (POF3-345)

Appears in the scientific report 2010

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Database coverage:
; BIOSIS Previews ; BIOSIS Reviews Reports And Meetings ; Clarivate Analytics Master Journal List ; IF < 5 ; JCR ; NCBI Molecular Biology Database ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Web of Science Core Collection

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