Literature DB >> 30746424

99mTc-TRODAT-1 SPECT Showing Dopaminergic Deficiency in a Patient with Spinocerebellar Ataxia Type 10 and Parkinsonism.

Giorgio Fabiani1,2, Raul Martins3, Tetsuo Ashizawa4, Francisco M B Germiniani2, Hélio A G Teive2.   

Abstract

Entities:  

Keywords:  99Tc‐TRODAT‐1 SPECT; SCA10; parkinsonism; spinocerebellar ataxia type 10

Year:  2018        PMID： 30746424      PMCID： PMC6335547          DOI： 10.1002/mdc3.12700

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN： 2330-1619


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  2 in total

1.  Meta-Analysis of Differentially Expressed Genes in the Substantia Nigra in Parkinson's Disease Supports Phenotype-Specific Transcriptome Changes.

Authors:  Duong My Phung; Jinwoo Lee; SangKyoon Hong; Young Eun Kim; Jeehee Yoon; Yun Joong Kim
Journal:  Front Neurosci       Date:  2020-12-18       Impact factor: 4.677

2.  The Protein-Protein Interaction Network of Hereditary Parkinsonism Genes Is a Hierarchical Scale-Free Network.

Authors:  Yun Joong Kim; Kiyong Kim; Heonwoo Lee; Junbeom Jeon; Jinwoo Lee; Jeehee Yoon
Journal:  Yonsei Med J       Date:  2022-08       Impact factor: 3.052
  2 in total

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