No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra-Reference-Cited by-同舟云学术

No parkinsonism in SCA2 and SCA3 despite severe neurodegeneration of the dopaminergic substantia nigra

Published:2015-09-11 Issue:11 Volume:138 Page:3316-3326
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Schöls Ludger,Reimold Matthias,Seidel Kay,Globas Christoph,Brockmann Kathrin,Karsten Hauser Till,Auburger Georg,Bürk Katrin,den Dunnen Wilfred,Reischl Gerald,Korf Horst-Werner,Brunt Ewout R.,Rüb Udo

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/138/11/3316/13798602/awv255.pdf

Reference47 articles.

1. Subthalamic nucleus and its connections: Anatomic substrate for the network effects of deep brain stimulation

2. Abnormalities of dopaminergic neurotransmission in SCA2: A combined123I-βCIT and123I-IBZM SPECT study

3. Staging of brain pathology related to sporadic Parkinson’s disease

4. Involvement of precerebellar nuclei in multiple system atrophy

5. Lesion of the pedunculopontine nucleus reverses hyperactivity of the subthalamic nucleus and substantia nigra pars reticulata in a 6-hydroxydopamine rat model

Cited by 51 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Specific Biomarkers in Spinocerebellar Ataxia Type 3: A Systematic Review of Their Potential Uses in Disease Staging and Treatment Assessment;International Journal of Molecular Sciences;2024-07-24

2. The characteristic and biomarker value of transcranial sonography in cerebellar ataxia;Annals of Clinical and Translational Neurology;2024-06-24

3. Nigrostriatal dysfunction in RFC1-related disorder/CANVAS;Parkinsonism & Related Disorders;2023-10

4. Genetic Epidemiology and Clinical Characteristics of Patients with Spinocerebellar Ataxias in an Unexplored Brazilian State, Using Strategies for Resource-Limited Settings;The Cerebellum;2023-07-15

5. Genetic Movement Disorders Commonly Seen in Asians;Movement Disorders Clinical Practice;2023-05-08