Spinal cord atrophy in early Huntington's disease-Reference-Cited by-同舟云学术

Spinal cord atrophy in early Huntington's disease

Published:2014-03-24 Issue:4 Volume:1 Page:302-306
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Mühlau Mark¹²³,Engl Christina¹²,Boucard Christine C.¹²,Schmidt Paul¹²⁴,Biberacher Viola¹²,Görsch Isabel¹⁵,Sorg Christian²⁶⁷,Wohlschläger Afra²⁶,Zimmer Claus⁶,Hemmer Bernhard¹³,Weindl Adolph¹

Affiliation:

1. Department of Neurology Klinikum rechts der Isar Technische Universität München Munich Germany

2. TUM–Neuroimaging Center Klinikum rechts der Isar Technische Universität München Munich Germany

3. Munich Cluster for Systems Neurology (SyNergy) Munich Germany

4. Department of Statistics Ludwig‐Maximilians‐University München Munich Germany

5. Department of Ophthalmology University Hospital Hamburg Hamburg Germany

6. Department of Neuroradiology Klinikum rechts der Isar Technische Universität München Munich Germany

7. Department of Psychiatry Klinikum rechts der Isar Technische Universität München Munich 81675 Germany

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.52

Reference20 articles.

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

2. Huntington's disease

3. The human dorsal spinocerebellar tract: myelinated fiber spectrum and fiber density in controls, autosomal dominant spinocerebellar atrophy, Huntington's chorea, radiation myelopathy, and diseases with peripheral sensory nerve involvement;Ringelstein EB;Clin Neuropathol,1982

4. Linkage to the Huntington's disease locus in a family with unusual clinical and pathological features

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3. Progressive spinal cord atrophy in manifest and premanifest Huntington’s disease;Journal of Neurology, Neurosurgery & Psychiatry;2017-02-16