Optical coherence tomography in autosomal recessive spastic ataxia of Charlevoix-Saguenay-Reference-Cited by-同舟云学术

Optical coherence tomography in autosomal recessive spastic ataxia of Charlevoix-Saguenay

Published:2018-03-12 Issue:4 Volume:141 Page:989-999
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:

Author:

Parkinson Michael H¹²,Bartmann Ana P²,Clayton Lisa M S²,Nethisinghe Suran¹,Pfundt Rolph³,Chapple J Paul⁴,Reilly Mary M¹²⁵,Manji Hadi²,Wood Nicholas J¹²,Bremner Fion²,Giunti Paola¹²^ORCID

Affiliation:

1. Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK

2. National Hospital for Neurology and Neurosurgery, Queen Square, London, UK

3. Department of Human Genetics, Radboud University, Nijmegen Medical Centre, Nijmegen, The Netherlands

4. William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, UK

5. MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, London, UK

Funder

Ataxia UK

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/141/4/989/25082983/awy028.pdf

Reference43 articles.

1. Retinal nerve fibre layer thinning is associated with drug resistance in epilepsy;Balestrini;J Neurol Neurosurg Psychiatry,2016

2. Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy;Barboni;Ophthalmology,2005

3. Recessive spastic ataxia of Charlevoix-Saguenay;Bouchard;Handb Clin Neurol,1991

4. Autosomal recessive spastic ataxia of Charlevoix-Saguenay;Bouchard;Can J Neurol Sci,1978

5. Autosomal recessive spastic ataxia of Charlevoix-Saguenay;Bouchard;Neuromuscul Disord,1998

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