Are Leber’s mitochondial DNA mutations associated with aquaporin-4 autoimmunity?-Reference-Cited by-同舟云学术

Are Leber’s mitochondial DNA mutations associated with aquaporin-4 autoimmunity?

Published:2015-07-24 Issue:3 Volume:22 Page:393-394
ISSN:1352-4585
Container-title:Multiple Sclerosis Journal
language:en
Short-container-title:Mult Scler

Author:

Dujmovic I¹,Jancic J²,Dobricic V³,Jankovic M³,Novakovic I⁴,Comabella M⁵,Drulovic J¹

Affiliation:

1. Clinic of Neurology, Clinical Centre of Serbia, University of Belgrade School of Medicine, Belgrade, Serbia

2. Clinic of Neurology and Psychiatry for Children and Youth, University of Belgrade School of Medicine, Belgrade, Serbia

3. Clinic of Neurology, Clinical Centre of Serbia, Belgrade, Serbia

4. Institute for Human Genetics, University of Belgrade School of Medicine, Belgrade, Serbia

5. Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (Cemcat), Institut de Receca Vall d’Hebron (VHIR), Hospital Universitari Vall d’Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

Link

http://journals.sagepub.com/doi/pdf/10.1177/1352458515590649

Reference4 articles.

1. Neuromyelitis optica antibody in Leber hereditary optic neuropathy: case report

2. A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber’s hereditary optic neuropathy

3. Devic?s neuromyelitis optica and mitochondrial DNA mutation: a case report

4. Devic’s Neuromyelitis Optica: A Case with Mitochondrial DNA Mutations

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2. Leber’s hereditary optic neuropathy companied with multiple-related diseases;Frontiers in Human Neuroscience;2022-11-03

3. Recurrent Bilateral Myelin Oligodendrocyte Glycoprotein Antibody Optic Neuritis in a Leber Hereditary Optic Neuropathy Carrier;Journal of Neuro-Ophthalmology;2019-12-13

4. Myelin Oligodendrocyte Glycoprotein Antibody–Associated Demyelination Comorbid With Leber Hereditary Optic Neuropathy;JAMA Neurology;2019-02-01

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