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Evolution of brain lesions in a patient with TREX1 cerebroretinal vasculopathy

Neurology. 2015 Nov 3;85(18):1633-4. doi: 10.1212/WNL.0000000000002092.

Authors

Radhika Dhamija¹, David Schiff², M Beatriz S Lopes², Joanna C Jen², Doris D Lin², Bradford B Worrall²

Affiliations

¹ From the University of Virginia (R.D., D.S., M.B.S.L., B.B.W.), Charlottesville; the UCLA School of Medicine (J.C.J.), Los Angeles, CA; and the Johns Hopkins University School of Medicine (D.D.L.), Baltimore, MD. rd3gz@virginia.edu.
² From the University of Virginia (R.D., D.S., M.B.S.L., B.B.W.), Charlottesville; the UCLA School of Medicine (J.C.J.), Los Angeles, CA; and the Johns Hopkins University School of Medicine (D.D.L.), Baltimore, MD.

PMID: 26527794
DOI: 10.1212/WNL.0000000000002092

No abstract available

Publication types

Case Reports

MeSH terms

Adult
Brain / pathology*
Disease Progression
Exodeoxyribonucleases / genetics
Female
Hereditary Central Nervous System Demyelinating Diseases / genetics
Hereditary Central Nervous System Demyelinating Diseases / pathology*
Humans
Magnetic Resonance Imaging
Phosphoproteins / genetics
Retinal Diseases / genetics
Retinal Diseases / pathology*
Vascular Diseases / genetics
Vascular Diseases / pathology*

Substances

Phosphoproteins
Exodeoxyribonucleases
three prime repair exonuclease 1

Supplementary concepts

Vasculopathy, Retinal, With Cerebral Leukodystrophy