Title
Pearls & Oy-sters: A Novel Presentation of Ataxia With Vitamin E Deficiency Caused by TTPA Gene Mutation
Date Issued
26 January 2021
Access level
metadata only access
Resource Type
journal article
Author(s)
Cincinnati Children's Hospital Medical Center
Publisher(s)
Lippincott Williams and Wilkins
Abstract
Ataxia with isolated vitamin E deficiency can present with a phenotype similar to a complex hereditary spastic paraplegia with dystonia and bradykinesia, but absent cerebellar ataxia or proprioceptive deficits. © American Academy of Neurology.
Start page
e640
End page
e642
Volume
96
Issue
4
Language
English
OCDE Knowledge area
Neurociencias
Scopus EID
2-s2.0-85100445696
PubMed ID
Source
Neurology
Resource of which it is part
Neurology
Sponsor(s)
A. Zea Vera, W. Liu, and C. Thomas report no financial disclosures. D.L. Gilbert has received honoraria and/or travel support from the Tourette Association of America/Centers for Disease Control and Prevention, the Child Neurology Society, and the American Academy of Neurology; compensation for expert testimony for the US National Vaccine Injury Compensation Program through the Department of Health and Human Services; and payment for medical expert opinions through Advanced Medical/Teladoc. D.L. Gilbert has received research support from the NIH (NIMH, NINDS); salary compensation through Cincinnati Children's for work as a clinical trial site investigator from Emalex (clinical trial, Tourette syndrome) and EryDel (clinical trial, Ataxia Telangiectasia); and book royalties from Elsevier and Wolters Kluwer. Go to Neurology.org/N for full disclosures.
Sources of information:
Directorio de Producción Científica
Scopus