Clinical and genetic study of ataxia with vitamin E deficiency: A case report-Reference-Cited by-同舟云学术

Clinical and genetic study of ataxia with vitamin E deficiency: A case report

Published:2022-08-16 Issue:23 Volume:10 Page:8271-8276
ISSN:2307-8960
Container-title:World Journal of Clinical Cases
language:
Short-container-title:WJCC

Author:

Zhang Lin-Wei,Liu Bing,Peng Dan-Tao

Publisher

Baishideng Publishing Group Inc.

Subject

General Medicine

Reference20 articles.

1. Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency

2. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia

3. Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families

4. Esmer C, Salazar MA, Rentería PE, Bravo OA. Clinical and molecular findings in a patient with ataxia with vitamin E deficiency, homozygous for the c.205-1G>C mutation in the TTPA gene. Bol Med Hos Infant Mex 2013; 70: 313-317

5. Vitamin E and Phosphoinositides Regulate the Intracellular Localization of the Hepatic α-Tocopherol Transfer Protein

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1. Are age-related neurodegenerative diseases caused by a lack of the diet-derived compound ergothioneine?;Free Radical Biology and Medicine;2024-05

2. α-Tocopherol: New Perspectives and Challenges for Achieving the Sustainable Development Goals (SDG) Target;Journal of Oleo Science;2024

3. Genetically proven Ataxia with Vitamin-E deficiency with predominant cervico-brachial dystonic presentation: A case report from India;Journal of Movement Disorders;2023-12-18

4. Isolated Head Tremor as an Initial Presentation of Ataxia with Vitamin E Deficiency: A Case Report;Movement Disorders Clinical Practice;2023-09-29

5. Inborn Errors of Metabolism with Ataxia: Current and Future Treatment Options;Cells;2023-09-19