Literature DB >> 30072240

Dramatic Improvement of a Rare Syndrome With High Dose Riboflavin Treatment.

Eva B Forman1, A Reghan Foley2, Mary D King3.   

Abstract

Entities:  

Keywords:  Brown-Vialetto-Van Laere syndrome; Neuronopathy; Riboflavin; SLC52A2

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Year:  2018        PMID： 30072240     DOI： 10.1016/j.pediatrneurol.2018.05.005

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN： 0887-8994            Impact factor:   3.372


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  1 in total

1.  Successful treatment of a genetic childhood ataxia due to riboflavin transporter deficiency.

Authors:  Judy Fan; Brent L Fogel
Journal:  Cerebellum Ataxias       Date:  2018-10-20
  1 in total

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