Remarkable motor recovery after riboflavin therapy in adult-onset Brown—Vialetto—Van Laere syndrome

Author:

Bashford James A,Chowdhury Fahmida A,Shaw Chris E

Funder

Motor Neurone Disease Association

Publisher

BMJ

Subject

Neurology (clinical),General Medicine

Reference10 articles.

1. Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54;Green;Am J Hum Genet,2010

2. Brown-vialetto-van laere syndrome;Sathasivam;Orphanet J Rare Dis,2008

3. Clinical presentation and outcome of riboflavin transporter deficiency: mini review after five years of experience;Jaeger;J Inherit Metab Dis,2016

4. The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives;Bosch;Orphanet J Rare Dis,2012

5. Exome sequencing reveals riboflavin transporter mutations as a cause of motor neurone disease;Johnson;Brain,2012

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