Full article: Brown–Vialetto–Van Laere syndrome: Egyptian case report
Brown-Vialetto-Van Laere Syndrome 2 | Hereditary Ocular Diseases
A luta contra a Síndrome rara de Brown-Vialetto-Van Laere - YouTube
Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
Orphanet Journal of Rare Diseases
Town mobilizes to help woman with rare disease ACN | Barcelona Only 80 people worldwide have rare Brown-Vialetto-Van Laere Syndrome November 9, 2017 06:42 PM
Brown-Vialetto-Van-Laere Syndrome - YouTube
Padre Márlon Múcio, mss - Hoje o dia foi muito difícil. Talvez um dos mais puxados nesta atual exacerbação da Síndrome de Brown-Vialetto-van Laere. Pude tomar um banho de sol, por ordem
Brown-Vialetto-Van Laere syndrome | Pakistan Pediatric Journal
The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives | springermedizin.de
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
Identification of residues/sequences in the human riboflavin transporter-2 that is important for function and cell biology – topic of research paper in Biological sciences. Download scholarly article PDF and read for free
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics
Frontiers | First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic
Bebê luta contra doença neurodegenerativa raríssima: "Minha filha está em teste com canabidiol para diminuir as dores", diz mãe - Revista Crescer | Saúde
Brown–Vialetto–Van Laere syndrome: Egyptian case report – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
Brown-Vialetto-Van Laere syndrome and Fazio-Londe syndrome: A novel mutation and in silico analyses - Journal of Clinical Neuroscience
