Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
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: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
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
A luta contra a Síndrome rara de Brown-Vialetto-Van Laere - YouTube
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
![PDF] Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/bfe13b005ba8661ccc7f28e621b83313adc67899/2-Figure1-1.png "PDF] Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings | Semantic Scholar")
PDF] Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings | Semantic Scholar
Phenotypic characteristics of Brown-Vialetto-Van Laere syndrome caused... | Download Scientific Diagram
Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core
PDF) Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series
Full article: Brown–Vialetto–Van Laere syndrome: Egyptian case report
Brown-Vialetto-Van Laere syndrome | Pakistan Pediatric Journal
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma | Semantic Scholar
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
Finding the Genes Associated with Brown-Vialetto-Van Laere Syndrome (BVVLS) – bria varner
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
Orphanet Journal of Rare Diseases
brown vialetto van laere syndrome | Vans, Brown, Syndrome
The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives | springermedizin.de
Brown-Vialetto-Van Laere Syndrome 1 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
