Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
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
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
Riboflavin treatment in genetically proven Brown–Vialetto–Van Laere syndrome Garg M, Kulkarni SD, Hegde AU, Shah KN - J Pediatr Neurosci
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics
PDF) Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series
PDF) A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
Brown-Vialetto-Van Laere Syndrome 1 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Clinical features and neurophysiological follow-up in a case of Brown- Vialetto-Van Laere syndrome - Neuromuscular Disorders
The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma | Semantic Scholar
Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula | Human Genome Variation
Brown‐Vialetto‐Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance? - Mégarbané - 2000 - American Journal of Medical Genetics - Wiley Online Library
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
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 | Vans, Brown, Syndrome
Brown-Vialetto-Van Laere syndrome | Pakistan Pediatric Journal
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
![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
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
