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: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
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
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
PDF) Brown-Vialetto-Van Laere syndrome
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 2 | Hereditary Ocular Diseases
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
Brown–Vialetto–Van Laere syndrome Archives - Global Genes
Brown-Vialetto-Van-Laere-Syndrom - Ursachen, Symptome & Behandlung | MedLexi.de
Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
![Brown–Vialetto–Van Laere [BVVL] Syndrome | SpringerLink](https://media.springernature.com/lw685/springer-static/image/chp%3A10.1007%2F978-981-10-5361-0_21/MediaObjects/420252_1_En_21_Fig1_HTML.jpg "Brown–Vialetto–Van Laere [BVVL] Syndrome | SpringerLink")
Brown–Vialetto–Van Laere [BVVL] Syndrome | SpringerLink
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
Pontobulbar Palsy and Neurosensory Deafness (Brown-Vialetto-van Laere Syndrome) With Hyperintense Brainstem Nuclei on Magnetic Resonance Imaging: New Finding in Three Siblings | Semantic Scholar
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics
![PDF] Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/b96021c4ddde4755a31468327b3ada14ceeeaa56/7-Figure3-1.png "PDF] Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 | Semantic Scholar")
PDF] Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 | Semantic Scholar
Rare diseases: How patients and parents cope with with little-known illnesses - Daily Record
Phenotypic characteristics of Brown-Vialetto-Van Laere syndrome caused... | Download Scientific Diagram
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Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
Genetic study identifies treatable pathway in childhood motor neuron disease | UCL News - UCL – University College London
Riboflavin treatment in genetically proven Brown–Vialetto–Van Laere syndrome Garg M, Kulkarni SD, Hegde AU, Shah KN - J Pediatr Neurosci
Brown‐Vialetto‐Van Laere and Fazio Londe syndromes: defects of riboflavin transport with biochemical similarities to multiple acyl‐CoA dehydrogenation defects (MADD) - Bennett - 2012 - Journal of Inherited Metabolic Disease - Wiley Online Library
