![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
![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
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
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma | Semantic Scholar
Brown-Vialetto-Van-Laere-Syndrom - Ursachen, Symptome & Behandlung | MedLexi.de
Pedigree of Lebanese family with Brown-Vialetto-Van Laere syndrome.... | Download Scientific Diagram
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
Brown-Vialetto-Van Laere Syndrome 2 | Hereditary Ocular Diseases
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
PDF) Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance? | Andre Megarbane - Academia.edu
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.
Phenotypic characteristics of Brown-Vialetto-Van Laere syndrome caused... | Download Scientific Diagram
Rare diseases: How patients and parents cope with with little-known illnesses - Daily Record
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - 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
Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula | Human Genome Variation
Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance - Gayathri - 2021 - European Journal of Neurology - Wiley Online Library
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 syndrome | Van, Brown, Syndrome
Brown–Vialetto–Van Laere syndrome Archives - Global Genes
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics
MarkerDB
Finding the Genes Associated with Brown-Vialetto-Van Laere Syndrome (BVVLS) – bria varner
