PDF) Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series
brown vialetto van laere syndrome | Van, Brown, Syndrome
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.
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma | Semantic Scholar
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, a fatal disease with a simple solution: a case series | 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
MarkerDB
Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
Genetic study identifies treatable pathway in childhood motor neuron disease | UCL News - UCL – University College London
Finding the Genes Associated with Brown-Vialetto-Van Laere Syndrome (BVVLS) – bria varner
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PDF] Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 | Semantic Scholar
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics
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-Syndrom - Ursachen, Symptome & Behandlung | MedLexi.de
PDF) Brown-Vialetto-van Laere syndrome; the first Turkish case | Omer Aydin - Academia.edu
![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
Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance - Gayathri - 2021 - European Journal of Neurology - Wiley Online Library
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: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
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
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
