PDF) Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance? | Andre Megarbane - Academia.edu
Finding the Genes Associated with Brown-Vialetto-Van Laere Syndrome (BVVLS) – bria varner
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma | Semantic Scholar
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
PDF) Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series
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PDF] Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 | Semantic Scholar
MarkerDB
Brown–Vialetto–Van Laere syndrome Archives - Global Genes
Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance - Gayathri - 2021 - European Journal of Neurology - Wiley Online Library
Brown-Vialetto-Van-Laere-Syndrom - Ursachen, Symptome & Behandlung | MedLexi.de
brown vialetto van laere syndrome | Van, Brown, Syndrome
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
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Brown–Vialetto–Van Laere [BVVL] Syndrome | SpringerLink
PDF) Brown-Vialetto-van Laere syndrome; the first Turkish case | Omer Aydin - Academia.edu
Genetic study identifies treatable pathway in childhood motor neuron disease | UCL News - UCL – University College London
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.
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
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 fatal disease with a simple solution: a case series | Semantic Scholar
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - 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
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
Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula | Human Genome Variation
Riboflavin treatment in genetically proven Brown–Vialetto–Van Laere syndrome Garg M, Kulkarni SD, Hegde AU, Shah KN - J Pediatr Neurosci
