Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
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Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
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PDF] Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 | Semantic Scholar
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Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
Phenotypic characteristics of Brown-Vialetto-Van Laere syndrome caused... | Download Scientific Diagram
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Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula | Human Genome Variation
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Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
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Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma | Semantic Scholar
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Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
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The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core
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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
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Genetic study identifies treatable pathway in childhood motor neuron disease | UCL News - UCL – University College London
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PDF) A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin
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Riboflavin treatment in genetically proven Brown–Vialetto–Van Laere syndrome Garg M, Kulkarni SD, Hegde AU, Shah KN - J Pediatr Neurosci
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Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
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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
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