Phenotypic characteristics of Brown-Vialetto-Van Laere syndrome caused... | Download Scientific Diagram
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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 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 syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
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The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core
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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 Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
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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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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
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Remarkable motor recovery after riboflavin therapy in adult-onset Brown— Vialetto—Van Laere syndrome | Practical Neurology
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Alex's Story - Riboflavin Transporter Deficiency Type 2 | Please watch this powerful video that Cure RTD's media director, Lauren Fitzgerald, made about her son Alex with Riboflavin Transporter Deficiency type...
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PDF) Brown-Vialetto-Van Laere Syndrome-report of three cases | Adel Mahmoud, Tamer Rizk,, and Abdulaziz Alsaman - Academia.edu
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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
Brown-Vialetto-Van Laere Syndrome: Clinical and Neuropathologic Findings with Immunohistochemistry for C20orf54 in Three Affecte
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma
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