Πέννες Αγριος Επίμονος brown vialetto van laere syndrome Υλισμός Πρόθυμος Σόφη
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
Rare diseases: How patients and parents cope with with little-known illnesses - Daily Record
PDF) Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance? | Andre Megarbane - Academia.edu
PDF] Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings | Semantic Scholar
Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
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
PDF) Brown-Vialetto-Van Laere syndrome
PDF) Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
PDF) Brown-Vialetto-van Laere syndrome; the first Turkish case | Omer Aydin - Academia.edu
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
Frontiers | First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core
PDF] Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2 | 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: Egyptian case report – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
Genetic study identifies treatable pathway in childhood motor neuron disease | UCL News - UCL – University College London
PDF) A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin
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: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
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-report of three cases. | Semantic Scholar
Brown–Vialetto–Van Laere syndrome Archives - Global Genes
Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance - Gayathri - 2021 - European Journal of Neurology - Wiley Online Library