Four novel C20orf54 mutations identified in Brown–Vialetto–Van Laere syndrome patients | Journal of Human Genetics
Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
![PDF] Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/bfe13b005ba8661ccc7f28e621b83313adc67899/2-Figure1-1.png "PDF] Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings | Semantic Scholar")
PDF] Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings | Semantic Scholar
Raising a Family With Brown-Vialetto-Van Laere Syndrome
The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core
Brown–Vialetto–Van Laere syndrome Archives - Global Genes
Thirteen‐month‐old girl with hyporegenerative macrocytic anemia due to Brown –Vialetto–Van Laere syndrome 2 - Naami - 2022 - American Journal of Hematology - Wiley Online Library
PDF) Brown-Vialetto-Van Laere Syndrome-report of three cases | Adel Mahmoud, Tamer Rizk,, and Abdulaziz Alsaman - Academia.edu
Brown–Vialetto–Van Laere syndrome: Egyptian case report
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
MarkerDB
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...
Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula | Human Genome Variation
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma
Remarkable motor recovery after riboflavin therapy in adult-onset Brown— Vialetto—Van Laere syndrome | Practical Neurology
A riboflavin-responsive neuronopathy with unique characteristics: Brown- Vialetto- Van Laere syndrome | Journal de la faculté de médecine d'Oran
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics
Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
Brown-Vialetto-Van-Laere Syndrome - YouTube
Riboflavin treatment in genetically proven Brown–Vialetto–Van Laere syndrome Garg M, Kulkarni SD, Hegde AU, Shah KN - J Pediatr Neurosci
SYNDROME DE BROWN VIALETTO VAN LAERE : CAUSE CURABLE DE SMA BULBAIRE CHEZ L'ENFANT - Santedz
![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
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
Clinical features and neurophysiological follow-up in a case of Brown- Vialetto-Van Laere 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
