Brown-Vialetto-Van Laere syndrome | springermedizin.de
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
Four novel C20orf54 mutations identified in Brown–Vialetto–Van Laere syndrome patients | Journal of Human Genetics
The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
PDF) Brown-Vialetto-Van Laere Syndrome-report of three cases | Adel Mahmoud, Tamer Rizk,, and Abdulaziz Alsaman - Academia.edu
Remarkable motor recovery after riboflavin therapy in adult-onset Brown— Vialetto—Van Laere syndrome | Practical Neurology
PDF) Brown-Vialetto-Van Laere syndrome
Brown–Vialetto–Van Laere syndrome: Egyptian case report
Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders
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...
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
Phenotypic characteristics of Brown-Vialetto-Van Laere syndrome caused... | Download Scientific Diagram
Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics
![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
![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
A riboflavin-responsive neuronopathy with unique characteristics: Brown- Vialetto- Van Laere syndrome | Journal de la faculté de médecine d'Oran
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma
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
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
What is SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test ?
Clinical features and neurophysiological follow-up in a case of Brown- Vialetto-Van Laere syndrome
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 - YouTube
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
Raising a Family With Brown-Vialetto-Van Laere Syndrome
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
