Brown-Vialetto-Van Laere syndrome | springermedizin.de
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
What is SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test ?
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma
Brown-Vialetto-Van Laere Syndrome: Clinical and Neuropathologic Findings with Immunohistochemistry for C20orf54 in Three Affecte
A riboflavin-responsive neuronopathy with unique characteristics: Brown- Vialetto- Van Laere syndrome | Journal de la faculté de médecine d'Oran
![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
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: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
PDF) 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
Clinical features and neurophysiological follow-up in a case of Brown- Vialetto-Van Laere syndrome
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
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
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: Egyptian case report
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 - YouTube
Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders
PDF) Brown-Vialetto-Van Laere Syndrome-report of three cases | Adel Mahmoud, Tamer Rizk,, and Abdulaziz Alsaman - Academia.edu
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
Remarkable motor recovery after riboflavin therapy in adult-onset Brown— Vialetto—Van Laere syndrome | Practical Neurology
Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula | Human Genome Variation
