Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders
The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
Four novel C20orf54 mutations identified in Brown–Vialetto–Van Laere syndrome patients | Journal of Human Genetics
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
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
Clinical features and neurophysiological follow-up in a case of Brown- Vialetto-Van Laere syndrome
Raising a Family With Brown-Vialetto-Van Laere Syndrome
SYNDROME DE BROWN VIALETTO VAN LAERE : CAUSE CURABLE DE SMA BULBAIRE CHEZ L'ENFANT - Santedz
Riboflavin treatment in genetically proven Brown–Vialetto–Van Laere syndrome Garg M, Kulkarni SD, Hegde AU, Shah KN - J Pediatr Neurosci
PDF) Brown-Vialetto-Van Laere Syndrome-report of three cases | Adel Mahmoud, Tamer Rizk,, and Abdulaziz Alsaman - Academia.edu
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma
Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect
Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
Brown-Vialetto-Van Laere syndrome | springermedizin.de
What is SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test ?
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
Brown-Vialetto-Van-Laere Syndrome - YouTube
A riboflavin-responsive neuronopathy with unique characteristics: Brown- Vialetto- Van Laere syndrome | Journal de la faculté de médecine d'Oran
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
PDF) Brown-Vialetto-Van Laere syndrome
