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
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 2 | Hereditary Ocular Diseases
PDF) 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
Brown-Vialetto-Van Laere syndrome | springermedizin.de
Brown–Vialetto–Van Laere syndrome: Egyptian case report
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: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India
Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin
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
Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma
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
Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar
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...
Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC
SYNDROME DE BROWN VIALETTO VAN LAERE : CAUSE CURABLE DE SMA BULBAIRE CHEZ L'ENFANT - Santedz
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
Riboflavin treatment in genetically proven Brown–Vialetto–Van Laere syndrome Garg M, Kulkarni SD, Hegde AU, Shah KN - J Pediatr Neurosci
Four novel C20orf54 mutations identified in Brown–Vialetto–Van Laere syndrome patients | Journal of Human Genetics
Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula | Human Genome Variation
Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar
Phenotypic characteristics of Brown-Vialetto-Van Laere syndrome caused... | Download Scientific Diagram
