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Brown-Vialetto-Van Laere syndrome: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin

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

What is SLC52A3 Gene Brown-Vialetto-Van Laere syndrome 1 NGS Genetic DNA Test ?

Brown–Vialetto–Van Laere [BVVL] Syndrome | SpringerLink

Brown-Vialetto-Van-Laere Syndrome - YouTube

Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma | Semantic Scholar

Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula | Human Genome Variation

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

Phenotypic characteristics of Brown-Vialetto-Van Laere syndrome caused... | Download Scientific Diagram

Brown-Vialetto-Van Laere Syndrome: Clinical and Neuropathologic Findings with Immunohistochemistry for C20orf54 in Three Affecte

Brown-Vialetto-Van Laere Syndrome: A Riboflavin-Unresponsive Patient With a Novel Mutation in the C20orf54 Gene - ScienceDirect

Brown-Vialetto-Van Laere syndrome | springermedizin.de

SYNDROME DE BROWN VIALETTO VAN LAERE : CAUSE CURABLE DE SMA BULBAIRE CHEZ L'ENFANT - Santedz

Motor neuron disease in a young female, Madras pattern or Brown-Vialetto Van Laere syndrome? - A diagnostic dilemma

Brown–Vialetto–Van Laere syndrome Archives - Global Genes

Remarkable motor recovery after riboflavin therapy in adult-onset Brown— Vialetto—Van Laere syndrome | Practical Neurology

Brown-Vialetto-Van Laere Syndrome 2 | Hereditary Ocular Diseases

Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series | Semantic Scholar

PDF] Four cases of brown-vialetto-van laere syndrome from Iran: Clinical and electrophysiologic findings | Semantic Scholar

Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritance. - Abstract - Europe PMC

PDF) Brown-Vialetto-Van Laere Syndrome-report of three cases | Adel Mahmoud, Tamer Rizk,, and Abdulaziz Alsaman - Academia.edu

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Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar

Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disorders

Late-onset and acute presentation of Brown-Vialetto-Van Laere syndrome in a Brazilian family | Neurology Genetics

Brown-Vialetto-Van Laere Syndrome-report of three cases. | Semantic Scholar

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