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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 Archives - Global Genes

Finding the Genes Associated with Brown-Vialetto-Van Laere Syndrome (BVVLS) – bria varner

Brown-Vialetto-Van Laere syndrome | Orphanet Journal of Rare Diseases | Full Text

Frontiers | First report of paternal uniparental disomy of chromosome 8 with SLC52A2 mutation in Brown-vialetto-van laere syndrome type 2 and an analysis of genotype-phenotype correlations

A luta contra a Síndrome rara de Brown-Vialetto-Van Laere - YouTube

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: two siblings with a new mutation and dramatic therapeutic effect of high-dose riboflavin

PDF) Brown Vialetto Van Laere syndrome, a fatal disease with a simple solution: a case series

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

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

Clinical features and neurophysiological follow-up in a case of Brown- Vialetto-Van Laere syndrome - Neuromuscular Disorders

The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives | springermedizin.de

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Brown–Vialetto–Van Laere syndrome: A rare case report of MND mimic

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

The audiovestibular profile of Brown-Vialetto-Van Laere syndrome | The Journal of Laryngology & Otology | Cambridge Core

Orphanet Journal of Rare Diseases

Town mobilizes to help woman with rare disease ACN | Barcelona Only 80 people worldwide have rare Brown-Vialetto-Van Laere Syndrome November 9, 2017 06:42 PM

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

Brown–Vialetto–Van Laere syndrome: Egyptian case report – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.

Full article: Brown–Vialetto–Van Laere syndrome: Egyptian case report

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

Riboflavin treatment in genetically proven Brown–Vialetto–Van Laere syndrome Garg M, Kulkarni SD, Hegde AU, Shah KN - J Pediatr Neurosci