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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: A rare case report of MND mimic Kranthi P, Garuda BR, Gopi S, Kumar T S Neurol India

Brown-Vialetto-Van-Laere Syndrome - YouTube
Brown-Vialetto-Van-Laere Syndrome - YouTube

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

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

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

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

Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect
Genetic, Radiologic, and Clinical Variability in Brown-Vialetto-van Laere Syndrome - ScienceDirect

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

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

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
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

Brown-Vialetto-Van Laere syndrome and Fazio-Londe syndrome: A novel mutation and in silico analyses - Journal of Clinical Neuroscience
Brown-Vialetto-Van Laere syndrome and Fazio-Londe syndrome: A novel mutation and in silico analyses - Journal of Clinical Neuroscience

Bebê luta contra doença neurodegenerativa raríssima: "Minha filha está em teste com canabidiol para diminuir as dores", diz mãe - Revista Crescer | Saúde
Bebê luta contra doença neurodegenerativa raríssima: "Minha filha está em teste com canabidiol para diminuir as dores", diz mãe - Revista Crescer | Saúde

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

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.
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.

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

Brown-Vialetto-Van Laere syndrome | Pakistan Pediatric Journal
Brown-Vialetto-Van Laere syndrome | Pakistan Pediatric Journal

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

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

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

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
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

Genetic study identifies treatable pathway in childhood motor neuron disease | UCL News - UCL – University College London
Genetic study identifies treatable pathway in childhood motor neuron disease | UCL News - UCL – University College London

PDF) A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin
PDF) A Chinese pedigree with Brown-Vialetto-Van Laere syndrome due to two novel mutations of SLC52A2 gene: Clinical course and response to riboflavin

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

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