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PDF) Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance? | Andre Megarbane - Academia.edu
PDF) Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance? | Andre Megarbane - Academia.edu

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

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

Pontobulbar Palsy and Neurosensory Deafness (Brown-Vialetto-van Laere Syndrome) With Hyperintense Brainstem Nuclei on Magnetic Resonance Imaging: New Finding in Three Siblings | Semantic Scholar
Pontobulbar Palsy and Neurosensory Deafness (Brown-Vialetto-van Laere Syndrome) With Hyperintense Brainstem Nuclei on Magnetic Resonance Imaging: New Finding in Three Siblings | Semantic Scholar

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

brown vialetto van laere syndrome | Van, Brown, Syndrome
brown vialetto van laere syndrome | Van, Brown, Syndrome

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

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

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

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

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

PDF) Brown-Vialetto-van Laere syndrome; the first Turkish case | Omer Aydin - Academia.edu
PDF) Brown-Vialetto-van Laere syndrome; the first Turkish case | Omer Aydin - Academia.edu

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

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

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.

Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance - Gayathri - 2021 - European Journal of Neurology - Wiley Online Library
Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance - Gayathri - 2021 - European Journal of Neurology - Wiley Online Library

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

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

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

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

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

Rare diseases: How patients and parents cope with with little-known illnesses - Daily Record
Rare diseases: How patients and parents cope with with little-known illnesses - Daily Record

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