BVVL

(redirected from Brown-Vialetto-Van Laere)
AcronymDefinition
BVVLBrown-Vialetto-Van Laere (neurological disorder)
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References in periodicals archive ?
Brown-Vialetto-Van Laere (BVVL) syndrome and related disorders have prominent bulbar weakness.
Brown-Vialetto-Van Laere (BVVL) Syndrome and Other Bulbar SMA Syndromes.
Crow et al., "Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54," American Journal of Human Genetics, vol.
Ijlst et al., "Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment," Journal of Inherited Metabolic Disease, vol.
Shaw, "Remarkable motor recovery after riboflavin therapy in adult-onset Brown-Vialetto-Van Laere syndrome," Practical Neurology, vol.
Shaw, "Brown-Vialetto-Van Laere syndrome: case report and literature review," Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders, vol.
Chian et al., "Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS," Neurobiology of Disease, vol.
Brown-Vialetto-Van Laere syndrome 2 (BWLS2) is an excellent example of this potential, said panel member David Goldstein, Ph.D., of Columbia University.
Laura, 43, is the full time carer for Ava who has extremely rare Brown-Vialetto-Van Laere syndrome.
On April 30, 2007, she and her husband John lost their two-year old daughter Elenna "Thisbe" to Brown-Vialetto-Van Laere (BVLL) syndrome.