Add to ORKGTitle 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 treatmen
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial ne...
Riboflavin transporter deficiency (RTD) is a neurodegenerative disorder that presents from infancy t...
Brown-Vialetto-Van-Laere syndrome (BVVL), is a rare autosomal recessive degenerative disorder, assoc...
We report on three patients (two siblings and one unrelated) presenting in infancy with progressive ...
The Brown-Vialetto-Van Laere syndrome is a rare neurological disorder which may present at all ages ...
Brown-Vialetto-Van Laere syndrome (BVVLS) is a genetic condition caused by a mutation in the C20orf5...
Brown-Vialetto-Van Laere syndrome (BVVLS [MIM 211530]) is a rare neurological disorder characterized...
Riboflavin Transporter Deficiency (RTD) is a rare neurological condition that encompasses the Brown-...
Riboflavin transporter deficiency (RTD) is a rare neurological condition that encompasses the Brown-...
Brown-Vialetto-Van Laere syndrome (BVVLS) or riboflavin transporter deficiency (OMIM 211530) is a ra...
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutati...
Investigators at Great Ormond Street Hospital, London, UK, and multiple centers internationally repo...
Brown-Vialetto-Van Laere syndrome is a rare disorder characterized by motor, sensory, and cranial ne...
Background: Brown-Vialetto-Van Laere (BVVL) syndrome is a rare disorder characterised by progressive...
PubMedID: 26444347Brown-Vialetto-Van Laere syndrome (BVVLS) is a rare and severe neurometabolic dise...
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial ne...
Riboflavin transporter deficiency (RTD) is a neurodegenerative disorder that presents from infancy t...
Brown-Vialetto-Van-Laere syndrome (BVVL), is a rare autosomal recessive degenerative disorder, assoc...
We report on three patients (two siblings and one unrelated) presenting in infancy with progressive ...
The Brown-Vialetto-Van Laere syndrome is a rare neurological disorder which may present at all ages ...
Brown-Vialetto-Van Laere syndrome (BVVLS) is a genetic condition caused by a mutation in the C20orf5...
Brown-Vialetto-Van Laere syndrome (BVVLS [MIM 211530]) is a rare neurological disorder characterized...
Riboflavin Transporter Deficiency (RTD) is a rare neurological condition that encompasses the Brown-...
Riboflavin transporter deficiency (RTD) is a rare neurological condition that encompasses the Brown-...
Brown-Vialetto-Van Laere syndrome (BVVLS) or riboflavin transporter deficiency (OMIM 211530) is a ra...
Riboflavin transporter 3 involvement in infantile Brown-Vialetto-Van Laere disease: two novel mutati...
Investigators at Great Ormond Street Hospital, London, UK, and multiple centers internationally repo...
Brown-Vialetto-Van Laere syndrome is a rare disorder characterized by motor, sensory, and cranial ne...
Background: Brown-Vialetto-Van Laere (BVVL) syndrome is a rare disorder characterised by progressive...
PubMedID: 26444347Brown-Vialetto-Van Laere syndrome (BVVLS) is a rare and severe neurometabolic dise...
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial ne...
Riboflavin transporter deficiency (RTD) is a neurodegenerative disorder that presents from infancy t...
Brown-Vialetto-Van-Laere syndrome (BVVL), is a rare autosomal recessive degenerative disorder, assoc...