Studies aimed at supporting different treatment approaches for pantothenate kinase-associated neurodegeneration (PKAN) have revealed the complexity of coenzyme A (CoA) metabolism and the limits of our current knowledge about disease pathogenesis. Here we offer a foundation for critically evaluating the myriad approaches, argue for the importance of unbiased disease models, and highlight some of the outstanding questions that are central to our understanding and treating PKAN.</p
Abstract Pantothenate kinase‐associated neurodegeneration (PKAN) is an inborn error of CoA metabolis...
Pantothenate kinase-associated neurodegeneration (PKAN) is a hereditary progressive disorder and the...
Pantothenate kinase-associated neurodegeneration (PKAN, OMIM 234200) is an autosomal recessive, prog...
Studies aimed at supporting different treatment approaches for pantothenate kinase-associated neurod...
Therapeutics Development for Pantothenate Kinase-Associated NeurodegenerationLay summaryFor more tha...
Pantothenate kinase-associated neurodegeneration (PKAN) is an inborn error of CoA metabolism causing...
Pantothenate kinase-associated neurodegeneration (PKAN) is a hereditary progressive disorder and the...
Mutations in the pantothenate kinase 2 gene (PANK2) are the cause of pantothenate kinase-associated ...
Pantothenate kinase-associated neurodegeneration (PKAN) is a rare, inborn error of metabolism charac...
CITATION: Di Meo, I., et al. 2017. Acetyl-4′-phosphopantetheine is stable in serum and prevents phen...
Pantothenate kinase-associated neurodegeneration (PKAN is a neurodegenerative disease with unresolve...
Inborn errors of CoA (coenzyme A) biosynthesis lead to neurodegenerative disorders in humans. PKAN (...
Coenzyme A (CoA) is a key molecule involved in several metabolic processes such as tricarboxylic aci...
Abstract Pantothenate kinase‐associated neurodegeneration (PKAN) is an inborn error of CoA metabolis...
Pantothenate kinase-associated neurodegeneration (PKAN) is a hereditary progressive disorder and the...
Pantothenate kinase-associated neurodegeneration (PKAN, OMIM 234200) is an autosomal recessive, prog...
Studies aimed at supporting different treatment approaches for pantothenate kinase-associated neurod...
Therapeutics Development for Pantothenate Kinase-Associated NeurodegenerationLay summaryFor more tha...
Pantothenate kinase-associated neurodegeneration (PKAN) is an inborn error of CoA metabolism causing...
Pantothenate kinase-associated neurodegeneration (PKAN) is a hereditary progressive disorder and the...
Mutations in the pantothenate kinase 2 gene (PANK2) are the cause of pantothenate kinase-associated ...
Pantothenate kinase-associated neurodegeneration (PKAN) is a rare, inborn error of metabolism charac...
CITATION: Di Meo, I., et al. 2017. Acetyl-4′-phosphopantetheine is stable in serum and prevents phen...
Pantothenate kinase-associated neurodegeneration (PKAN is a neurodegenerative disease with unresolve...
Inborn errors of CoA (coenzyme A) biosynthesis lead to neurodegenerative disorders in humans. PKAN (...
Coenzyme A (CoA) is a key molecule involved in several metabolic processes such as tricarboxylic aci...
Abstract Pantothenate kinase‐associated neurodegeneration (PKAN) is an inborn error of CoA metabolis...
Pantothenate kinase-associated neurodegeneration (PKAN) is a hereditary progressive disorder and the...
Pantothenate kinase-associated neurodegeneration (PKAN, OMIM 234200) is an autosomal recessive, prog...