Krabbe Disease (KD) is an autosomal metabolic disorder that affects both the central and peripheral nervous systems. It is caused by a functional deficiency of the lysosomal enzyme, galactocerebrosidase (GALC), resulting in an accumulation of the toxic metabolite, psychosine. Psychosine accumulation affects many different cellular pathways, leading to severe demyelination. Although there is currently no effective therapy for Krabbe disease, recent gene therapy-based approaches in animal models have indicated a promising outlook for clinical treatment. This review highlights recent findings in the pathogenesis of Krabbe disease, and evaluates AAV-based gene therapy as a promising strategy for treating this devastating pediatric disease
Krabbe disease is a severe, fatal neurodegenerative disorder caused by defects in the lysosomal enzy...
This study characterized the therapeutic benefits of combining hematogenous cell replacement with le...
Background: Krabbe disease (KD) or globoid cell leukodystrophy is an autosomal recessive lysosomal d...
Krabbe disorder was autophagosome collection disorder leading to gradual as well as eloquent neurode...
Krabbe disease is an autosomal recessive leukodystrophy caused by pathogenic variants in the galacto...
Infantile globoid cell leukodystrophy (GLD, Krabbe disease) is a demyelinating disease caused by the...
This is a brief report of the 19th Annual Meeting of the American Society of Gene and Cell Therapy t...
Krabbe disease (KD), also known as globoid cell leukodystrophy (GLD), is a rare (one in 100,000 birt...
Introduction: Krabbe disease (KD) or globoid cell leukodystrophy (GLD) is one of the lysosomal disor...
Missense mutations in the lysosomal hydrolase β-galactocerebrosidase (GALC) account for at least 40%...
Krabbe disease (KD) is a lysosomal storage disease (LSD) caused by mutations in the galc gene. There...
Azzam A Maghazachi Research Department, ImmnoProfiling and Boosting, Oslo, NorwayCorrespondence: Azz...
Krabbe disease (KD) is a rare and genetic lysosomal storage disorder (LSD) caused by different mutat...
Krabbe disease is a lysosomal storage disorder that affects several species including humans, mice a...
Neonatal AAV9-gene therapy of the lysosomal enzyme galactosylceramidase (GALC) significantly amelior...
Krabbe disease is a severe, fatal neurodegenerative disorder caused by defects in the lysosomal enzy...
This study characterized the therapeutic benefits of combining hematogenous cell replacement with le...
Background: Krabbe disease (KD) or globoid cell leukodystrophy is an autosomal recessive lysosomal d...
Krabbe disorder was autophagosome collection disorder leading to gradual as well as eloquent neurode...
Krabbe disease is an autosomal recessive leukodystrophy caused by pathogenic variants in the galacto...
Infantile globoid cell leukodystrophy (GLD, Krabbe disease) is a demyelinating disease caused by the...
This is a brief report of the 19th Annual Meeting of the American Society of Gene and Cell Therapy t...
Krabbe disease (KD), also known as globoid cell leukodystrophy (GLD), is a rare (one in 100,000 birt...
Introduction: Krabbe disease (KD) or globoid cell leukodystrophy (GLD) is one of the lysosomal disor...
Missense mutations in the lysosomal hydrolase β-galactocerebrosidase (GALC) account for at least 40%...
Krabbe disease (KD) is a lysosomal storage disease (LSD) caused by mutations in the galc gene. There...
Azzam A Maghazachi Research Department, ImmnoProfiling and Boosting, Oslo, NorwayCorrespondence: Azz...
Krabbe disease (KD) is a rare and genetic lysosomal storage disorder (LSD) caused by different mutat...
Krabbe disease is a lysosomal storage disorder that affects several species including humans, mice a...
Neonatal AAV9-gene therapy of the lysosomal enzyme galactosylceramidase (GALC) significantly amelior...
Krabbe disease is a severe, fatal neurodegenerative disorder caused by defects in the lysosomal enzy...
This study characterized the therapeutic benefits of combining hematogenous cell replacement with le...
Background: Krabbe disease (KD) or globoid cell leukodystrophy is an autosomal recessive lysosomal d...