Secondary Mitochondrial Dysfunction as a Cause of Neurodegenerative Dysfunction in Lysosomal Storage Diseases and an Overview of Potential Therapies.

Stepien, Karolina M; Cufflin, Neve; Donald, Aimee; Jones, Simon; Church, Heather; Hargreaves, Iain P

Stepien, Karolina M; Cufflin, Neve; Donald, Aimee; Jones, Simon; Church, Heather; Hargreaves, Iain P.

Afiliação

Stepien KM; Adult Inherited Metabolic Disorders, Salford Royal NHS Foundation Trust, Salford M6 8HD, UK.
Cufflin N; School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool L3 3AF, UK.
Donald A; Willink Biochemical Genetics, St Mary's Hospital, Manchester Foundation Trust, Manchester M13 9WL, UK.
Jones S; Willink Biochemical Genetics, St Mary's Hospital, Manchester Foundation Trust, Manchester M13 9WL, UK.
Church H; Willink Biochemical Genetics, St Mary's Hospital, Manchester Foundation Trust, Manchester M13 9WL, UK.
Hargreaves IP; School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool L3 3AF, UK.

Int J Mol Sci ; 23(18)2022 Sep 12.

Article em En | MEDLINE | ID: mdl-36142486

Assuntos

Doença de Gaucher; Doenças por Armazenamento dos Lisossomos; Doenças de Niemann-Pick; Doença de Gaucher/metabolismo; Humanos; Hidrolases/metabolismo; Doenças por Armazenamento dos Lisossomos/metabolismo; Lisossomos/metabolismo; Mitocôndrias; Doenças de Niemann-Pick/metabolismo

Palavras-chave

Gaucher disease; NiemannPick disease; lysosomal storage diseases; mucopolysaccharidosis; neurodegeneration; secondary mitochondrial dysfunction; type C

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças de Niemann-Pick / Doenças por Armazenamento dos Lisossomos / Doença de Gaucher Limite: Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

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