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Plasma Glucosylsphingosine in GBA1 Mutation Carriers with and without Parkinson's Disease.

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第一作者： Matthew,Surface

第一单位： Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, New York, USA.

作者： Matthew,Surface ^[1] ; Manisha,Balwani ^[2] ; Cheryl,Waters ^[1] ; Alexander,Haimovich ^[1] ; Ziv,Gan-Or ^[3] ; Karen S,Marder ^[1] ; Tammy,Hsieh ^[4] ; Linxia,Song ^[4] ; Shalini,Padmanabhan ^[5] ; Frank,Hsieh ^[4] ; Kalpana M,Merchant ^[6] ; Roy N,Alcalay ^[1]

作者单位： Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, New York, USA. ^[1] Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, USA. ^[2] The Neuro (Montreal Neurological Institute-Hospital), McGill University, Montreal, Quebec, Canada.;Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.;Department of Human Genetics, McGill University, Montreal, Quebec, Canada. ^[3] Nextcea, Inc., Woburn, Massachusetts, USA. ^[4] The Michael J. Fox Foundation for Parkinson's Research, New York, New York, USA. ^[5] Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA. ^[6]

关键词 Gaucher's Parkinson's glucocerebrosidase lipidomics

医学主题词戈谢病(Gaucher Disease);葡糖苷酰鞘氨醇酶(Glucosylceramidase);人类(Humans);突变(Mutation);帕金森病(Parkinson Disease);鞘氨醇半乳糖苷(Psychosine)

DOI 10.1002/mds.28846

PMID 34741486

发布时间 2022-09-01

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