Drug Targets from Genetics: Alpha-Synuclein [PDF]
Karin M. Danzer, Pamela J. McLean
openalex +1 more source
Reply: “PGRN Manifesting as Parkinson's Disease: Counseling and Treatment Implications”
Movement Disorders Clinical Practice, EarlyView.
Angelo Antonini +2 more
wiley +1 more source
Allogeneic Bone Marrow‐Derived Mesenchymal Stem Cells for Parkinson's Disease: A Randomized Trial
Abstract Background Neuroinflammation contributes to Parkinson's disease (PD) progression and motor dysfunction. Allogeneic human mesenchymal stem cells (allo‐hMSCs) may reduce neuroinflammation and improve motor symptoms. Objectives To evaluate the efficacy of repeated intravenous doses of 10 × 106/kg allo‐hMSCs in improving motor symptoms in patients
Mya C. Schiess +15 more
wiley +1 more source
A novel alpha-synuclein G14R missense variant is associated with atypical neuropathological features. [PDF]
Brücke C +19 more
europepmc +1 more source
P2‐372: Development of oligomer‐specific alpha‐synuclein antibodies
Therese Wahlberg +6 more
openalex +1 more source
Transcript expression levels of full-length alpha-synuclein and its three alternatively spliced variants in Parkinson's disease brain regions and in a transgenic mouse model of alpha-synuclein overexpression [PDF]
Jesse R. McLean +4 more
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Abstract Background Mitochondrial membrane protein–associated neurodegeneration (MPAN) from the neurodegeneration with brain iron accumulation (NBIA) family is a rare neurodegenerative disease marked by α‐synuclein aggregation, brain iron accumulation, and midbrain dopaminergic neuron degeneration.
Leonie M. Heger +18 more
wiley +1 more source
Analysis of striatal transcriptome in mice overexpressing human wild-type alpha-synuclein supports synaptic dysfunction and suggests mechanisms of neuroprotection for striatal neurons [PDF]
Yofre Cabeza-Arvelaiz +5 more
openalex +1 more source
A Novel α‐Synuclein K58N Missense Variant in a Patient with Parkinson's Disease
Abstract Background Parkinson's disease (PD) is a complex multifactorial disorder with a genetic component in about 15% of cases. Multiplications and point mutations in SNCA gene, encoding α‐synuclein (aSyn), are linked to rare familial forms of PD. Objective Our goal was to assess the clinical presentation and the biological effects of a novel K58N ...
Mohammed Al‐Azzani +24 more
wiley +1 more source

