NeuralCipher Open access
Riboflavin deficiency induces a significant change in proteomic profiles in HepG2 cells.
DOI: 10.1038/srep45861PMID: 28367977
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187.286 articles found
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Editorial Expression of Concern: <i>Parkin</i>, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27.
DOI: 10.1073/pnas.1704295114PMID: 28373549
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A randomized trial of a low-dose Rasagiline and Pramipexole combination (P2B001) in early Parkinson's disease.
DOI: 10.1002/mds.26941PMID: 28370340
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Sequencing TMEM230 in Chinese patients with sporadic or familial Parkinson's disease.
DOI: 10.1002/mds.26996PMID: 28370613
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Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population.
DOI: 10.1016/j.neulet.2017.04.003PMID: 28380328
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Intrastriatal Transplantation of Human Neural Stem Cells Restores the Impaired Subventricular Zone in Parkinsonian Mice.
DOI: 10.1002/stem.2616PMID: 28328168
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Statins may facilitate Parkinson's disease: Insight gained from a large, national claims database.
DOI: 10.1002/mds.27006PMID: 28370314
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A sensitive assay reveals structural requirements for α-synuclein fibril growth.
DOI: 10.1074/jbc.m116.767053PMID: 28373279
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In vivo evaluation of central cholinergic circuits in Parkinson's disease using transcranial magnetic stimulation.
DOI: 10.1016/j.clinph.2017.03.037PMID: 28427894
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Transcranial magnetic stimulation in developmental stuttering: Relations with previous neurophysiological research and future perspectives.
DOI: 10.1016/j.clinph.2017.03.039PMID: 28431323
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Frequency of <i>GBA</i> variants in autopsy-proven multiple system atrophy.
DOI: 10.1002/mdc3.12481PMID: 28966932
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Cost-effectiveness of focused ultrasound, radiosurgery, and DBS for essential tremor.
DOI: 10.1002/mds.26997PMID: 28370272
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