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au.\*:("FINCH, Nicole")

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Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRADEMAKERS, Rosa; BAKER, Matt; ADAMSON, Jennifer et al.Nature genetics. 2012, Vol 44, Num 2, pp 200-205, issn 1061-4036, 6 p.Article

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementiaRADEMAKERS, Rosa; ERIKSEN, Jason L; BOEVE, Bradley F et al.Human molecular genetics (Print). 2008, Vol 17, Num 23, pp 3631-3642, issn 0964-6906, 12 p.Article

Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human PlasmaCARRASQUILLO, Minerva M; NICHOLSON, Alexandra M; SINGLETON, Andrew et al.American journal of human genetics. 2010, Vol 87, Num 6, pp 890-897, issn 0002-9297, 8 p.Article

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family membersFINCH, Nicole; BAKER, Matt; DICKSON, Dennis W et al.Brain. 2009, Vol 132, pp 583-591, issn 0006-8950, 9 p., 3Article

Hippocampal Sclerosis in the Elderly: Genetic and Pathologic Findings, Some Mimicking Alzheimer Disease ClinicallyPAO, Winnie C; DICKSON, Dennis W; CROOK, Julia E et al.Alzheimer disease and associated disorders. 2011, Vol 25, Num 4, pp 364-368, issn 0893-0341, 5 p.Article

Progranulin protein levels are differently regulated in plasma and CSFNICHOLSON, Alexandra M; FINCH, Nicole A; RADEMAKERS, Rosa et al.Neurology. 2014, Vol 82, Num 21, pp 1871-1878, issn 0028-3878, 8 p.Article

CSF1R mutations link POLD and HDLS as a single disease entityNICHOLSON, Alexandra M; BAKER, Matt C; KNOPMAN, David S et al.Neurology. 2013, Vol 80, Num 11, pp 1033-1040, issn 0028-3878, 8 p.Article

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