About: Bradley F Boeve

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
field of work	wds:Q67501037-20E1CC33-A6C6-406E-9FCA-2068165C59EC wds:Q67501037-4853A7F8-0455-45F3-8BA4-77F7A46308D4 wds:Q67501037-D04BFE1B-9450-4264-9270-4CF2B0757EF4
field of work	neurology neurodegeneration sleep disorder
description	researcher (en) wetenschapper (nl) дослідник (uk) Americký profesor neurologie, specialista v oblasti neurodegenerativních nemocí a poruch spánku. (cs)
rdfs:label	B.F. Boeve (es) B.F. Boeve (ast) Bradley F Boeve (en) Bradley F Boeve (nl) Bradley F Boeve (sl) Bradley F. Boeve (cs) Bradley F. Boeve (de)
skos:prefLabel	B.F. Boeve (es) B.F. Boeve (ast) Bradley F Boeve (en) Bradley F Boeve (nl) Bradley F Boeve (sl) Bradley F. Boeve (cs) Bradley F. Boeve (de)
name	B.F. Boeve (es) B.F. Boeve (ast) Bradley F Boeve (en) Bradley F Boeve (nl) Bradley F Boeve (sl) Bradley F. Boeve (cs) Bradley F. Boeve (de)
given name	wds:Q67501037-E05DB8C2-882C-40C8-B56C-7C75D7DC1304
given name	Bradley
instance of	wds:Q67501037-FA712C98-C858-4D4A-A105-8A6FBB55E4E9
NL CR AUT ID	wds:Q67501037-2D9F2391-0CB7-4FDC-861E-99D8CFF44743
instance of	Homo sapiens
NL CR AUT ID	mub20221159241
Semantic Scholar author ID	wds:Q67501037-3475F193-3061-41D2-92CB-8B400F7FEEBA
Semantic Scholar author ID	2744779
skos:altLabel	B.F. Boeve (en) B.F. Boeve (nl) Boeve BF (en) Boeve BF (es) Boeve BF (nl) Boeve BF (ast) Bradley F. Boeve (en)
occupation	wds:Q67501037-16546f7e-5db7-449a-9d19-31f7e7368257 wds:Q67501037-61c53499-8769-4c9a-9c04-1b8dbbd8f5fd
CONOR.SI ID	wds:Q67501037-565A8123-A188-49F1-ADC4-119D6916255A
languages spoken, written or signed	wds:Q67501037-79bc990b-55a7-4c52-85c6-57d11058ec2c
sex or gender	wds:Q67501037-0fd52b6d-9ece-4a4b-9226-85445ddb7418
VIAF ID	wds:Q67501037-DBD57041-92FB-4B61-B534-DFACEB2B3117
IdRef ID	wds:Q67501037-266d70bb-c1f5-4d0c-8f15-6400d27caf40
National Library of Israel J9U ID	wds:Q67501037-8D328447-ADB9-4C8E-9C7F-24AC95B51800
VIAF ID	http://viaf.org/viaf/271823455
IdRef ID	http://www.idref.fr/229909760/id
occupation	university teacher neurologist
CONOR.SI ID	164881251
languages spoken, written or signed	English
sex or gender	male
VIAF ID	271823455
IdRef ID	229909760
National Library of Israel J9U ID	987012330339405171
is owl:sameAs of	Bradley F Boeve Bradley F Boeve
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q67501037
is author of	Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids Mild cognitive impairment associated with limbic and neocortical Lewy body disease: a clinicopathological study Neuropsychological characterization of evolving cognitive decline in idiopathic REM sleep behavior disorder is important, but not easy REM sleep behavior disorder and dementia: cognitive differences when compared with AD. Age, family history, and memory and future risk for cognitive impairment. Cognitive measures predict pathologic Alzheimer disease Rarity of the Alzheimer disease-protective APP A673T variant in the United States Baseline neuropsychiatric symptoms and the risk of incident mild cognitive impairment: a population-based study Inclusion of RBD improves the diagnostic classification of dementia with Lewy bodies Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases Incidence of dementia among participants and nonparticipants in a longitudinal study of cognitive aging Early Alzheimer's disease neuropathology detected by proton MR spectroscopy Risk of dementia in MCI: combined effect of cerebrovascular disease, volumetric MRI, and 1H MRS Mild cognitive impairment due to Alzheimer disease in the community Vegetables, unsaturated fats, moderate alcohol intake, and mild cognitive impairment Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis Discovery of a biomarker and lead small molecules to target r(GGGGCC)-associated defects in c9FTD/ALS. Pathologically confirmed corticobasal degeneration presenting with visuospatial dysfunction Alzheimer disease: postmortem neuropathologic correlates of antemortem 1H MR spectroscopy metabolite measurements 1H magnetic resonance spectroscopy, cognitive function, and apolipoprotein E genotype in normal aging, mild cognitive impairment and Alzheimer's disease Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin Prominent phenotypic variability associated with mutations in Progranulin Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations Non-stationarity in the "resting brain's" modular architecture The Mayo Clinic Study of Aging: design and sampling, participation, baseline measures and sample characteristics Age-related changes in the default mode network are more advanced in Alzheimer disease An operational approach to National Institute on Aging-Alzheimer's Association criteria for preclinical Alzheimer disease Association of low plasma Abeta42/Abeta40 ratios with increased imminent risk for mild cognitive impairment and Alzheimer disease. Comparison of the short test of mental status and the mini-mental state examination in mild cognitive impairment. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS Physical exercise, aging, and mild cognitive impairment: a population-based study

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