About: Andrea Calvo

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

researcher (ORCID 0000-0002-5122-7243)

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) 研究者 (ja) investigador (es) chercheur (fr) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) İtalyan bilim insanı (tr) italienischer Neurologe (de) researcher (ORCID 0000-0002-5122-7243) (en)
rdfs:label	Andrea Calvo (de) Andrea Calvo (en) Andrea Calvo (es) Andrea Calvo (it) Andrea Calvo (nl) Andrea Calvo (ast)
skos:prefLabel	Andrea Calvo (de) Andrea Calvo (en) Andrea Calvo (es) Andrea Calvo (it) Andrea Calvo (nl) Andrea Calvo (ast)
name	Andrea Calvo (de) Andrea Calvo (en) Andrea Calvo (es) Andrea Calvo (it) Andrea Calvo (nl) Andrea Calvo (ast)
Scopus author ID	wds:Q56862908-140A6EBB-8173-4C4B-BBEF-B6BA143CBA4B wds:Q56862908-5539FFAD-0FA6-4E79-8C2A-BB6691B424C1
Scopus author ID	57208095998 7005236400
given name	wds:Q56862908-7D86FBD5-6C54-4996-B194-33703CE55D9C
given name	Andrea
instance of	wds:Q56862908-1FB6A286-372D-4E96-8C54-2A9525B1B2A8
instance of	Homo sapiens
Loop ID	wds:Q56862908-9A1D3837-3B65-4568-A2A1-6AB66E72D5E4
Loop ID	529728
skos:altLabel	Andrea CALVO (en)
occupation	wds:Q56862908-EABEAB5E-7927-4DCC-96FC-97A338E7F64C
employer	wds:Q56862908-D2DC5547-D3A9-42CC-A427-97AB93DD0255
CERL Thesaurus ID	wds:Q56862908-AA1A8BF3-7B22-4F0E-9A9D-849F1FC156F2
VIAF ID	wds:Q56862908-2CA1C813-8DD1-459E-8A78-58494116F1B7
GND ID	wds:Q56862908-4C5260EA-ECF3-4F40-B13D-A84B46AA2694
Library of Congress authority ID	wds:Q56862908-49FEE2E7-1C1F-437F-BDB6-4A69611B254B
country of citizenship	wds:Q56862908-C0DD043C-7B5D-4712-BAF9-F59029881945
educated at	wds:Q56862908-4C003038-4FA5-4274-ABC6-22B8CE4FB27D wds:Q56862908-A60C0C84-E222-47B9-9908-D64297620E66 wds:Q56862908-E74729D2-E245-46DF-90C1-65FB3AAD9992
family name	wds:Q56862908-C98669B9-FDA6-4DDE-9C1D-18D59CC5A7E1
WorldCat Identities ID (superseded)	wds:Q56862908-FE06FEAE-CC7E-4DBE-BC2D-70A9F3559502
CERL Thesaurus ID	http://thesaurus.cerl.org/record/cnp00574901
VIAF ID	http://viaf.org/viaf/47666361
GND ID	https://d-nb.info/gnd/1307112560
Library of Congress authority ID	http://id.loc.gov/authorities/names/n2020018045
occupation	researcher
employer	University of Turin
CERL Thesaurus ID	cnp00574901
VIAF ID	47666361
GND ID	1307112560
Library of Congress authority ID	n2020018045
country of citizenship	Italy
educated at	University of Palermo University of Turin
family name	Calvo
WorldCat Identities ID (superseded)	viaf-47666361
ORCID iD	wds:Q56862908-AB51F686-E8E8-45E0-BE6A-7F9BE0CF6DC6 wds:Q56862908-D7209D0C-E637-4F63-8620-0E5A83B551A4
ORCID iD	https://orcid.org/0000-0001-8249-1226 https://orcid.org/0000-0002-5122-7243
ORCID iD	0000-0001-8249-1226 0000-0002-5122-7243
ResearcherID	wds:Q56862908-D7628F17-178B-4A33-AFF5-3A5731CBA917
ResearcherID	K-4141-2016
is owl:sameAs of	Andrea Calvo
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56862908
is author of	Brain hypermetabolism in amyotrophic lateral sclerosis: a FDG PET study in ALS of spinal and bulbar onset. The metabolic signature of C9ORF72-related ALS: FDG PET comparison with nonmutated patients Genetic counselling in ALS: facts, uncertainties and clinical suggestions Amyotrophic lateral sclerosis/frontotemporal dementia with predominant manifestations of obsessive-compulsive disorder associated to GGGGCC expansion of the c9orf72 gene Neurobehavioral dysfunction in ALS has a negative effect on outcome and use of PEG and NIV. Large proportion of amyotrophic lateral sclerosis cases in Sardinia due to a single founder mutation of the TARDBP gene Amyotrophic lateral sclerosis-frontotemporal lobar dementia in 3 families with p.Ala382Thr TARDBP mutations Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72. Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation Prevalence of SOD1 mutations in the Italian ALS population Idiopathic chronic inflammatory demyelinating polyneuropathy: an epidemiological study in Italy Pain in amyotrophic lateral sclerosis: a population-based controlled study. A longitudinal study on quality of life and depression in ALS patient-caregiver couples A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels Exome sequencing reveals VCP mutations as a cause of familial ALS C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population Non-invasive ventilation in amyotrophic lateral sclerosis: a 10 year population based study Validity of hospital morbidity records for amyotrophic lateral sclerosis. A population-based study

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