About: Antonio Gambardella

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

neuromedicine researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) investigador (es) araştırmacı (tr) chercheur (fr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (en-ca) researcher (en-gb) researcher (en-us) investigador (ca) investigador (gl) investigador (ast) investigador (pt) neuromedicine researcher (en)
rdfs:label	Antonio Gambardella (en) Antonio Gambardella (es) Antonio Gambardella (it) Antonio Gambardella (nl) Antonio Gambardella (sl) Antonio Gambardella (ast)
skos:prefLabel	Antonio Gambardella (en) Antonio Gambardella (es) Antonio Gambardella (it) Antonio Gambardella (nl) Antonio Gambardella (sl) Antonio Gambardella (ast)
name	Antonio Gambardella (en) Antonio Gambardella (es) Antonio Gambardella (it) Antonio Gambardella (nl) Antonio Gambardella (sl) Antonio Gambardella (ast)
Scopus author ID	wds:Q30500568-26FD7F5A-95A5-44C3-856E-D02F1151EB5E wds:Q30500568-61225F0F-AF39-4635-BEA8-391DEE588D30 wds:Q30500568-64B73A23-C319-4C3C-8717-A325C6720373 wds:Q30500568-9673B3E8-572B-4730-A089-7D6A602138D2 wds:Q30500568-C44441FD-9918-442E-9E35-C5F9E39DC58D
Scopus author ID	7103208295
given name	wds:Q30500568-E67A22F0-5B52-41B5-A0B8-862B8C5906D0
given name	Antonio
instance of	wds:Q30500568-5E13512F-2864-450B-BDB7-B82904F1300D
instance of	Homo sapiens
Loop ID	wds:Q30500568-B74BB5A6-0F4E-4C76-B046-0A65BA196486
Loop ID	127621
occupation	wds:Q30500568-1F6BC5EF-5910-400F-B264-D214E2BFD497
employer	wds:Q30500568-60185F18-7A21-4525-A030-2E20D9A1D962 wds:Q30500568-987E9179-4AB0-4FC7-8E7F-77EB784D97AA
different from	wds:Q30500568-c0d7501e-4f96-c0fb-8562-48b3fa65e160
sex or gender	wds:Q30500568-505B3A26-6E3D-4087-9EF4-E39D0943633B
educated at	wds:Q30500568-27763F21-C8D9-4E31-9C18-1AB2A4EBC1A3
occupation	researcher
employer	Consiglio Nazionale delle Ricerche Magna Græcia University
different from	Antonio Gambardella
sex or gender	male
educated at	Montreal Neurological Institute and Hospital
Springer Nature person ID	wds:Q30500568-A249B23A-17BA-49E5-81E3-FED4B9FCA9E6
ORCID iD	wds:Q30500568-87E3FEA0-D1D0-49C0-B3F2-C7744A12B090
Dimensions author ID	wds:Q30500568-26EF5651-4B67-4471-9764-2C2038F51AEF
ORCID iD	https://orcid.org/0000-0001-7384-3074
Springer Nature person ID	013226624020.93
ORCID iD	0000-0001-7384-3074
Dimensions author ID	013226624020.93
ResearcherID	wds:Q30500568-84124BE4-2BCE-4DB4-98D0-21E50D74D2E2
ResearcherID	F-5295-2012
IRIS UNICZ author ID	wds:Q30500568-3C07B943-B8CA-419F-BB0B-7C35195FABA7
IRIS UNICZ author ID	15047
IRIS UNICAMPANIA author ID	wds:Q30500568-2853D4CF-BB47-4885-991A-C8F567A8E815
IRIS UNICAMPANIA author ID	00967
is owl:sameAs of	Antonio Gambardella
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q30500568
is author of	Idiopathic generalized epilepsies with versive or circling seizures. Usefulness of focal rhythmic discharges on scalp EEG of patients with focal cortical dysplasia and intractable epilepsy. APOE and risk of cognitive impairment in multiple sclerosis Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy Relationship between atrophy of the amygdala and ictal fear in temporal lobe epilepsy. Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. TARDBP gene mutations in south Italian patients with amyotrophic lateral sclerosis A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1. Open label, long-term, pragmatic study on levetiracetam in the treatment of juvenile myoclonic epilepsy Alteration of the in vivo nicotinic receptor density in ADNFLE patients: a PET study. A Novel Mutation in the Notch3 Gene in an Italian Family With Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Silent celiac disease in patients with childhood localization-related epilepsies. Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2. Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus Randomized trial comparing two different high doses of methylprednisolone in MS: a clinical and MRI study. Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations. Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease. Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly

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