About: Catherine Chiron

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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
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідниця (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtuese (sq)
rdfs:label	Catherine Chiron (en) Catherine Chiron (es) Catherine Chiron (nl) Catherine Chiron (ast)
skos:prefLabel	Catherine Chiron (en) Catherine Chiron (es) Catherine Chiron (nl) Catherine Chiron (ast)
name	Catherine Chiron (en) Catherine Chiron (es) Catherine Chiron (nl) Catherine Chiron (ast)
given name	wds:Q56923847-77B6703E-98FC-4D49-A5DF-4BBB1F399DA4
given name	Catherine
instance of	wds:Q56923847-BFE4BD12-6C8F-4D7E-9593-6EBE1FE9E742
instance of	Homo sapiens
occupation	wds:Q56923847-5C31FAFA-AA55-4BD2-AF15-A3F0CD5C572B
sex or gender	wds:Q56923847-3D86AEF1-9A09-467E-A4EE-BE2B9FE94177
ISNI	wds:Q56923847-3F73B509-2D59-4036-B4D2-8BFC8D232B63
VIAF ID	wds:Q56923847-36575A3D-A42F-4F4F-BE64-7262E39852A9
IdRef ID	wds:Q56923847-C75561B6-8821-4FA6-8A13-43AE73EAF55D
family name	wds:Q56923847-D4BCD229-4F23-4C7F-8D07-264376F19733
WorldCat Identities ID (superseded)	wds:Q56923847-76A68F49-3FDA-4934-BE20-0B834D22D28F
VIAF ID	http://viaf.org/viaf/22152851
IdRef ID	http://www.idref.fr/028259424/id
occupation	researcher
sex or gender	female organism
ISNI	0000000000789487
VIAF ID	22152851
IdRef ID	028259424
family name	Chiron
WorldCat Identities ID (superseded)	viaf-22152851
ORCID iD	wds:Q56923847-25478954-3C02-407A-B964-512DDB165D14
ORCID iD	https://orcid.org/0000-0002-9096-1694
ORCID iD	0000-0002-9096-1694
ResearcherID	wds:Q56923847-C8A7C2CB-EDE0-4B9D-BC82-49060EA11889
ResearcherID	E-8506-2016
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56923847
is author of	Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-up Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy. Current therapeutic procedures in Dravet syndrome. Study of regional cerebral blood flow in West syndrome. Stiripentol: efficacy and tolerability in children with epilepsy A revisited strategy for antiepileptic drug development in children: designing an initial exploratory step. Stiripentol. In vitro and in vivo inhibitory effect of stiripentol on clobazam metabolism. Vigabatrin and epilepsy: lessons learned Magnetic resonance imaging abnormalities associated with vigabatrin in patients with epilepsy Randomized trial comparing vigabatrin and hydrocortisone in infantile spasms due to tuberous sclerosis The three stages of epilepsy in patients with CDKL5 mutations Myoclonic epilepsy with non-progressive encephalopathy Autism and visual agnosia in a child with right occipital lobectomy STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients. Effect of stiripentol on carbamazepine plasma concentration and metabolism in epileptic children Severe relapse of epilepsy after vigabatrin withdrawal: for how long should we treat symptomatic infantile spasms? Cryptogenic late-onset epileptic spasms: an overlooked syndrome of early childhood? Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene. A conserved switch in sensory processing prepares developing neocortex for vision. Is refractory epilepsy preventable? Guidelines for imaging infants and children with recent-onset epilepsy Functional integration changes in regional brain glucose metabolism from childhood to adulthood. Presurgical language mapping in children with epilepsy: clinical usefulness of functional magnetic resonance imaging for the planning of cortical stimulation Callosotomy for epilepsy after West syndrome Topiramate: efficacy and tolerability in children according to epilepsy syndromes. Late plasticity for language in a child’s non‐dominant hemisphere Misleading effects of clonazepam in symptomatic electrical status epilepticus during sleep syndrome. Devastating epileptic encephalopathy in school-aged children (DESC): a pseudo encephalitis. Unusual consequences of status epilepticus in Dravet syndrome. The ketogenic diet improves recently worsened focal epilepsy Persistent epileptiform activity induced by low Mg2+ in intact immature brain structures. Taurine deficiency is a cause of vigabatrin-induced retinal phototoxicity Modulation of encoding and retrieval by recollection and familiarity: mapping the medial temporal lobe networks. An unexpected EEG course in Dravet syndrome. Auditory stimuli mimicking ambient sounds drive temporal "delta-brushes" in premature infants. Epilepsy in Menkes disease: analysis of clinical stages. Bumetanide for the treatment of seizures in newborn babies with hypoxic ischaemic encephalopathy (NEMO): an open-label, dose finding, and feasibility phase 1/2 trial Reassessment of stiripentol pharmacokinetics in healthy adult volunteers. The c.429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia The pharmacologic treatment of Dravet syndrome Long term response to steroid therapy in Rasmussen encephalitis Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsy Subependymal giant-cell astrocytomas in pediatric tuberous sclerosis disease: when should we operate? Memory functions following surgery for temporal lobe epilepsy in children. Topiramate pharmacokinetics in infants and young children: contribution of population analysis. Pharmacology aspects during transition and at transfer in patients with epilepsy

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