About: Charalampos Tzoulis

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Charalampos Tzoulis Goto Sponge NotDistinct Permalink

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

Greek neurodegeneration researcher

Attributes	Values
rdf:type	Item
owl:sameAs	Charalampos Tzoulis
description	forskare (sv) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) araştırmacı (tr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) Greek neurodegeneration researcher (en)
rdfs:label	Charalampos Tzoulis (en) Charalampos Tzoulis (es) Charalampos Tzoulis (nb) Charalampos Tzoulis (nl) Charalampos Tzoulis (sl) Charalampos Tzoulis (ast)
skos:prefLabel	Charalampos Tzoulis (en) Charalampos Tzoulis (es) Charalampos Tzoulis (nb) Charalampos Tzoulis (nl) Charalampos Tzoulis (sl) Charalampos Tzoulis (ast)
name	Charalampos Tzoulis (en) Charalampos Tzoulis (es) Charalampos Tzoulis (nb) Charalampos Tzoulis (nl) Charalampos Tzoulis (sl) Charalampos Tzoulis (ast)
instance of	wds:Q43095051-91948491-25C8-4559-8256-43974D3107CA
instance of	Homo sapiens
Google Knowledge Graph ID	wds:Q43095051-F1D2C746-1573-44B3-9C8C-63AAE8CE5F50
Google Knowledge Graph ID	http://g.co/kg/g/11fyxpw03g
Google Knowledge Graph ID	/g/11fyxpw03g
CRIStin ID	wds:Q43095051-91ec22b3-4bf0-e648-351b-f52cbcade382
CRIStin ID	44838
NORAF ID	wds:Q43095051-96e91240-43cb-2c01-f478-0071b9b3a0a6
occupation	wds:Q43095051-F7A58BA3-92F7-4C67-8130-86A16F8D285D
employer	wds:Q43095051-4497F907-D180-4C43-BB27-629ABB73C844 wds:Q43095051-E6A18CA2-ECD3-4622-AD66-DD97E08C1C24
sex or gender	wds:Q43095051-8A949973-7025-4CDC-AB1C-48D150641054
ISNI	wds:Q43095051-6d825c49-47e6-8c53-0dd7-5131dc7ff572
VIAF ID	wds:Q43095051-0d11e787-434e-84da-b5a1-cffb24562b76
NORAF ID	https://livedata.bibsys.no/authority/11001329
VIAF ID	http://viaf.org/viaf/2765149108447668780005
NORAF ID	11001329
occupation	researcher
employer	University of Bergen Haukeland University Hospital
sex or gender	male
ISNI	0000000481390476
VIAF ID	2765149108447668780005
ORCID iD	wds:Q43095051-6E30B7FE-256B-4609-9DF3-48D6FB40699D
ORCID iD	https://orcid.org/0000-0003-0341-5191
ORCID iD	0000-0003-0341-5191
Mendeley person ID	wds:Q43095051-2443486E-1AEB-4865-8E9E-AC68F1BF4ABF
Mendeley person ID	charalampos-tzoulis2
is about of	Charalampos Tzoulis https://www.wikidata.org/wiki/Special:EntityData/Q43095051 Charalampos Tzoulis https://no.wikipedia.org/wiki/Charalampos_Tzoulis
is author of	MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease Novel SACS mutations identified by whole exome sequencing in a norwegian family with autosomal recessive spastic ataxia of Charlevoix-Saguenay POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection Molecular pathogenesis of polymerase γ-related neurodegeneration Practical guidance for CD management involving treatment of botulinum toxin: a consensus statement The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases. Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes Serial Diffusion Imaging in a Case of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions The angiogenic switch leads to a metabolic shift in human glioblastoma. Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations Mitochondrial DNA homeostasis is essential for nigrostriatal integrity. Progressive striatal necrosis associated with anti-NMDA receptor antibodies A multicenter study on Leigh syndrome: disease course and predictors of survival Neuropsychological performance in patients with POLG1 mutations and the syndrome of mitochondrial spinocerebellar ataxia and epilepsy. Excellent response of intramedullary Erdheim-Chester disease to vemurafenib: a case report Subcellular Parkinson's Disease-Specific Alpha-Synuclein Species Show Altered Behavior in Neurodegeneration. Hereditary spastic paraplegia caused by the novel mutation 1047insC in the SPG7 gene No evidence of ischemia in stroke-like lesions of mitochondrial POLG encephalopathy. ADCK3 mutations with epilepsy, stroke-like episodes and ataxia: a POLG mimic? Management of dystonia in Europe: a survey of the European network for the study of the dystonia syndromes. Differences in RNA processing underlie the tissue specific phenotype of ISCU myopathy. PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema. Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease Simvastatin is associated with decreased risk of Parkinson disease. Acute mitochondrial encephalopathy reflects neuronal energy failure irrespective of which genome the genetic defect affects Beta-propeller protein-associated neurodegeneration: a case report and review of the literature. Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy Increased levels of cell-free mitochondrial DNA in the cerebrospinal fluid of patients with multiple sclerosis. Leukoencephalopathy with brainstem and spinal cord involvement caused by a novel mutation in the DARS2 gene. MELAS ASSOCIATED WITH MUTATIONS IN THE POLG1 GENE Migrainous cerebral infarction in a previously healthy 93-year-old female patient with no risk factors for stroke. Glitazone use associated with reduced risk of Parkinson's disease.

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 196 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software