About: Juan P Kaski

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

About: Juan P Kaski Goto Sponge NotDistinct Permalink

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) researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Juan P Kaski (en) Juan P Kaski (es) Juan P Kaski (nl) Juan P Kaski (ast)
skos:prefLabel	Juan P Kaski (en) Juan P Kaski (es) Juan P Kaski (nl) Juan P Kaski (ast)
name	Juan P Kaski (en) Juan P Kaski (es) Juan P Kaski (nl) Juan P Kaski (ast)
Scopus author ID	wds:Q57078572-E5625F31-EFAD-4952-9293-64DEF3281479
Scopus author ID	16204898600
given name	wds:Q57078572-B393F9FC-7E91-49AF-8C5E-9C0D427F85E3
given name	Juan
instance of	wds:Q57078572-822B5935-4EDA-44F4-B124-7AED7D4A39CA
instance of	Homo sapiens
skos:altLabel	Juan Kaski (en)
occupation	wds:Q57078572-C218FCEE-A402-4F06-968A-1F6634C8D82D
employer	wds:Q57078572-2AF3023A-5184-4D1A-8C32-BDF3050FC238 wds:Q57078572-31761A96-17E9-43BC-8474-4A96C8FE8D1F
sex or gender	wds:Q57078572-64E07E5F-2F74-4E0C-B3C5-F968D0D0A666
educated at	wds:Q57078572-0922890D-F8A7-42B2-B1EE-687E7C76AA23 wds:Q57078572-0C1A2C64-84A2-4F5C-8B51-A4D80A4778C2 wds:Q57078572-48DB913F-F450-474D-88B1-D4B7501CBCAC wds:Q57078572-D61A13FE-5F6F-4DE6-B9C7-408806FD55BE
family name	wds:Q57078572-20AEE751-D664-4B36-AF01-B03285E1196B
occupation	researcher
employer	Great Ormond Street Hospital University College London
sex or gender	male
educated at	University College London Royal College of Paediatrics and Child Health University College London Medical School
family name	Kaski
ORCID iD	wds:Q57078572-EEDC8E2A-5296-4237-93B0-3B7C72B40033
ORCID iD	https://orcid.org/0000-0002-0014-9927
ORCID iD	0000-0002-0014-9927
Gateway to Research person ID	wds:Q57078572-4281AB10-75E9-47DE-AC9B-6B0C62FEF1C6
Gateway to Research person ID	4BDF41E9-7C4A-46E8-AA29-5200977ACB7D
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57078572
is author of	Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes De novo mutations in histone-modifying genes in congenital heart disease. Mutations in the cardiac Troponin C gene are a cause of idiopathic dilated cardiomyopathy in childhood. Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy Prevalence of sequence variants in the RAS-mitogen activated protein kinase signaling pathway in pre-adolescent children with hypertrophic cardiomyopathy. Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle. Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene. Thioredoxin Reductase 2 (TXNRD2) mutation associated with familial glucocorticoid deficiency (FGD). Cardiac disease in adolescents with delayed diagnosis of vertically acquired HIV infection The classification concept of the ESC Working Group on myocardial and pericardial diseases for dilated cardiomyopathy Outcomes after implantable cardioverter-defibrillator treatment in children with hypertrophic cardiomyopathy. Long-term Safety and Efficacy of Mexiletine for Patients With Skeletal Muscle Channelopathies. Pacemaker therapy in hypertrophic obstructive cardiomyopathy: still awaiting the evidence Epidemiology and Clinical Aspects of Genetic Cardiomyopathies Outcomes following general anaesthesia in children with hypertrophic cardiomyopathy Pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus (PHID) syndrome is associated with severe chronic inflammation and cardiomyopathy, and represents a new monogenic autoinflammatory syndrome. Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype Hypertrophic cardiomyopathy in children Normalization of echocardiographically derived paediatric cardiac dimensions to body surface area: time for a standardized approach Feasibility and outcomes of ajmaline provocation testing for Brugada syndrome in children in a specialist paediatric inherited cardiovascular diseases centre Nomenclature and systems of classification for cardiomyopathy in children B-type natriuretic peptide predicts disease severity in children with hypertrophic cardiomyopathy Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study Cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results. Becker muscular dystrophy associated with sarcomeric hypertrophic cardiomyopathy in a paediatric patient: a case report The Cardiomyopathy Registry of the EURObservational Research Programme of the European Society of Cardiology: baseline data and contemporary management of adult patients with cardiomyopathies Can atrioventricular septal defects exist with intact septal structures? Sudden Arrhythmic Death Syndrome: Diagnostic Yield of Comprehensive Clinical Evaluation of Pediatric First-Degree Relatives High prevalence of early repolarization in the paediatric relatives of sudden arrhythmic death syndrome victims and in normal controls Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry Echocardiographic reference ranges in older children and adolescents in sub-Saharan Africa Anxiety in children attending a specialist inherited cardiac arrhythmia clinic: a questionnaire study Obliteration of left superior caval vein draining to the left atrium during spontaneous closure of ventricular septal defect Clinical presentation and survival of childhood hypertrophic cardiomyopathy: a retrospective study in United Kingdom High prevalence of echocardiographic abnormalities in older HIV-infected children taking antiretroviral therapy Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry Data on cardiac defects, morbidity and mortality in patients affected by RASopathies. CARNET study results. Semi-supine exercise stress echocardiography in children and adolescents: feasibility and safety Rare diseases hiding in the cardiomyopathy clinic - The importance of seeing and observing Cardiomyopathy in children: importance of aetiology in prognosis SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups Atrial fibrillation, anticoagulation management and risk of stroke in the Cardiomyopathy/Myocarditis registry of the EURObservational Research Programme of the European Society of Cardiology Risk stratification in childhood hypertrophic cardiomyopathy How to use...the paediatric ECG. Racial Variation in Echocardiographic Reference Ranges for Left Chamber Dimensions in Children and Adolescents: A Systematic Review. Echocardiographic diagnosis of anomalous origin of the left coronary artery from the right coronary sinus. Current use of cardiac magnetic resonance in tertiary referral centres for the diagnosis of cardiomyopathy: the ESC EORP Cardiomyopathy/Myocarditis Registry

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, 188 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software