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Wyszukujesz frazę ""Ting TW"" wg kryterium: Autor


Wyświetlanie 1-5 z 5
Tytuł:
Cluster analysis and visualisation of electronic health records data to identify undiagnosed patients with rare genetic diseases.
Autorzy:
Moynihan D; Curtin University, Perth, Australia.
Monaco S; Health Catalyst, Utah, USA.
Ting TW; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore.; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Narasimhalu K; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.; Department of Neurology, National Neuroscience Institute (Singapore General Hospital), Singapore, Singapore.
Hsieh J; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.; Department of Internal Medicine, Singapore General Hospital, Singapore, Singapore.
Kam S; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore.; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Lim JY; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore.; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.
Lim WK; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore.; Cancer & Stem Cell Biology Program, Duke-NUS Medical School, Singapore, Singapore.; Laboratory of Genome Variation Analytics, Genome Institute of Singapore, Singapore, Singapore.
Davila S; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore.
Bylstra Y; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore.
Balakrishnan ID; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore.; National Heart Centre Singapore, Singapore, Singapore.
Heng M; SingHealth Office of Insights and Analytics, Singapore, Singapore.
Chia E; SingHealth Office of Insights and Analytics, Singapore, Singapore.
Yeo KK; National Heart Centre Singapore, Singapore, Singapore.
Goh BK; Data Analytics Office, KK Women's and Children's Hospital, Singapore, Singapore.
Gupta R; Curtin University, Perth, Australia.
Tan T; Curtin University, Perth, Australia.
Baynam G; Rare Care Centre, Perth Children's Hospital, Perth, WA, Australia.; Western Australian Register of Developmental Anomalies, Perth, WA, Australia.
Jamuar SS; Genetics Service, Department of Paediatrics, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore. .; SingHealth Duke-NUS Genomic Medicine Centre, Singapore, Singapore. .; SingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore. .
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Źródło:
Scientific reports [Sci Rep] 2024 Mar 01; Vol. 14 (1), pp. 5056. Date of Electronic Publication: 2024 Mar 01.
Typ publikacji:
Journal Article
MeSH Terms:
Fabry Disease*
Hyperlipoproteinemia Type II*/genetics
Undiagnosed Diseases*
Humans ; Rare Diseases/diagnosis ; Rare Diseases/epidemiology ; Rare Diseases/genetics ; Electronic Health Records ; Cluster Analysis
Czasopismo naukowe
Tytuł:
Sex differences in proteomic correlates of coronary microvascular dysfunction among patients with heart failure and preserved ejection fraction.
Autorzy:
Chandramouli C; National Heart Centre Singapore, Singapore.; Duke-National University of Singapore, Singapore.
Ting TW; National Heart Centre Singapore, Singapore.
Tromp J; National Heart Centre Singapore, Singapore.; Department of Cardiology, University Medical Center Groningen, Groningen, The Netherlands.
Agarwal A; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Svedlund S; Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.
Saraste A; Heart Center, Turku University Hospital, University of Turku, Turku, Finland.
Hage C; Department of Medicine, Cardiology Unit and Heart and Vascular Theme, Karolinska Institutet, Stockholm, Sweden.
Tan RS; National Heart Centre Singapore, Singapore.
Beussink-Nelson L; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Lagerström Fermer M; Early Clinical Development, Research and Early Development, Cardiovascular, Renal and Metabolism (CVRM), BioPhamaceuticals R&D AstraZeneca, Gothenburg, Sweden.
Gan LM; Early Clinical Development, Research and Early Development, Cardiovascular, Renal and Metabolism (CVRM), BioPhamaceuticals R&D AstraZeneca, Gothenburg, Sweden.
Lund L; Department of Medicine, Cardiology Unit and Heart and Vascular Theme, Karolinska Institutet, Stockholm, Sweden.
Shah SJ; Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Lam CSP; National Heart Centre Singapore, Singapore.; Duke-National University of Singapore, Singapore.; Department of Cardiology, University Medical Center Groningen, Groningen, The Netherlands.; The George Institute for Global Health, Sydney, Australia.
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Źródło:
European journal of heart failure [Eur J Heart Fail] 2022 Apr; Vol. 24 (4), pp. 681-684. Date of Electronic Publication: 2022 Jan 31.
Typ publikacji:
Journal Article
MeSH Terms:
Heart Failure*/epidemiology
Myocardial Ischemia*
Biomarkers ; Female ; Humans ; Ligands ; Male ; Prospective Studies ; Proteomics ; Receptors, Tumor Necrosis Factor ; Sex Characteristics ; Stroke Volume/physiology
Czasopismo naukowe
Tytuł:
Loeys-Dietz syndrome in a Southeast Asian Hospital: a case series.
Autorzy:
Ting TW; Genetics Service, Department of Paediatric Medicine, KK Women's and Children's Hospital, 100 Bukit Timah Road, Singapore, 229899, Singapore, ting..
Lai AH
Choo JT
Tan TH
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Źródło:
European journal of pediatrics [Eur J Pediatr] 2014 Mar; Vol. 173 (3), pp. 387-91. Date of Electronic Publication: 2013 Oct 22.
Typ publikacji:
Journal Article
MeSH Terms:
Mutation*
Loeys-Dietz Syndrome/*genetics
Protein Serine-Threonine Kinases/*genetics
Receptors, Transforming Growth Factor beta/*genetics
Asian People/genetics ; Child ; Child, Preschool ; Ductus Arteriosus, Patent/diagnosis ; Ductus Arteriosus, Patent/epidemiology ; Female ; Humans ; Loeys-Dietz Syndrome/surgery ; Male ; Receptor, Transforming Growth Factor-beta Type I ; Receptor, Transforming Growth Factor-beta Type II ; Retrospective Studies
Czasopismo naukowe
Tytuł:
Prevalence of cataract surgery and visual outcomes in Indian immigrants in Singapore: the Singapore Indian eye study.
Autorzy:
Gupta P; Singapore Eye Research Institute and Singapore National Eye Centre, Singapore, Singapore.
Zheng Y
Ting TW
Lamoureux EL
Cheng CY
Wong TY
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Źródło:
PloS one [PLoS One] 2013 Oct 07; Vol. 8 (10), pp. e75584. Date of Electronic Publication: 2013 Oct 07 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cataract Extraction/*statistics & numerical data
Emigrants and Immigrants/*statistics & numerical data
Vision Disorders/*diagnosis
Visually Impaired Persons/*statistics & numerical data
Adult ; Aged ; Aged, 80 and over ; Cataract/complications ; Diabetic Retinopathy/complications ; Female ; Humans ; India/ethnology ; Macular Degeneration/complications ; Male ; Middle Aged ; Postoperative Period ; Prevalence ; Singapore/epidemiology ; Treatment Outcome
Czasopismo naukowe
    Wyświetlanie 1-5 z 5

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