Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Caroline Vuong"'
Autor:
Caroline Vuong, Kumar Utkarsh, Rebecca Stojancic, Arvind Subramaniam, Olivia Fernandez, Tanvi Banerjee, Daniel M. Abrams, Karin Fijnvandraat, Nirmish Shah
Publikováno v:
Frontiers in Digital Health, Vol 5 (2023)
BackgroundIn sickle cell disease (SCD), unpredictable episodes of acute severe pain, known as vaso-occlusive crises (VOC), disrupt school, work activities and family life and ultimately lead to multiple hospitalizations. The ability to predict VOCs w
Externí odkaz:
https://doaj.org/article/644037667f1a47df99547a0a319f4b71
Autor:
Caroline Vuong, Kumar Utkarsh, Rebecca Stojancic, Arvind Mallikarjunan, Olivia Fernandez, Karin Fijnvandraat, Nirmish Shah
Publikováno v:
HemaSphere, Vol 7, p e6358685 (2023)
Externí odkaz:
https://doaj.org/article/36d5327475074111816e68ef096e2610
Autor:
Rebecca Sofia Stojancic, Arvind Subramaniam, Caroline Vuong, Kumar Utkarsh, Nuran Golbasi, Olivia Fernandez, Nirmish Shah
Publikováno v:
JMIR Formative Research, Vol 7, p e45355 (2023)
BackgroundSickle cell disease (SCD) is a genetic red blood cell disorder associated with severe complications including chronic anemia, stroke, and vaso-occlusive crises (VOCs). VOCs are unpredictable, difficult to treat, and the leading cause of hos
Externí odkaz:
https://doaj.org/article/641b1ab79e764311a7a9931e7db115cf
Autor:
Caroline Vuong, Ibtissame Moussa, Maud van Muilekom, Harriët Heijboer, Eva Rettenbacher, Lotte Haverman, Jos Twisk, Karin Fijnvandraat, Corien L. Eckhardt
Background: Sickle cell disease (SCD) is characterized by vaso-occlusive crises (VOCs), that impair the health-related quality of life (HRQoL). The aim of this study is to evaluate the impact of hospitalization for VOCs on HRQoL in children with SCD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3dd2c605685cb0e09876067ea8b24b2
https://doi.org/10.22541/au.168415034.45346461/v1
https://doi.org/10.22541/au.168415034.45346461/v1
Autor:
Sarah van Veelen, Caroline Vuong, Jorn J. Gerritsma, Corien L. Eckhardt, Sophie E. M. Verbeek, Marjolein Peters, Karin Fijnvandraat
Background: Pain is the clinical hallmark of sickle cell disease (SCD) leading to hospitalization, psychological sequelae and a decreased health-related quality of life. The aim of this systematic literature review is to evaluate the efficacy of non-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ff1e87bdb24ef13eefab637e655cc29
https://doi.org/10.22541/au.167282157.72069736/v1
https://doi.org/10.22541/au.167282157.72069736/v1
Autor:
Rebecca Sofia Stojancic, Arvind Subramaniam, Caroline Vuong, Kumar Utkarsh, Nuran Golbasi, Olivia Fernandez, Nirmish Shah
BACKGROUND Sickle cell disease (SCD) is a genetic red blood cell disorder associated with severe complications including chronic anemia, stroke, and vaso-occlusive crises (VOCs). VOCs are unpredictable, difficult to treat, and the leading cause of ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1129ec75a013db10bb62d79cb8bcd28a
https://doi.org/10.2196/preprints.45355
https://doi.org/10.2196/preprints.45355
Publikováno v:
Blood. 140:2578-2579
Autor:
Michiel Coppens, Qun Hu, Caroline Vuong, Karin Fijnvandraat, Xiao-Qin Feng, Julie J Jansen, Soon K Kim, Samantha C. Gouw, Johanna G. van der Bom, Anne-Fleur Zwagemaker
Publikováno v:
Zwagemaker, A-F, Gouw, S C, Jansen, J S, Vuong, C, Coppens, M, Hu, Q, Feng, X, Kim, S K, van der Bom, J G & Fijnvandraat, K 2021, ' Incidence and mortality rates of intracranial hemorrhage in hemophilia : a systematic review and meta-analysis ', Blood, vol. 138, no. 26, pp. 2853-2873 . https://doi.org/10.1182/blood.2021011849
Blood, 138(26), 2853-2873. American Society of Hematology
Blood, 138(26), 2853-2873. AMER SOC HEMATOLOGY
Blood, 138(26), 2853-2873. American Society of Hematology
Blood, 138(26), 2853-2873. AMER SOC HEMATOLOGY
Intracranial hemorrhage (ICH) is a severe complication that is relatively common among patients with hemophilia. This systematic review aimed to obtain more precise estimates of ICH incidence and mortality in hemophilia, which may be important for pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244d3efb386488565d5b463c17607f02
https://research.vumc.nl/en/publications/580dbce1-97e0-4a4d-8442-893a4bcfff2a
https://research.vumc.nl/en/publications/580dbce1-97e0-4a4d-8442-893a4bcfff2a
Autor:
Caroline Vuong, Ibtissame Moussa, Lotte Haverman, Eva Rettenbacher, Harriet Heijboer, Jos W.R. Twisk, Karin Fijnvandraat, Corien L. Eckhardt
Publikováno v:
Blood. 140:13145-13145
Autor:
Christoph Male, Michiel Coppens, Maria Elisa Mancuso, Samantha C. Gouw, Cedric Hermans, Daniel P. Hart, Britta A P Laros-van Gorkom, Johanna G. van der Bom, Johannes Oldenburg, Amal Abdi, Caroline Vuong, Giancarlo Castaman, Maria Gabriella Mazzucconi, Corien L. Eckhardt, Alice S. van Velzen, Simon McRae, Frank W.G. Leebeek, Karin Fijnvandraat
Publikováno v:
Journal of Thrombosis and Haemostasis, 19, 9, pp. 2171-2181
Journal of thrombosis and haemostasis, 19(9), 2171-2181. Wiley-Blackwell
Journal of Thrombosis and Haemostasis
Journal of Thrombosis and Haemostasis, 19(9), 2171-2181. WILEY
Journal of thrombosis and haemostasis, Vol. 19, no. 9, p. 2171-2181 (2021)
Journal of Thrombosis and Haemostasis, 19(9), 2171-2181. Wiley-Blackwell Publishing Ltd
Journal of Thrombosis and Haemostasis, 19, 2171-2181
Journal of thrombosis and haemostasis, 19(9), 2171-2181. Wiley-Blackwell
Journal of Thrombosis and Haemostasis
Journal of Thrombosis and Haemostasis, 19(9), 2171-2181. WILEY
Journal of thrombosis and haemostasis, Vol. 19, no. 9, p. 2171-2181 (2021)
Journal of Thrombosis and Haemostasis, 19(9), 2171-2181. Wiley-Blackwell Publishing Ltd
Journal of Thrombosis and Haemostasis, 19, 2171-2181
Background: Non-severe hemophilia A patients have a life-long inhibitor risk. Yet, no studies have analyzed risk factors for inhibitor development after 50 factor VIII (FVIII) exposure days (EDs). Objectives: This case-control study investigated trea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dd4e1e9eab275305819e25645eb7caf
https://doi.org/10.1111/jth.15419
https://doi.org/10.1111/jth.15419