Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Jenny Y. Zhou"'
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-6 (2019)
Abstract Background Hemophagocytic lymphohistiocytosis is a rare hematological syndrome characterized by excessive and uncontrolled activation of the immune system. The often nonspecific nature of early symptoms and the potential for progression to m
Externí odkaz:
https://doaj.org/article/d73343be2baf4436a25595593bd1884b
Autor:
Nicolas Gallastegui MD, Jenny Y. Zhou MD, Annette von Drygalski MD, PharmD, RMSK, Richard F. W. Barnes PhD, Timothy M. Fernandes MD, MPH, Timothy A. Morris MD, FCCP
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
Introduction: Acute respiratory illnesses from COVID19 infection are increasing globally. Reports from earlier in the pandemic suggested that patients hospitalized for COVID19 are at particularly high risk for pulmonary embolism (PE). To estimate the
Externí odkaz:
https://doaj.org/article/fc8d72a551234263934288bdfa2ea5c0
Autor:
Jenny Y. Zhou MD, Richard F. W. Barnes PhD, Gary Foster PhD, Alfonso Iorio MD, PhD, Thomas J. Cramer PhD, Annette von Drygalski MD, PharmD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)
Hemophilic arthropathy from joint bleeding remains a complication with major morbidity in the increasingly aging patients with hemophilia. Prophylactic clotting factor infusions, based on pharmacokinetic dosing to reduce bleeding rates, are being exp
Externí odkaz:
https://doaj.org/article/5c4df386c30a40df91c9703007c6c435
Autor:
Jonathan C Roberts, Annette von Drygalski, Jenny Y Zhou, George M Rodgers, Kristin Ansteatt, Michael D Tarantino
Publikováno v:
Journal of Blood Medicine. 13:611-618
Jonathan C Roberts,1 Annette von Drygalski,2 Jenny Y Zhou,2 George M Rodgers,3 Kristin Ansteatt,1 Michael D Tarantino1 1Bleeding & Clotting Disorders Institute, University of Illinois College of Medicine â Peoria, Peoria, IL, USA; 2Hemophilia an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64bb0281827760dd2c69dc46c1bdb8a9
https://doi.org/10.2147/jbm.s365996
https://doi.org/10.2147/jbm.s365996
Autor:
Jonathan Wong, Annette von Drygalski, Alecio F Lombardi, Zachary Berman, Jenny Y Zhou, Eric Y. Chang
Publikováno v:
Haemophilia
Introduction Joint iron accumulation is the incendiary factor triggering osteochondral destruction, synovial hypertrophy, inflammation, and vascular remodelling in haemophilic arthropathy (HA). Hemosiderin depositions have been described in synovium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2dd2c2f45f3ab799eea458066d0030a
https://doi.org/10.1111/hae.14417
https://doi.org/10.1111/hae.14417
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-6 (2019)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Hemophagocytic lymphohistiocytosis is a rare hematological syndrome characterized by excessive and uncontrolled activation of the immune system. The often nonspecific nature of early symptoms and the potential for progression to multiorgan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85a8e517f5fbb9a268fc5c10dc7379e9
http://link.springer.com/article/10.1186/s13256-019-2295-1
http://link.springer.com/article/10.1186/s13256-019-2295-1
Autor:
Srila Gopal, Morten A. Karsdal, Tine Wyseure, Chanond A Nasamran, Esther J Cooke, Kathleen M. Fisch, Tina Manon-Jensen, Jenny Y Zhou, Annette von Drygalski, Laurent O. Mosnier
Publikováno v:
J Thromb Haemost
Background Vascular remodeling associated with hemophilic arthropathy (HA) may contribute to bleed propagation, but the mechanisms remain poorly understood. Objectives To explore molecular mechanisms of HA and the effects of hemostasis correction on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa34b7c33e059a07f5465a26bbd28d37
https://doi.org/10.1111/jth.14567
https://doi.org/10.1111/jth.14567
Publikováno v:
Case Reports in Hematology, Vol 2019 (2019)
Case Reports in Hematology
Case Reports in Hematology
Acquired hemophilia A (AHA) is a rare autoimmune disorder caused by autoantibodies against Factor VIII (FVIII). It has a high mortality due to bleeding complications. FVIIa-based bypassing agents are the first line of treatment but not always effecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34df501d496cd01000ac0681a2abe205
https://doi.org/10.1155/2019/9026121
https://doi.org/10.1155/2019/9026121
Autor:
Jenny Y Zhou, Nicolas Gallastegui, Timothy A. Morris, Timothy M. Fernandes, Richard F. W. Barnes, Annette von Drygalski
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
Introduction:Acute respiratory illnesses from COVID19 infection are increasing globally. Reports from earlier in the pandemic suggested that patients hospitalized for COVID19 are at particularly high risk for pulmonary embolism (PE). To estimate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18072a269a9dfc7f53884b29f7e9c4b0
https://pubmed.ncbi.nlm.nih.gov/33689493
https://pubmed.ncbi.nlm.nih.gov/33689493
Autor:
Samantha Ruiz, Esther J Cooke, Annette von Drygalski, Jenny Y Zhou, Bilgimol Chumappumkal Joseph, Sonha Nguyen
Publikováno v:
Blood. 138:3175-3175
Introduction Local and systemic molecular responses to hemarthroses in hemophilia are not well understood. Emerging clinical evidence suggests that treatment with FVIII-Fc Fusion protein (FcFVIII), using the Fc-portion of immunoglobulin for half-life
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::461de036bb1d1a9cff08815d42ad723a
https://doi.org/10.1182/blood-2021-149923
https://doi.org/10.1182/blood-2021-149923