Zobrazeno 1 - 10
of 52
pro vyhledávání: '"hemophilia A and B"'
Publikováno v:
مجله دانشگاه علوم پزشکی بیرجند, Vol 30, Iss 3, Pp 204-215 (2023)
Hemophilia is an inherited bleeding disorder caused by malfunctioning or lacking blood coagulation factor VIII (hemophilia A) or IX (hemophilia B). Currently, the main treatments for these X-linked diseases are replacement therapy using periodic and
Externí odkaz:
https://doaj.org/article/36ff2be09b344c3fbb735199bb022f5f
Autor:
Emre Basar, Henry Mead, Bennett Shum, Ingrid Rauter, Cihan Ay, Adriane Skaletz-Rorowski, Norbert H. Brockmeyer
Publikováno v:
Pharmaceutics, Vol 16, Iss 9, p 1207 (2024)
Biological barriers remain a major obstacle for the development of innovative therapeutics. Depending on a disease’s pathophysiology, the involved tissues, cell populations, and cellular components, drugs often have to overcome several biological b
Externí odkaz:
https://doaj.org/article/b68d5b539a7b435b916a13d0a113e935
Publikováno v:
International Journal of Women's Health, Vol Volume 14, Pp 1307-1313 (2022)
Maissaa Janbain,1 Peter Kouides2 1Deming Department of Internal Medicine, Section of Hematology and Medical Oncology, Tulane School of Medicine, New Orleans, LA, USA; 2Department of Medicine, University of Rochester School of Medicine and Dentistry,
Externí odkaz:
https://doaj.org/article/2f0889d5c3b4458c86bd7cb86d424de0
Publikováno v:
Althea Medical Journal, Vol 7, Iss 2, Pp 95-98 (2020)
Background: The clinical manifestations of hemophilia A (HA) and hemophilia B (HB)are quite similar; however, the bleeding characteristics of these two hemophilia types have been reported to be different. This study aimed to explore the bleeding patt
Externí odkaz:
https://doaj.org/article/2dbe3a347e6c4264b0800ede1c86373e
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Althea Medical Journal, Vol 7, Iss 2, Pp 95-98 (2020)
Background : The clinical manifestations of hemophilia A (HA) and hemophilia B (HB)are quite similar; however, the bleeding characteristics of these two hemophilia types have been reported to be different. This study aimed to explore the bleeding pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c26b91d8de5f4797e1e97557437a472
https://doi.org/10.15850/amj.v7n2.1941
https://doi.org/10.15850/amj.v7n2.1941
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Abbonizio, Francesca, Hassan, Hamisa J, Riccioni, Roberta, Santagostino, Elena, Arcieri, Romano, Giampaolo, Adele, on behalf of the Italian Association of Haemophilia Centres, Sergio, Siragusa
BACKGROUND: In Italy, the National Register of Congenital Coagulopathies (NRCC) collects epidemiological and therapeutic data from patients affected by haemophilia A (HA), haemophilia B (HB), von Willebrand’s disease (vWD) and other rare coagulatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::aae271d842c727517345451b137c6f5a
http://hdl.handle.net/10447/510173
http://hdl.handle.net/10447/510173
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
While observed for centuries, the diseases that we call hemophilia have been clarified and elucidated in the past 50 to 60 years. We now know the genetics and transmission of the various types of hemophilia and are greatly facilitated by their labora
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13dca5046428a71bec6ccf72340af844
https://doi.org/10.1016/b978-0-323-46202-0.00003-0
https://doi.org/10.1016/b978-0-323-46202-0.00003-0