Results 251 to 260 of about 69,645 (303)

Surgical and Medical Co-Management in an 82-Year-Old Patient With Hemophilia a Undergoing Pancreaticoduodenectomy. [PDF]

Health Care Sci
Lu W, Liu C, He J, Cheng R.
europepmc   +1 more source

Large intramuscular hematoma due to acquired Factor VIII inhibitors in post Polycythemia Vera-Myelofibrosis. [PDF]

Clin Hematol Int
Prabhu RS, V S SR, S N R.
europepmc   +1 more source

Mild or moderate hemophilia is not always a mild or moderate bleeding disorder: Back to the clinical phenotype. [PDF]

Hemasphere
Rodeghiero F, Ghiotto L, Pontalto L, Casini A, Castaman G, Abdul-Kadir R, Berntorp E, Bodó I, Degenaar-Dujardin M, Fijnvandraat K, Gresele P, Key NS, Lassila R, Leebeek FWG, Lillicrap D, Makris M, Meijer S, Mezzano D, Noris P, Pabinger I, Ragni MV, Silva D, Srivastava A, Tosetto A, Windyga J, Zieger B.   +25 more
europepmc   +1 more source

Venous Thromboembolism Prophylaxis in Hemophilic Patients Undergoing Total Hip or Knee Arthroplasty: Insights from a Single-Center Experience. [PDF]

Medicina (Kaunas)
Badulescu OV, Sirbu PD, Ciocoiu M, Vladeanu MC, Plesoianu CE, Bojan A, Iliescu-Halitchi D, Tudor R, Huzum B, Sirbu MT, Forna N, Sofron G, Friedl W, Bararu-Bojan I.   +13 more
europepmc   +1 more source

2025 ASH ISTH NBDF WFH monitoring report on the 2021 clinical guidelines on the diagnosis and management of von Willebrand disease. [PDF]

Blood Adv
James PD, Flood VH, Connell NT.
europepmc   +1 more source

An Observational Study of Glycopegylated Extended Half-Life Factor Prophylaxis in Hemophilia A and B in a Tertiary Care Center in India. [PDF]

Cureus
Bhatt P, Patel H.
europepmc   +1 more source

Comparison of Efficiency of Closed Kinetic Chain Exercises Versus Proprioceptive Exercises in Improving Balance and Gait in People With Hemophilia: Protocol for a Randomized Controlled Trial.

JMIR Res Protoc
Poyraz Isleyen T, Tarakci E, Leblebici G, Yeldan I, Zulfikar B.   +4 more
europepmc   +1 more source

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The More Recent History of Hemophilia Treatment.

Seminars in Thrombosis and Hemostasis, 2022
The availability first in the 1970s of plasma-derived and then in the 1990s of recombinant clotting factor concentrates represented a milestone in hemophilia care, enabling not only treatment of episodic bleeding events but also implementation of ...
M. Franchini, P. Mannucci
semanticscholar   +1 more source

Hemophilia

Pediatrics In Review, 1991
Hemophilia is a hereditary bleeding disorder characterized by Factor VIII (F-VIII) or Factor IX (F-IX) deficiency, bleeding into joints and soft tissues, and an X-linked mode of inheritance. Approximately one third of new cases occur as spontaneous mutations, with no family history of hemophilia.
J M, Lusher, I, Warrier
openaire   +2 more sources

Hemophilia

Emergency Medicine Clinics of North America, 1993
Hemophilia and von Willebrand's disease are the most common hereditary bleeding disorders. A variety of treatment modalities of these disorders are discussed. Common organ system bleeding and its treatment and disposition are outlined. Finally, potential complications of both the disease and treatment are reviewed.
J A, Pfaff, M, Geninatti
openaire   +2 more sources