Results 171 to 180 of about 83,381 (315)

Dose Requirement for Substitution Therapy in Hemophilia A. [PDF]

, 1977
Jean‐Pierre Allain
openalex   +1 more source

Promise, Pitfalls, and Precision: Standardizing Clinical Framework for Hereditary Hemorrhagic Telangiectasia and a Call for Cost‐Conscious Innovation

American Journal of Hematology, Volume 100, Issue 10, Page 1719-1721, October 2025.
Magdalena Lewandowska
wiley   +1 more source

Early Hemostatic Treatment Could Improve 30‐Day Survival After Spontaneous Rupture of Hepatocellular Carcinoma

Liver International, Volume 45, Issue 10, October 2025.
ABSTRACT Introduction Spontaneous rupture of hepatocellular carcinoma (SRHCC) presents a critical clinical challenge, with early haemostasis often difficult to achieve and limited data available on subsequent treatment strategies. This study aims to evaluate whether the initial hemostatic approach influences early prognosis and facilitates further ...
Apolline Commin, Chloé Metivier, Manon Allaire, Jean Lubrano, Amandine Claudinot, Audrey Coilly, Marc‐Antoine Allard, Charles Roux, Olivier Scatton, Jean Charles Nault, Olivier Sutter, Nathalie Ganne‐Carrié, Thuy Vi Ngo, Valérie Le Goff, Zeineb Ben Ali, Husni Tedlaouti, Josephine Papin, Marion Habireche, Louise Lebedel, Claire Pérignon, Thông Dao, Rémy Morello, Isabelle Ollivier‐Hourmand   +22 more
wiley   +1 more source

Carrier Detection in Hemophilia B. [PDF]

, 1977
E Briët, Rogier M. Bertina, Nico H. van Tilburg, J.J. Veltkamp   +3 more
openalex   +1 more source

Radionuclides in the postoperative management of orthotopic human organ transplantation. [PDF]

, 1969
Brown, DW, Starzl, TE
core   +1 more source

Postoperative bleeding complicated by hemophilia A following anal fistula surgery: A case report. [PDF]

Medicine (Baltimore)
Chen X, Tian R, Chen Z, Quan L, Bei S.
europepmc   +1 more source

Deficiency of the autologous mixed lymphocyte reaction in patients with classic hemophilia treated with commercial factor VIII concentrate. Correlation with T cell subset distribution, antibodies to lymphadenopathy-associated or human T lymphotropic virus, and analysis of the cellular basis of the deficiency. [PDF]

, 1985
Josef S Smolen, Peter Bettelheim, Ursula Köller, Sarah J McDougal, W. Graninger, Thomas A. Luger, Walter Knapp, Klaus Lechner   +7 more
openalex   +1 more source

Characterization and management of patients with hereditary factor X deficiency: A case series

Transfusion, Volume 65, Issue 10, Page 1786-1792, October 2025.
Abstract Background Hereditary factor X deficiency (HFXD) is an ultra‐rare, autosomal recessive bleeding disorder that results in reduced factor X coagulant activity (FX:C). HFXD is traditionally classified by severity as severe (FX:C <1%), moderate (FX:C = 1%–5%), or mild (FX:C = 6%–10%).
Meera Chitlur, Lauren E. Amos, Mark T. Reding, Cynthia Sabo, Suchitra S. Acharya   +4 more
wiley   +1 more source

A qualitative study on the impact of hemophilia on sexual functioning and well-being in Dutch men. [PDF]

J Patient Rep Outcomes
van Gastel TCM, Teela L, Lehmann V, Brands MR, Marchal JP, Gravendeel K, Peters M, Fijnvandraat K, Haverman L.   +8 more
europepmc   +1 more source

Medical haematology trial eligibility and the Duffy null‐associated neutrophil count: A cross‐sectional study

HemaSphere, Volume 9, Issue 10, October 2025.
Olga Tsiamita, Laura Aiken, Mohsin Badat, Gill Lowe, Funmi Oyesanya, Sonia Wolf, Lauren E. Merz, Andrew Hantel, Stephen P. Hibbs   +8 more
wiley   +1 more source