Results 81 to 90 of about 13,745 (204)
Successful Vaginal Delivery in a Pregnant Woman With Bernard–Soulier Syndrome: A Case Report
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Bernard–Soulier syndrome (BSS) is a rare inherited platelet disorder that poses major risks during pregnancy because of potential bleeding complications. Managing such cases in low‐resource settings is especially challenging. We report the case of a 23‐year‐old Afghan woman with BSS who achieved a successful full‐term vaginal delivery at a ...
Monireh Yaghoubi +2 more
wiley +1 more source
Overview of the use of recombinant factor VIIa in children
Pediatric Health, Medicine and Therapeutics, 2014 John Puetz Department of Pediatrics, Division of Hematology/Oncology, Cardinal Glennon Children's Medical Center, Saint Louis University, St Louis, MO, USA Abstract: Recombinant factor VIIa (rFVIIa) was initially developed as a bypassing agent to ...
Puetz J
doaj
Expression and purification of recombinant human coagulation Factor VII fused to His-Tag through Gateway technology [PDF]
Background. Factor VII is a plasma glycoprotein that participates in the coagulation process leading to generation of fibrin. Construction, expression and purification of recombinant FVII fused to poly histidin tag through gateway technology ...
حلبیان, راحله +6 more
core +1 more source
روشهای مورد استفاده در کنترل خونریزی کبدی [PDF]
, 2014 برقراری هموستاز سریع و مناسب در ارگان¬های پارانشیمی، خصوصاً در بافت کبدی کار بسیار دشواری می¬باشد. مشکل اصلی در کنترل خونریزی کبد، توقف تراوش خون از ساختار سینوزوئیدال بافت کبد می¬باشد که دارای عروق بسیار کوچکی می¬باشد و در نتیجه بستـن عـروق بسیار مشکل ...
شریف, محمد رضا +1 more
core
Tissue factor pathway inhibitor-2 is a novel inhibitor of matrix metalloproteinases with implications for atherosclerosis [PDF]
, 2014 Degradation of ECM, particularly interstitial collagen, promotes plaque instability, rendering atheroma prone to rupture. Previous studies implicated matrix metalloproteinases (MMPs) in these processes, suggesting that dysregulated MMP activity, probably
Foster, Don +6 more
core +1 more source
PlateletsMutations in the ITGA2B or ITGB3 gene that encodes for the αIIbβ3 platelet integrin usually cause Glanzmann thrombasthenia (GT). This study aims to investigate the clinical characteristics of a pedigree exhibiting an inherited hemorrhagic disorder ...
Xiangcheng Liao +7 more
doaj +1 more source
Management of neonatal massive hemorrhage: A narrative review
Transfusion, Volume 66, Issue 5, Page 1012-1022, May 2026.
Cheryl S. L. Chooi +7 more
wiley +1 more source
BMC Infectious Diseases, 2007 Background This report discusses a case of unsuccessful treatment with recombinant factor VIIa (rFVIIa) in off-label use. The need for international guidelines concerning the off-label use of rFVIIa is outlined as well as the need for methods to control ...
Tsakiris Dimitrios A +3 more
doaj +1 more source
Combined Factor VII and X Deficiency [PDF]
, 2011 Factor VII deficiency and factor X deficiency and very rare disorders individually. Combined Factor VII and X is a rare congenital blood disorder with very few cases reported in the literature.
Arora, Sunita +2 more
core
Management of anticoagulant-related intracranial hemorrhage: An evidence-based review [PDF]
, 2014 The increased use of anticoagulants for the prevention and treatment of thromboembolic diseases has led to a rising incidence of anticoagulant-related intracranial hemorrhage (AICH) in the aging western population. High mortality accompanies this form of
Keyrouz, Salah G, Ray, Bappaditya
core +3 more sources