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Resuscitative adjuncts and alternative products when blood supplies are limited. [PDF]
Trauma Surg Acute Care OpenLoss L, Tinoco-Garcia L, Schreiber M.
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Congenital afibrinogenemia presenting with cellulitis in the lower back: A case report
Journal of Hematology and Allied Sciences, 2023Afibrinogenemia is a rare inherited bleeding disorder characterized by the complete absence of fibrinogen, a clotting protein essential for normal blood coagulation.
L. Shamanur +3 more
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Blood Coagulation and Fibrinolysis, 2023
Background Congenital fibrinogen deficiencies (CFD) are a group of rare bleeding disorders (RBD). Afibrinogenemia as a subclass of these disorders would occurs as a result of mutations in fibrinogen gene. Here in, the sequences of Aα chain of fibrinogen (
Ali Moazzeni +3 more
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Background Congenital fibrinogen deficiencies (CFD) are a group of rare bleeding disorders (RBD). Afibrinogenemia as a subclass of these disorders would occurs as a result of mutations in fibrinogen gene. Here in, the sequences of Aα chain of fibrinogen (
Ali Moazzeni +3 more
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Pediatrics, 1954
A case of congenital afibrinogenemia is described. Despite the absolute incoagulability of afibrinogenemic blood, this type of hemorrhagic diathesis is not accompanied by hemarthrosis. Systematic studies of this patient's blood revealed that all other known clotting factors are present in normal concentration.
P G, FRICK, I, McQUARRIE
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A case of congenital afibrinogenemia is described. Despite the absolute incoagulability of afibrinogenemic blood, this type of hemorrhagic diathesis is not accompanied by hemarthrosis. Systematic studies of this patient's blood revealed that all other known clotting factors are present in normal concentration.
P G, FRICK, I, McQUARRIE
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Acta Paediatrica, 1963
SUMMARYTwo patients, brother and sister, suffering from congenital afibrinogenemia are reported. This condition has previously not been described from Scandinavia. Both suffered from severe umbilical hemorrhage soon after birth and a continuing bleeding tendency.
S, OSEID, H M, SVENDSEN
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SUMMARYTwo patients, brother and sister, suffering from congenital afibrinogenemia are reported. This condition has previously not been described from Scandinavia. Both suffered from severe umbilical hemorrhage soon after birth and a continuing bleeding tendency.
S, OSEID, H M, SVENDSEN
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American Journal of Hematology, 1994
AbstractCongenital afibrinogenemia is a rare disorder with unusual clinical manifestations. The disease is inherited as an autosomal recessive trait and consanguinity is common among affected families. Clinical manifestations range from minimal bleeding to catastrophic hemorrhage.
H, al-Mondhiry, W C, Ehmann
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AbstractCongenital afibrinogenemia is a rare disorder with unusual clinical manifestations. The disease is inherited as an autosomal recessive trait and consanguinity is common among affected families. Clinical manifestations range from minimal bleeding to catastrophic hemorrhage.
H, al-Mondhiry, W C, Ehmann
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Thrombosis and Haemostasis, 2022
INTRODUCTION Inherited afibrinogenemia is a very rare disease characterized by complete absence of fibrinogen in the circulation and an increased risk in both thrombosis and bleeding.
C. Djambas Khayat +5 more
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INTRODUCTION Inherited afibrinogenemia is a very rare disease characterized by complete absence of fibrinogen in the circulation and an increased risk in both thrombosis and bleeding.
C. Djambas Khayat +5 more
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Blood Coagulation and Fibrinolysis, 2022
Introduction Congenital afibrinogenemia treatment with plasma-derived fibrinogen concentrates in pediatric patients is limited. This study investigated the pharmacokinetics, surrogate efficacy, and safety of a plasma-derived fibrinogen concentrate (FIB ...
C. Khayat +7 more
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Introduction Congenital afibrinogenemia treatment with plasma-derived fibrinogen concentrates in pediatric patients is limited. This study investigated the pharmacokinetics, surrogate efficacy, and safety of a plasma-derived fibrinogen concentrate (FIB ...
C. Khayat +7 more
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Dental management of a 4-year-old child with congenital afibrinogenemia-A rare case report.
Special Care in Dentistry: managing special patients, settings, and situations, 2022Congenital afibrinogenemia is a rare hematologic disorder with an estimated incidence of 1-2 per million people worldwide. It is inherited as an autosomal recessive trait and is characterized by the inability to synthesize fibrinogen.
Shreya Khodke +7 more
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afibrinogenemia or dysfibrinogenemia, fibrinogen deficiency in kids and lambs
CABI Compendium, 2022This datasheet on afibrinogenemia or dysfibrinogenemia, fibrinogen deficiency in kids and lambs covers Identity, Hosts/Species Affected, Diagnosis.
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