Results 121 to 130 of about 239,927 (172)
Are all fibrinogen concentrates the same? The effects of two fibrinogen therapies in an afibrinogenemic patient and in a fibrinogen deficient plasma model. A clinical and laboratory case report. [PDF]
Front Med (Lausanne)Goodarzi S +5 more
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An exploratory plasma-based functional assay for phenotypic characterization of fibrinolysis in dysfibrinogenemia. [PDF]
Res Pract Thromb HaemostSuzuki A +7 more
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The Swiss Haemophilia Registry-Report From the First 8 Years. [PDF]
HaemophiliaBosch A +8 more
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The fibrinogen αC region promotes arterial thrombosis in the context of hypofibrinogenemia.
BloodLee RH +11 more
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About Congenital Afibrinogenemia.
Turkish journal of haematology : official journal of Turkish Society of Haematology, 2016 openaire +1 more source
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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
openaire +3 more sources
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
exaly +3 more sources
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
exaly +3 more sources
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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Congenital Afibrinogenemia in Goats
Zentralblatt für Veterinärmedizin Reihe A, 2010Summary A case of congenital afibrinogenemia in goats is described. The animal shows severe haemorrhagic diathesis with joint bleedings. The patient's blood was absolutely incoagulable. Immunologically no fibrinogen could be demonstrated in the plasma. The other clotting factors were present in normal concentrations.
H J, Breukink +4 more
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Thrombosis and Haemostasis, 1971
SummaryA case of congenital afibrinogenemia is reported.The patient is a 2 month old white female infant who presented bleeding from the umbilical stump a few days after birth. Subsequently other hemorrhagic manifestations were hematomas at the site of venipunctures.All routine plasmatic tests gave values greater than 1000 sec. The prothrombin time was
A Girolami, G Zacchello, R D’Elia
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SummaryA case of congenital afibrinogenemia is reported.The patient is a 2 month old white female infant who presented bleeding from the umbilical stump a few days after birth. Subsequently other hemorrhagic manifestations were hematomas at the site of venipunctures.All routine plasmatic tests gave values greater than 1000 sec. The prothrombin time was
A Girolami, G Zacchello, R D’Elia
openaire +1 more source