Results 131 to 140 of about 1,227 (170)
A Review of Desmopressin Use in Bleeding Disorders: An Unsung Hero? [PDF]
BiomoleculesReardon B, Pasalic L, Favaloro EJ.
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Evaluating the clinical validity of genes related to hemostasis and thrombosis using the Clinical Genome Resource gene curation framework. [PDF]
J Thromb HaemostRoss JE +22 more
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About Congenital Afibrinogenemia.
Turkish journal of haematology : official journal of Turkish Society of Haematology, 2016 openaire +1 more source
Laboratory and Clinical Analysis of Rare Coagulation Factor Deficiencies-A Respective Study of a Single Center from Northwest China. [PDF]
Clin Appl Thromb HemostLi J, Liu Y, Yuan L.
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Determination of Fibrinogen Ratio Cutoff Limits Using Indirect Reference Interval Methodology. [PDF]
Int J Lab HematolSaadalla A, Doyle K, Moser K, Smock K.
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[Congenital afibrinogenemia. A clinical case].
Archivos de pediatria del Uruguay, 1998 J, RODRIGUEZ, S, BIDEGAIN
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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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