...Marganit Benish; Adi Shitrit Yarhi; Ivan Budnik; Chagit Klieger; Noah Gruber; Yael Harel; Gili Kenet; Assaf Arie Barg; Sarina Levy-Mendelovich Introduction: Heavy menstrual bleeding (HMB) poses a significant concern among adolescents and can arise from bleeding disorders. This study aimed...

... Platelet aggregation Bleeding disorders Platelets Venlafaxine (VEN) is a selective norepinephrine reuptake inhibitor (SNRI) that mainly helps treat major depressive disorder and anxiety and panic disorders [ 1 ]. It is one of the most widely prescribed antidepressants in the USA; more than 15...

...” with a particular statement. Haemophilia Haematology Bleeding disorders Multidisciplinary care Gene therapy Hemophilia A, a hereditary bleeding disorder characterized by a deficiency of clotting factor VIII (FVIII), presents a significant health challenge in Kuwait, Oman, Saudi Arabia, and the UAE...

..., instructions or products referred to in the content or advertisements. 2022 Chronic myeloid leukemia Acquired factor V deficiency Acquired prothrombin deficiency Acquired factor XI deficiency Megakaryocytes Bleeding disorders Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm...

... compared to prior treatment with pdVWF. Causal treatment has been reported to resolve the bleeding disorder. Treatment options for acute bleeding include desmopressin, antifibrinolytics, and plasma-derived (pd)VWF [1]. Recently, recombinant von Willebrand factor (rVWF) has become available...

... to in the content or advertisements. Bleeding Bleeding disorders Pregnancy von Willebrand disease Type 2B von Willebrand disease is a rare condition in which the large von Willebrand factor (VWF) multimers have a gain-of-function mutation resulting in an increased affinity for GpIb receptors...

...Peter Cashin; Lars Göran Lundberg; Hans Hagberg; Elisabeth Ejerblad; Urban Karlbom Background: Acquired haemophilia A (AHA) is a rare bleeding disorder caused by an imbalance in the immune system leading to the production of factor VIII antibodies. In half of the cases, the underlying cause...

... history for bleeding disorders and a normal mother who had an antihaemophilic globulin concentration of 200%. Family history revealed no bleeding disorder in 3 successive generations of the maternal side. This together with AHF activity exceeding slightly AHF-like antigen concentration provides good...

... responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Bleeding disorders Blood coagulation Platelet factor 3 deficiency Thrombocytopathy Acta Haemat. 50: 116-123 (1973) Congenital Thrombocytopathy...

... and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Abnormal factor X Bleeding disorders Blood coagulation Acta Haemat. 49: 114-122 (1973) Abnormal Factor X (Factor X...

...Sinasi Özsoylu; Faruk L. Özer Coagulation studies in 2 patients revealed decreased factor IX activity. Family history of factor IX deficiency or bleeding disorder was not present and the past history of the patients did not disclose any evidence of congenital hemorrhagic disorder. They did...

... of heparin in the medium markedly reduced the inhibitory effect of the paraprotein on platelet aggregation by ADP. Anti-heparins Bleeding disorders Macroglobulin Paraproteinemia Platelet aggregation Acta haemat. 53: 249-255 (1975) Anti-Heparin Activity of a Macroglobulin from a Patient with Breast...

... or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Bleeding disorders Blood coagulation Factor VII deficiency Hypoproconvertinemia Acta Haemat. 50: 228-237 (1973) Congenital Hypoproconvertinemia (Factor VII Deficiency) A Report...

..., quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Bleeding disorders Blood lipids Lipoproteins Platelet functions Purpura...

.... Abnormal factor X Bleeding disorders Blood coagulation Factor X Friuli Acta Haemat. 51: 40-50 (1974) Abnormal Factor X (Factor X Friuli) Coagulation Disorder. The Heterozygote Population A Study of 57 Subjects A ntonio G iroi.ami, A driano Brunetti, G iovanna Bareggi and G iu­ seppe Cella Institute...

..., instructions or products referred to in the content or advertisements. Angiohaemophilia Aspirin tolerance test Bleeding disorders Factor VIII Platelet aggregation Von Willebrand’s disease Acta Haemat. 52: 29-39 (1974) Von Willebrand s Disease in Italy A Study of 13 Families from a Small Area...

... advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Bleeding disorders Disseminated intravascular...

... coagulation Bleeding disorders Factor X Friuli Factor X survival 4 3 2009 Acta Haemat. 52: 223-231 (1974) Factor X Survival and Therapeutic Factor X Levels in the Abnormal Factor X (Factor X Friuli) Coagulation Disorder1 A. G irolami, G. M olaro and L. D e Marco Institute of Semeiotica Medica...

...(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Bleeding disorders Blood coagulation Electroimmunoassay Electrosyneresis Factor X deficiency Acta haemat. 53: 118...

... or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Age effect on factor XI Bleeding disorders Coagulation Factor XI...