scholarly article | Q13442814 |
review article | Q7318358 |
P356 | DOI | 10.1016/S0190-9622(81)70035-5 |
P698 | PubMed publication ID | 7012204 |
P2093 | author name string | Taylor RE | |
Blatt PM | |||
P2860 | cites work | Disorders of hemostatic function in patients with systemic lupus erythematosus | Q33333344 |
Platelet physiology and abnormalities of platelet function (second of two parts). | Q33334020 | ||
Thrombotic thrombocytopenic purpura: combined treatment with plasmapheresis and antiplatelet agents | Q33484996 | ||
Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant agains | Q34055947 | ||
Biologic and clinical significance of cryoglobulins. A report of 86 cases | Q34204386 | ||
WATERFALL SEQUENCE FOR INTRINSIC BLOOD CLOTTING. | Q34257361 | ||
Syndrome of acquired factor X deficiency and systemic amyloidosis in vivo studies of the metabolic fate of factor X. | Q34733324 | ||
Actions and Interactions of Antithrombin and Heparin | Q35148665 | ||
Natural inhibitors of fibrinolysis | Q35898900 | ||
Secretable Storage Pools in Platelets | Q38077642 | ||
Passovoy factor: A hitherto unrecognised factor necessary for haemostasis | Q39338610 | ||
Relationships Between Platelets and Coagulation Factors in Hemostasis | Q39722730 | ||
Behçet disease (Behçet syndrome) | Q39804316 | ||
Molecular assembly in the contact phase of the Hageman factor system | Q39811219 | ||
Molecular mechanism of physiological fibrinolysis | Q39861594 | ||
The Genetics of Hereditary Disorders of Blood Coagulation | Q39922946 | ||
Blood coagulation factor VIII (antihemophilic factor): with comments on von Willebrand's disease and Christmas disease | Q39938846 | ||
Platelet physiology and abnormalities of platelet function (first of two parts). | Q39944486 | ||
Benign hypergammaglobulinemic purpura of Waldenström | Q40004569 | ||
Arachidonic Acid Metabolites and the Interactions between Platelets and Blood-Vessel Walls | Q40219524 | ||
The mechanism of clot dissolution by plasmin | Q40330962 | ||
Clinical manifestations of ascorbic acid deficiency in man | Q40926713 | ||
Disseminated Intravascular Coagulation: A Reappraisal | Q41208362 | ||
Platelets and Experimental Scurvy | Q46569786 | ||
Relationship of plasminogen activator to fibrin. | Q47859101 | ||
Factor XIII. | Q54565389 | ||
THROMBOTIC THROMBOCYTOPENIC PURPURA | Q56286858 | ||
Aggregation of Blood Platelets by Adenosine Diphosphate and its Reversal | Q59065336 | ||
On the "easy bruising" syndrome with normal platelet count. A study of 75 patients | Q66877957 | ||
Factor X deficiency in primary amyloidosis: resolution after splenectomy | Q66946958 | ||
Products Containing Aspirin | Q69815632 | ||
Psychogenic purpura: a re-evaluation of the syndrome of autoerythrocyte sensitization | Q72234296 | ||
COLD-PRECIPITABLE FIBRINOGEN, "CRYOFIBRINOGEN" | Q76721846 | ||
THE CUTANEOUS MANIFESTATION OF CRYOGLOBULINEMIA | Q76726848 | ||
Plasmin-antiplasmin complex as a reservoir of fibrinolytic enzyme | Q78770726 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 348-368 | |
P577 | publication date | 1981-03-01 | |
P1433 | published in | Journal of the American Academy of Dermatology | Q15757046 |
P1476 | title | Clinical evaluation of the patient with bruising and bleeding | |
P478 | volume | 4 |
Q37111243 | Newer hemostatic agents used in the practice of dermatologic surgery | cites work | P2860 |
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