Coagulation Tools

References


A    B    C    D    E    F    G    H    I    J    K    L    M    N    O    P    Q    R    S    T   U    V    W    X    Y    Z

A

Agarwal N, Spahr JE, Werner TL, Newton DL, Rodgers GM. Acquired amegakaryocytic thrombocytopenic purpura. Am J Hematol. 2006;81(2):132-135.

Anwar R, Miloszewski KJA. Factor XIII deficiency. Br J Haematol. 1999;107(3):468-484.

Arepally G, Rebbeck TR, Song W, Gilliland G, Maris JM, Poncz M. Evidence for genetic homogeneity in a familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML) [letter]. Blood. 1998;92(7):2600-2602.

Arepally GM, Ortel TL. Heparin-induced thrombocytopenia. N Engl J Med. 2006;355(8):809-817.

B

Bain BJ. Diagnosis from the blood smear. N Engl J Med. 2005;353(5):498-507.

Balduini CL, Cattaneo M, Fabris F, et al; Italian Gruppo di Studio delle Piastrine. Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle Piastrine. Haematologica. 2003;88(5):582-592.

Bambrah RK, Pham DC, Zaiden R, Vu H, Tai S. Heparin-induced thrombocytopenia. Clin Adv Hematol Oncol. 2011;9(8):594-599.

Baudo F, de Cataldo F. Acquired hemophilia: a critical bleeding syndrome. Haematologica. 2004;89(1):96-100.

Bauer KA. Laboratory markers of coagulation and fibrinolysis. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:835-850.

Bitting RL, Bent S, Li Y, Kohlwes J. The prognosis and treatment of acquired hemophilia: a systematic review and meta-analysis. Blood Coagul Fibrinolysis. 2009;20(7):517-523.

Bleeker JS, Hogan WJ. Thrombocytosis: diagnostic evaluation, thrombotic risk stratification, and risk-based management strategies. Thrombosis. 2011; 2011. doi: 10.1155/2011/536062.

Blood smear. In: Pagana KD, Pagana TJ, eds. Mosby’s Diagnostic and Laboratory Test Reference. 2nd ed. St. Louis, MO: Mosby-Year Book, Inc; 1995:125-127.

Boggio LN, Kessler CM. Hemophilia A and B. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:45-59.

Bolton-Maggs PHB, Chalmers EA, Collins PW, et al. A review of inherited platelet disorders with guidelines for their management on behalf of the UKHCDO. Br J Haematol. 2006;135(5):603-633.

Bolton-Maggs PHB, Perry DJ, Chalmers EA, et al. The rare coagulation disorders—review with guidelines for management from the United Kingdom Haemophilia Centre Doctors’ Organisation. Haemophilia. 2004;10(5):593-628.

Bone marrow biopsy. In: Pagana KD, Pagana TJ, eds. Mosby’s Diagnostic and Laboratory Test Reference. 2nd ed. St. Louis, MO: Mosby-Year Book, Inc; 1995:130-133.

Bonnar J. Coagulation effects of oral contraception. Am J Obstet Gynecol. 1987;157(4, pt 2):1042-1048.

Bose P, Hussein KK, Terrell DR, Berger D, Rice L, George JN. Successful treatment of cyclic thrombocytopenia with thrombopoietin-mimetic agents: a report of two patients [letter]. Am J Hematol. 2009;84(7):459-461.

Brasic GM, Meyer LA, Bottner WA, Go RS. Cyclic thrombocytopenia: an important but often-neglected differential diagnosis in patients with suspected idiopathic immune thrombocytopenia. Gundersen Lutheran Med J. 2006;4(1):26-28.

C

Camire RM, Pollak ES. Genetics of coagulation. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:59-89.

Cantor AB. Developmental hemostasis: relevance to newborns and infants. In: Orkin SH, Nathan DG, Ginsburg D, Look AT, Fisher DE, Lux SE IV, eds. Nathan and Oski’s Hematology of Infancy and Childhood. 7th ed. Philadelphia, PA: Saunders Elsevier; 2009:147-191.

Cattaneo M. The platelet P2Y12 receptor for adenosine diphosphate: congenital and drug-induced defects. Blood. 2011;117(7):2102-2112.

Chandler WL. Fibrinolysis testing. In: Kottke-Marchant K, ed. An Algorithmic Approach to Hemostasis Testing. Northfield, IL: College of American Pathologists; 2008:113-124.

Chandler WL. Fibrinolytic bleeding disorders. In: Kottke-Marchant K, ed. An Algorithmic Approach to Hemostasis Testing. Northfield, IL: College of American Pathologists; 2008:175-183.

Clauser S, Cramer-Bordé E. Role of platelet electron microscopy in the diagnosis of platelet disorders. Semin Thromb Hemost. 2009;35(2):213-223.

Coagulation factor assays. In: Jacobs DS, DeMott WR, Oxley DK, eds. Lexi-Comp's Laboratory Test Handbook Concise With Disease Index. 3rd ed. Hudson, OH: Lexi-Comp; 2004:418-424.

Coller BS, Schneiderman PI. Clinical evaluation of hemorrhagic disorders: the bleeding history and differential diagnosis of purpura. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:1851-1876.

Collins PW, Hirsch S, Baglin TP, et al; for UK Haemophilia Centre Doctors' Organisation. Acquired hemophilia A in the United Kingdom: a 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors' Organisation. Blood. 2007;109(5):1870-1877.

Collins PW, Percy CL. Advances in the understanding of acquired haemophilia A: implications for clinical practice. Br J Haematol. 2010;148(2):183-194.

Colman RW, Clowes AW, George JN, Goldhaber SZ, Marder VJ. Overview of hemostasis. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:3-16.

Colman RW, Marder VJ, Clowes AW. Overview of coagulation, fibrinolysis, and their regulation. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:17-20.

Cooney MF. Heparin-induced thrombocytopenia: advances in diagnosis and treatment. Crit Care Nurse. 2006;26(6):30-36.

Cox K, Price V, Kahr WHA. Inherited platelet disorders: a clinical approach to diagnosis and management. Expert Rev Hematol. 2011;4(4):455-472.

D

D-dimers and fibrin degradation products. In: Jacobs DS, DeMott WR, Oxley DK, eds. Lexi-Comp's Laboratory Test Handbook Concise With Disease Index. 3rd ed. Hudson, OH: Lexi-Comp; 2004:502-504.

Dame C, Sutor AH. Primary and secondary thrombocytosis in childhood. Br J Haematol. 2005;129(2):165-177.

Deloughery TG. Management of acute hemorrhage. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1159-1171.

DeSantis Parsons D, Marty J, Strauss RG. Cell biology, disorders of neutrophils, infectious mononucleosis, and reactive lymphocytosis. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:251-271.

Dorsam RT, Kunapuli SP. Central role of the P2Y12 receptor in platelet activation. J Clin Invest. 2004;113(3):340-345.

Drachman JG. Inherited thrombocytopenia: when a low platelet count does not mean ITP. Blood. 2004;103(2):390-398.

Dvorak HF, Rickles FR. Malignancy and hemostasis. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:851-873.

E

Eby CS, Joist JH. Hemostatic abnormalities in liver disease. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1025-1033.

Ehsan A, Plumbley JA. Introduction to thrombosis and anticoagulant therapy. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:534-562.

Escobar CE, Harmening DM, Joiner Maier DM, Simmons VL, Smith-Moore KM, Wyrick-Glatzel J. Introduction to hemostasis. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:441-470.

Ewenstein BM. Nonhemophilic inhibitors of coagulation. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:81-95.

F

Favaloro EJ, Lippi G, Franchini M. Contemporary platelet function testing. Clin Chem Lab Med. 2010;48(5):579-598.

Favaloro EJ. Phenotypic identification of platelet-type von Willebrand disease and its discrimination from type 2B von Willebrand disease: a question of 2B or not 2B? A story of nonidentical twins? Or two sides of a multidenominational or multifaceted primary-hemostasis coin? Semin Thromb Hemost. 2008;34(1):113-127.

Feinstein DI. Lupus anticoagulant and acquired inhibitors of blood coagulation. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:1979-1997.

Feinstein DI. Lupus anticoagulant and acquired inhibitors of blood coagulation. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:1979-1997.

Fink LM, Marlar RA, Miller JL. Antithrombotic therapy. In: McPherson RA, Pincus MR, eds. Henry's Clinical Diagnosis and Management by Laboratory Methods. 21st ed. Philadelphia, PA: Saunders Elsevier; 2007:778-788.

Franchini M, Lippi G, Favaloro EJ. Advances in hematology: etiology and diagnosis of acquired von Willebrand syndrome. Clin Adv Hematol Oncol. 2010;8(1):20-24.

Franchini M, Montagnana M, Lippi G. Clinical, laboratory and therapeutic aspects of platelet-type von Willebrand disease. Int J Lab Hematol. 2008;30(2):91-94.

Franchini M. Heparin-induced thrombocytopenia: an update. Thromb J. 2005;3:14.

Francis CW. Antithrombotic agents. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:449-460.

Furie BC, Furie B. Vitamin K: metabolism and disorders. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:1973-1977.

G

Garcia D, Libby E, Crowther MA. The new oral anticoagulants. Blood. 2010;115(1):15-20.

Gelfand EV, Cannon CP. Acute coronary syndromes. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1387-1404.

George JN, Vesely SK, Lämmle B. Thrombotic thrombocytopenic purpura–hemolytic uremic syndrome. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1613-1620.

Gerwitz AM. Thrombocytopenia due to decreased platelet production. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:411-423.

Giannini S, Cecchetti L, Mezzasoma AM, Gresele P. Diagnosis of platelet-type von Willebrand disease by flow cytometry. Haematologica. 2010;95(6):1021-1024.

Giers G, Wenzel F, Stockschläder M, Riethmacher R, Lorenz H, Tutschek B. Fetal alloimmune thrombocytopenia and maternal intravenous immunoglobulin infusion. Haematologica. 2010;95(11):1921-1926.

Giugliano GR, Lotfi A, Simon DI. Antithrombotic therapy for percutaneous coronary intervention. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1405-1432.

Glassman AB. Anemia: diagnosis and clinical considerations. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:74-83.

Go RS. Idiopathic cyclic thrombocytopenia. Blood Rev. 2005;19(1):53-59.

Gonzalez CE, Pengetze YM. Post-transfusion purpura. Curr Hematol Rep. 2005;4(2):154-159.

Granger CB, Alexander JH, McMurray JJV, et al; ARISTOTLE Committees and Investigators. Apixaban versus warfarin in patients with atrial fibrillation. N Engl J Med. 2011;365(11):981-992.

Greenberg DL, Davie EW. The blood coagulation factors: their complementary DNAs, genes, and expression. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:21-57.

H

Haberichter SL, Montgomery RR. Structure and function of von Willebrand factor. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:707-722.

Hagger D, Wolff S, Owen J, Samson D. Changes in coagulation and fibrinolysis in patients with sickle cell disease compared with healthy black controls. Blood Coagul Fibrinolysis. 1995;6(2):93-99.

Haram K, Svendsen E, Abildgaard U. The HELLP syndrome: clinical issues and management: a review. BMC Pregnancy Childbirth. 2009;9:8.

Hayes TE. Normal prothrombin time and activated partial thromboplastin time. In: Kottke-Marchant K, ed. An Algorithmic Approach To Hemostasis Testing. Northfield, IL: College of American Pathologists; 2008:169-173.

Heit JA. Thrombophilia: clinical and laboratory assessment and management. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:213-244.

Hematology. In: Wallach J, ed. Interpretation of Diagnostic Tests. 8th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2007:368-560.

Heparin antifactor Xa assay. In: Jacobs DS, DeMott WR, Oxley DK, eds. Lexi-Comp’s Laboratory Test Handbook Concise With Disease Index. 3rd ed. Hudson, OH: Lexi-Comp; 2004:693-695.

Hillarp A, Baghaei F, Fagerberg Blixter I, et al. Effects of the oral, direct factor Xa inhibitor rivaroxaban on commonly used coagulation assays. J Thromb Haemost. 2011;9(1):133-139.

Hsieh L, Nugent D. Factor XIII deficiency. Haemophilia. 2008;14(6):1190-1200.

Huth-Kühne A, Baudo F, Collins P, et al. International recommendations on the diagnosis and treatment of patients with acquired hemophilia A. Haematologica. 2009;94(4):566-575.

I

Introduction to normal values (reference ranges). In: Wallach J, ed. Interpretation of Diagnostic Tests. 8th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2007:3-25.

Israels SJ, Kahr WHA, Blanchette VS, Luban NLC, Rivard GE, Rand ML. Platelet disorders in children: a diagnostic approach. Pediatr Blood Cancer. 2011;56(6):975-983.

Ivaskevicius V, Seitz R, Kohler HP, et al; and The Study Group. International registry on factor XIII deficiency: a basis formed mostly on European data. Thromb Haemost. 2007;97(6):914-921.

J

Jang JJ, Olin JW. Medical therapy for peripheral arterial disease. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1441-1451.

Jobe S, Di Paola J. Congenital and acquired disorders of platelet function and number. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:139-157.

Johns CS, Ens GE. Coagulation. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:658-681.

Jong E, van Gorp ECM, Levi M, ten Cate H. The cross-talk of inflammation and coagulation in infectious disease and their roles in disseminated intravascular coagulation. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:199-209.

K

Kacena MA, Chou ST, Weiss MJ, Raskind WH. GATA1-related x-linked cytopenia. In: Pagon RA, Bird TD, Dolan CR, et al, eds. GeneReviewsTM [internet]. Seattle, WA: University of Washington, Seattle; 1993. http://www.ncbi.nlm.nih.gov/books/NBK1364/. Published November 22, 2006. Revised March 22, 2011. Accessed May 30, 2012.

Karimi M, Bereczky Z, Cohan N, Muszbek L. Factor XIII deficiency. Semin Thromb Hemost. 2009;35(4):426-438.

Kessler CM, Acs P, Mariani G. Acquired disorders of coagulation: the immune coagulopathies. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1061-1084.

Kessler CM, Khokhar N, Liu M. A systematic approach to the bleeding patient: correlation of clinical symptoms and signs with laboratory testing. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:17-33.

Kim H-H, Liao JK. Translational therapeutics of dipyridamole. Arterioscler Thromb Vasc Biol. 2008;28(8):s39-s42.

King JAC, Elkhalifa MY, Latour LF. Rapid progression of acquired amegakaryocytic thrombocytopenia to aplastic anemia. South Med J. 1997;90(1):91-94.

Kitchens CS. Surgery and hemostasis. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:613-634.

Kohler HP, Ichinose A, Seitz R, Ariens RAS, Muszbek L; Factor XIII and Fibrinogen SSC Subcommittee of the ISTH. Diagnosis and classification of factor XIII deficiencies. J Thromb Haemost. 2011;9(7):1404-1406.

Konkle BA. Clinical approach to the bleeding patient. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1147-1158.

Kottke-Marchant K. Platelet disorders. In: Kottke-Marchant K, ed. An Algorithmic Approach to Hemostasis Testing. Northfield, IL: College of American Pathologists; 2008:185-216.

Kottke-Marchant K. Platelet testing. In: Kottke-Marchant K, ed. An Algorithmic Approach to Hemostasis Testing. Northfield, IL: College of American Pathologists; 2008:93-112.

Kubitza D, Becka M, Mueck W, Zuehlsdorf M. Rivaroxaban (BAY 59-7939)—an oral, direct factor Xa inhibitor—has no clinically relevant interaction with naproxen. Br J Clin Pharmacol. 2007;63(4):469-476.

Kumar V, Abbas AK, Fausto N, Aster JC, eds. Diseases of white blood cells, lymph nodes, spleen, and thymus. In: Kumar V, Abbas AK, Fausto N, Aster JC, eds. Robbins and Cotran Pathologic Basis of Disease, Professional Edition. 8th ed. Philadelphia, PA: Saunders Elsevier; 2010.

Kuter DJ. General aspects of thrombocytopenia, platelet transfusions, and thrombopoietic growth factors. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:111-122.

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LaBelle C, Kitchens CS. Disseminated intravascular coagulation. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:183-198.

Laubach J, Bendell J. Hematologic changes of pregnancy. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:2385-2396.

Lawrie AS, Green L, Mackie IJ, Liesner R, Machin SJ, Peyvandi F. Factor XIII—an under diagnosed deficiency—are we using the right assays? J Thromb Haemost. 2010;8(11):2478-2482.

Lazarchick J. Interaction of the fibrinolytic, coagulation, and kinin systems; disseminated intravascular coagulation; and related pathology. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:521-533.

Lefkowitz JB. Heparin-induced thrombocytopenia. In: Kottke-Marchant K, ed. An Algorithmic Approach to Hemostasis Testing. Northfield, IL: College of American Pathologists; 2008:287-294.

Liles DK, Knupp CL. Disorders of primary hemostasis: quantitative and qualitative platelet disorders and vascular disorders. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:471-494.

Long JM. Multiple myeloma and related plasma cell disorders. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:379-397.

López JA, Lockhart E. Acquired disorders of platelet function. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:2145-2159.

Lorand L, Losowsky MS, Miloszewski KJM. Human factor XIII: fibrin-stabilizing factor. Prog Hemost Thromb. 1980;5:245-290.

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Marder VJ, Feinstein DI, Colman RW, Levi M. Consumptive thrombohemorrhagic disorders. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1571-1600.

Marder VJ, Francis CW. Physiologic regulation of fibrinolysis. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:419-436.

Marder VJ. Foundations of thrombolytic therapy. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1739-1751.

Marks PW, Rosenthal DS. Hematologic manifestations of systemic disease: infection, chronic inflammation, and cancer. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:2309-2319.

Marks PW. Obstetric hemorrhage. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:1121-1127.

Mehta R, Shapiro AD. Plasminogen activator inhibitor type 1 deficiency. Haemophilia. 2008;14(6):1255-1260.

Metjian A, Konkle BA. Inhibitors in hemophilia A and B. In: Hoffman R, Benz EJ Jr, Shattil SJ, et al, eds. Hematology: Basic Principles and Practice. 5th ed. Philadelphia, PA: Churchill Livingstone Elsevier; 2009:1931-1938.

Mhawech P, Saleem A. Inherited giant platelet disorders: classification and literature review. Am J Clin Pathol. 2000;113(2):176-190.

Mihu D, Costin N, Mihu CM, Seicean A, Ciortea R. HELLP syndrome—a multisystemic disorder. J Gastrointestin Liver Dis. 2007;16(4):419-424.

Moake JL. Thrombotic thrombocytopenic purpura. In: Kitchens CS, Alving BM, Kessler CM, eds. Consultative Hemostasis and Thrombosis. 2nd ed. Philadelphia, PA: Saunders Elsevier; 2007:405-420.

Murawaki A, Nakayasu H, Doi M, et al. Heparin-induced thrombocytopenia in essential thrombocytosis [published online ahead of print March 17, 2012]. J Stroke Cerebrovasc Dis. doi:10.1016/j.jstrokecerebrovasdis.2012.02.011.

Muszbek L, Bagoly Z, Cairo A, Peyvandi F. Novel aspects of factor XIII deficiency. Curr Opin Hematol. 2011;18(5):366-372.

N

Ng VL. Anticoagulation monitoring. Clin Lab Med. 2009;29(2):283-304.

Nugent DJ. Prophylaxis in rare coagulation disorders—factor XIII deficiency. Thromb Res. 2006;118(suppl 1):S23-S28.

Nurden AT, George JN. Inherited abnormalities of the platelet membrane: Glanzmann thrombasthenia, Bernard-Soulier syndrome, and other disorders. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:987-1010.

Nurden P, George JN, Nurden AT. Inherited thrombocytopenias. In: Colman RW, Marder VJ, Clowes AW, George JN, Goldhaber SZ, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. 5th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2006:975-986.

O

Othman M, Lopez JA, Ware J. Platelet-type von Willebrand disease update: the disease, the molecule and the animal model. Expert Rev Hematol. 2011;4(5):475-477.

Othman M. Platelet-type von Willebrand disease: three decades in the life of a rare bleeding disorder. Blood Rev. 2011;25(4):147-153.

P

Peerschke EIB. The laboratory evaluation of platelet dysfunction. Clin Lab Med. 2002;22(2):405-420.

Perkins SL. Aplastic anemia (including pure red cell aplasia and congenital dyserythropoietic anemia). In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. 4th ed. Philadelphia, PA: F.A. Davis Company; 2002:129-140.

Platelet count. In: Pagana KD, Pagana TJ, eds. Mosby’s Diagnostic and Laboratory Test Reference. 2nd ed. St. Louis, MO: Mosby-Year Book, Inc; 1995:622-624.

Platelet function testing. In: Kitchen S, McCraw A, Echenagucia M, eds. Diagnosis of Hemophilia and Other Bleeding Disorders: A Laboratory Manual. 2nd ed. Montréal, Québec: World Federation of Hemophilia; 2010:124-134. http://www.wfh.org/2/docs/Publications/Diagnosis_and_Treatment/Lab_Manual2010/Lab_Manual_Nov2010.pdf. Updated September 2011. Accessed May 30, 2012.

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