Benign Hematology Reading List

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A. Hematopoiesis

• Lee et al. Wintrobe’s Clinical Hematology, 11th edition. Galter Library Quick Reference WH 100 W794 2004
• Tenen, DG, Hromas, R, Licht, JD, Zhang, DE. Transcription factors, normal myeloid development, and leukemia. Blood 1997; 90:489-519
• Jacob, J, Haug, JS, Raptis, S, Link, DC. Specific signals generated by the cytoplasmic domain of the granulocyte colony-stimulating factor (G-CSF) receptor are not required for G-CSF-dependent granulocytic differentiation. Blood 1998; 92:353-61

B. B 12 and Folic Acid

• Pruthi, RK, Tefferi, A. Pernicious anemia revisited. Mayo Clin Proc 1994; 69:144
• Stabler, SP, Allen, RH, Savage, DG, Lindenbaum, J. Clinical spectrum and diagnosis of cobalamin deficiency. Blood 1990; 76:871-81
• Naurath, HJ, Joosten, E, Riezler, R, et al. Effects of vitamin B12, folate, and vitamin B6 supplements in elderly people with normal serum vitamin concentrations. Lancet 1995; 346:85-9

C. Iron Metabolism

• Brittenham, GM. Disorders of iron metabolism: Iron deficiency and Overload. In: Hematology Basic Principles and Practice, 3rd ed, Hoffman, R, Benz, EJ Jr, Shattil, SJ, et al (Eds), Churchill Livingstone, New York 2000 Galter Library Level 2 WH 120 H487 1999
• Annibale, B, Capurso, G, Chistolini, A, D'Ambra, G. Gastrointestinal causes of refractory iron deficiency anemia in patients without gastrointestinal symptoms. Am J Med 2001; 111:439-45
• Cook, JD, Skikne, BS. Iron deficiency: Definition and diagnosis. J Intern Med 1989; 226:349
• Levin, SM, Goldberg, M. Clinical evaluation and management of lead-exposed construction workers. Am J Ind Med 2000; 37:23-43

D. RBC membrane disorders

• Mohandas, N, Evans, E. Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects. Annu Rev Biophys Biomol Struct 1994; 23:787-818
• Lux, SE, Palek, J. Disorders of the red cell membrane. In: Blood. Principles and Practice of Hematology, Handin RI, Lux SE, Stossel TP, (Eds), Lippincott, Philadelphia 1995. p.1701. Galter Library Level 2 WH 100 B654 1995
• Jacobasch, G, Rapoport, SM. Hemolytic anemias due to erythrocyte enzyme deficiencies. Mol Aspects Med 1996; 17:143.
• Socie, G, Mary, JY, de Gramont, A, et al. Paroxysmal nocturnal haemoglobinuria: Long term follow-up and prognostic factors. French Society of Haematology. Lancet 1996; 348:573-7

E. Disorders of globin synthesis

• Forget, BG. Thalassemia syndromes. In: Hematology: Basic principles and practice, 3rd Edition, Hoffman, R, Benz, Jr EJ, Shattil, SJ, et al (Eds), Churchill Livingstone, New York 2000. p.485-511. Galter Library WH 120 H487 1999
• Olivieri, NF. The beta-thalassemias. N Engl J Med 1999; 341:99-109 [published erratum appears in N Engl J Med 1999 Oct 28;341(18):1407]
• Steinberg, MH. Management of sickle cell disease. N Engl J Med 1999; 340:1021-1030
• Weatherall, DJ, Clegg, JB. The Thalassaemia Syndromes. 4th ed, Blackwell Scientific, Oxford, 2001 Galter Library Level 2 WH 170 W362t

F. Enzyme deficiencies

• Oski, F, Marshall, B, Cohen, P, et al. Exercise with anemia. The role of the left shifted or right-shifted oxygen-hemoglobin equilibrium curve. Ann Intern Med 1971; 74:44-6
• Glader, BE. Glucose-6-phosphate dehydrogenase deficiency and related disorders of hexose monophosphate shunt and glutathione metabolism. In: Wintrobe's Clinical Hematology, 11th ed, Lee, GR, Foerster, J, Lukens, J, et al (Eds), Williams Wilkins, Baltimore. Galter Library Quick Reference WH 100 W794 2004
• Beutler, E. Red blood cell enzyme disorders. In: Hematologic disorders in maternal-fetal medicine, Bern, M, Frigoletto, F Jr, (Eds), Wiley-Liss, Inc, New York, 1990, p. 199 Galter Library Level 2 WQ 252 H4865 1990

ABO compatibility

A. Blood banking

• Reid, MR, Lomas-Francis, C. The blood group antigen facts book. 2004 Academic Press. Harcourt Brace and Company, Publishers. Galter Library Quick Reference QW 539 R357b 2004
• Avent, ND, Reid, ME. The Rh blood group system: a review. Blood 2000; 95:375-87
• Van Buren, NL, Stroncek, DF, Clay, ME, et al. Transfusion-related acute lung injury caused by an NB2 granulocyte-specific antibody in a patient with thrombotic thrombocytopenic purpura. Transfusion 1990; 30:42
• Vogelsang, G, Kickler, TS, Bell, WR. Post-transfusion purpura: A report of five patients and a review of the pathogenesis and management. Am J Hematol 1986; 21:259
• Shulman, IA, Petz, LD. Red cell compatibility testing: Clinical significance and laboratory methods. In: Clinical practice of transfusion medicine, Petz, LD, Swisher, SN, Kleinman, S, et al (Eds), Churchill and Livingstone, San Francisco 1996

B. Immune hemolysis

• Marchand, A, Galen, RS, Van Lente, F. The predictive value of serum haptoglobin in hemolytic disease. JAMA 1980; 243:1909
• Prevention of D isoimmunization. In: ACOG Technical Bulletin, Number 147, American College of Obstetrics and Gynecology, Washington, DC, 1990
• Gehrs, BC, Friedberg, RC. Autoimmune hemolytic anemia. Am J Hematol 2002; 69:258-71.
• Horwitz, CA, Moulds, J, Henle, W, et al. Cold agglutinins in infectious mononucleosis and heterophil-antibody-negative mononucleosis-like syndromes. Blood 1977; 50:195
• Petz, LD, Fudenberg, HH. Coombs-positive hemolytic anemia caused by penicillin administration. N Engl J Med 1966; 274:171

A. Thrombocytopenia

• Sixma, JJ, van Zanten, GH, Huizinga, EG, et al. Platelet adhesion to collagen: an update. Thromb Haemost 1997; 78:434
• Shcherbina, A, Rosen, FS, Remold-O'Donnell, E. Pathological events in platelets of Wiskott-Aldrich syndrome patients. Br J Haematol 1999; 106:875-883
• George, JN, Woolf, SH, Raskob, GE, et al. Idiopathic thrombocytopenic purpura: A practice guideline developed by explicit methods for the American Society of Hematology. Blood 1996; 88:3-40

B. Other

• Moake, JL. Thrombotic microangiopathies. N Engl J Med 2002; 347:589-600
• Remuzzi, G, Galbusera, M, Noris, M, et al. von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Blood 2002; 100:778-85
• Warkentin, TE, Chong, BH, Greinacher, A. Heparin-induced thrombocytopenia: towards consensus. Thromb Haemost 1998; 79:1
• Kroll, MH, Sullivan, R. Mechanisms of platelet activation. In: Thrombosis and Hemorrhage, Loscalzo, J, Schafer, AI (Eds), Blackwell Science, Boston 1993 Galter Library Level 2 WH 322 T5312 1993
• Rabelink, TJ, Zwaginga, JJ, Koomans, HA, Sixma, JJ. Thrombosis and hemostasis in renal disease. Kidney Int 1994; 46:287

A. Coagulation Cascade

• Lee et al. Wintrobe’s Clinical Hematology, 11th edition Galter Library Reserve Desk WH 100 W794 2004
• Clouse, LH, Comp, PC. The regulation of hemostasis: The protein C system. N Engl J Med 1986; 314:1298
• Hirsh, J, Anand, SS, Halperin, JL, Fuster, V. Guide to anticoagulant therapy: heparin: a statement for healthcare professionals from the American Heart Association. Circulation 2001; 103:2994-3018

B. Thrombosis

• Bertina, RM. Genetic approach to thrombophilia. Thromb Haemost 2001; 86:92
• Samama, MM. An epidemiologic study of risk factors for deep vein thrombosis in medical outpatients: the Sirius study. Arch Intern Med 2000; 160:3415-20
• Ames, PR, Khamashta, MA, Hughes, GR. Clinical and therapeutic aspects of the antiphospholipid syndrome. Lupus 1995; 4 Suppl 1:S23-25.

C. Bleeding

• White, GC 2nd, Rosendaal, F, Aledort, LM, et al. Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Factor VII and Factor IX Subcommittee. Thromb Haemost 2001; 85:560
• Sadler, JE. A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 1994; 71:520
• Kumar, S, Pruthi, RK, Nichols, WL. Acquired von Willebrand disease. Mayo Clin Proc 2002; 77:181-8
• Boggio L, Green D. Acquired Hemophilia. Rev Clin Exper Hem. 5(4): 389-404, 2001.

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