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Sadler JE, Poncz M
Antibody-mediated thrombotic disorders: thrombotic thrombocytopenic purpura and heparin induced thrombocytopenia.
In: Williams Hematology, Eighth Edition (MA Lichtman, E Beutler, K Kaushansky, TJ Kipps, U Seligsohn, JT Prchal, eds.) McGraw-Hill, New York, in press
Sadler JE Low vWF: sometimes a risk factor and sometimes a disease.
Hematology (Am Soc Hematol Educ Program) 2009: in press
Nichols WL, Rick ME, Ortel TL, Montgomery RR, Sadler JE, Yawn BP, James AH, Hultin MB, Manco-Johnson MJ, Weinstein M
Clinical and laboratory diagnosis of von Willebrand disease: a synopsis of the 2008 NHLBI/NIH guidelines.
Am J Hematol 2009 Jun;84(6):366-70
McCrae KR, Sadler JE, Cines D
Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.
In: Hematology: Basic Principles and Practice, Fifth Edition (R Hoffman, EJ Benz, SJ Shattil, B Furie, LE Silberstein, P McGlave, HE Heslop, eds.) Elsevier Churchill Livingstone, Philadelphia, 2009; 2099-2111
White GC II, Sadler JE Von Willebrand disease: clinical aspects and therapy.
In: Hematology: Basic Principles and Practice, Fifth Edition (R Hoffman, EJ Benz, SJ Shattil, B Furie, LE Silberstein, P McGlave, HE Heslop, eds.) Elsevier Churchill Livingstone, Philadelphia, 2009; 1961-1972
Nichols WL, Hultin MB, James AH, Manco-Johnson MJ, Montgomery RR, Ortel TL, Rick ME, Sadler JE, Weinstein M, Yawn BP
Von Willebrand factor content in Alphanate (Laurence J. Logan) – reply.
Haemophilia 2009;15:370-1
Sadler JE Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura.
Blood 2008 Jul 1;112(1):11-8
Sadler JE Diagnosing VWD type 1: when is it useful and when illogical?
Blood 2007;109:4106
Sadler JE Interesting variations on how a disease is defined: comparisons of von Willebrand disease and Glanzmann thrombasthenia. Reply to a rebuttal.
J Thromb Haemost 2007 Mar;5(3):649-51
Sadler JE VWD data worth 10,000 words.
Blood 2007;109:3
McCrae KR, Cines DB, Sadler JE Thrombotic microangiopathies: thrombotic thrombocytopenic purpura and the hemolytic uremic syndrome.
In: Thrombocytopenia (KR McCrae, ed.) Taylor and Francis, London, UK, 2006; 247-265
Zheng XL, Sadler JE Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.
In: Clinical Hematology (NS Young, SL Gerson, KA High, eds) Mosby Elsevier, Philadelphia, 2006; 802-813
Sadler JE, Blinder M
von Willebrand disease.
In: Hemostasis and Thrombosis: Basic Principles and Clinical Practice, Fifth Edition (RW Colman, VJ Marder, AW Clowes, JN George, and SZ Goldhaber, eds) Lippincott Williams & Wilkins, Philadelphia, 2006; 905-921
Sadler JE, Poncz M
Antibody-mediated thrombotic disorders: thrombotic thrombocytopenic purpura and heparin induced thrombocytopenia.
In: Williams Hematology, Seventh Edition (MA Lichtman, E Beutler, K Kaushansky, TJ Kipps, U Seligsohn, JT Prchal, eds) McGraw-Hill, New York, 2006; 2031-2054
McCrae KR, Sadler JE, Cines D
Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome.
In: Hematology: Basic Principles and Practice, Fourth Edition (R Hoffman, EJ Benz, SJ Shattil, B Furie, HJ Cohen, LE Silberstein, P McGlave, eds) Elsevier Churchill Livingstone, Philadelphia, 2005; 2287-2304
White GC II, Sadler JE Von Willebrand disease: Clinical aspects and therapy.
In: Hematology: Basic Principles and Practice, Fourth Edition (R Hoffman, EJ Benz, SJ Shattil, B Furie, HJ Cohen, LE Silberstein, P McGlave, eds) Elsevier Churchill Livingstone, Philadelphia, 2005; 2121-2136
Sadler JE More to TTP than VWFCP.
Blood 2002;99:397-398
Sadler JE von Willebrand factor.
In: Encyclopedia of Molecular Medicine (T.E. Creighton, ed.) John Wiley & Sons, New York, 2002; 3392-3395
Moake JL, Sadler JE, Mannucci P, Ganguly P
Report on the workshop: Von Willebrand factor and Thrombotic Thrombocytopenic Purpura.
Am J Hematol 2001 Oct;68(2):122-6
Sadler JE Boosting a natural anticoagulant.
Blood 2001;97:1523-1524
Sadler JE von Willebrand disease.
In: The Metabolic and Molecular Bases of Inherited Disease, Eighth Edition (C.R. Scriver, A.L. Beaudet, W.S. Sly, and D. Valle, eds) McGraw-Hill Book Co., New York, 2001; 4415-4431
Sadler JE, and Davie EW
Hemophilia A, hemophilia B, and von Willebrand disease.
In: The Molecular Basis of Blood Diseases, Third Edition (G. Stamatoyannopoulos, P.W. Majerus, R. M. Perlmutter, and H. Varmus, eds) W.B. Saunders Co., Philadelphia 2001; 680-718
Sadler JE, Blinder M
von Willebrand disease.
In: Hemostasis and Thrombosis Basic Principles and Clinical Practice, Fourth Edition (R.W. Colman, J. Hirsh, V.J. Marder, A.W. Clowes, and J.N. George, eds) Lippincott Williams & Wilkins, Philadelphia 2001; 825-837
Sadler JE, Matsushita T, Dong Z, Tuley EA, Westfield LA
Molecular mechanism and classification of von Willebrand disease.
Thromb Haemost 1995 Jul;74(1):161-6
Sadler JE von Willebrand disease.
In: The Metabolic and Molecular Basis of Inherited Disease, Seventh Edition (C.R. Scriver, A.L. Beaudet, W.S. Sly, and D. Valle, eds) McGraw-Hill Book Co., New York 1995; 3269-3287
Sadler JE, Gralnick HR
Commentary: a new classification for von Willebrand disease.
Blood 1994 Aug 1;84(3):676-9
Lentz SR, Sadler JE The molecular basis of thrombomodulin function.
In: Thrombomodulin (J.C. Giddings, ed.) R.G. Landes Co, Austin, TX, 1994; 91-120
Sadler JE von Willebrand disease.
In: Haemostasis and Thrombosis, Third Edition (A.L. Bloom, C.D. Forbes, D.P. Thomas, and E.G.D. Tuddenham, eds) Churchill-Livingstone, Edinburgh 1994; 843-857
Sadler JE, Davie EW
Hemophilia A, hemophilia B, and von Willebrand disease.
In: Molecular Basis of Blood Diseases, Second Edition (G. Stamatoyannopoulos, A.W. Nienhuis, P.W. Majerus, and H. Varmus, eds) W.B. Saunders Co., Philadelphia 1994; 657-700
Sadler JE, Lentz SR, Sheehan JP, Tsiang M, Wu Q
Structure-function relationships of the thrombin-thrombomodulin interaction.
Haemostasis 1993 Mar;23 Suppl 1:183-93
Lebo RV, Conneally PM, Flandermeyer RR, Christian C, Bolbus MS, Lovelace RE, Anderson LA, Chance PF, Bird TD, Bruce BD, Slotnick RN, Dyckoff D, Sadler JE, Carver V, Schonberg SA, Fowler WM, Ionasescu V, Kadasi L, Dyck PJ
The multilocus Charcot-Marie-Tooth syndrome.
In: Charcot-Marie-Tooth Disorders Pathophysiology, Molecular Genetics, and Therapy (R.E. Lovelace and H.K. Shapiro, eds) Neurology and Neurobiology 53, Alan R. Liss, New York 1990; 307-334
Mancuso DJ, Sadler JE Molekularbiologie des von-Willebrand-Faktors [German].
Hämostaseologie 1989;9:122-129
Sadler JE Von Willebrand disease.
In: The Metabolic Basis of Inherited Disease, Sixth Edition (C.R. Scriver, A.L. Beaudet, W.S. Sly, and D. Valle, eds) McGraw-Hill Book Co., New York 1989; 2171-2188
Sadler JE Molecular biology of von Willebrand factor.
In: Coagulation and Bleeding Disorders The Role of Factor VIII and von Willebrand Factor (T.S. Zimmerman and Z. Ruggeri, eds) Marcel Dekker, Inc., New York 1989; 117-135
Sadler JE The molecular biology of von Willebrand factor.
In Thrombosis and Haemostasis 1987 (M. Verstraete, J. Vermylen, R. Lijnen, and J. Arnout, eds) International Society on Thrombosis and Haemostasis and Leuven University Press, Leuven, Belgium 1987; 61-79
Sadler JE, Davie EW
Hemophilia A, hemophilia B, and von Willebrand's disease.
In: Molecular Basis of Blood Diseases (G. Stamatoyannopoulos, A.W. Nienhuis, P. Leder, and P.W. Majerus, eds) W.B. Saunders Co., Philadelphia 1987; 575-630
Sadler JE, Shelton-Inloes BB, Sorace JM, Harlan JM, Titani K, Davie EW
Characterization of two cDNAs coding for human von Willebrand factor and the implications for biosynthesis and evolution.
In: Factor VIII/von Willebrand Factor: Biological and Clinical Advances (N. Ciavarella, Z.M. Ruggeri, and T.S. Zimmerman, eds) Wichtig Editore, Milan 1986; 103-109
Sadler JE, Malinowski DP, Davie EW
Cloning and structural characterization of the gene for human plasminogen.
In: Progress in Fibrinolysis, Vol. 7 (J.F. Davidson, M.B. Donati, and S. Coccheri, eds) Churchill Livingstone, Edinburgh 1985; 201-204
Sadler JE Biosynthesis of glycoproteins Formation of O-linked oligosaccharides.
In: Biology of Carbohydrates, Vol. 2 (V. Ginsburg and P.W. Robbins, eds) John Wiley and Sons, New York 1984; 199-288
Sadler JE, Beyer TA, Oppenheimer CL, Paulson JC, Prieels JP, Rearick JI, Hill RL
Purification of mammalian glycosyltransferases.
Methods Enzymol 1982;83:458-514
Beyer TA, Sadler JE, Rearick JI, Paulson JC, Hill RL
Glycosyltransferases and their use in assessing oligosaccharide structure and structure-function relationships.
Adv Enzymol Relat Areas Mol Biol 1981;52:23-175
Hill RL, Beyer TA, Paulson JC, Prieels J-P, Rearick JI, Sadler JE Glycosyltransferases in oligosaccharide biosynthesis and their use in structure-function analysis of glycoproteins.
In: (IUPAC) Frontiers of Bioorganic Chemistry and Molecular Biology (S.N. Ananchenko, ed.) Pergamon Press, New York 1980; 63-71
Hill RL, Beyer TA, Rearick JI, Sadler JE, Prieels J-P, Paulson JC
Glycosyl transferases in glycoconjugate biosynthesis and their use in assessing oligosaccharide structure and function.
In: Glycoconjugates: Proceedings of the Fifth International Symposium, Kiel, Federal Republic of Germany, (R. Schauer, P. Boer, E. Buddecke, M.F. Kramer, J.F.G. Vliegenthart, and H. Wiegandt, eds) Georg Thieme Publishers, Stuttgart, September 1979; 274-275
Sadler JE, Rearick JI, Paulson JC, Hill RL
Purification of two sialyltransferase activities from porcine submaxillary glands.
In: Glycoconjugate Research Proceedings of the Fourth International Symposium on Glycoconjugates (J.D. Gregory and R.W. Jeanloz, eds) Academic Press, New York 1979; Vol. II: 763-766