Page 1316 - Hall et al (2015) Principles of Critical Care-McGraw-Hill
P. 1316
Chapter 91
REFERENCES
1. Moschcowitz E. Hyaline thrombosis of the terminal arterioles 15. Noris M, Mescia F, Remuzzi G. STEC-HUS, atypical HUS and
and capillaries: a hitherto undescribed disease. Proc N Y Pathol TTP are all diseases of complement activation. Nat Rev Nephrol.
Soc. 1924;24:21-24. 2012;8(11):622-633.
2. Amorosi EL, Ultmann JE. Thrombocytopic purpura: report 16. Zheng XL, Sadler JE. Pathogenesis of thrombotic microangiopa-
of 16 cases and review of the literature. Medicine (Baltimore). thies. Annu Rev Path Mech Dis. 2008;3:249-277.
1966;45:139-159. 17. Tsai HM. Current concepts in thrombotic thrombocytopenic
3. Schulman I, Pierce M, Lukens A, Currimbhoy Z. Studies on purpura. Annu Rev Med. 2006;57:419-436.
thrombopoiesis. I. A factor in normal human plasma required 18. Moake JL. Thrombotic microangiopathies. N Engl J Med.
for platelet production; chronic thrombocytopenia due to its 2002;347(8):589-600.
deficiency. Blood. 1960;16:943-957. 19. Fujimura Y, Matsumoto M, Yagi H, Yoshioka A, Matsui T,
4. Upshaw JD Jr. Congenital deficiency of a factor in normal Titani K. Von Willebrand factor-cleaving protease and Upshaw-
plasma that reverses microangiopathic hemolysis and thrombo- Schulman syndrome. Int J Hematol. 2002;75(1):25-34.
cytopenia. N Engl J Med. 1978;298(24):1350-1352. 20. Schultz DR, Arnold PI, Jy W, et al. Anti-CD36 autoantibodies in
5. Fujikawa K, Suzuki H, McMullen B, Chung D. Purification of thrombotic thrombocytopenic purpura and other thrombotic
human von Willebrand factor-cleaving protease and its identifi- disorders: identification of an 85 kD form of CD36 as a target
cation as a new member of the metalloproteinase family. Blood. antigen. Br J Haematol. 1998;103(3):849-857.
2001;98(6):1662-1666. 21. Fujimura Y, Matsumoto M. Registry of 919 patients with throm-
6. Gerritsen HE, Robles R, Lammle B, Furlan M. Partial amino botic microangiopathies across Japan: database of Nara Medical
acid sequence of purified von Willebrand factor-cleaving University during 1998-2008. Intern Med. 2010;49(1):7-15.
protease. Blood. 2001;98(6):1654-1661. 22. Furlan M, Lammle B. Deficiency of von Willebrand factor-
7. Levy GG, Nichols WC, Lian EC, et al. Mutations in a member of cleaving protease in familial and acquired thrombotic thrombo-
the ADAMTS gene family cause thrombotic thrombocytopenic cytopenic purpura. Baillieres Clin Haematol. 1998;11(2):509-514.
purpura. Nature. 2001;413(6855):488-494. 23. Fujimura Y, Matsumoto M, Kokame K, et al. Pregnancy-
8. Zheng XL, Chung D, Takayama T, Majerus E, Sadler J, Fujikawa K. induced thrombocytopenia and TTP, and the risk of fetal death,
Structure of von Willebrand factor-cleaving protease in Upshaw-Schulman syndrome: a series of 15 pregnancies in
(ADAMTS13), a metalloprotease involved in thrombotic throm- 9 genotyped patients. Br J Haematol. 2009;144(5):742-754.
bocytopenic purpura. J Biol Chem. 2001;276(44):41059-41063. 24. Kato R, Shinohara A, Sato J. ADAMTS13 deficiency, an impor-
9. Gasser C, Gautier E, Steck A, Siebenmann RE, Oechslin R. tant cause of thrombocytopenia during pregnancy. Int J Obstet
[Hemolytic-uremic syndrome: bilateral necrosis of the renal Anesth. 2009;18(1):73-77.
cortex in acute acquired hemolytic anemia]. Schweiz Med
Wochenschr. 1955;85(38-39):905-909. 25. Richter J, Strandberg K, Lindblom A, Strevens H, Karpman D,
Wide-Swensson D. Successful management of a planned pregnancy
10. Kaplan BS. Another step forward in our understanding of in severe congenital thrombotic thrombocytopaenic purpura: the
the hemolytic uremic syndromes: tieing up some loose ends. Upshaw-Schulman syndrome. Transfus Med. 2011;21(3):211-213.
Pediatr Nephrol. 1995;9(1):30-32. 26. Yagi H, Matsumoto M, Fujimura Y. Paradigm shift of child-
11. George JN. How I treat patients with thrombotic thrombocyto- hood thrombotic thrombocytopenic purpura with severe
penic purpura: 2010. Blood. 2010;116(20):4060-4069. ADAMTS13 deficiency. Presse Med. 2012;41(3, pt 2):e137-e155.
12. Kaplan BS, Chesney RW, Drummond KN. Hemolytic uremic 27. Furlan M, Lammle B. Aetiology and pathogenesis of thrombotic
syndrome in families. N Engl J Med. 1975;292(21):1090-1093. thrombocytopenic purpura and haemolytic uraemic syndrome:
13. Kavanagh D, Goodship TH. Atypical hemolytic uremic syn- the role of von Willebrand factor-cleaving protease. Best Pract
drome. Curr Opin Hematol. 2010;17(5):432-438. Res Clin Haematol. 2001;14(2):437-454.
14. Moake JL. Haemolytic-uraemic syndrome: basic science. Lancet. 28. Terrell DR, Williams LA, Vesely SK, Lammle B, Hovinga JA,
1994;343(8894):393-397. George JN. The incidence of thrombotic thrombocytopenic
Section07-O-ref.indd 1 1/21/2015 11:26:48 AM

