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2072           Part XII:  Hemostasis and Thrombosis                                                                                                                                                         <CN>:  <ct>             PB




                 560. Favier R, Jondeau K, Boutard P, et al: Paris-Trousseau syndrome: Clinical, hematologi-    588. Kobrinsky NL, Israels ED, Gerrard JM, et al: Shortening of bleeding time by 1-deamino-
                  cal, molecular data of ten new cases. Thromb Haemost 90:893–897, 2003.  8-d-arginine vasopressin in various bleeding disorders. Lancet 1:1145–1148, 1984.
                 561. Raslova H, Komura E, Le Couedic JP, et al: FLI1 monoallelic expression combined with     589. Schulman S, Johnson H, Egberg N, Blombäck M: DDAVP-induced correction of pro-
                  its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia.  J Clin Invest   longed bleeding time in patients with congenital platelet function defects. Thromb Res
                  114:77–84, 2004.                                       45:165–174, 1987.
                 562. Shivdasani RA: Lonely in Paris: When one gene copy isn’t enough. J Clin Invest 114:     590. DiMichele DM, Hathaway WE: Use of DDAVP in inherited and acquired platelet
                  17–19, 2004.                                           dysfunction. Am J Hematol 33:39–45, 1990.
                 563. Kurstjens R, Bolt C, Vossen M, Haanen C: Familial thrombopathic thrombocytopenia.     591. Nieuwenhuis HK, Sixma JJ: 1-Desamino-8-d-arginine vasopressin (Desmopressin)
                  Br J Haematol 15:305–317, 1968.                        shortens the bleeding time in storage pool deficiency. Ann Intern Med 108:65–67, 1988.
                 564. Estes JW: Platelet abnormalities in heritable disorders of connective tissue. Ann N Y     592. Colucci G, Stutz M, Rochat S, et al: The effect of desmopressin on platelet function: A
                  Acad Sci 201:445–450, 1972.                            selective enhancement of procoagulant COAT platelets in patients with primary plate-
                 565. Evensen SA, Myhre L, Stormorken H: Haemostatic studies in osteogenesis imperfecta.   let function defects. Blood 123:1905–1916, 2014.
                  Scand J Haematol 33:177–179, 1984.                    593. Almeida AM, Khair K, Hann  I, Liesner R:  The use  of recombinant  factor VIIa in
                 566. Akkerman JWN, Rijksen G, Gorter G, al e. Platelet functions and energy metabolism in   children with inherited platelet function disorders. Br J Haematol 121:477–481, 2003.
                  a patient with hexokinase deficiency. Blood 63:147–153, 1984.    594. Poon  MC,  d’Oiron  R.  Recombinant  activated  factor  VII  (NovoSeven)  treatment  of
                 567. Corby DG, Putnam CW, Greene HL: Impaired platelet function in glucose-   platelet-related bleeding disorders. International Registry on Recombinant Factor
                  6-phosphatase deficiency. J Pediatr 85:71–76, 1974.    VIIa and Congenital Platelet Disorders Group. Blood Coagul Fibrinolysis 11 (Suppl 1:)
                 568. Czapek EE, Deykin D, Salzman EW: Platelet dysfunction in glycogen storage disease   S55–S68, 2000.
                  type I. Blood 41:235–247, 1973.                       595. Poon MC, Demers C, Jobin F, Wu JW: Recombinant factor VIIa is effective for bleed-
                 569. Boullin DJ, O’Brien RA. Abnormalities of 5-hydroxytryptamine uptake and binding by   ing and surgery in patients with Glanzmann thrombasthenia. Blood 94:3951–3953,
                  blood platelets from children with Down’s syndrome. J Physiol 212:287–297, 1971.  1999.
                 570. Lott IT, Chase TN, Murphy DL: Down’s syndrome: Transport, storage, and metabolism     596. del Pozo Pozo AI, Jimenez-Yuste V, Villar A, et al: Successful thyroidectomy in a patient
                  of serotonin in blood platelets. Pediatr Res 6:730–735, 1972.  with Hermansky-Pudlak syndrome treated with recombinant activated factor VII and
                 571. McCoy EE, Sneddon JM: Decreased calcium content and 45Ca2+ uptake in Down’s   platelet concentrates. Blood Coagul Fibrinolysis 13:551–553, 2002.
                  syndrome blood platelets. Pediatr Res 18:914–916, 1984.    597. Sindet-Pedersen S, Ramstrom G, Bernvil S, Blomback M: Hemostatic effect of tranex-
                 572. More R, Amir N, Meyer S, et al: Platelet abnormalities in Down’s syndrome. Clin Genet   amic acid mouthwash in anticoagulant-treated patients undergoing oral surgery. N Engl
                  22:128–136, 1982.                                      J Med 320:840–843, 1989.
                 573. Sheppard JR, Schumacher W, White JG, et al: The alpha adrenergic response of Down’s     598. Mielke CH Jr, Levine PH, Zucker S: Preoperative prednisone therapy in platelet func-
                  syndrome platelets. J Pharmacol Exp Ther 225:584–588, 1983.  tion disorders. Thromb Res 21:655–662, 1981.
                 574. Hamilton RW, Shaikh BS, Ottie JN, et al: Platelet function, ultrastructure, and survival     599. Spotnitz WD, Burks S: Hemostats, sealants, and adhesives: Components of the surgical
                  in the May-Hegglin anomaly. Am J Clin Pathol 74:663–668, 1980.  toolbox. Transfusion 48:1502–1516, 2008.
                 575. Lusher JM, Schneider J, Mizukami I, et al: The May-Hegglin anomaly: Platelet function,     600. Chuansumrit A, Suwannuraks M, Sri-Udomporn N, et al: Recombinant activated
                  ultrastructure and chromosome studies. Blood 32:950–961, 1968.  factor VII combined with local measures in preventing bleeding from invasive dental
                 576. Coller BS, Zarrabi MH: Platelet membrane studies in the May-Hegglin anomaly. Blood   procedures in patients with Glanzmann thrombasthenia. Blood Coagul Fibrinolysis 14:
                  58:279–284, 1981.                                      187–190, 2003.
                 577. Freson K, Hashimoto H, Thys C, et al: The pituitary adenylate cyclase-activating poly-    601. Singla NK, Foster KN, Alexander WA, Pribble JP: Safety and immunogenicity
                  peptide is a physiological inhibitor of platelet activation. J Clin Invest 113:905–912,   of recombinant human thrombin: A pooled analysis of results from 10 clinical trials.
                  2004.                                                  Pharmacotherapy 32:998–1005, 2012.
                 578. Sandrock K, Nakamura L, Vraetz T, et al: Platelet secretion defect in patients with     602. Wilcox DA, Olsen JC, Ishizawa L, et al: Integrin alphaIIb promoter-targeted expres-
                  familial hemophagocytic lymphohistiocytosis type 5 (FHL-5). Blood 116:6148–6150,   sion of gene products in megakaryocytes derived from retrovirus-transduced human
                  2010.                                                  hematopoietic cells. Proc Natl Acad Sci U S A 96:9654–9659, 1999.
                 579. Al Hawas R, Ren Q, Ye S, et al: Munc18b/STXBP2 is required for platelet secretion.     603. Wilcox  DA,  White  GC  2nd:  Gene  therapy  for  platelet  disorders:  Studies  with
                  Blood 120:2493–2500, 2012.                             Glanzmann’s thrombasthenia. J Thromb Haemost 1:2300–2311, 2003.
                 580. Ye S, Karim ZA, Al Hawas R, et al: Syntaxin-11, but not syntaxin-2 or syntaxin-4, is     604. Fang J, Jensen ES, Boudreaux MK, et al: Platelet gene therapy improves hemostatic
                  required for platelet secretion. Blood 120:2484–2492, 2012.  function for integrin alphaIIbbeta3-deficient dogs.  Proc Natl Acad Sci U S A 108:
                 581. Alamelu J, Liesner R: Modern management of severe platelet function disorders. Br     9583–9588, 2011.
                  J Haematol 149:813–823, 2010.                         605. Hodivala-Dilke KM, Tsakiris DA, Rayburn H, et al: Beta3-integrin-deficient mice are a
                 582. Seligsohn U: Treatment of inherited platelet disorders.  Haemophilia 18 (Suppl 4:)   model for Glanzmann thrombasthenia showing placental defects and reduced survival.
                  161–165, 2012.                                         J Clin Invest 103:229–238, 1999.
                 583. Bolton-Maggs PH, Chalmers EA, Collins PW, et al: A review of inherited platelet disor-    606. Boudreaux MK, Lipscomb DL: Clinical, biochemical, and molecular aspects of
                  ders with guidelines for their management on behalf of the UKHCDO. Br J Haematol   Glanzmann’s thrombasthenia in humans and dogs. Vet Pathol 38:249–260, 2001.
                  135:603–633, 2006.                                    607. Niemeyer GP, Boudreaux MK, Goodman-Martin SA, et al: Correction of a large
                 584. Fiore M, Firah N, Pillois X, et al: Natural history of platelet antibody formation against   animal model of type I Glanzmann’s thrombasthenia by nonmyeloablative bone marrow
                  alphaIIbbeta3 in a French cohort of Glanzmann thrombasthenia patients. Haemophilia   transplantation. Exp Hematol 31:1357–1362, 2003.
                  18:e201–9, 2012.                                      608. Schlosser RJ: Clinical practice. Epistaxis. N Engl J Med 360:784–789, 2009.
                 585. Mannucci PM: Desmopressin (DDAVP) in the treatment of bleeding disorders: The     609. Siddiq S, Clark A, Mumford A: A systematic review of the management and outcomes
                  first 20 years. Blood 90:2515–2521, 1997.              of pregnancy in Glanzmann thrombasthenia. Haemophilia 17:e858–e869, 2011.
                 586. Mannucci PM: Hemostatic Drugs. N Engl J Med 339:245–253, 1998.    610. Peitsidis P, Datta T, Pafilis I, et al: Bernard Soulier syndrome in pregnancy: A systematic
                 587. Rao AK, Ghosh S, Sun L, et al: Effect of mechanism of platelet dysfunction on response   review. Haemophilia 16:584–591, 2010.
                  to  DDAVP  in  patients  with  congenital  platelet  function  defects.  A  double-blind      611. Coller BS: Inherited disorders of platelet function, in  Hemostasis and Thrombosis,
                  placebo-controlled trial. Thromb Haemost 74:1071–1078, 1995.  edited by AL Bloom, p. 721–766. Churchill Livingstone, Edinburgh, 1992.



























          Kaushansky_chapter 120_p2039-2072.indd   2072                                                                 9/21/15   2:22 PM
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