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Plenary Paper

Diagnostic laboratory standardization and validation of platelet transmission electron microscopy

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Pages 574-582 | Received 08 Feb 2018, Accepted 01 Apr 2018, Published online: 04 Jun 2018

References

  • Philipp CS, Dilley A, Miller CH, Evatt B, Baranwal A, Schwartz R, Bachmann G, Saidi P. Platelet functional defects in women with unexplained menorrhagia. J Thromb Haemost. 2003;1(3):477–484.
  • Quiroga T, Goycoolea M, Munoz B, Morales M, Aranda E, Panes O, Pereira J, Mezzano D. Template bleeding time and PFA-100 have low sensitivity to screen patients with hereditary mucocutaneous hemorrhages: comparative study in 148 patients. J Thromb Haemost. 2004;2(6):892–898.
  • Perez Botero J, Pruthi RK, Majerus JA, Coon LM, Uhl CB, Chen D, Patnaik MM. Practice patterns in the diagnosis of inherited platelet disorders within a single institution. Blood Coagul Fibrinolysis. 2017;28(4):303–308.
  • Nurden AT, Nurden P. Congenital platelet disorders and understanding of platelet function. Br J Haematol. 2014;165(2):165–178.
  • Gresele P, Harrison P, Bury L, Falcinelli E, Gachet C, Hayward CP, Kenny D, Mezzano D, Mumford AD, Nugent D and others. Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey. J Thromb Haemost. 2014;12(9):1562–1569.
  • De Robertis E. Electron microscope observations of the platelet-fibrin relationship in blood clotting. Blood. 1955;10(5):528–533.
  • White JG. Electron microscopy methods for studying platelet structure and function. Methods Mol Biol. 2004;272:47–63.
  • White JG. The dense bodies of human platelets. Origin of serotonin storage particles from platelet granules. Am J Pathol. 1968;53(5):791–808.
  • White JG. The dense bodies of human platelets: inherent electron opacity of the serotonin storage particles. Blood. 1969;33(4):598–606.
  • White JG. Giant electron-dense chains, clusters and granules in megakaryocytes and platelets with normal dense bodies: an inherited thrombocytopenic disorder. Platelets. 2003;14(2):109–121.
  • White JG. Electron-dense chains and clusters in platelets from patients with storage pool-deficiency disorders. J Thromb Haemost. 2003;1(1):74–79.
  • Bull BS. The ultrastructure of negatively stained platelets. Some physiologic implications. Blood. 1966;28(6):901–912.
  • Witkop CJ, Krumwiede M, Sedano H, White JG. Reliability of absent platelet dense bodies as a diagnostic criterion for Hermansky–Pudlak syndrome. Am J Hematol. 1987;26(4):305–311.
  • White JG, Keel S, Reyes M, Burris SM. Alpha-delta platelet storage pool deficiency in three generations. Platelets. 2007;18(1):1–10.
  • Ferreira CR, Chen D, Abraham SM, Adams DR, Simon KL, Malicdan MC, Markello TC, Gunay-Aygun M, Gahl WA. Combined alpha-delta platelet storage pool deficiency is associated with mutations in GFI1B. Mol Genet Metab. 2017;120(3):288–294.
  • White JG. Platelet storage pool deficiency in Jacobsen syndrome. Platelets. 2007;18(7):522–527.
  • Grottum KA, Hovig T, Holmsen H, Abrahamsen AF, Jeremic M, Seip M. Wiskott–Aldrich syndrome: qualitative platelet defects and short platelet survival. Br J Haematol. 1969;17(4):373–388.
  • Day HJ, Holmsen H. Platelet adenine nucleotide “storage pool deficiency” in thrombocytopenic absent radii syndrome. Jama. 1972;221(9):1053–1054.
  • Page AR, Berendes H, Warner J, Good RA. The Chediak–Higashi syndrome. Blood. 1962;20:330–343.
  • Hamilton RW, Shaikh BS, Ottie JN, Storch AE, Saleem A, White JG. Platelet function, ultrastructure, and survival in the May-Hegglin anomaly. Am J Clin Pathol. 1980;74(5):663–668.
  • White JG. Platelet microtubules and giant granules in the Chediak–Higashi syndrome. Am J Med Technol. 1978;44(4):273–278.
  • Christie DJ, Avari T, Carrington LR, Cohen E, DeBiase BA, Harrison P, Kickler TS, Kottke-Marchant K, Ledford-Kraemer M, Rand ML, Schmaier AH, McCabe White M. Plate-let Function Testing by Aggregometry; Approved Guideline. Wayne, PA: Clinical and Laboratory Standards Institute; 2008;28:1–45.
  • Koenker R, Hallock K. Quantile regression. J Econ Perspect. 2001;15(4):143–156.
  • Weiss HJ, Ames RP. Ultrastructural findings in storage pool disease and aspirin-like defects of platelets. Am J Pathol. 1973;71(3):447–466.
  • Israels SJ, McNicol A, Robertson C, Gerrard JM. Platelet storage pool deficiency: diagnosis in patients with prolonged bleeding times and normal platelet aggregation. Br J Haematol. 1990;75(1):118–121.
  • White JG. Electron opaque structures in human platelets: which are or are not dense bodies? Platelets. 2008;19(6):455–466.
  • White JG. Effects of ethylenediamine tetracetic acid (EDTA) on platelet structure. Scand J Haematol. 1968;5(4):241–254.
  • Markello T, Chen D, Kwan JY, Horkayne-Szakaly I, Morrison A, Simakova O, Maric I, Lozier J, Cullinane AR, Kilo T and others. York platelet syndrome is a CRAC channelopathy due to gain-of-function mutations in STIM1. Mol Genet Metab. 2015;114(3):474–482.
  • White JG. Use of the electron microscope for diagnosis of platelet disorders. Semin Thromb Hemost. 1998;24(2):163–168.
  • Hayward CP, Moffat KA, Plumhoff E, Timleck M, Hoffman S, Spitzer E, Van Cott EM, Meijer P. External quality assessment of platelet disorder investigations: results of international surveys on diagnostic tests for dense granule deficiency and platelet aggregometry interpretation. Semin Thromb Hemost. 2012;38(6):622–631.
  • Ingerman CM, Smith JB, Shapiro S, Sedar A, Silver MJ. Hereditary abnormality of platelet aggregation attributable to nucleotide storage pool deficiency. Blood. 1978;52(2):332–344.
  • Weiss HJ, Lages B, Vicic W, Tsung LY, White JG. Heterogeneous abnormalities of platelet dense granule ultrastructure in 20 patients with congenital storage pool deficiency. Br J Haematol. 1993;83(2):282–295.
  • Sorokin V, Alkhoury R, Al-Rawabdeh S, Houston RH, Thornton D, Kerlin B, O’Brien S, Baker P, Boesel C, Uddin M and others. Reference range of platelet delta granules in the pediatric age group: an ultrastructural study of platelet whole mount preparations from healthy volunteers. Pediatr Dev Pathol. 2016;19(6):498–501.
  • Zarzour W, Kleta R, Frangoul H, Suwannarat P, Jeong A, Kim SY, Wayne AS, Gunay-Aygun M, White J. Filipovich AH and others. Two novel CHS1 (LYST) mutations: clinical correlations in an infant with Chediak–Higashi syndrome. Mol Genet Metab. 2005;85(2):125–132.
  • Paulus JM. Platelet size in man. Blood. 1975;46(3):321–336.
  • White JG, de Alarcon PA. Platelet spherocytosis: a new bleeding disorder. Am J Hematol. 2002;70(2):158–166.
  • White JG, Clawson CC. Development of giant granules in platelets during prolonged storage. Am J Pathol. 1980;101(3):635–646.
  • White JG, Key NS, King RA, Vercellotti GM. The White platelet syndrome: a new autosomal dominant platelet disorder. Platelets. 2004;15(3):173–184.
  • White JG. Medich giant platelet disorder: a unique alpha granule deficiency I. Structural abnormalities. Platelets. 2004;15(6):345–353.
  • White JG. Platelet pathology in carriers of the X-linked GATA-1 macrothrombocytopenia. Platelets. 2007;18(8):620–627.
  • Lev EI. Immature platelets: clinical relevance and research perspectives. Circulation. 2016;134(14):987–988.

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