References
- Raccuglia G. Gray platelet syndrome: a variety of qualitative platelet disorder. Am J Med 1971; 51: 818–28.
- White J G. Ultrastructural studies of the gray platelet syndrome. Am J Pathol 1971; 95: 445–54.
- Gerrard J M, Phillips D R, Rao G H, Plow E F, Walz D A, Ross R, Harker L A, White J G. Biochemical studies of two patients with the gray platelet syndrome. J Clin Invest 1980; 66(1): 102–9.
- Breton-Gorius J, Vainchenker W, Nurden A, Levy-Toledano S, Caen J. Defective a-granule production in megakaryocytes from gray platelet syndrome: ultrastructural studies of bone marrow cells and megakaryocytes growing in culture from bloodprecursors. Am J Pathol 1981; 102: 10–9.
- Cramer E M, Vainchenker W, Vinci G, Guichard J, Breton- Gorius J. Gray platelet syndrome: immunoelectron microscopic localization of fibrinogen and von Willebrand factor in platelets and megakaryocytes. Blood 1985; 66: 1309–16.
- Rosa J P, George J N, Bainton D F, Nurden A T, Caen J P, McEver R P. Gray platelet syndrome: demonstration of a-granule membranes that can fuse with the cell surface. J Clin Invest 1987; 80: 1138–46.
- Drouin A, Favier R M, Masse´ J M, Debili N, Schmitt A, Elbim C, Grichard J, Adam M, Gougerot-Pocidalo M A, Cramer M. Newly recognized cellular abnormalities in the gray platelet syndrome. Blood 2001; 98: 1382–91.
- Sengelov H, Kjeldsen L, Kroeze W, Berger M, Borregaard N. Secretory vesicles are the intracellular reservoir of complement receptor 1 in human neutrophils. J Immunol 1994; 153: 804–10.
- Borregaard N, Lollike K, Kjeldsen L, et al. Human neutrophil granules and secretory vesicles. Eur J Haematol 1993; 4: 187–98.
- Borregaard N, Cowland J B. Granules of the human neutrophilic polymorphonuclear leukocyte. Blood 1997; 89: 3503–21.
- Gregoire C, Welch H, Astarie-Dequeker C, Mari-donneau- Parini I. Expression of azurophil and specific granule proteins during differentiation of NB4 cells in neutrophils. J Cell Physiol 1998; 175: 203–10.
- Kaplow L S. Simplified myeloperoxidase stain using benzidine dihydrochloride. Blood 1965; 26: 215–9.
- Hayhoe F G J, Quaglina D. Cytochemical demonstra- tion and measurement of leukocyte alkaline phosphatase activity in normal and pathological states by a modified azo-dye coupling technique. Br J Haematol 1958; 4: 375–89.
- White J G. Interaction of membrane systems in blood platelets. Am J Pathol 1972; 66(2): 295–312.
- White J G. A simple method for preservation of fine struc- ture of blood cells. Thromb Diath Haemorrh 1967; 18(3–4): 745–53.
- White J G. The Chediak-Higashi syndrome: a possible lysosomal disease. Blood 1966; 28(2): 143–56.
- White J G. The morphology of platelet function. In: Harker L A, Zimmerman T S, eds. Methods in hematology, series 8L: measurements of platelet function. New York: Churchill- Livingstone, 1983; 1–25.
- Ganz T, Metcalf J A, Gallin J I, Boxer L A, Lehrer R I. Microbicidal/cytotoxic proteins of neutrophils are deficient in two disorders: Chediak-Higashi syndrome and ‘specific’ granule deficiency. J Clin Invest 1988; 82: 552–6.
- Mori K, Suzuki S, Sugai K. Electron microscope and functional studies on platelets in Gray Platelet Synrome. Tohoku J Exp Med 1984; 143: 261–87.
- White J G, Key N, King R, Vercellotti G. The White Platelet Syndrome. I. Structural defects. Blood 2003; 102–5.
- Hemmeler G. Thrombopathie familie. Schweiz Med Wschr1958; 88: 1018–9.
- Libanska J, Falcao L, Gautier A, Ammon J, Saphr A, Vainer H, Caen J P. Thrombocytope´ nie thrombocytopathique hypogranulaire he´ re´ ditaire. Nouv Rev Fr He´matol 1975; 15: 165–82.
- Kurstjens R, Bolt C, Vossen M, Haanen C. Familiar throm- bocytopathic thrombocytopenia. Br J Haematol 1968; 15: 305–17.