Journal articles on the topic 'Gray platelet syndrome'
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Wills, E. J. "Gray Platelet Syndrome." Ultrastructural Pathology 13, no. 4 (January 1989): 451–55. http://dx.doi.org/10.3109/01913128909048495.
Michelson, Alan D. "Gray platelet syndrome." Blood 121, no. 2 (January 10, 2013): 250. http://dx.doi.org/10.1182/blood-2012-09-455550.
Bain, Barbara J., and Manju Bhavnani. "Gray platelet syndrome." American Journal of Hematology 86, no. 12 (July 28, 2011): 1027. http://dx.doi.org/10.1002/ajh.22055.
Rosa, Jean-Philippe. "The gray platelet syndrome." Sang thrombose vaisseaux 26, no. 5 (September 2014): 240–54. http://dx.doi.org/10.1684/stv.2014.0854.
Rosa, Jean-Philippe. "The gray platelet syndrome." Hématologie 19, no. 2 (March 2013): 123–35. http://dx.doi.org/10.1684/hma.2013.0793.
Baruch, Dominique, Theo Lindhout, Evelyne Dupuy, and Jacques P. Caen. "Thrombin-Induced Platelet Factor Va Formation in Patients with a Gray Platelet Syndrome." Thrombosis and Haemostasis 58, no. 02 (1987): 768–71. http://dx.doi.org/10.1055/s-0038-1645967.
Tubman, Venée N., Jason E. Levine, Dean R. Campagna, Rita Monahan-Earley, Ann M. Dvorak, Ellis J. Neufeld, and Mark D. Fleming. "X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation." Blood 109, no. 8 (January 5, 2007): 3297–99. http://dx.doi.org/10.1182/blood-2006-02-004101.
Köhler, Michael. "Treatment of Gray Platelet Syndrome." Thrombosis and Haemostasis 60, no. 01 (1988): 123. http://dx.doi.org/10.1055/s-0038-1647649.
Nurden, Paquita, Martine Jandrot-Perrus, Robert Combrié, Joelle Winckler, Veronique Arocas, Christelle Lecut, Jean-Max Pasquet, Thomas J. Kunicki, and Alan T. Nurden. "Severe deficiency of glycoprotein VI in a patient with gray platelet syndrome." Blood 104, no. 1 (July 1, 2004): 107–14. http://dx.doi.org/10.1182/blood-2003-11-3842.
Rao, A. Koneti, and Deepak A. Rao. "Gray platelet syndrome: immunity goes awry." Blood 136, no. 17 (October 22, 2020): 1898–900. http://dx.doi.org/10.1182/blood.2020008196.
Tyagi, Seema, and Renu Saxena. "Gray Platelet Syndrome Presenting As Menorrhagia." International Journal of Hematology 77, no. 2 (February 2003): 201–2. http://dx.doi.org/10.1007/bf02983224.
Mues, Gabriele, Frank H. Wians, and Steven H. Kroft. "EDTA-Induced Pseudo–Gray Platelet Syndrome." Laboratory Medicine 32, no. 7 (July 1, 2001): 361–64. http://dx.doi.org/10.1309/7vbg-ym6h-am90-vnqt.
White, James G., and Richard D. Brunning. "Neutrophils in the gray platelet syndrome." Platelets 15, no. 5 (August 2004): 333–40. http://dx.doi.org/10.1080/09537100410001714872.
Berrebi, Alain, Abraham Klepfish, David Varon, Mordechai Shtalrid, Eliakim Vorst, Emanuel Nir, and Judith Lahav. "Gray platelet syndrome in the elderly." American Journal of Hematology 28, no. 4 (August 1988): 270–72. http://dx.doi.org/10.1002/ajh.2830280411.
Obydennyi, S. I., I. I. Kireev, and M. A. Panteleev. "The electron microscopy contribution to platelet structural pathology investigation." Pediatric Hematology/Oncology and Immunopathology 21, no. 3 (October 15, 2022): 142–46. http://dx.doi.org/10.24287/1726-1708-2022-21-3-142-146.
Drouin, Arnaud, Rémi Favier, Jean-Marc Massé, Najet Debili, Alain Schmitt, Carole Elbim, Josette Guichard, Mircea Adam, Marie-Anne Gougerot-Pocidalo, and Elisabeth M. Cramer. "Newly recognized cellular abnormalities in the gray platelet syndrome." Blood 98, no. 5 (September 1, 2001): 1382–91. http://dx.doi.org/10.1182/blood.v98.5.1382.
Van der Reijden, Bert A., Davide Monteferrario, Nikhita Bolar, Anna Marneth, Konnie Hebeda, Saskia Bergevoet, Hans Veenstra, et al. "A Dominant-Negative GFI1B Mutation in Gray Platelet Syndrome." Blood 122, no. 21 (November 15, 2013): LBA—3—LBA—3. http://dx.doi.org/10.1182/blood.v122.21.lba-3.lba-3.
Rensing-Ehl, Anne, Ulrich Pannicke, Stefanie-Yvonne Zimmermann, Myriam Ricarda Lorenz, Benedicte Neven, Ilka Fuchs, Ulrich Salzer, et al. "Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome." Blood 126, no. 16 (October 15, 2015): 1967–69. http://dx.doi.org/10.1182/blood-2015-06-654145.
Di Paola, Jorge. "Novel Congenital Platelet Disorders." Blood 128, no. 22 (December 2, 2016): SCI—39—SCI—39. http://dx.doi.org/10.1182/blood.v128.22.sci-39.sci-39.
MORI, KAZUO, SOZO SUZUKI, KOJI SUGAI, YASUYUKI AKUTSU, MASAAKI ISHIKAWA, and HIDEAKI SAKAI. "Morphological changes of platelets during the process of platelet aggregation in gray platelet syndrome." Tohoku Journal of Experimental Medicine 149, no. 4 (1986): 425–36. http://dx.doi.org/10.1620/tjem.149.425.
Aminkeng, F. "GFI1Bmutation causes autosomal dominant gray platelet syndrome." Clinical Genetics 85, no. 6 (April 9, 2014): 534–35. http://dx.doi.org/10.1111/cge.12380.
Di Paola, Jorge, and Jan Johnson. "Thrombocytopenias Due to Gray Platelet Syndrome orTHC2Mutations." Seminars in Thrombosis and Hemostasis 37, no. 06 (September 2011): 690–97. http://dx.doi.org/10.1055/s-0031-1291379.
White, James G., Asish Kumar, and Marjorie J. Hogan. "Gray Platelet Syndrome in a Somalian family." Platelets 17, no. 8 (January 2006): 519–27. http://dx.doi.org/10.1080/09537100600758636.
Monteferrario, Davide, Nikhita A. Bolar, Anna E. Marneth, Konnie M. Hebeda, Saskia M. Bergevoet, Hans Veenstra, Britta A. P. Laros-van Gorkom, et al. "A Dominant-NegativeGFI1BMutation in the Gray Platelet Syndrome." New England Journal of Medicine 370, no. 3 (January 16, 2014): 245–53. http://dx.doi.org/10.1056/nejmoa1308130.
Ido, Kentaro, Takahiko Nakane, Nao Tanizawa, Yosuke Makuuchi, Hiroshi Okamura, Shiro Koh, Satoru Nanno, et al. "Acquired Gray Platelet Syndrome Associated with Primary Myelofibrosis." Internal Medicine 59, no. 21 (November 1, 2020): 2751–56. http://dx.doi.org/10.2169/internalmedicine.4912-20.
McGinnis, Eric, and Kate M. Chipperfield. "Striking emperipolesis in megakaryocytes of gray platelet syndrome." Blood 133, no. 26 (June 27, 2019): 2809. http://dx.doi.org/10.1182/blood.2019000494.
Kahr, Walter H. A., and Yigal Dror. "Gray platelet syndrome: macrothrombocytopenia with deficient α-granules." Blood 120, no. 13 (September 27, 2012): 2543. http://dx.doi.org/10.1182/blood-2012-03-415778.
Tubman, Venée N., Jason E. Levine, Dean R. Campagna, Mark D. Fleming, and Ellis J. Neufeld. "X-Linked Gray Platelet Syndrome Due to a GATA1 Arg216Gln Mutation." Blood 106, no. 11 (November 16, 2005): 5. http://dx.doi.org/10.1182/blood.v106.11.5.5.
Perez-Pujol, Silvia, Lorraine B. Anderson, Michael B. Martinez, LeeAnn Higgins, James G. White, Gary L. Nelsestuen, and Nigel S. Key. "Proteomic Analysis of Gray Platelet Syndrome by iTRAQ Labelling and Mass Spectroscopy: A Potential New Diagnostic Strategy for Platelet Disorders." Blood 106, no. 11 (November 16, 2005): 2161. http://dx.doi.org/10.1182/blood.v106.11.2161.2161.
Sims, Matthew C., Louisa Mayer, Janine H. Collins, Tadbir K. Bariana, Karyn Megy, Cecile Lavenu-Bombled, Denis Seyres, et al. "Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome." Blood 136, no. 17 (October 22, 2020): 1956–67. http://dx.doi.org/10.1182/blood.2019004776.
Gootenberg, Joseph E., George R. Buchanan, Christine A. Holtkamp, and Catherine S. Casey. "Severe hemorrhage in a patient with gray platelet syndrome." Journal of Pediatrics 109, no. 6 (December 1986): 1017–19. http://dx.doi.org/10.1016/s0022-3476(86)80289-x.
Nurden, Alan T., and Paquita Nurden. "The gray platelet syndrome: Clinical spectrum of the disease." Blood Reviews 21, no. 1 (January 2007): 21–36. http://dx.doi.org/10.1016/j.blre.2005.12.003.
Bottega, Roberta, Elena Nicchia, Caterina Alfano, Ana C. Glembotsky, Annalisa Pastore, Debora Bertaggia-Calderara, Bettina Bisig, et al. "Gray platelet syndrome: Novel mutations of the NBEAL2 gene." American Journal of Hematology 92, no. 2 (January 17, 2017): E20—E22. http://dx.doi.org/10.1002/ajh.24610.
Riley, Roger, Asad Khan, Shella Pai, Laura Warmke, Marcus Winkler, and William Gunning. "A Case of Chronic Thrombocytopenia in a 17-Year-Old Female." Laboratory Medicine 50, no. 4 (June 22, 2019): 406–20. http://dx.doi.org/10.1093/labmed/lmz013.
Breton-Gorius, J., P. Clezardin, J. Guichard, N. Debili, L. Malaval, W. Vainchenker, EM Cramer, and PD Delmas. "Localization of platelet osteonectin at the internal face of the alpha- granule membranes in platelets and megakaryocytes." Blood 79, no. 4 (February 15, 1992): 936–41. http://dx.doi.org/10.1182/blood.v79.4.936.936.
Breton-Gorius, J., P. Clezardin, J. Guichard, N. Debili, L. Malaval, W. Vainchenker, EM Cramer, and PD Delmas. "Localization of platelet osteonectin at the internal face of the alpha- granule membranes in platelets and megakaryocytes." Blood 79, no. 4 (February 15, 1992): 936–41. http://dx.doi.org/10.1182/blood.v79.4.936.bloodjournal794936.
Aarts, Cathelijn E. M., Kate Downes, Arie J. Hoogendijk, Evelien G. G. Sprenkeler, Roel P. Gazendam, Rémi Favier, Marie Favier, et al. "Neutrophil specific granule and NETosis defects in gray platelet syndrome." Blood Advances 5, no. 2 (January 25, 2021): 549–64. http://dx.doi.org/10.1182/bloodadvances.2020002442.
Larocca, Luigi M., Paula G. Heller, Gianmarco Podda, Nuria Pujol-Moix, Ana C. Glembotsky, Alessandro Pecci, Maria Adele Alberelli, et al. "Megakaryocytic emperipolesis and platelet function abnormalities in five patients with gray platelet syndrome." Platelets 26, no. 8 (March 25, 2015): 751–57. http://dx.doi.org/10.3109/09537104.2014.994093.
K�hler, M., P. Hellstern, E. Morgenstern, C. Mueller-Eckhardt, R. Berberich, R. J. Meiser, P. Scheffler, and E. Wenzel. "Gray platelet syndrome: Selective ?-granule deficiency and thrombocytopenia due to increased platelet turnover." Blut 50, no. 6 (June 1985): 331–40. http://dx.doi.org/10.1007/bf00320926.
Gunay-Aygun, Meral, Yifat Zivony-Elboum, Fatma Gumruk, Dan Geiger, Mualla Cetin, Morad Khayat, Robert Kleta, et al. "Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p." Blood 116, no. 23 (December 2, 2010): 4990–5001. http://dx.doi.org/10.1182/blood-2010-05-286534.
Kasthuri, Raj S., Lorraine B. Anderson, LeeAnn Higgins, Jorge Di Paola, Georges E. Rivard, Catherine P. M. Hayward, and Nigel S. Key. "Proteomics in the Study of Qualitative Platelet Defects: Validation of the Approach in the Gray Platelet Syndrome and Quebec Platelet Disorder." Blood 110, no. 11 (November 16, 2007): 3900. http://dx.doi.org/10.1182/blood.v110.11.3900.3900.
Pfueller, Sharron L., Margaret A. Howard, James G. White, Chandrasekhara Menon, and Elizabeth W. Berry. "Shortening of Bleeding Time by 1-Deamino-8-Arginine Vasopressin (DDAVP) in the Absence of Platelet von Willebrand Factor in Gray Platelet Syndrome." Thrombosis and Haemostasis 58, no. 04 (1987): 1060–63. http://dx.doi.org/10.1055/s-0038-1646056.
Cramer, EM, W. Vainchenker, G. Vinci, J. Guichard, and J. Breton-Gorius. "Gray platelet syndrome: immunoelectron microscopic localization of fibrinogen and von Willebrand factor in platelets and megakaryocytes." Blood 66, no. 6 (December 1, 1985): 1309–16. http://dx.doi.org/10.1182/blood.v66.6.1309.1309.
Cramer, EM, W. Vainchenker, G. Vinci, J. Guichard, and J. Breton-Gorius. "Gray platelet syndrome: immunoelectron microscopic localization of fibrinogen and von Willebrand factor in platelets and megakaryocytes." Blood 66, no. 6 (December 1, 1985): 1309–16. http://dx.doi.org/10.1182/blood.v66.6.1309.bloodjournal6661309.
Yoo, Jaeeun, Yonggoo Kim, and Kyungja Han. "Pseudo gray platelet syndrome: the first case report in Korea." Blood Research 50, no. 2 (2015): 117. http://dx.doi.org/10.5045/br.2015.50.2.117.
Deppermann, Carsten, Paquita Nurden, Alan T. Nurden, Bernhard Nieswandt, and David Stegner. "TheNbeal2−/−mouse as a model for the gray platelet syndrome." Rare Diseases 1, no. 1 (January 2013): e26561. http://dx.doi.org/10.4161/rdis.26561.
Pluthero, Fred G., Jorge Di Paola, Manuel D. Carcao, and Walter H. A. Kahr. "NBEAL2 mutations and bleeding in patients with gray platelet syndrome." Platelets 29, no. 6 (June 5, 2018): 632–35. http://dx.doi.org/10.1080/09537104.2018.1478405.
Berger, G., JM Masse, and EM Cramer. "Alpha-granule membrane mirrors the platelet plasma membrane and contains the glycoproteins Ib, IX, and V." Blood 87, no. 4 (February 15, 1996): 1385–95. http://dx.doi.org/10.1182/blood.v87.4.1385.bloodjournal8741385.
Boulaftali, Yacine, Frédéric Adam, Laurence Venisse, Véronique Ollivier, Benjamin Richard, Sabrina Taieb, Denis Monard, et al. "Anticoagulant and antithrombotic properties of platelet protease nexin-1." Blood 115, no. 1 (January 7, 2010): 97–106. http://dx.doi.org/10.1182/blood-2009-04-217240.
Wang, Yuhuan, Ronghua Meng, Vincent Hayes, Rudy Fuentes, Xiang Yu, Charles S. Abrams, Harry F. G. Heijnen, Gerd A. Blobel, Michael S. Marks, and Mortimer Poncz. "Pleiotropic platelet defects in mice with disrupted FOG1-NuRD interaction." Blood 118, no. 23 (December 1, 2011): 6183–91. http://dx.doi.org/10.1182/blood-2011-06-363580.