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Original Article

Platelet pathology in carriers of the X-linked GATA-1 macrothrombocytopenia

Pages 620-627 | Received 19 Aug 2007, Accepted 04 Sep 2007, Published online: 07 Jul 2009

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Dong Chen, Cindy B. Uhl, Sandra C. Bryant, Marcy Krumwiede, Ryan L. Barness, Mary C. Olson, Susan C. Gossman, Sibel Erdogan Damgard, Scott I. Gamb, Lisa A. Cummins, Jon E. Charlesworth, Christina M. Wood-Wentz, Jeffrey L. Salisbury, Elizabeth A. Plumhoff, Elizabeth M. Van Cott, Rong He, Deepti M. Warad, Rajiv K. Pruthi, John A. Heit, William L. Nichols & James G. White. (2018) Diagnostic laboratory standardization and validation of platelet transmission electron microscopy. Platelets 29:6, pages 574-582.
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James G. White, Kourosh Pakzad & Lynn Meister. (2013) The York platelet syndrome: A fourth case with unusual pathologic features. Platelets 24:1, pages 44-50.
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Etheresia Pretorius, Hester M. Oberholzer, Wendy J. van der Spuy & Johannes H. Meiring. (2009) Macrothrombocytopenia: Investigating the Ultrastructure of Platelets and Fibrin Networks Using Scanning and Transmission Electron Microscopy. Ultrastructural Pathology 33:5, pages 216-221.
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James G. White, Steven M. Burris & Brian R. Crowe. (2009) GATA-1, G208S macrothrombocytes are deficient in talin: Immunofluorescence studies. Platelets 20:3, pages 216-224.
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J. G. White & A. Thomas. (2009) Platelet structural pathology in a patient with the X-linked GATA-1, R216Q mutation. Platelets 20:1, pages 41-49.
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Articles from other publishers (8)

Kerstin Jurk, Anke Adenaeuer, Stefanie Sollfrank, Kathrin Groß, Friederike Häuser, Andreas Czwalinna, Josef Erkel, Nele Fritsch, Dana Marandiuc, Martin Schaller, Karl J. Lackner, Heidi Rossmann & Frauke Bergmann. (2022) Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant. Cells 11:19, pages 3071.
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Kenneth J. Clemetson. 2019. Molecular Hematology 4e. Molecular Hematology 4e 251 266 .
Roger Riley, Asad Khan, Shella Pai, Laura Warmke, Marcus Winkler & William Gunning. (2019) A Case of Chronic Thrombocytopenia in a 17-Year-Old Female. Laboratory Medicine 50:4, pages 406-420.
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Juliana Perez Botero, Deepti M. Warad, Rong He, Cindy B. Uhl, Shulan Tian, Gregory E. Otteson, Ryan L. Barness, Mary C. Olson, Susan C. Gossman, Jon E. Charlesworth, William L. Nichols, Rajiv K. Pruthi & Dong Chen. (2017) Comprehensive Platelet Phenotypic Laboratory Testing and Bleeding History Scoring for Diagnosis of Suspected Hereditary Platelet Disorders. American Journal of Clinical Pathology 148:1, pages 23-32.
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Caroline J. Magri, Alaide Chieffo, Alessandro Durante, Azeem Latib, Matteo Montorfano, Francesco Maisano, Michela Cioni, Eustachio Agricola, Remo Daniel Covello, Chiara Gerli, Annalisa Franco, Pietro Spagnolo, Ottavio Alfieri & Antonio Colombo. (2013) Impact of Mean Platelet Volume on Combined Safety Endpoint and Vascular and Bleeding Complications following Percutaneous Transfemoral Transcatheter Aortic Valve Implantation. BioMed Research International 2013, pages 1-8.
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Giovanni de Gaetano, Iolanda Santimone, Francesco Gianfagna, Licia Iacoviello & Chiara Cerletti. 2012. Antiplatelet Agents. Antiplatelet Agents 395 434 .
Kenneth J Clemetson. 2010. Molecular Hematology. Molecular Hematology 246 258 .
Wendy A. Ciovacco, Wendy H. Raskind & Melissa A. Kacena. (2008) Human phenotypes associated with GATA-1 mutations. Gene 427:1-2, pages 1-6.
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