Citations (13)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (4)
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.
Read now
Read now
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.
Read now
Read now
James G. White, Nigel S. Key, Richard A. King & Gregory M. Vercellotti. (2004) The White platelet syndrome: a new autosomal dominant platelet disorderI. Structural abnormalities. Platelets 15:3, pages 173-184.
Read now
Read now
James G. White & Gilbert G. Ahlstrand. (2003) Giant electron dense chains, clusters and granules in megakaryocytes and platelets with normal dense bodies: an inherited thrombocytopenic disorder IV. Ultrastructural cytochemistry and analytical electron microscopy. Platelets 14:5, pages 313-324.
Read now
Read now
Articles from other publishers (9)
Alejandro Berna-Erro, Jose Sanchez-Collado, Joel Nieto-Felipe, Alvaro Macias-Diaz, Pedro C. Redondo, Tarik Smani, Jose J. Lopez, Isaac Jardin & Juan A. Rosado. (2023) The Ca2+ Sensor STIM in Human Diseases. Biomolecules 13:9, pages 1284.
Crossref
Crossref
Johann Böhm & Jocelyn Laporte. (2018) Gain-of-function mutations in STIM1 and ORAI1 causing tubular aggregate myopathy and Stormorken syndrome. Cell Calcium 76, pages 1-9.
Crossref
Crossref
Johann Böhm & Jocelyn Laporte. (2018) La myopathie à agrégats tubulaires et le syndrome de Stormorken. médecine/sciences 34, pages 26-31.
Crossref
Crossref
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.
Crossref
Crossref
Juliana Perez Botero, Rajiv K. Pruthi, Julie A. Majerus, Lea M. Coon, Cindy B. Uhl, Dong Chen & Mrinal M. Patnaik. (2017) Practice patterns in the diagnosis of inherited platelet disorders within a single institution. Blood Coagulation & Fibrinolysis 28:4, pages 303-308.
Crossref
Crossref
Rodrigo S. Lacruz & Stefan Feske. (2015)
Diseases caused by mutations in
ORAI1
and
STIM1
. Annals of the New York Academy of Sciences 1356:1, pages 45-79.
Crossref
Crossref
Thomas Markello, Dong Chen, Justin Y. Kwan, Iren Horkayne-Szakaly, Alan Morrison, Olga Simakova, Irina Maric, Jay Lozier, Andrew R. Cullinane, Tatjana Kilo, Lynn Meister, Kourosh Pakzad, William Bone, Sanjay Chainani, Elizabeth Lee, Amanda Links, Cornelius Boerkoel, Roxanne Fischer, Camilo Toro, James G. White, William A. Gahl & Meral Gunay-Aygun. (2015) York platelet syndrome is a CRAC channelopathy due to gain-of-function mutations in STIM1. Molecular Genetics and Metabolism 114:3, pages 474-482.
Crossref
Crossref
James G. White & Meral Gunay-Aygun. (2011) The York Platelet Syndrome: A third case. Platelets, pages 117-134.
Crossref
Crossref
Hezder van Nispen tot PannerdenFelix de HaasWillie Geerts, George PosthumaSuzanne van Dijk & Harry F. G. Heijnen. (2010) The platelet interior revisited: electron tomography reveals tubular α-granule subtypes. Blood 116:7, pages 1147-1156.
Crossref
Crossref