May-Hegglin anomaly: A rare cause of thrombocytopenia
- 1 September 1992
- journal article
- case report
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 151 (9) , 668-671
- https://doi.org/10.1007/bf01957570
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Sebastian platelet syndrome: A new variant of hereditary macrothrombocytopenia with leukocyte inclusionsAnnals of Hematology, 1990
- Hereditary types of thrombocytopenia with giant platelets and inclusion bodies in the leukocytesAnnals of Hematology, 1990
- Genetic thrombocytopenia with autosomal dominant transmission: a review of 54 casesBritish Journal of Haematology, 1990
- Congenital macrothrombocytopenia, leucocyte inclusions, deafness and proteinuria: functional and electron microscopic observations on platelets and megakaryocytesBritish Journal of Haematology, 1988
- Competitive Enzyme‐Linked Immunoassay for the Quantitation of Platelet‐Associated Immunoglobulins (IgG, IgM, IgA) and Complement (C3c, C3d) with Polyclonal and Monoclonal Reagents1Vox Sanguinis, 1987
- Kinetics, in vivo redistribution and sites of sequestration of indium-111-labelled platelets in giant platelet syndromesBritish Journal of Haematology, 1985
- Characterization of the platelet membrane glycoprotein abnormalities in Bernard-Soulier syndrome and comparison with normal by surface-labeling techniques and high-resolution two-dimensional gel electrophoresis.Journal of Clinical Investigation, 1982
- Congenital Disorders of the Functions of Polymorphonuclear NeutrophilsClinical Infectious Diseases, 1980
- Plasma and Platelet Beta-Thromboglobulin Levels in Patients with May-Hegglin AnomalyPathophysiology of Haemostasis and Thrombosis, 1980
- May-Hegglin Anomaly: A Defect in Megakaryocyte Fragmentation?British Journal of Haematology, 1974