To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribers receive full online access to your subscription and archive of back issues up to and including 2002.
Content published before 2002 is available via pay-per-view purchase only.
Subscribe:
Subscribe to Clinics in Laboratory MedicineAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- Thrombocytopenia in von Willebrand's disease.Thromb Res. 1983; 30: 391-393
- Evidence for genetic homogeneity in a familial platelet disorder with predisposition to acute myelogenous leukemia (FPD/AML).Blood. 1998; 92: 2600-2602
- Drug-induced immune thrombocytopenia: An overview of pathogenesis.Semin Hematol. 1999; 36: 2-6
- Can drugs cause autoimmune thrombocytopenic purpura?.Semin Hematol. 2000; 37: 229-238
- Alcohol-associated pancytopenia with hypocellular bone marrow.Am J Clin Pathol. 1986; 62: 333-344
- Kinetic studies of the mechanism of thrombocytopenia in patients with human immunodeficiency virus infection.N Engl J Med. 1992; 327: 1779-1784
- High-dose intravenous immunoglobulin for post-transfusion purpura.Br J Haematol. 1985; 61: 149-155
- Sur une nouvelle variete de dysthrophie thrombocytaire hemorrhagipare parse congenitale.Semin Hopitaux Paris. 1948; 24: 3217-3223
- Gray platelet syndrome in the elderly.Am J Hematol. 1988; 28: 270-272
- Platelet function studies in the Bernard-Soulier syndrome.Ann N Y Acad Med. 1972; 201: 145-160
- Platelet satellitosis to polymorphonuclears: Cytochemical, immunological and structural characterization of eight cases.Am J Hematol. 1991; 36: 235-242
- A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet alpha-granules and chromosome 11 deletion at 11q23.Blood. 1995; 85: 1805-1814
- Defective alpha-granule production in megakaryocytes from gray platelet syndrome: Ultrastructural studies of bone marrow cells and megakaryocytes growing in culture from blood precursors.Am J Pathol. 1981; 102: 10-19
- Gray platelet syndrome, an example of myelofi brosis of megakaryocytic origin.Bull Acad Natl Med. 1991; 175: 1145-1152
- Megakaryocytes and myelofibrosis in gray platelet syndrome.Nouv Rev Fr Hematol. 1987; 29: 109-114
- Italian Registry of Familial and Recurrent HUS/TTP.in: The molecular basis of familial hemolytic uremic syndrome: Mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20. Am Soc Nephrol. 12. 2001: 297-307
- Advances in the diagnosis of idiopathic thrombocytopenic purpura.Semin Hematol. 2000; 37: 249-260
- Post-transfusion purpura: Successful treatment by exchange transfusion.N Engl J Med. 1972; 287: 290-292
- Molecular abnormalities in Glanzmann's thromboasthenia, Bernard-Soulier syndrome, and platelet-type von Willebrand's disease.Curr Opin Hematol. 1994; 1: 388-393
- 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.J Clin Invest. 1982; 70: 304-311
- Thrombocytopenia of severe alcoholism.Ann Intern Med. 1971; 74: 37-43
- Effects of interleukin-1 and tumor necrosis factor on megakaryocytopoiesis: Mechanism of reactive thrombocytosis.Acta Haematol. 1995; 93: 67-72
- Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.Cell. 1994; 78: 635-644
- Adult idiopathic thrombocytopenic purpura: Clinical findings and response to therapy.Am J Med. 1982; 69: 430-442
- X-linked thrombocytopenia due to a novel mutation of GATA-1.Blood. 2000; 96 ([abstract 2422]): 564a
- Hereditary macrothrombocytopathia, nephritis and deafness.Am J Med. 1972; 52: 299-310
- Cytokines affecting megakaryocytopoiesis in rheumatoid arthritis with thrombocytosis.Rheumatol Int. 1996; 16: 5-8
- Primary thrombocytopenic purpura and acquired hemolytic anemia.Arch Intern Med. 1951; 87: 48-65
- Pathophysiology of heparin-induced thrombocytopenia: Clinical and diagnostic implications-a review.Arch Pathol Lab Med. 2000; 124: 1657-1666
- Platelet characteristics in patients with X-linked macrothrombocytopenia due to a novel GATA-1 mutation.in: [abstract 2420]. Blood. 96. 2000: 564a
- Physical, chemical and functional changes following plate let activation in normal and “giant” platelets.Blood Cells. 1983; 9: 359-382
- von Willebrand factor-cleaving protease in thrombocytopenic purpura and the hemolytic uremic syndrome.N Engl J Med. 1998; 339: 1578-1584
- Tirofiban and Eptifibatide, but not abciximab, induce leukocyte-platelet aggregation.Circulation. 1999; 100 ([abstract]): 1-681
- Platelets: Acute thrombocytopenia.in: Hematology 1999. American Society of Hematology Education Program Book. American Society of Hematology, Washington, DC1999: 371-383
- Idiopathic thrombocytopenic purpura: A concise summary of the pathophysiology and diagnosis in children and adults.Semin Hematol. 1998; 1: 5-8
- Drug-induced thrombocytopenia: A systematic review of published case reports.Ann Intern Med. 1998; 129: 886-890
- Bernard-Soulier disease: A study of four patients and their parents.Br J Haematol. 1981; 48: 459-467
- Idiopathic thrombocytopenic purpura: A practice guideline developed by explicit methods for the American Society of Hematology.Blood. 1996; 88: 3-40
- Assay of von Willebrand factor (vWF)-cleaving protease based on decreased collagen binding affinity of degraded vWF: A tool for the diagnosis of thrombotic thrombocytopenic purpura (TTP).Thromb Haemost. 1999; 82: 1386-1389
- Management of idiopathic thrombocytopenic purpura in pregnancy.Semin Hematol. 2000; 37: 275-289
- Drug-induced thrombocytopenia: Is it a serious concern for glycoprotein IIb/IIIa receptor inhibitors?.J Thromb Thrombolysis. 1998; 5: 191-202
- Thrombocytopenia with GP IIb/IIIa inhibitors: A meta-analysis.JACC. 1998; 31: 185A
- Haemorrhagic thrombocytopathy associated with dilatation of the platelet-membrane complex.Br J Haematol. 1981; 48: 595-600
- Heparin-induced thrombocytopenia-pathogenesis and treatment.Thromb Haemost. 1999; 82: 148-156
- May-Hegglin anomaly: A rare cause of thrombocytopenia.Eur J Pediatr. 1992; 151: 668-671
- Sebastian platelet syndrome: A new variant of hereditary macrothrombocytopenia with leukocyte inclusions.Blut. 1990; 61: 282-288
- Platelet to leukocyte adherence phenomena associated with thrombocytopenia.Blood. 1976; 47: 513-521
- Static and functional morphology of the pathological platelets in myelofibrosis and myeloproliferative syndrome.Ser Haematol. 1975; 8: 126-150
- Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1–22.2.Blood. 1996; 15: 5218-5224
- Hereditary giant platelet syndrome: A new disorder of platelet function.BMJ. 1973; 2: 586-588
- The use of electron microscopy in the investigation of the ultrastructural morphology of immune thrombocytopenic purpura platelets.Semin Hematol. 2000; 37: 222-228
- Gray platelet syndrome with splenomegaly and signs of extramedullary hematopoiesis: A case report with review of the literature.Am J Hematol. 1994; 46: 218-224
- Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-13.Hum Genet. 2000; 106: 557-564
- Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.Nat Genet. 2000; 26: 106-108
- Gray platelet syndrome: Selective alpha-granule deficiency and thrombocytopenia due to increased platelet turnover.Blut. 1985; 50: 331-340
- Partial clinical improvement in Upshaw-Schulman syndrome following prostacyclin infusion.Acta Paediatr Jpn. 1995; 37: 97-100
- Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).Blood. 2001; 97: 1147-1149
- Mapping of a gene for May-Hegglin anomaly to chromosome 22q.Hum Genet. 1999; 105: 379-383
- Acute idiopathic thrombocytopenic purpura presenting a high serum level of immunoglobulin E and eosinophilia in an elderly patient.J Med. 1998; 29: 93-96
- IIB von Willebrand's disease: Pathogenetic and therapeutic studies.Br J Haematol. 1988; 69: 55-59
- Post-transfusion purpura treated with plasma exchange by Haemonetics Cell Separator.Acta Med Scand. 1978; 203: 539-543
- Laboratory hemostatic abnormalities in massively transfused patients given red blood cells and crystalloid.Am J Clin Pathol. 1991; 96: 770-773
- Effect of ethanol on thrombopoiesis.Br J Haematol. 1986; 62: 345-354
- Thrombocytopenia caused by immunologic platelet destruction.in: Lee GR Lukens J Greer JP ed 10. Wintrobe's Clinical Hematology. vol 12. Williams and Wilkins, Baltimore1999: 1596-1597
- Gray platelet syndrome: Alpha-granule deficiency.in: Its influence on platelet function. J Lab Clin Med. 98. 1981: 831-848
- Bernard-Soulier syndrome.Blood. 1998; 91: 4397-4418
- Splenectomy in the management of the thrombocytopenia of the Wiskott-Aldrich syndrome.N Engl J Med. 1980; 302: 892-896
- The May-Hegglin anomaly: Platelet function, ultrastructure and chromosome studies.Blood. 1968; 32: 950-961
- Gray platelet syndrome.Arch Fr Pediatr. 1992; 49: 637-640
- Dysplastic platelets and circulating megakaryocytes in chronic myeloproliferative disease.Blood. 1974; 43: 797-809
- Hemostasis testing during massive blood replacement: A study of 172 cases.Vox Sang. 1982; 42: 113-123
- Fechtner syndrome: Physiologic analysis of macrothrombocytopenia.Blood Coagul Fibrinolysis. 2000; 11: 243-247
- Refractory thrombocytopenia: A myelodysplastic syndrome that may mimic immune thrombocytopenic purpura.Am J Clin Pathol. 1992; 98: 473-475
- Shape-changing agents produce abnormally large platelets in a hereditary “giant platelets syndrome (MPS)”.J Lab Clin Med. 1979; 93: 154-161
- Images in cardiovascular medicine: Pseudothrombocytopenia after abciximab (Reopro) treatment.Circulation. 1999; 100: 1460
- Diagnosis of Bernard-Soulier syndrome and Glanzmann's thromboasthenia with a monoclonal assay in whole blood.J Clin Invest. 1983; 71: 385-389
- Nat Genet. 2000; 26: 103-105
- Normal distribution of collagen IV in renal basement membranes in Epstein's syndrome.J Clin Pathol. 1997; 50: 919-922
- Preeclampsia effect on platelet count.Am J Perinatol. 1972; 9: 378-380
- Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1.Nat Gen. 2000; 24: 266-270
- Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: Role of factor H abnormalities.in: Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura. J Am Soc Nephrol. 10. 1999: 281-293
- Thrombocytopenia, giant platelets, and leukocyte inclusion bodies (May-Hegglin anomaly): Clinical and laboratory findings.Am J Med. 1998; 104: 355-360
- The analytical basis for the use of platelet estimates from peripheral blood smears.Am J Clin Pathol. 1978; 69: 383-387
- Platelet ultrastructural abnormalities in three patients with type 2B von Willebrand disease.Br J Haematol. 2000; 110: 704-714
- The Wiskott-Aldrich syndrome.Semin Hematol. 1998; 35: 332-345
- Wiskott-Aldrich syndrome protein and platelets.Immunol Rev. 2000; 178: 111-117
- Montreal platelet syndrome: A defect in calcium-activated neutral proteinase (calpain).Blood. 1989; 74: 715-721
- Fechtner syndrome: A variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia.Blood. 1985; 65: 397-406
- Gray platelet syndrome: A variety of qualitative platelet disorder.Am J Med. 1971; 51: 818-828
- Thrombotic thrombocytopenia purpura: Report of 25 cases and a review of the literature.Medicine. 1981; 60: 413-428
- Drug-induced thrombocytopenia.Curr Opin Hematol. 1999; 6: 349-353
- Upshaw-Schulman syndrome in two siblings.Acta Paediatr Jpn. 1990; 32: 373-376
- Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome.Blood. 2001; 97: 1330-1335
- Clinical and laboratory aspects of disseminated intravascular coagulation (DIC): A study of 118 cases.Thromb Haemost. 1978; 9: 122-134
- Megakaryocytes and platelets in alpha-granule disorders.Ballieres Clin Haematol. 1997; 10: 125-148
- Thrombasthenic-thrombopathic thrombocytopenia with giant, “Swiss-cheese” platelets: A case report.Ann Intern Med. 1973; 79: 828-834
- Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukemia.Nat Genet. 1999; 23: 134-135
- Disseminated intravascular coagulation: Findings in 346 patients.Thromb Haemost. 1980; 43: 28-33
- Recent advances in our understanding of Wiskott-Aldrich syndrome.Curr Opin Hematol. 1999; 6: 8-14
- Suppression of hematopoiesis by ethanol.J Clin Invest. 1964; 43: 2048-2062
- Plasma interleukin-6 and C-reactive protein levels in reactive versus clonal thrombocytosis.Am J Med. 1994; 97: 374-378
- Bernard-Soulier syndrome: Quantitative characterization of megakaryocytes and platelets by flow cytometry and platelet kinetic measurements.Eur J Haematol. 1994; 52: 193-200
- Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13.Am J Hum Genet. 1999; 65: 1711-1717
- Autosomal-dominant giant platelet syndromes: A hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13.Blood. 2000; 96: 3447-3451
- Disseminated intravascular coagulation and the syndrome of hemolysis, elevated liver enzymes and low platelet in severe preeclampsia.Obstet Gynecol. 1989; 73: 97-102
- Longitudinal analysis of platelet count and volume in normal pregnancy.Thromb Haemost. 1997; 77: 806-807
- Post-transfusion purpura: A report of five cases and review of the pathogenesis and management.Am J Hematol. 1986; 21: 259-267
- Heparin-induced thrombocytopenia: A ten-year retrospective.Annu Rev Med. 1999; 50: 129-147
- Thrombocytopenia due to platelet destruction and hypersplenism.in: Hoffman R Benz Jr, EJ Shattil SJ Hematology, Basic Principles and Practice. Churchill Livingstone, Philadelphia2000: 21-47
- Structural characterization and chromosomal location of the gene encoding human platelet glycoprotein Ib beta.J Biol Chem. 1994; 269: 17424-17427
- Increased serum level of interleukin-6 in patients with psoriatic arthritis and thrombocytosis.J Dermatol. 1995; 22: 718-722
- Thrombocytopenia induced by human parvovirus B19 infections.Eur J Haematol. 1993; 50: 255-257
Article info
Identification
Copyright
© 2002 W.B. Saunders Company. Published by Elsevier Inc. All rights reserved.