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3. 2B or not to be--the 45-year saga of the Montreal Platelet Syndrome. Poon MC; Rand ML; Jackson SC Thromb Haemost; 2010 Nov; 104(5):903-10. PubMed ID: 20838735 [TBL] [Abstract][Full Text] [Related]
4. [Type IIB von Willebrand Jürgens syndrome as the cause of neonatal thrombocytopenia]. Zeitler P; von Stockhausen HB Klin Padiatr; 1998; 210(2):85-8. PubMed ID: 9561963 [TBL] [Abstract][Full Text] [Related]
6. A second report of platelet-type von Willebrand disease with a Gly233Ser mutation in the GPIBA gene. Nurden P; Lanza F; Bonnafous-Faurie C; Nurden A Thromb Haemost; 2007 Feb; 97(2):319-21. PubMed ID: 17264965 [No Abstract] [Full Text] [Related]
7. The platelet aggregation defect in the von Willebrand-Jürgens-Syndrom on the Aland Islands. The possible existence of an "anti-Willebrand-Factor". Jürgens J; Lehmann W; Eriksson A Hemostase; 1966 Oct; 6(4):225-31. PubMed ID: 5299356 [No Abstract] [Full Text] [Related]
8. Metabolic disorders of platelets. Hellem AJ Adv Intern Med; 1973; 17():171-87. PubMed ID: 4593928 [No Abstract] [Full Text] [Related]
9. The hemostatic mechanism and its defects. Macfarlane RG Int Rev Exp Pathol; 1968; 6():55-133. PubMed ID: 4884086 [No Abstract] [Full Text] [Related]
11. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders. Gupta PK; Charan VD; Saxena R Ann Hematol; 2007 Jun; 86(6):403-7. PubMed ID: 17375300 [TBL] [Abstract][Full Text] [Related]
12. [Thrombocyte function and its disorders]. Gugler E Med Lab (Stuttg); 1979 Apr; 32(4):88-94. PubMed ID: 312419 [No Abstract] [Full Text] [Related]
13. Diagnostic and therapeutic considerations on inherited platelet disorders in neonates and children. Schlegel N; Bardet V; Kenet G; Muntean W; Zieger B; Nowak-Göttl U; Klin Padiatr; 2010 May; 222(3):209-14. PubMed ID: 20535670 [TBL] [Abstract][Full Text] [Related]
14. Metabolic disorders of platelets. Hellem AJ Adv Intern Med; 1971; 17():171-87. PubMed ID: 4950245 [No Abstract] [Full Text] [Related]
15. The White platelet syndrome: a new autosomal dominant platelet disorder. White JG; Key NS; King RA; Vercellotti GM Platelets; 2004 May; 15(3):173-84. PubMed ID: 15203719 [TBL] [Abstract][Full Text] [Related]
16. [A case of hereditary hemorrhagic disease which may be defined as "thrombasthenia with functional thrombopathy"]. Torsellini A; Lombardi V Haematologica; 1970; 55(10):621-36. PubMed ID: 4996530 [No Abstract] [Full Text] [Related]
18. Inherited abnormalities of platelets. Nurden AT Thromb Haemost; 1999 Aug; 82(2):468-80. PubMed ID: 10605738 [No Abstract] [Full Text] [Related]
19. Platelet-vessel wall interaction: from the bedside to molecules. Caen JP; Rosa JP Thromb Haemost; 1995 Jul; 74(1):18-24. PubMed ID: 8578453 [TBL] [Abstract][Full Text] [Related]
20. The bleeding time as a screening test for evaluation of platelet function. Harker LA; Slichter SJ N Engl J Med; 1972 Jul; 287(4):155-9. PubMed ID: 4537519 [No Abstract] [Full Text] [Related] [Next] [New Search]