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131 related items for PubMed ID: 429863
21. [Congenital anomalies of the human blood platelet, models for understanding mechanisms of platelet secretion: gray platelet disease]. Caen JP, Nurden AT, Levy-Toledano S. C R Seances Acad Sci III; 1981 Oct 26; 293(7):363-6. PubMed ID: 6797688 [Abstract] [Full Text] [Related]
32. Detection of carriers in Glanzmann's thrombasthenia. Zonneveld GT, van Leeuwen EF, Sturk A, ten Cate JW. Thromb Haemost; 1983 Jun 28; 49(3):182-6. PubMed ID: 6224309 [Abstract] [Full Text] [Related]
33. [The Bernard-Soulier syndrome. A hereditary functional and structural disorder of blood platelets]. Cieslar P, Holada K, Dyr JE, Smetana K, Matousková O, Spicka I. Cas Lek Cesk; 1997 Apr 02; 136(7):210-4. PubMed ID: 9221196 [Abstract] [Full Text] [Related]
39. Survival and function of transfused platelets. Studies in two patients with congenital deficiencies of platelet membrane glycoproteins. Cesar JM, Vecino AM. Platelets; 2009 May 02; 20(3):158-62. PubMed ID: 19437332 [Abstract] [Full Text] [Related]
40. Deletion of the platelet-specific alloantigen PlA1 from platelets in Glanzmann's thrombasthenia. Kunicki TJ, Aster RH. J Clin Invest; 1978 May 02; 61(5):1225-31. PubMed ID: 566280 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]