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2. Molecular abnormalities in Glanzmann's thrombasthenia, Bernard-Soulier syndrome, and platelet-type von Willebrand's disease. Clemetson KJ, Clemetson JM. Curr Opin Hematol; 1994 Sep; 1(5):388-93. PubMed ID: 9371310 [Abstract] [Full Text] [Related]
3. Platelet-vessel wall interaction: from the bedside to molecules. Caen JP, Rosa JP. Thromb Haemost; 1995 Jul; 74(1):18-24. PubMed ID: 8578453 [Abstract] [Full Text] [Related]
4. Identification of a homozygous single base pair deletion in the gene coding for the human platelet glycoprotein Ib alpha causing Bernard-Soulier syndrome. Simsek S, Admiraal LG, Modderman PW, van der Schoot CE, von dem Borne AE. Thromb Haemost; 1994 Sep; 72(3):444-9. PubMed ID: 7855797 [Abstract] [Full Text] [Related]
8. The use of fluorescence flow cytometry in the characterization of Bernard-Soulier syndrome and Glanzmann's thrombasthenia. Fabris F, Casonato A, Randi ML, Luzzatto G, De Silvestro G, Ongaro G, Girolami A. Haematologica; 1989 Sep; 74(1):39-44. PubMed ID: 2498181 [Abstract] [Full Text] [Related]
9. Are patients with Glanzmann thrombasthenia and the Bernard-Soulier syndrome protected against atherosclerosis? Nurden AT, Nurden P, George JN. Adv Exp Med Biol; 2001 Sep; 489():13-29. PubMed ID: 11554587 [No Abstract] [Full Text] [Related]
12. [Membrane glycoproteins of human platelets: structures, functions, and abnormalities in Glanzmann's thrombasthenia and Bernard-Soulier syndrome]. Ando Y, Fusegawa H, Kawada T, Tanaka Y, Watanabe K, Kobayashi N. Rinsho Byori; 1989 Dec; 37(12):1344-52. PubMed ID: 2614964 [Abstract] [Full Text] [Related]
17. Evidence that an abnormality in the glycoprotein Ib alpha gene is not the cause of abnormal platelet function in a family with classic Bernard-Soulier disease. Finch CN, Miller JL, Lyle VA, Handin RI. Blood; 1990 Jun 15; 75(12):2357-62. PubMed ID: 1972029 [Abstract] [Full Text] [Related]