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24. [Clinical and laboratory findings in 6 cases of Glanzmann's thrombasthenia]. Inceman S; Tangün Y Turk Tip Cemiy Mecm; 1970; 36(7):235-43. PubMed ID: 5534885 [No Abstract] [Full Text] [Related]
25. [Glanzmann's thrombasthenia. Apropos of 22 cases]. Meddeb B; Ben Abid H; Hafsia R; Hafsia A; Khaier R; Ben Hafsa R Tunis Med; 1986 Jan; 64(1):29-34. PubMed ID: 3715990 [No Abstract] [Full Text] [Related]
26. [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]
27. [A new family displaying ophthalmic changes overlapping Epstein's triad (macrothrombocytopathia, nephritis and deafness) (author's transl)]. Kuroda M; Kametani T; Morise T; Kita T; Sakato S; Miyazaki R; Tofuku Y; Takeda R Nihon Naika Gakkai Zasshi; 1982 Apr; 71(4):485-96. PubMed ID: 7202033 [No Abstract] [Full Text] [Related]
29. Classification of hereditary platelet function disorders and diagnostic criteria: an inductive study based on a nation-wide survey in Japan. Yasunaga K Nihon Ketsueki Gakkai Zasshi; 1978 Oct; 41(5):946-54. PubMed ID: 735707 [No Abstract] [Full Text] [Related]
30. Congenital qualitative platelet disorders in children. Hiçsönmez G Turk J Pediatr; 1982; 24(1):21-8. PubMed ID: 7112689 [No Abstract] [Full Text] [Related]
31. [Dysfunction of platelets in uremia]. Hryszko T; Małyszko J; Myśliwiec M Przegl Lek; 1999; 56(9):599-603. PubMed ID: 10695367 [TBL] [Abstract][Full Text] [Related]
32. An inherited hemorrhagic trait with characteristics resembling both mild hemophilia of type A and Von Willebrand's disease. Egeberg O Scand J Clin Lab Invest; 1965; 17():Suppl 84:25-32. PubMed ID: 5295420 [No Abstract] [Full Text] [Related]
33. Abnormalities of platelet function in patients with polycythemia vera. Berger S; Aledort LM; Gilbert HS; Hanson JP; Wasserman LR Cancer Res; 1973 Nov; 33(11):2683-7. PubMed ID: 4748429 [No Abstract] [Full Text] [Related]