193 related articles for article (PubMed ID: 3689696)
1. Familial bleeding disorder associated with deficiencies in platelet signal processing and glycoproteins.
Holmsen H; Walsh PN; Koike K; Murphy S; Holme S; Johnson MM; Dangelmaier CA; Egan JJ; Benzel JE; Tuszynski GP
Br J Haematol; 1987 Nov; 67(3):335-44. PubMed ID: 3689696
[TBL] [Abstract][Full Text] [Related]
2. [Aspirin-like defect - a hereditary thrombocytopathy due to impaired release of platelet adenosine diphosphate].
Elezović I; Mijović A; Rolović Z
Bilt Hematol Transfuz; 1979; 7(2-3):165-74. PubMed ID: 263623
[TBL] [Abstract][Full Text] [Related]
3. Deficiency of (33P)2MeS-ADP binding sites on platelets with secretion defect, normal granule stores and normal thromboxane A2 production. Evidence that ADP potentiates platelet secretion independently of the formation of large platelet aggregates and thromboxane A2 production.
Cattaneo M; Lombardi R; Zighetti ML; Gachet C; Ohlmann P; Cazenave JP; Mannucci PM
Thromb Haemost; 1997 May; 77(5):986-90. PubMed ID: 9184415
[TBL] [Abstract][Full Text] [Related]
4. Abnormalities of platelet adenine nucleotides in patients with myeloproliferative disorders.
Nishimura J; Okamoto S; Ibayashi H
Thromb Haemost; 1979 Jun; 41(4):787-95. PubMed ID: 483250
[TBL] [Abstract][Full Text] [Related]
5. Impairment of phosphatidylinositol metabolism in a patient with a bleeding disorder associated with defects of initial platelet responses.
Lages B; Weiss HJ
Thromb Haemost; 1988 Apr; 59(2):175-9. PubMed ID: 2838922
[TBL] [Abstract][Full Text] [Related]
6. Platelets from bleeding Simmental cattle mobilize calcium, phosphorylate myosin light chain and bind normal numbers of fibrinogen molecules but have abnormal cytoskeletal assembly and aggregation in response to ADP.
Searcy GP; Frojmovic MM; McNicol A; Robertson C; Wong T; Gerrard JM
Thromb Haemost; 1994 Feb; 71(2):240-6. PubMed ID: 8191406
[TBL] [Abstract][Full Text] [Related]
7. The Hermansky-Pudlak syndrome. Evidence for a lowered 5-hydroxytryptamine content in platelets of heterozygotes.
Gerritsen SM; Akkerman JW; Nijmeijer B; Sixma JJ; Witkop CJ; White J
Scand J Haematol; 1977 Mar; 18(3):249-56. PubMed ID: 847398
[TBL] [Abstract][Full Text] [Related]
8. Hereditary abnormality of platelet aggregation attributable to nucleotide storage pool deficiency.
Ingerman CM; Smith JB; Shapiro S; Sedar A; Silver MJ
Blood; 1978 Aug; 52(2):332-44. PubMed ID: 667360
[TBL] [Abstract][Full Text] [Related]
9. Newborn platelet dysfunction: a storage pool and release defect.
Corby DG; Zuck TF
Thromb Haemost; 1976 Aug; 36(1):200-7. PubMed ID: 1036810
[TBL] [Abstract][Full Text] [Related]
10. Platelet aggregation by thimerosal: role of ADP and SH groups.
Leone G; Boni P; Vincenti A
Thromb Haemost; 1976 Feb; 35(1):249-57. PubMed ID: 989191
[TBL] [Abstract][Full Text] [Related]
11. Spontaneous platelet aggregation in a hereditary giant platelet syndrome (MPS).
Milton JG; Frojmovic MM; Tang SS; White JG
Am J Pathol; 1984 Feb; 114(2):336-45. PubMed ID: 6696046
[TBL] [Abstract][Full Text] [Related]
12. The in-vitro effect of tirofiban, glycoprotein IIb/IIIa antagonist, on various responses of porcine blood platelets.
Ciborowski M; Tomasiak M; Rusak T; Winnicka K; Dobrzycki S
Blood Coagul Fibrinolysis; 2008 Sep; 19(6):557-67. PubMed ID: 18685439
[TBL] [Abstract][Full Text] [Related]
13. Essential athrombia: study of a new case.
Inceman S; Tangün Y
Thromb Diath Haemorrh; 1975 Apr; 33(2):278-85. PubMed ID: 1138423
[TBL] [Abstract][Full Text] [Related]
14. Hereditary thrombocytopathy: a familial bleeding disorder due to impaired platelet coagulant activity.
Ardlie NG; Coupland WW; Schoefl GI
Aust N Z J Med; 1976 Feb; 6(1):37-45. PubMed ID: 1065298
[TBL] [Abstract][Full Text] [Related]
15. Role of platelet membrane glycoproteins Ib/IX and IIb/IIIa, and of platelet alpha-granule proteins in platelet aggregation induced by human osteosarcoma cells.
Clezardin P; Drouin J; Morel-Kopp MC; Hanss M; Kehrel B; Serre CM; Kaplan C; Delmas PD
Cancer Res; 1993 Oct; 53(19):4695-700. PubMed ID: 7691402
[TBL] [Abstract][Full Text] [Related]
16. A familial platelet function disorder associated with abnormal signalling through the glycoprotein VI pathway.
Dunkley S; Arthur JF; Evans S; Gardiner EE; Shen Y; Andrews RK
Br J Haematol; 2007 Jun; 137(6):569-77. PubMed ID: 17539777
[TBL] [Abstract][Full Text] [Related]
17. Platelet size and shape in hereditary giant platelet syndromes on blood smear and in suspension: evidence for two types of abnormalities.
Milton JG; Hutton RA; Tuddenham EG; Frojmovic MM
J Lab Clin Med; 1985 Sep; 106(3):326-35. PubMed ID: 4031633
[TBL] [Abstract][Full Text] [Related]
18. Detection of carriers in Glanzmann's thrombasthenia.
Zonneveld GT; van Leeuwen EF; Sturk A; ten Cate JW
Thromb Haemost; 1983 Jun; 49(3):182-6. PubMed ID: 6224309
[TBL] [Abstract][Full Text] [Related]
19. Gray platelet syndrome: alpha-granule deficiency. Its influence on platelet function.
Levy-Toledano S; Caen JP; Breton-Gorius J; Rendu F; Cywiner-Golenzer C; Dupuy E; Legrand Y; Maclouf J
J Lab Clin Med; 1981 Dec; 98(6):831-48. PubMed ID: 6458643
[TBL] [Abstract][Full Text] [Related]
20. Failure to mobilize intracellular calcium in response to thrombin in a patient with familial thrombocytopathy characterized by macrothrombocytopenia and abnormal platelet membrane complexes.
Parker RI; Bray GL; McKeown LP; White JG
J Lab Clin Med; 1993 Oct; 122(4):441-9. PubMed ID: 8228559
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
