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291 related items for PubMed ID: 6156948

  • 1. Biochemical studies of two patients with the gray platelet syndrome. Selective deficiency of platelet alpha granules.
    Gerrard JM, Phillips DR, Rao GH, Plow EF, Walz DA, Ross R, Harker LA, White JG.
    J Clin Invest; 1980 Jul; 66(1):102-9. PubMed ID: 6156948
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Evidence that abnormal platelet functions in human Chédiak-Higashi syndrome are the result of a lack of dense bodies.
    Rendu F, Breton-Gorius J, Lebret M, Klebanoff C, Buriot D, Griscelli C, Levy-Toledano S, Caen JP.
    Am J Pathol; 1983 Jun; 111(3):307-14. PubMed ID: 6222656
    [Abstract] [Full Text] [Related]

  • 4. Correlation between prolonged bleeding time and depletion of platelet dense granule ADP in patients with myelodysplastic and myeloproliferative disorders.
    Malpass TW, Savage B, Hanson SR, Slichter SJ, Harker LA.
    J Lab Clin Med; 1984 Jun; 103(6):894-904. PubMed ID: 6233383
    [Abstract] [Full Text] [Related]

  • 5. Medich giant platelet disorder: a unique alpha granule deficiency I. Structural abnormalities.
    White JG.
    Platelets; 2004 Sep; 15(6):345-53. PubMed ID: 15370096
    [Abstract] [Full Text] [Related]

  • 6. Ultrastructural studies of the gray platelet syndrome.
    White JG.
    Am J Pathol; 1979 May; 95(2):445-62. PubMed ID: 453324
    [Abstract] [Full Text] [Related]

  • 7. Membrane defects in inherited disorders of platelet function.
    White JG.
    Am J Pediatr Hematol Oncol; 1982 May; 4(1):83-94. PubMed ID: 7091581
    [Abstract] [Full Text] [Related]

  • 8.
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  • 9. Congenital deficiency of alpha-2-adrenoceptors on human platelets: description of two cases.
    Tamponi G, Pannocchia A, Arduino C, Bazzan M, Della Dora N, Schinco P, Buraglio M, Eandi M.
    Thromb Haemost; 1987 Dec 18; 58(4):1012-6. PubMed ID: 2832962
    [Abstract] [Full Text] [Related]

  • 10.
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  • 11. Human platelet storage organelles. A review.
    Fukami MH, Salganicoff L.
    Thromb Haemost; 1977 Dec 15; 38(4):963-70. PubMed ID: 579698
    [Abstract] [Full Text] [Related]

  • 12. A 'touch' of the White platelet syndrome.
    White JG, Key NS, King RA, Vercellotti GM.
    Platelets; 2005 Sep 15; 16(6):346-61. PubMed ID: 16194865
    [Abstract] [Full Text] [Related]

  • 13. Phosphotyrosine proteins in platelets from patients with storage pool disease: direct relation between granule defects and defective signal transduction.
    Arderiu G, Díaz-Ricart M, Domenech P, Escolar G, Ordinas A, Pujol-Moix N.
    Haematologica; 2002 Jun 15; 87(6):629-36. PubMed ID: 12031920
    [Abstract] [Full Text] [Related]

  • 14. Characterization of platelet abnormalities of Tester Moriyama (TM) rats with storage pool deficiency.
    Fujimori H, Ozaki K, Nomura S, Nishikawa T, Pan-Hou H, Nishimura M, Narama I.
    Lab Anim Sci; 1998 Oct 15; 48(5):490-5. PubMed ID: 10090063
    [Abstract] [Full Text] [Related]

  • 15. [Gray-platelet syndrome associated with Marfan disease in a Mexican family].
    Martínez-Murillo C, Payns Borrego E, Arzate Hernández G, Soriano Rosas J, Ambriz Fernández R, Marín Palomares T, Quintana González S.
    Sangre (Barc); 1994 Aug 15; 39(4):287-91. PubMed ID: 7985059
    [Abstract] [Full Text] [Related]

  • 16. Conditions influencing release of granule contents from human platelets in citrated plasma induced by ADP or the thrombin receptor activating peptide SFLLRN: direct measurement of percent release of beta-thromboglobulin and assessment by flow cytometry of P-selectin expression.
    Rand ML, Perry DW, Packham MA, Gemmell CH, Yeo EL, Kinlough-Rathbone RL.
    Am J Hematol; 1996 Aug 15; 52(4):288-94. PubMed ID: 8701947
    [Abstract] [Full Text] [Related]

  • 17. [Gray platelet syndrome].
    Lutz P, Roth-Pougheon A, Wiesel ML, Albert A, Brisson C, Grunebaum L, Cazenave JP, Lévy JM.
    Arch Fr Pediatr; 1992 Aug 15; 49(7):637-40. PubMed ID: 1476482
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 77(5):986-90. PubMed ID: 9184415
    [Abstract] [Full Text] [Related]

  • 19. [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]

  • 20. Inherited prolonged bleeding time and platelet storage pool deficiency in the subtle gray (sut) mouse.
    Swank RT, Reddington M, Novak EK.
    Lab Anim Sci; 1996 Feb 26; 46(1):56-60. PubMed ID: 8699821
    [Abstract] [Full Text] [Related]

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