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Journal Abstract Search

387 related items for PubMed ID: 24237983

  • 1. Inherited disorders of platelet function.
    Matthews DC.
    Pediatr Clin North Am; 2013 Dec; 60(6):1475-88. PubMed ID: 24237983
    [Abstract] [Full Text] [Related]

  • 2. Inherited disorders of platelet function in pediatric clinical practice: a diagnostic challenge.
    Streif W, Knöfler R, Eberl W.
    Klin Padiatr; 2010 May; 222(3):203-8. PubMed ID: 20514633
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  • 6. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders.
    Gupta PK, Charan VD, Saxena R.
    Ann Hematol; 2007 Jun; 86(6):403-7. PubMed ID: 17375300
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  • 7. von Willebrand disease and platelet disorders.
    Favaloro EJ, Bodó I, Israels SJ, Brown SA.
    Haemophilia; 2014 May; 20 Suppl 4():59-64. PubMed ID: 24762277
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  • 8. Inherited platelet function disorders. Diagnostic approach and management.
    Gresele P, Falcinelli E, Bury L.
    Hamostaseologie; 2016 Nov 07; 36(4):265-278. PubMed ID: 27484722
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  • 9. ISTH bleeding assessment tool and platelet function analyzer in children with mild inherited platelet function disorders.
    Alhaj D, Hagedorn N, Cuntz F, Reschke M, Schuldes J, Ruthenberg J, Bakchoul T, Greinacher A, Holzhauer S.
    Eur J Haematol; 2024 Jul 07; 113(1):54-65. PubMed ID: 38549165
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  • 10. Screening women with menorrhagia for underlying bleeding disorders: the utility of the platelet function analyser and bleeding time.
    Philipp CS, Miller CH, Faiz A, Dilley A, Michaels LA, Ayers C, Bachmann G, Dowling N, Saidi P.
    Haemophilia; 2005 Sep 07; 11(5):497-503. PubMed ID: 16128894
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  • 11. Laboratory assessment of familial, nonthrombocytopenic mucocutaneous bleeding: a definitive diagnosis is often not possible.
    Pereira J, Quiroga T, Mezzano D.
    Semin Thromb Hemost; 2008 Oct 07; 34(7):654-62. PubMed ID: 19085766
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  • 12. Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment.
    Hayward CP, Rao AK, Cattaneo M.
    Haemophilia; 2006 Jul 07; 12 Suppl 3():128-36. PubMed ID: 16684008
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  • 13. Platelet disorders in children: A diagnostic approach.
    Israels SJ, Kahr WH, Blanchette VS, Luban NL, Rivard GE, Rand ML.
    Pediatr Blood Cancer; 2011 Jun 07; 56(6):975-83. PubMed ID: 21294245
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  • 14. High prevalence of bleeders of unknown cause among patients with inherited mucocutaneous bleeding. A prospective study of 280 patients and 299 controls.
    Quiroga T, Goycoolea M, Panes O, Aranda E, Martínez C, Belmont S, Muñoz B, Zúñiga P, Pereira J, Mezzano D.
    Haematologica; 2007 Mar 07; 92(3):357-65. PubMed ID: 17339185
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  • 15. Evaluation of desmopressin effect on primary haemostasis in pediatric patients with aspirin-like defect as hereditary thrombocytopathy.
    Tauer JT, Gneuss A, Lohse JE, Jürgens T, Knöfler R.
    Klin Padiatr; 2011 May 07; 223(3):169-72. PubMed ID: 21509710
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  • 16. Platelet function disorders and menorrhagia in adolescents: a review of laboratory diagnosis.
    Sokkary NA, Venkateswaran L, Dietrich JE, Teruya J.
    J Pediatr Adolesc Gynecol; 2012 Aug 07; 25(4):233-7. PubMed ID: 22840932
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  • 17. Dozing and bruising due to abnormal platelet function (thrombocytopathia). A family study of the syndrome.
    Zucker S, Mielke CH, Durocher JR, Crosby WH.
    Ann Intern Med; 1972 May 07; 76(5):725-31. PubMed ID: 5025323
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  • 18. Bleeding disorders: A common cause of menorrhagia in adolescents.
    Bevan JA, Maloney KW, Hillery CA, Gill JC, Montgomery RR, Scott JP.
    J Pediatr; 2001 Jun 07; 138(6):856-61. PubMed ID: 11391329
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  • 20. Use of ISTH bleeding assessment tool to predict inherited platelet dysfunction in resource constrained settings.
    Rashid A, Moiz B, Karim F, Shaikh MS, Mansoori H, Raheem A.
    Scand J Clin Lab Invest; 2016 Sep 07; 76(5):373-8. PubMed ID: 27215135
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