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Journal Abstract Search

804 related items for PubMed ID: 19002043

  • 1. The spectrum of inherited bleeding disorders in pediatrics.
    El-Bostany EA, Omer N, Salama EE, El-Ghoroury EA, Al-Jaouni SK.
    Blood Coagul Fibrinolysis; 2008 Dec; 19(8):771-5. PubMed ID: 19002043
    [Abstract] [Full Text] [Related]

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

  • 3. Inherited bleeding disorders: a 14-year retrospective study.
    Eid SS, Kamal NR, Shubeilat TS, Wael AG.
    Clin Lab Sci; 2008 Jun; 21(4):210-4. PubMed ID: 19174980
    [Abstract] [Full Text] [Related]

  • 4. The condensed MCMDM-1 VWD bleeding questionnaire as a predictor of bleeding disorders in women with unexplained menorrhagia.
    Azzam HA, Goneim HR, El-Saddik AM, Azmy E, Hassan M, El-Sharawy S.
    Blood Coagul Fibrinolysis; 2012 Jun; 23(4):311-5. PubMed ID: 22450545
    [Abstract] [Full Text] [Related]

  • 5. A longitudinal prospective study of bleeding diathesis in Egyptian pediatric patients: single-center experience.
    Mokhtar GM, Tantawy AA, Adly AA, Telbany MA, El Arab SE, Ismail M.
    Blood Coagul Fibrinolysis; 2012 Jul; 23(5):411-8. PubMed ID: 22610136
    [Abstract] [Full Text] [Related]

  • 6. Multiple congenital coagulopathies co-expressed with Von Willebrand's disease: the experience of Hemophilia Region III Treatment Centers over 25 years and review of the literature.
    Asatiani E, Kessler CM, Directors of the Comprehensive Hemophilia Treatment Centers in Region III.
    Haemophilia; 2007 Nov; 13(6):685-96. PubMed ID: 17973844
    [Abstract] [Full Text] [Related]

  • 7. Clinical audit of inherited bleeding disorders in a developing country.
    Sajid R, Khalid S, Mazari N, Azhar WB, Khurshid M.
    Indian J Pathol Microbiol; 2010 Nov; 53(1):50-3. PubMed ID: 20090222
    [Abstract] [Full Text] [Related]

  • 8. Prevalence and spectrum of von Willebrand disease in Eastern Uttar Pradesh.
    Kumar S, Kishore R, Gupta V, Jain M, Shukla J.
    Indian J Pathol Microbiol; 2010 Nov; 53(3):486-9. PubMed ID: 20699508
    [Abstract] [Full Text] [Related]

  • 9. Inherited platelet function disorders versus other inherited bleeding disorders: an Indian overview.
    Ahmad F, Kannan M, Ranjan R, Bajaj J, Choudhary VP, Saxena R.
    Thromb Res; 2008 Nov; 121(6):835-41. PubMed ID: 17850851
    [Abstract] [Full Text] [Related]

  • 10. Spectrum of inherited bleeding disorders in southern Iran, before and after the establishment of comprehensive coagulation laboratory.
    Karimi M, Haghpanah S, Amirhakimi A, Afrasiabi A, Dehbozorgian J, Nasirabady S.
    Blood Coagul Fibrinolysis; 2009 Dec; 20(8):642-5. PubMed ID: 19710607
    [Abstract] [Full Text] [Related]

  • 11. Congenital bleeding disorders in Karachi, Pakistan.
    Borhany M, Shamsi T, Naz A, Khan A, Parveen K, Ansari S, Farzana T.
    Clin Appl Thromb Hemost; 2011 Dec; 17(6):E131-7. PubMed ID: 21247962
    [Abstract] [Full Text] [Related]

  • 12. Multimeric analysis in diagnosis of vWD variants in Indians.
    Gupta PK, Kumar H, Saxena R.
    Indian J Pathol Microbiol; 2007 Jul; 50(3):636-9. PubMed ID: 17883169
    [Abstract] [Full Text] [Related]

  • 13. von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA).
    Nichols WL, Hultin MB, James AH, Manco-Johnson MJ, Montgomery RR, Ortel TL, Rick ME, Sadler JE, Weinstein M, Yawn BP.
    Haemophilia; 2008 Mar; 14(2):171-232. PubMed ID: 18315614
    [Abstract] [Full Text] [Related]

  • 14. Laboratory diagnosis and molecular classification of von Willebrand disease.
    Gadisseur A, Hermans C, Berneman Z, Schroyens W, Deckmyn H, Michiels JJ.
    Acta Haematol; 2009 Mar; 121(2-3):71-84. PubMed ID: 19506352
    [Abstract] [Full Text] [Related]

  • 15. Genetic diagnosis of haemophilia and other inherited bleeding disorders.
    Peyvandi F, Jayandharan G, Chandy M, Srivastava A, Nakaya SM, Johnson MJ, Thompson AR, Goodeve A, Garagiola I, Lavoretano S, Menegatti M, Palla R, Spreafico M, Tagliabue L, Asselta R, Duga S, Mannucci PM.
    Haemophilia; 2006 Jul; 12 Suppl 3():82-9. PubMed ID: 16684001
    [Abstract] [Full Text] [Related]

  • 16. Registry of inherited coagulopathies in Brazil: first report.
    Rezende SM, Pinheiro K, Caram C, Genovez G, Barca D.
    Haemophilia; 2009 Jan; 15(1):142-9. PubMed ID: 18976255
    [Abstract] [Full Text] [Related]

  • 17. Coagulation disorders and inhibitors of coagulation in children from Mansoura, Egypt.
    Abdelrazik N, Rashad H, Selim T, Tharwat L.
    Hematology; 2007 Aug; 12(4):309-14. PubMed ID: 17654057
    [Abstract] [Full Text] [Related]

  • 18. [Von Willebrand's disease in the IX Region of Chile].
    Cabrera ME, Artigas CG, Páez E, Monsalve V, Zolezzi P, Arauco G, Espinoza R, Hevia C, Villegas J.
    Rev Med Chil; 1989 Apr; 117(4):423-30. PubMed ID: 2519397
    [Abstract] [Full Text] [Related]

  • 19. Predictors of von Willebrand disease in children.
    Sidonio RF, Gunawardena S, Shaw PH, Ragni M.
    Pediatr Blood Cancer; 2012 May; 58(5):736-40. PubMed ID: 22237978
    [Abstract] [Full Text] [Related]

  • 20. Laboratory diagnosis of von Willebrand disease type 1/2E (2A subtype IIE), type 1 Vicenza and mild type 1 caused by mutations in the D3, D4, B1-B3 and C1-C2 domains of the von Willebrand factor gene. Role of von Willebrand factor multimers and the von Willebrand factor propeptide/antigen ratio.
    Gadisseur A, Berneman Z, Schroyens W, Michiels JJ.
    Acta Haematol; 2009 May; 121(2-3):128-38. PubMed ID: 19506359
    [Abstract] [Full Text] [Related]

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