These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

456 related items for PubMed ID: 19408195

  • 21. Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment.
    Hayward CP, Rao AK, Cattaneo M.
    Haemophilia; 2006 Jul; 12 Suppl 3():128-36. PubMed ID: 16684008
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. Bernard-Soulier-like functional platelet defect in myelodysplastic syndrome and in acute myeloblastic leukemia associated with trilineage myelodysplasia.
    Hiçsönmez G, Gümrük F, Cetin M, Ozbek N, Tuncer M, Gürsel T.
    Turk J Pediatr; 1995 May; 37(4):425-9. PubMed ID: 8560614
    [Abstract] [Full Text] [Related]

  • 24. A case of Bernard-Soulier syndrome: study of platelet glycoprotein Ib in a kindred.
    Ingerslev J, Stenbjerg S, Taaning E.
    Eur J Haematol; 1987 Aug; 39(2):182-4. PubMed ID: 3666106
    [Abstract] [Full Text] [Related]

  • 25. [Differential diagnosis of platelet disorders].
    Rothe G.
    Dtsch Med Wochenschr; 2006 Feb 03; 131(5):219-22. PubMed ID: 16440270
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Diagnosis of heterozygotes in Glanzmann's thrombasthenia.
    Stormorken H, Gogstad GO, Solum NO, Pande H.
    Thromb Haemost; 1982 Oct 29; 48(2):217-21. PubMed ID: 6217584
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. [A case from practice (270). 1. Bernard Soulier syndrome (heterozygote form). 2. Iron deficiency anemia of uncertain etiology. 3. Lactose intolerance].
    Roth R.
    Schweiz Rundsch Med Prax; 1993 Jun 15; 82(24):721-3. PubMed ID: 8327810
    [No Abstract] [Full Text] [Related]

  • 35. What's new in using platelet research? To unravel thrombopathies and other human disorders.
    Freson K, Labarque V, Thys C, Wittevrongel C, Geet CV.
    Eur J Pediatr; 2007 Dec 15; 166(12):1203-10. PubMed ID: 17619901
    [Abstract] [Full Text] [Related]

  • 36. Diagnostic assessment of platelet disorders: what are the challenges to standardization?
    Pai M, Hayward CP.
    Semin Thromb Hemost; 2009 Mar 15; 35(2):131-8. PubMed ID: 19408186
    [Abstract] [Full Text] [Related]

  • 37. Congenital platelet function disorders: survey findings and pathophysiology.
    Yasunaga K.
    Nihon Ketsueki Gakkai Zasshi; 1986 Dec 15; 49(8):1499-508. PubMed ID: 3564845
    [No Abstract] [Full Text] [Related]

  • 38. Detection and identification of platelet antibodies in clinical disorders.
    McFarland JG.
    Transfus Apher Sci; 2003 Jun 15; 28(3):297-305. PubMed ID: 12725957
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 23.