Literature DB >> 20725709

[Congenital thrombocytopathies].

C M Kirchmaier1, D Pillitteri.   

Abstract

Inherited thrombocytopathies are much less frequent in comparison to acquired platelet function disorders. However, congenital disorders can lead to severe bleeding tendency and are often not diagnosed. They are induced by different platelet defects based on disorders of platelet adhesion, receptors, secretion and signal transduction. In some cases they are associated with thrombocytopenia, giant platelets and various comorbidities. This article gives an overview regarding diverse defects, their diagnosis and treatment options.

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Year:  2010        PMID: 20725709     DOI: 10.1007/s00108-010-2596-3

Source DB:  PubMed          Journal:  Internist (Berl)        ISSN: 0020-9554            Impact factor:   0.743


  19 in total

1.  Platelet membrane glycoprotein Ib: genetic polymorphism detected in the intact molecule and in proteolytic fragments.

Authors:  M Meyer; I Schellenberg
Journal:  Thromb Res       Date:  1990-05-01       Impact factor: 3.944

2.  [Clinical assessment of potential fields of application of recombinant factor VIIa in internal and pediatric diseases. Recommendations of an expert group].

Authors:  Carl-Erik Dempfle; Dietrich Gulba; Carl M Kirchmaier; Robert Klamroth; Wolfgang Korte; Reinhard Lorenz; Markus Peck-Radosavljevic; Alex Veldman; Rainer B Zotz
Journal:  Med Klin (Munich)       Date:  2007-01-15

3.  Gray platelet syndrome. A variety of qualitative platelet disorder.

Authors:  G Raccuglia
Journal:  Am J Med       Date:  1971-12       Impact factor: 4.965

Review 4.  Clues for understanding the structure and function of a prototypic human integrin: the platelet glycoprotein IIb/IIIa complex.

Authors:  J J Calvete
Journal:  Thromb Haemost       Date:  1994-07       Impact factor: 5.249

5.  Role of ADP receptor P2Y(12) in platelet adhesion and thrombus formation in flowing blood.

Authors:  Jasper A Remijn; Ya-Ping Wu; Ellen H Jeninga; Martin J W IJsseldijk; Gijsbert van Willigen; Philip G de Groot; Jan J Sixma; Alan T Nurden; Paquita Nurden
Journal:  Arterioscler Thromb Vasc Biol       Date:  2002-04-01       Impact factor: 8.311

6.  Another link between phospholipid transmembrane migration and ABC transporter gene family, inferred from a rare inherited disorder of phosphatidylserine externalization.

Authors:  F Toti; V Schindler; J F Riou; G Lombard-Platet; E Fressinaud; D Meyer; A Uzan; J B Le Pecq; J L Mandel; J M Freyssinet
Journal:  Biochem Biophys Res Commun       Date:  1997-12-18       Impact factor: 3.575

Review 7.  Molecular basis of Glanzmann's Thrombasthenia and current strategies in treatment.

Authors:  S Bellucci; J Caen
Journal:  Blood Rev       Date:  2002-09       Impact factor: 8.250

8.  Patients with a prolonged bleeding time and normal aggregation tests may have storage pool deficiency: studies on one hundred six patients.

Authors:  H K Nieuwenhuis; J W Akkerman; J J Sixma
Journal:  Blood       Date:  1987-09       Impact factor: 22.113

9.  Platelet-type von Willebrand's disease: characterization of a new bleeding disorder.

Authors:  J L Miller; A Castella
Journal:  Blood       Date:  1982-09       Impact factor: 22.113

10.  Bleeding risks associated with inheritance of the Quebec platelet disorder.

Authors:  Heather McKay; Francine Derome; M Anwar Haq; Susan Whittaker; Emmy Arnold; Frédéric Adam; Nancy M Heddle; Georges E Rivard; Catherine P M Hayward
Journal:  Blood       Date:  2004-03-16       Impact factor: 22.113

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