نتایج جستجو برای: bernard soulier syndrome

تعداد نتایج: 627301  

2014
Stuart Bisland Frank Smith

INTRODUCTION The management of patients with coagulopathic disorders undergoing orthopaedic surgery requires a dedicated, multi-disciplinary team with detailed perioperative planning. Bernard-Soulier Syndrome (BSS) is an extremely rare disorder, affecting 1 in 1 million individuals worldwide. It is caused by a deficiency in glycoprotein 1b-V-IX which is required for normal platelet-mediated clo...

Journal: :The Journal of clinical investigation 1980
I Hagen A Nurden O J Bjerrum N O Solum J Caen

Crossed immunoelectrophoresis of Triton X-100 solubilized proteins from normal and abnormal platelets was performed with rabbit antibodies raised against normal platelets. In Bernard-Soulier platelets protein 13 was not detected, and neither the amphiphilic (probably GP Ib) nor the hydrophilic (glycocalicin) glycocalicin-related proteins were seen when monospecific antiglycocalicin antiserum wa...

Journal: :Haematologica 2011
Anna Savoia Annalisa Pastore Daniela De Rocco Elisa Civaschi Mariateresa Di Stazio Roberta Bottega Federica Melazzini Valeria Bozzi Alessandro Pecci Silvana Magrin Carlo L Balduini Patrizia Noris

BACKGROUND Bernard-Soulier syndrome is a severe bleeding disease due to a defect of GPIb/IX/V, a platelet complex that binds the von Willebrand factor. Due to the rarity of the disease, there are reports only on a few cases compromising any attempt to establish correlations between genotype and phenotype. In order to identify any associations, we describe the largest case series ever reported, ...

Journal: :Blood 1996
G Sae-Tung J F Dong J A López

To evaluate the biosynthetic basis for decreased glycoprotein (GP) Ib-IX expression resulting from GP IX mutations described in three siblings with Bernard-Soulier syndrome, we introduced each mutation into the cDNA for GP IX by site-directed mutagenesis (GP IX Asp21 --> Gly and GP IX Asn45 --> Ser) and examined the associations of the mutants with the two other subunits of the GP Ib-IX complex...

2005
Harvey R. Gralnick

This study demonstrates that when platelets are stimulated by thrombin in the presence of low concentrations of purified human fibrinogen (10 to 20 Lg/mL. final concentration) binding of released platelet von Willebrand factor (plt-vWF) to the platelet membrane is enhanced. This effect appears to be mediated by fibrin monomer produced by the action of thrombin on the fibrinogen in the incubatio...

Journal: :Seminars in thrombosis and hemostasis 1982
M Andrew R D Barr

The number of platelets in the peripheral blood of healthy children, full-term, and premature infants falls into the same range as that of adults. Thrombocytopenia, defined as a platelet count of less than 150,000/mm(<150 × 10/L), may be due to decreased production, splenic sequestration, or increased platelet destruction. The following is a review of disorders involving the last mechanism, all...

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