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1.
Platelets ; 25(8): 636-8, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24245489

RESUMO

Prasugrel is a widely used antiplatelet agent in the setting of percutaneous coronary intervention. In case of resistance to this third-generation thienopyridine, choices of alternative drugs remain limited. Here, we describe a case of a 49-year-old man with stent thrombosis occurring 5 days after drug-eluting stent implantation despite a well-conducted antiplatelet therapy with aspirin and prasugrel. Evaluation of platelet functions by different tests revealed prasugrel resistance. Genotyping for various CYP single-nucleotide polymorphisms showed that the patient carried mutant alleles encoding enzymes CYP2B6 and CYP2C9 involved in prasugrel metabolic pathway. Strikingly, an adequate platelet response was rapidly obtained after switching from prasugrel to ticagrelor.


Assuntos
Adenosina/análogos & derivados , Piperazinas/efeitos adversos , Antagonistas do Receptor Purinérgico P2Y/uso terapêutico , Tiofenos/efeitos adversos , Trombose/tratamento farmacológico , Adenosina/uso terapêutico , Resistência a Medicamentos , Humanos , Masculino , Pessoa de Meia-Idade , Cloridrato de Prasugrel , Trombose/etiologia , Ticagrelor
2.
Blood ; 118(22): 5928-37, 2011 Nov 24.
Artigo em Inglês | MEDLINE | ID: mdl-21960593

RESUMO

Filaminopathies A caused by mutations in the X-linked FLNA gene are responsible for a wide spectrum of rare diseases including 2 main phenotypes, the X-linked dominant form of periventricular nodular heterotopia (FLNA-PVNH) and the otopalatodigital syndrome spectrum of disorders. In platelets, filamin A (FLNa) tethers the principal receptors ensuring the platelet-vessel wall interaction, glycoprotein Ibα and integrin αIIbß3, to the underlying cytoskeleton. Hemorrhage, coagulopathy, and thrombocytopenia are mentioned in several reports on patients with FLNA-PVNH. Abnormal platelet morphology in 2 patients with FLNA-PVNH prompted us to examine a third patient with similar platelet morphology previously diagnosed with immunologic thrombocytopenic purpura. Her enlarged platelets showed signs of FLNa degradation in Western blotting, and a heterozygous missense mutation in FLNA was detected. An irregular distribution of FLNa within the total platelet population was shown by confocal microscopy for all 3 patients. In vitro megakaryocyte cultures showed an abnormal differentiation, including an irregular distribution of FLNa with a frayed aspect, the presence of enlarged α-granules, and an abnormal fragmentation of the cytoplasm. Mutations in FLNA may represent an unrecognized cause of macrothrombocytopenia with an altered platelet production and a modified platelet-vessel wall interaction.


Assuntos
Proteínas Contráteis/genética , Proteínas dos Microfilamentos/genética , Mutação , Trombocitopenia/classificação , Trombocitopenia/genética , Idoso , Células Cultivadas , Feminino , Filaminas , Predisposição Genética para Doença , Humanos , Pessoa de Meia-Idade , Mutação/fisiologia , Contagem de Plaquetas , Síndrome , Trombocitopenia/sangue , Trombocitopenia/diagnóstico
3.
Opt Express ; 13(4): 1275-80, 2005 Feb 21.
Artigo em Inglês | MEDLINE | ID: mdl-19495000

RESUMO

We report a novel and efficient method for the laser direct writing of two-dimensional silver structures. Multiphoton absorption of a small fraction of the output of a Ti:sapphire oscillator is sufficient to photoreduce silver nitrate in a thin film of polyvinylpyrrolidone that has been spin-coated on a substrate. The polymer can then be washed away, leaving a pattern consisting of highly interconnected silver nanoparticles. We report the characterization of the silver patterns using scanning electron and atomic force microscopies, and demonstrate the application of this technique in the creation of diffraction gratings.

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