Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH.
about
Inherited platelet disorders: toward DNA-based diagnosisPre-analytical issues in the haemostasis laboratory: guidance for the clinical laboratoriesThe European Hematology Association Roadmap for European Hematology Research: a consensus documentProgress in understanding the diagnosis and molecular genetics of macrothrombocytopenias.Dawning of the age of genomics for platelet granule disorders: improving insight, diagnosis and management.A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersGenomic approaches to bleeding disorders.Current status and future prospects for platelet function testing in the diagnosis of inherited bleeding disorders.Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding.A diagnostic approach to mild bleeding disorders.Diagnosis of inherited bleeding disorders in the genomic era.Variability in platelet dense granule adenosine triphosphate release findings amongst patients tested multiple times as part of an assessment for a bleeding disorder.Platelet type von Willebrand disease and registry report: communication from the SSC of the ISTH.Bleeding risk of surgery and its prevention in patients with inherited platelet disordersMassive intoxication with rivaroxaban, phenprocoumon, and diclofenac: A case report.Prevalence of hemostatic alterations in patients with recurrent spontaneous subconjunctival hemorrhage.Decreased numbers of dense granules in fetal and neonatal platelets.Research at the heart of hematology: thrombocytopenias and platelet function disorders.Allogeneic hematopoietic cell transplantation in an adult patient with Glanzmann thrombasthenia.Diagnosis of platelet function disorders: A standardized, rational, and modular flow cytometric approach.Screening for platelet function disorders with Multiplate and platelet function analyzer.Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders.Standardization and reference ranges for whole blood platelet function measurements using a flow cytometric platelet activation test.High-throughput sequencing approaches for diagnosing hereditary bleeding and platelet disorders.Mean platelet diameter measurements to classify inherited thrombocytopenias.Flow cytometry-based platelet function testing is predictive of symptom burden in a cohort of bleeders.Effects of pH and concentration of sodium citrate anticoagulant on platelet aggregation measured by light transmission aggregometry induced by adenosine diphosphate.Comparison of multiple electrode aggregometry with lumi-aggregometry for the diagnosis of patients with mild bleeding disorders.Challenges on the diagnostic approach of inherited platelet function disorders: Is a paradigm change necessary?Preoperative screening for bleeding disorders: A comprehensive laboratory assessment of clinical practice
P2860
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P2860
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH.
@en
type
label
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH.
@en
prefLabel
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH.
@en
P2860
P356
P1476
Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH.
@en
P2093
Subcommittee on Platelet Physi ...... y on Thrombosis and Hemostasis
P2860
P304
P356
10.1111/JTH.12792
P577
2015-01-22T00:00:00Z