How we treat the platelet glycoprotein defects; Glanzmann thrombasthenia and Bernard Soulier syndrome in children and adults

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

(2017) Sara Orsini et al.   HAEMATOLOGICA

ITGA2B and ITGB3 gene mutations associated with Glanzmann thrombasthenia

(2017) Alan T. Nurden et al.   PLATELETS

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

(2017) Sara Orsini et al.   HAEMATOLOGICA

Guidelines for the use of platelet transfusions

(2016) Lise J. Estcourt et al.   BRITISH JOURNAL OF HAEMATOLOGY

Use of ISTH bleeding assessment tool to predict inherited platelet dysfunction in resource constrained settings

(2016) Anila Rashid et al.   SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION

New Insights Into the Treatment of Glanzmann Thrombasthenia

(2016) Man-Chiu Poon et al.   TRANSFUSION MEDICINE REVIEWS

Detection of septic transfusion reactions to platelet transfusions by active and passive surveillance

(2015) H. Hong et al.   BLOOD

Analysis of 65 pregnancies in 34 women with five different forms of inherited platelet function disorders

(2015) Elisa Civaschi et al.   BRITISH JOURNAL OF HAEMATOLOGY

Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH

(2015) P. Gresele et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Accuracy of a New Platelet Count System (PLT-F) Depends on the Staining Property of Its Reagents

(2015) Atsushi Wada et al.   PLoS One

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

(2014) P. Noris et al.   HAEMATOLOGICA

The Sysmex XN-2000 Hematology Autoanalyzer Provides a Highly Accurate Platelet Count than the Former Sysmex XE-2100 System Based on Comparison with the CD41/CD61 Immunoplatelet Reference Method of Flow Cytometry

(2014) Sang Hyuk Park et al.   Annals of Laboratory Medicine

Heavy menstrual bleeding significantly affects quality of life

(2013) Trine S. Karlsson et al.   ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA

Inherited thrombocytopenias frequently diagnosed in adults

(2013) C. L. Balduini et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Bernard-Soulier Syndrome: An Update

(2013) Robert Andrews et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Gray platelet syndrome: macrothrombocytopenia with deficient  -granules

(2012) W. H. A. Kahr et al.   BLOOD

May-Hegglin anomaly

(2012) C. C. Hsia et al.   BLOOD

Natural history of platelet antibody formation against αIIbβ3 in a French cohort of Glanzmann thrombasthenia patients

(2012) M. FIORE et al.   HAEMOPHILIA

Inherited platelet disorders

(2012) A. T. NURDEN et al.   HAEMOPHILIA

Understanding the genetic basis of Glanzmann thrombasthenia: implications for treatment

(2012) Alan T Nurden et al.   Expert Review of Hematology

Guidelines for the laboratory investigation of heritable disorders of platelet function

(2011) Paul Harrison et al.   BRITISH JOURNAL OF HAEMATOLOGY

Evaluation and management of acute menorrhagia in women with and without underlying bleeding disorders: consensus from an international expert panel

(2011) Andra H. James et al.   European Journal of Obstetrics & Gynecology and Reproductive Biology

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIb  (Bolzano mutation)

(2011) P. Noris et al.   HAEMATOLOGICA

Modern management of severe platelet function disorders

(2010) Jayanthi Alamelu et al.   BRITISH JOURNAL OF HAEMATOLOGY

The impact of menstrual disorders on quality of life in women with inherited bleeding disorders

(2010) R. A. KADIR et al.   HAEMOPHILIA

Prevalence of allo-immunization anti-HLA and anti-integrin αIIbβ3 in Glanzmann Thromboasthenia patients

(2010) C. SANTORO et al.   HAEMOPHILIA

Trends in postpartum hemorrhage in high resource countries: a review and recommendations from the International Postpartum Hemorrhage Collaborative Group

(2009) Marian Knight et al.   BMC Pregnancy and Childbirth

Novel point mutation in a leucine-rich repeat of the GPIb  chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant

(2008) S. Vettore et al.   HAEMATOLOGICA

Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent

(2008) M. VIJAPURKAR et al.   HAEMOPHILIA