(Q33393990)

26 July 2017

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title

Platelet disorders in children: A diagnostic approach (English)

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26 July 2017

Sara J Israels

1

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Victor S. Blanchette

3

object named as

Victor S Blanchette

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26 July 2017

Walter H A Kahr

2

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26 July 2017

Naomi L C Luban

4

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Georges E Rivard

5

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Margaret L Rand

6

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publication date

3 February 2011

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26 July 2017

published in

Pediatric Blood Cancer

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volume

56

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issue

6

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page(s)

975-983

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Inherited disorders of platelet function in pediatric clinical practice: a diagnostic challenge

26 July 2017

cites work

1 reference

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Contemporary platelet function testing

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21 January 2018

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Bleeding risks associated with inheritance of the Quebec platelet disorder

21 January 2018

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Inherited disorders of platelet function and challenges to diagnosis of mucocutaneous bleeding

21 January 2018

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The gray platelet syndrome: clinical spectrum of the disease

21 January 2018

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MYH9-related platelet disorders

21 January 2018

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21 January 2018

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The role of PFA-100 testing in the investigation and management of haemostatic defects in children and adults

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Screening tests of platelet function: update on their appropriate uses for diagnostic testing

21 January 2018

1 reference

Identification and characterization of a novel P2Y 12 variant in a patient diagnosed with type 1 von Willebrand disease in the European MCMDM-1VWD study

21 January 2018

1 reference

Light transmission aggregometry and ATP release for the diagnostic assessment of platelet function.

21 January 2018

1 reference

Methodology and outcomes of platelet aggregation testing in Australia, New Zealand and the Asia-Pacific region: results of a survey from the Royal College of Pathologists of Australasia Haematology Quality Assurance Program

21 January 2018

1 reference

Results of a worldwide survey on the assessment of platelet function by light transmission aggregometry: a report from the platelet physiology subcommittee of the SSC of the ISTH.

21 January 2018

1 reference

Whole blood platelet aggregometry and platelet function testing

21 January 2018

1 reference

Variables influencing Multiplate(TM) whole blood impedance platelet aggregometry and turbidimetric platelet aggregation in healthy individuals.

21 January 2018

1 reference

Multiplate whole blood impedance point of care aggregometry: preliminary reference values in healthy infants, children and adolescents

21 January 2018

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Platelet function disorders

21 January 2018

1 reference

Diagnostic approach to platelet function disorders

21 January 2018

1 reference

Phenotypic identification of platelet-type von Willebrand disease and its discrimination from type 2B von Willebrand disease: a question of 2B or not 2B? A story of nonidentical twins? Or two sides of a multidenominational or multifaceted primary-he

21 January 2018

1 reference

The genetic basis of von Willebrand disease

21 January 2018

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Genetic testing in the diagnostic evaluation of inherited platelet disorders

21 January 2018

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Disorders of lysosome-related organelle biogenesis: clinical and molecular genetics

21 January 2018

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Wiskott-Aldrich syndrome: diagnosis, clinical and laboratory manifestations, and treatment

21 January 2018

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21 January 2018

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Congenital amegakaryocytic thrombocytopenia and thrombocytopenia with absent radii

21 January 2018

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c-mpl mutations are the cause of congenital amegakaryocytic thrombocytopenia

21 January 2018

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Giant platelet disorders in African-American children misdiagnosed as idiopathic thrombocytopenic purpura

21 January 2018

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International consensus report on the investigation and management of primary immune thrombocytopenia

21 January 2018

1 reference

von Willebrand disease type 2B must be always considered in the differential diagnosis of genetic thrombocytopenias with giant platelets.

21 January 2018

1 reference

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder.

21 January 2018

1 reference

Genotype-phenotype correlation in MYH9-related thrombocytopenia

21 January 2018

1 reference

Role of platelet electron microscopy in the diagnosis of platelet disorders

21 January 2018

1 reference

Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p

21 January 2018

1 reference

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21 January 2018

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Requirement of VPS33B, a member of the Sec1/Munc18 protein family, in megakaryocyte and platelet alpha-granule biogenesis

21 January 2018

1 reference

Platelets from patients with the Quebec platelet disorder contain and secrete abnormal amounts of urokinase-type plasminogen activator

21 January 2018

1 reference

Insights into abnormal hemostasis in the Quebec platelet disorder from analyses of clot lysis.

21 January 2018

1 reference

Antithrombotic thrombocytes: ectopic expression of urokinase-type plasminogen activator in platelets

21 January 2018

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Increased expression of urokinase plasminogen activator in Quebec platelet disorder is linked to megakaryocyte differentiation

21 January 2018

1 reference

Quebec platelet disorder is linked to the urokinase plasminogen activator gene (PLAU) and increases expression of the linked allele in megakaryocytes

21 January 2018

1 reference

Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator gene.

21 January 2018

1 reference

The Montreal platelet syndrome kindred has type 2B von Willebrand disease with the VWF V1316M mutation

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PBC.22988

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26 July 2017

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