List of works - Sandrine Meunier

A single-centre study of management of pregnant women with von Willebrand disease

scientific article published on 18 December 2018

Benefits of thromboelastometry for monitoring replacement therapy in patients with severe inherited factor XIII deficiency: 3 illustrative cases

scientific article published on 30 July 2019

Chemistry approach for therapeutic education of children with hemophilia and their parents: Representation of complex phenomena related to treatment

scientific article published on 23 June 2016

Contribution of genetical analysis for diagnosis of von Willebrand's disease type 2B.

scientific article

Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): study protocol for a multicentric French national observational cross-sectional study

article

Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements

scientific article published on 12 February 2014

Differential diagnosis of neonatal alloimmune thrombocytopenia: Type 2B von Willebrand disease.

scientific article

Impact of prophylaxis on health-related quality of life of boys with hemophilia: An analysis of pooled data from 9 countries

scientific article published on 23 April 2019

Individualized PK-based prophylaxis in severe haemophilia

scientific article published on 01 March 2018

Intramuscular vaccination of haemophiliacs: Is it really a risk for bleeding?

scientific article published on 14 June 2019

Major surgery in a severe haemophilia A patient with high titre inhibitor: use of the thrombin generation test in the therapeutic decision.

scientific article

Management of a child with von Willebrand disease (type 2A) and extensive burns: a case report

scientific article published on 25 November 2011

Patient resources in the therapeutic education of haemophiliacs in France: their skills and roles as defined by consensus of a working group.

scientific article published on 18 January 2010

Safety and efficacy of a glycoPEGylated rFVIII (turoctocog alpha pegol, N8-GP) in paediatric patients with severe haemophilia A

scientific article published on 06 July 2017

Spectrum of the mutations in Bernard-Soulier syndrome

scientific article

Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability.

scientific article published in August 2016

Two novel factor V null mutations associated with activated protein C resistance phenotype/genotype discrepancy.

scientific article

Use of clinical practice guidelines on long-term prophylaxis in severe hemophilia in France: a retrospective audit.

scientific article

[Collagen gastritis, an unusual cause of anemia in children. Report of 2 cases].

scientific article

[Diagnostic strategy in the face of a coagulation abnormality]

scientific article published on 01 April 2015

[French guidelines. Long-term prophylaxis for severe haemophilia A and B children to prevent haemophiliac arthropathy]

scientific article published on 01 December 2009

[Hemorrhagic syndrome with hematologic origin]

scientific article published on 01 April 2015

[Varicella-associated purpura fulminans and deep vein thrombosis: a pediatric case report]

scientific article published on 26 May 2011

List of works by Sandrine Meunier

A single-centre study of management of pregnant women with von Willebrand disease

Benefits of thromboelastometry for monitoring replacement therapy in patients with severe inherited factor XIII deficiency: 3 illustrative cases

Chemistry approach for therapeutic education of children with hemophilia and their parents: Representation of complex phenomena related to treatment

Contribution of genetical analysis for diagnosis of von Willebrand's disease type 2B.

Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): study protocol for a multicentric French national observational cross-sectional study

Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements

Differential diagnosis of neonatal alloimmune thrombocytopenia: Type 2B von Willebrand disease.

Impact of prophylaxis on health-related quality of life of boys with hemophilia: An analysis of pooled data from 9 countries

Individualized PK-based prophylaxis in severe haemophilia

Intramuscular vaccination of haemophiliacs: Is it really a risk for bleeding?

Major surgery in a severe haemophilia A patient with high titre inhibitor: use of the thrombin generation test in the therapeutic decision.

Management of a child with von Willebrand disease (type 2A) and extensive burns: a case report

Patient resources in the therapeutic education of haemophiliacs in France: their skills and roles as defined by consensus of a working group.

Safety and efficacy of a glycoPEGylated rFVIII (turoctocog alpha pegol, N8-GP) in paediatric patients with severe haemophilia A

Spectrum of the mutations in Bernard-Soulier syndrome

Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability.

Two novel factor V null mutations associated with activated protein C resistance phenotype/genotype discrepancy.

Use of clinical practice guidelines on long-term prophylaxis in severe hemophilia in France: a retrospective audit.

[Collagen gastritis, an unusual cause of anemia in children. Report of 2 cases].

[Diagnostic strategy in the face of a coagulation abnormality]

[French guidelines. Long-term prophylaxis for severe haemophilia A and B children to prevent haemophiliac arthropathy]

[Hemorrhagic syndrome with hematologic origin]

[Varicella-associated purpura fulminans and deep vein thrombosis: a pediatric case report]