Homozygous Factor V Leiden mutation in sickle cell anaemia

Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group.

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An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF study.

Journal of thrombosis and haemostasis : JTH·2018

Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami.

Journal of thrombosis and haemostasis : JTH·2016

Platelet-type von Willebrand Disease: Diagnostic Challenges. Flaws and Pitfalls Experienced in the THROMKID Quality Project.

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Successful second ITI with factor IX and combined immunosuppressive therapy. A patient with severe haemophilia B and recurrence of a factor IX inhibitor.

Hamostaseologie·2014

[Therapy of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)].

Hamostaseologie·2014

Variation in antenatal anaemia guidelines across the NHS in the United Kingdom: A cross-sectional study.

British journal of haematology·2026

Minimal residual disease-guided ibrutinib and venetoclax in patients with chronic lymphocytic leukaemia and complex karyotype.

British journal of haematology·2026

Danburstotug, an anti-PD-L1 antibody, in relapsed/refractory extra-nodal natural killer/T-cell lymphoma: The phase 2 DISTINKT study.

British journal of haematology·2026

External validation of the AAA+ survival model in a large Chinese cohort with essential thrombocythaemia.

British journal of haematology·2026

Treatment sequence with gilteritinib and allogeneic haematopoietic stem cell transplantation in relapsed/refractory FMS-like tyrosine kinase 3 (FLT3)-mutated acute myeloid leukaemia patients: A multicentre real-world study.

British journal of haematology·2026

Salvage treatment patterns in multiple myeloma patients progressing after lenalidomide maintenance: A real-life study from European Myeloma Network (EMN) Italy.

British journal of haematology·2026

Intrahepatic Platelets Orchestrate Microenvironmental Remodelling and Cellular Crosstalk in Liver Fibrosis.

Liver international : official journal of the International Association for the Study of the Liver·2026

Homocysteine, cysteine and methionine are associated with 90-day prognosis in intracerebral hemorrhage patients.

Annals of medicine·2026

Inflammatory markers and the systemic immune-inflammation index in endometrial carcinoma and hyperplasia: a retrospective cohort study.

Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology·2026

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Homozygous Factor V Leiden mutation in sickle cell anaemia

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Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group.

An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF study.

Identification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami.

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Successful second ITI with factor IX and combined immunosuppressive therapy. A patient with severe haemophilia B and recurrence of a factor IX inhibitor.

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Homozygous Factor V Leiden mutation in sickle cell anaemia

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