[The genetics of thrombosis]

Antiplatelet glycoprotein autoantibodies in patients with autoimmune diseases with and without thrombocytopenia.

Journal of clinical immunology·1996

Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasma.

Blood·1996

Homozygous patients with APC resistance may remain paucisymptomatic or asymptomatic during oral contraception.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis·1996

Inhibitory effect of prostacyclin and nitroprusside on type IIB von Willebrand factor-promoted platelet activation.

Thrombosis and haemostasis·1996

Deep venous thrombosis and lupus anticoagulant. A case-control study.

Thrombosis and haemostasis·1996

DDAVP infusion in haemophilia A carriers: different behaviour of plasma factor VIII and von Willebrand factor.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis·1996

Neurodegenerative Langerhans cell histiocytosis: building the evidence for prospective monitoring and early treatment. Response to Comment on: "Neurodegenerative Langerhans cell histiocytosis: longterm follow-up of 63 patients from the Italian Registry".

Haematologica·2026

What's liver got to do with it? Hepatic response and survival in AL amyloidosis.

Haematologica·2026

Bridging periodontitis and clonal hematopoiesis: implications for solid tumor metastasis, clinical trial design, and microbiome dynamics. Comment on: "Ligature-induced periodontitis promotes Dnmt3aR878H-driven clonal hematopoiesis".

Haematologica·2026

Comparison and combination of prognostic scores for nodular lymphocytepredominant Hodgkin lymphoma: an analysis from the German Hodgkin Study Group.

Haematologica·2026

Elevated on-treatment D-dimer level is associated with major bleeding during extended anticoagulation for venous thromboembolism.

Haematologica·2026

Short-term emicizumab in patients with acquired hemophilia A.

Haematologica·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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[The genetics of thrombosis]

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Antiplatelet glycoprotein autoantibodies in patients with autoimmune diseases with and without thrombocytopenia.

Compound heterozygous protein C deficiency resulting in the presence of only the beta-form of protein C in plasma.

Homozygous patients with APC resistance may remain paucisymptomatic or asymptomatic during oral contraception.

Inhibitory effect of prostacyclin and nitroprusside on type IIB von Willebrand factor-promoted platelet activation.

Deep venous thrombosis and lupus anticoagulant. A case-control study.

DDAVP infusion in haemophilia A carriers: different behaviour of plasma factor VIII and von Willebrand factor.

Neurodegenerative Langerhans cell histiocytosis: building the evidence for prospective monitoring and early treatment. Response to Comment on: "Neurodegenerative Langerhans cell histiocytosis: longterm follow-up of 63 patients from the Italian Registry".

What's liver got to do with it? Hepatic response and survival in AL amyloidosis.

Bridging periodontitis and clonal hematopoiesis: implications for solid tumor metastasis, clinical trial design, and microbiome dynamics. Comment on: "Ligature-induced periodontitis promotes Dnmt3aR878H-driven clonal hematopoiesis".

Comparison and combination of prognostic scores for nodular lymphocytepredominant Hodgkin lymphoma: an analysis from the German Hodgkin Study Group.

Elevated on-treatment D-dimer level is associated with major bleeding during extended anticoagulation for venous thromboembolism.

Short-term emicizumab in patients with acquired hemophilia A.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

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[The genetics of thrombosis]

Related Concept Videos

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