Genetics of classic von Willebrand's disease. I. Phenotypic variation within families

Impact of trauma centre capacity and volume on the mortality risk of incoming new admissions.

BMJ military health·2020

Mathematical model of thrombin generation and bleeding phenotype in Amish carriers of Factor IX:C deficiency vs. controls.

Thrombosis research·2019

Distinguishing lupus anticoagulants from factor VIII inhibitors in haemophilic and non-haemophilic patients.

Haemophilia : the official journal of the World Federation of Hemophilia·2018

Effects of pre-analytical heat treatment in factor VIII (FVIII) inhibitor assays on FVIII antibody levels.

Haemophilia : the official journal of the World Federation of Hemophilia·2018

Laboratory testing for factor VIII and IX inhibitors in haemophilia: A review.

Haemophilia : the official journal of the World Federation of Hemophilia·2018

Limit of detection and threshold for positivity of the Centers for Disease Control and Prevention assay for factor VIII inhibitors.

Journal of thrombosis and haemostasis : JTH·2017

You Are Already Trained for This: The Hematologist/Oncologist's Role in Radiation Mass Casualty Response.

Blood·2026

Venetoclax plus Inotuzumab Ozogamicin for Relapsed and Refractory Acute Lymphoblastic Leukemia.

Blood·2026

Multipotent Progenitor-3 Cells Are Reprogrammed by Bone-derived DKK1 to Drive Myelopoiesis in Breast Cancer.

Blood·2026

Characterization of disease-initiating hematopoietic stem cells in calreticulin-mutated myeloproliferative neoplasms.

Blood·2026

HIF-1α/ADPGK-driven glycolytic reprogramming provokes platelet hyperactivation by fueling RHOA lactylation.

Blood·2026

Development of Inno8, an orally administered factor VIIIa-mimetic antibody fragment for treatment of hemophilia A.

Blood·2026

Large-scale genetic profiling of hereditary ataxias in China: implications for a stepwise molecular diagnostic strategy.

Translational neurodegeneration·2026

Monoallelic variants in BRSK1 are associated with a neurodevelopmental disorder with or without epilepsy.

American journal of human genetics·2026

Parent-of-origin dependent allelic regulation of social behaviors in mice by noncanonically imprinted monoamine synthesis genes.

Genetics·2026

Identification of Four Novel HLA-C Alleles.

HLA·2026

Biallelic Variants in KMO Cause a Novel Form of Congenital NAD Deficiency.

medRxiv : the preprint server for health sciences·2026

Circulating asparagine and short stature: A case-control study and exploratory two-sample Mendelian randomization analysis.

Medicine·2026

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Genetics of classic von Willebrand's disease. I. Phenotypic variation within families

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Impact of trauma centre capacity and volume on the mortality risk of incoming new admissions.

Mathematical model of thrombin generation and bleeding phenotype in Amish carriers of Factor IX:C deficiency vs. controls.

Distinguishing lupus anticoagulants from factor VIII inhibitors in haemophilic and non-haemophilic patients.

Effects of pre-analytical heat treatment in factor VIII (FVIII) inhibitor assays on FVIII antibody levels.

Laboratory testing for factor VIII and IX inhibitors in haemophilia: A review.

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Multipotent Progenitor-3 Cells Are Reprogrammed by Bone-derived DKK1 to Drive Myelopoiesis in Breast Cancer.

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HIF-1α/ADPGK-driven glycolytic reprogramming provokes platelet hyperactivation by fueling RHOA lactylation.

Development of Inno8, an orally administered factor VIIIa-mimetic antibody fragment for treatment of hemophilia A.

Large-scale genetic profiling of hereditary ataxias in China: implications for a stepwise molecular diagnostic strategy.

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