Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and "true" prothrombin deficiency

High incidence of anti-FVIII antibodies against non-coagulant epitopes in haemophilia A patients: a possible role for the half-life of transfused FVIII.

British journal of haematology·1996

Type I factor XIII deficiency is caused by a genetic defect of its b subunit: insertion of triplet AAC in exon III leads to premature termination in the second Sushi domain.

Blood·1996

"Pseudo homozygous" activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds.

Thrombosis and haemostasis·1996

The risk of abortion and stillbirth in antithrombin-, protein C-, and protein S-deficient women.

Thrombosis and haemostasis·1996

Prothrombin fragment 1+2 and thrombin-antithrombin complex levels in patients with inherited APC resistance due to factor V Leiden mutation.

British journal of haematology·1996

Mutations which introduce free cysteine residues in the Gla-domain of vitamin K dependent proteins result in the formation of complexes with alpha 1-microglobulin.

Thrombosis and haemostasis·1996

KPNA2-Mediated MYC Nuclear Import Enhances CAR-T Cell Memory and Potentiates Antitumor Efficacy.

Blood·2026

How I Identify and Diagnose Carriers of Hemophilia and Women and Girls with Hemophilia.

Blood·2026

The origins of rare glycosylphosphatidylinositol-deficient cells in normal and immune-mediated hematopoiesis.

Blood·2026

How I Treat Heavy Menstrual Bleeding in Patients with Bleeding Disorder of Unknown Cause.

Blood·2026

Choice of a different donor reduces relapse risk after second allogeneic SCT for MDS.

Blood·2026

A multicenter phase II study of glofitamab plus polatuzumab-R-CHP for patients with diffuse large B-cell lymphoma.

Blood·2026

Five ways to find a parasite: comparison of five molecular assays for the detection of Strongyloides spp.

Journal of clinical microbiology·2026

Mpox (Formerly Known as Monkeypox) in Dermatological Practice: Presentation of a Series of Four Clinical Cases at a Referral Hospital.

Cureus·2026

Nutrient Sensing and Growth Control in Plasmodium: Beyond mTOR Signaling.

Molecular microbiology·2026

[Myiasis: a practical approach].

Dermatologie (Heidelberg, Germany)·2026

Molecular detection of Bartonella dromedarii-like in Microthoracius spp. (Phthiraptera: Microthoraciidae) associated with alpacas from the southern Andes of Peru.

Comparative immunology, microbiology and infectious diseases·2026

Comparison of signal drop on T2-weighted and post-contrast T1-weighted Dixon MRI in spinal bone marrow lesions.

European journal of radiology·2026

Related Experiment Videos

Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and

Related Concept Videos

High incidence of anti-FVIII antibodies against non-coagulant epitopes in haemophilia A patients: a possible role for the half-life of transfused FVIII.

Type I factor XIII deficiency is caused by a genetic defect of its b subunit: insertion of triplet AAC in exon III leads to premature termination in the second Sushi domain.

"Pseudo homozygous" activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds.

The risk of abortion and stillbirth in antithrombin-, protein C-, and protein S-deficient women.

Prothrombin fragment 1+2 and thrombin-antithrombin complex levels in patients with inherited APC resistance due to factor V Leiden mutation.

Mutations which introduce free cysteine residues in the Gla-domain of vitamin K dependent proteins result in the formation of complexes with alpha 1-microglobulin.

KPNA2-Mediated MYC Nuclear Import Enhances CAR-T Cell Memory and Potentiates Antitumor Efficacy.

How I Identify and Diagnose Carriers of Hemophilia and Women and Girls with Hemophilia.

The origins of rare glycosylphosphatidylinositol-deficient cells in normal and immune-mediated hematopoiesis.

How I Treat Heavy Menstrual Bleeding in Patients with Bleeding Disorder of Unknown Cause.

Choice of a different donor reduces relapse risk after second allogeneic SCT for MDS.

A multicenter phase II study of glofitamab plus polatuzumab-R-CHP for patients with diffuse large B-cell lymphoma.

Five ways to find a parasite: comparison of five molecular assays for the detection of Strongyloides spp.

Mpox (Formerly Known as Monkeypox) in Dermatological Practice: Presentation of a Series of Four Clinical Cases at a Referral Hospital.

Nutrient Sensing and Growth Control in Plasmodium: Beyond mTOR Signaling.

[Myiasis: a practical approach].

Molecular detection of Bartonella dromedarii-like in Microthoracius spp. (Phthiraptera: Microthoraciidae) associated with alpacas from the southern Andes of Peru.

Comparison of signal drop on T2-weighted and post-contrast T1-weighted Dixon MRI in spinal bone marrow lesions.

Related Experiment Videos

Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and...

Related Concept Videos

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Prothrombin Molise: a "new" congenital dysprothrombinemia, double heterozygosis with an abnormal prothrombin and