[Heparin-Ca is not identical with low molecular weight heparin (LMWH)]

Emergency care of patients receiving non-vitamin K antagonist oral anticoagulants.

British journal of anaesthesia·2018

Founder effect is responsible for the p.Leu131Phe heparin-binding-site antithrombin mutation common in Hungary: phenotype analysis in a large cohort.

Journal of thrombosis and haemostasis : JTH·2016

Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population.

Journal of thrombosis and haemostasis : JTH·2011

Accelerated clearance alone explains ultra-large multimers in von Willebrand disease Vicenza.

Journal of thrombosis and haemostasis : JTH·2010

Anti-factor V auto-antibody in the plasma and platelets of a patient with repeated gastrointestinal bleeding.

Journal of thrombosis and haemostasis : JTH·2003

[High-shear force-induced platelet aggregation in the screening and diagnosis of von Willebrand disease].

Orvosi hetilap·2001

[Structured data collection during neonatal anesthesia: Neo Somno Log - a self-developed digital event tracker].

Orvosi hetilap·2026

[Assessment of dietary habits in adolescents with inflammatory bowel disease].

Orvosi hetilap·2026

[Modern treatment of androgenetic alopecia].

Orvosi hetilap·2026

[A burning challenge in emergency care: burnout, secondary traumatic stress, and psychological immune competence].

Orvosi hetilap·2026

[Triptan treatment in migraine: a dose-based model for persistence and acute medication use patterns using nationwide health insurance data].

Orvosi hetilap·2026

[Patient satisfaction and complications following penile prosthesis implantation].

Orvosi hetilap·2026

Multiple Sclerosis Misdiagnosis in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: A Genotype-Misphenotype Study.

Neurology. Genetics·2026

Allogeneic hematopoietic stem cell transplantation for acute myeloid leukemia: the association of JACIE accreditation/preparation and center volume.

Haematologica·2026

Incidental findings of inherited thrombosis and hemostasis disorders in clinical exomes with unrelated indications.

Haematologica·2026

FLT3-directed therapy in acute myeloid leukemia: lessons from the final analysis of LACEWING.

Haematologica·2026

When genotype precedes phenotype: incidental findings in inherited disorders of hemostasis.

Haematologica·2026

Angiomatoid Fibrous Histiocytoma: An Exceptionally Rare Pulmonary Artery Tumor Presenting as an Asymptomatic Heart Murmur.

JACC. Case reports·2026

Related Experiment Videos

[Heparin-Ca is not identical with low molecular weight heparin (LMWH)]

Related Concept Videos

Emergency care of patients receiving non-vitamin K antagonist oral anticoagulants.

Founder effect is responsible for the p.Leu131Phe heparin-binding-site antithrombin mutation common in Hungary: phenotype analysis in a large cohort.

Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population.

Accelerated clearance alone explains ultra-large multimers in von Willebrand disease Vicenza.

Anti-factor V auto-antibody in the plasma and platelets of a patient with repeated gastrointestinal bleeding.

[High-shear force-induced platelet aggregation in the screening and diagnosis of von Willebrand disease].

[Structured data collection during neonatal anesthesia: Neo Somno Log - a self-developed digital event tracker].

[Assessment of dietary habits in adolescents with inflammatory bowel disease].

[Modern treatment of androgenetic alopecia].

[A burning challenge in emergency care: burnout, secondary traumatic stress, and psychological immune competence].

[Triptan treatment in migraine: a dose-based model for persistence and acute medication use patterns using nationwide health insurance data].

[Patient satisfaction and complications following penile prosthesis implantation].

Multiple Sclerosis Misdiagnosis in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: A Genotype-Misphenotype Study.

Allogeneic hematopoietic stem cell transplantation for acute myeloid leukemia: the association of JACIE accreditation/preparation and center volume.

Incidental findings of inherited thrombosis and hemostasis disorders in clinical exomes with unrelated indications.

FLT3-directed therapy in acute myeloid leukemia: lessons from the final analysis of LACEWING.

When genotype precedes phenotype: incidental findings in inherited disorders of hemostasis.

Angiomatoid Fibrous Histiocytoma: An Exceptionally Rare Pulmonary Artery Tumor Presenting as an Asymptomatic Heart Murmur.

Related Experiment Videos

[Heparin-Ca is not identical with low molecular weight heparin (LMWH)]

Related Concept Videos

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