Jan Hudecek
Martin, ZI 03601, Slovakia
Last Updated: 09/26/2026
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Found 8 publications
Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis.
Journal: Journal of clinical medicine
Published: December 22, 2021
Multimer Analysis of Von Willebrand Factor in Von Willebrand Disease with a Hydrasys Semi-Automatic Analyzer-Single-Center Experience.
Journal: Diagnostics (Basel, Switzerland)
Published: October 11, 2021
Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management.
Journal: Diagnostics (Basel, Switzerland)
Published: September 16, 2021
Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.
Journal: International journal of molecular sciences
Published: April 27, 2020
Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype.
Journal: Thrombosis research
Published: July 15, 2019
Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders.
Journal: International journal of molecular sciences
Published: November 15, 2017
Therapeutic angiogenesis for the critical limb ischemia decreases platelet activation.
Journal: Platelets
Published: March 29, 2013
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Last Updated: 09/26/2026