Radana Zachova

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 9 publications

Registry-Based Analysis of Treatment and Retreatment Attacks of Hereditary Angioedema.

Registry-Based Analysis of Treatment and Retreatment Attacks of Hereditary Angioedema.

Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology

Published: February 26, 2026

Systematic Approach Revealed SERPING1 Splicing-Affecting Variants to be Highly Represented in the Czech National HAE Cohort.

Systematic Approach Revealed SERPING1 Splicing-Affecting Variants to be Highly Represented in the Czech National HAE Cohort.

Journal: Journal of clinical immunology

Published: February 23, 2023

Myeloid lineage cells evince distinct steady-state level of certain gene groups in dependence on hereditary angioedema severity.

Myeloid lineage cells evince distinct steady-state level of certain gene groups in dependence on hereditary angioedema severity.

Journal: Frontiers in genetics

Published: December 14, 2022

Natural Course of Activated Phosphoinositide 3-Kinase Delta Syndrome in Childhood and Adolescence.

Natural Course of Activated Phosphoinositide 3-Kinase Delta Syndrome in Childhood and Adolescence.

Journal: Frontiers in pediatrics

Published: April 20, 2021

Acquired Angioedema with C1 Inhibitor Deficiency: Occurrence, Clinical Features, and Management: A Nationwide Retrospective Study in the Czech Republic Patients.

Acquired Angioedema with C1 Inhibitor Deficiency: Occurrence, Clinical Features, and Management: A Nationwide Retrospective Study in the Czech Republic Patients.

Journal: International archives of allergy and immunology

Published: October 02, 2020

Recombinant human C1 esterase inhibitor as short-term prophylaxis in patients with hereditary angioedema.

Recombinant human C1 esterase inhibitor as short-term prophylaxis in patients with hereditary angioedema.

Journal: The journal of allergy and clinical immunology. In practice

Published: April 25, 2019

Utility of Ruxolitinib in a Child with Chronic Mucocutaneous Candidiasis Caused by a Novel STAT1 Gain-of-Function Mutation.

Utility of Ruxolitinib in a Child with Chronic Mucocutaneous Candidiasis Caused by a Novel STAT1 Gain-of-Function Mutation.

Journal: Journal of clinical immunology

Published: December 26, 2017

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised? .

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised? .

Journal: Hormone research in paediatrics

Published: August 30, 2016

Genetic defects in PI3Kδ affect B-cell differentiation and maturation leading to hypogammaglobulineamia and recurrent infections.

Genetic defects in PI3Kδ affect B-cell differentiation and maturation leading to hypogammaglobulineamia and recurrent infections.

Journal: Clinical immunology (Orlando, Fla.)

Published: July 18, 2016

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Last Updated: 09/26/2026