R. Zachová

发表

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

T. Kalina, V. Kanderova, E. Froňková, 2018, Journal of Clinical Immunology.

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

V. Kanderova, A. Šedivá, Tomáš Milota, 2021, Frontiers in Pediatrics.

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

M. van der Burg, T. Kalina, M. Wentink, 2017, Clinical immunology.

High Prevalence of Likely Passively Acquired Anti-TPO and Anti-GAD Autoantibodies in Common Variable Immunodeficiency

A. Šedivá, J. Smetanova, R. Horváth, 2021, Journal of Clinical Immunology.

Recombinant Human C1 Esterase Inhibitor as Short-Term Prophylaxis in Patients With Hereditary Angioedema.

R. Shapiro, R. Tachdjian, M. Jesenak, 2020, The journal of allergy and clinical immunology. In practice.

No Evidence for Linkage between the Hereditary Angiooedema Clinical Phenotype and the BDKR1, BDKR2, ACE or MBL2 gene

J. Litzman, B. Ravčuková, Jirí Jarkovský, 2011, Scandinavian journal of immunology.

Abstracts from the 10th C1-inhibitor deficiency workshop

William H. Yang, A. Szilágyi, M. Margaglione, 2017, Allergy, Asthma & Clinical Immunology.

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

P. Kralickova, J. Bartůňková, I. Krčmová, 2021, International Archives of Allergy and Immunology.

Early development of immunity in diGeorge syndrome.

O. Hrusak, A. Šedivá, A. Janda, 2005, Medical science monitor : international medical journal of experimental and clinical research.

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

T. Kalina, V. Kanderova, E. Froňková, 2018, Journal of Clinical Immunology.

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

V. Kanderova, E. Froňková, A. Šedivá, 2017, Hormone Research in Paediatrics.

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

K. Réblová, M. Vlková, P. Kralickova, 2023, Frontiers in genetics.

Monogenic Early-Onset Lymphoproliferation and Autoimmunity: The Natural History of STAT3 GOF Syndrome.

K. Schwarz, M. Weinrich, F. Rieux-Laucat, 2022, The Journal of allergy and clinical immunology.

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

P. Kralickova, J. Litzman, B. Ravčuková, 2023, Journal of Clinical Immunology.

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

V. Kanderova, E. Froňková, Z. Šumník, 2017, Hormone Research in Paediatrics.

Recombinant Human C1 Esterase Inhibitor as Short‐Term Prophylaxis for Dental Procedures in Patients With Angioedema: A Case Series: 111

R. Shapiro, F. Hsu, T. Suiter, 2019, Journal of Allergy and Clinical Immunology.

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

M. van der Burg, T. Kalina, J. V. van Dongen, 2017, Clinical immunology.