Veronika Kanderova
Prague, PR, Czech Republic
Last Updated: 09/26/2026
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Found 28 publications
Revising pathogenesis of AP1S1-related MEDNIK syndrome: a missense variant in the AP1S1 gene as a causal genetic lesion.
Journal: Journal of molecular medicine (Berlin, Germany)
Published: May 06, 2024
Clinical Outcomes, Immunogenicity, and Safety of BNT162b2 Vaccine in Primary Antibody Deficiency.
Journal: The journal of allergy and clinical immunology. In practice
Published: June 29, 2022
Minimal Residual Disease-Guided Intermittent Dosing in Patients With Cancer: Successful Treatment of Chemoresistant Anaplastic Large Cell Lymphoma Using Intermittent Lorlatinib Dosing.
Journal: JCO precision oncology
Published: June 14, 2022
Impact of JAK Inhibitors in Pediatric Patients with STAT1 Gain of Function (GOF) Mutations-10 Children and Review of the Literature.
Journal: Journal of clinical immunology
Published: January 07, 2022
TLR8/TLR7 dysregulation due to a novel TLR8 mutation causes severe autoimmune hemolytic anemia and autoinflammation in identical twins.
Journal: American journal of hematology
Published: December 23, 2021
Somatic Mutations in Oncogenes Are in Chronic Myeloid Leukemia Acquired De Novo via Deregulated Base-Excision Repair and Alternative Non-Homologous End Joining.
Journal: Frontiers in oncology
Published: July 20, 2021
Partial RAG deficiency in humans induces dysregulated peripheral lymphocyte development and humoral tolerance defect with accumulation of T-bet+ B cells.
Journal: Nature immunology
Published: June 10, 2021
Natural Course of Activated Phosphoinositide 3-Kinase Delta Syndrome in Childhood and Adolescence.
Journal: Frontiers in pediatrics
Published: April 20, 2021
Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK.
Journal: The Journal of allergy and clinical immunology
Published: January 15, 2021
A Novel Case of Homozygous Interferon Alpha/Beta Receptor Alpha Chain (IFNAR1) Deficiency With Hemophagocytic Lymphohistiocytosis.
Journal: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
Published: June 08, 2020
Novel XIAP mutation causing enhanced spontaneous apoptosis and disturbed NOD2 signalling in a patient with atypical adult-onset Crohn's disease.
Journal: Cell death & disease
Published: January 23, 2020
Last Updated: 09/26/2026