J. Litzman

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Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia

T. Kalina, M. Vlková, J. Stuchly, 2017, Scientific Reports.

New and recurrent gain-of-function STAT1 mutations in patients with chronic mucocutaneous candidiasis from Eastern and Central Europe

J. Casanova, A. Šedivá, J. Litzman, 2013, Journal of Medical Genetics.

ICOS deficiency in patients with common variable immunodeficiency.

A. Plebani, J. Franco, C. Cunningham-Rundles, 2004, Clinical immunology.

Mannose‐binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency

J. Litzman, T. Pavlík, B. Grimbacher, 2008, Clinical and experimental immunology.

Phenotype, penetrance, and treatment of 133 cytotoxic T‐lymphocyte antigen 4–insufficient subjects

O. Elemento, T. Giese, A. Schulz, 2018, The Journal of allergy and clinical immunology.

Prognosis of Good syndrome: mortality and morbidity of thymoma associated immunodeficiency in perspective.

Smita Y. Patel, J. Litzman, Smita Y Patel, 2016, Clinical immunology.

The EUROclass trial: defining subgroups in common variable immunodeficiency.

Eren, M. Vihinen, M. Vlková, 2008, Blood.

Erratum: Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia

T. Kalina, M. Vlková, J. Stuchly, 2017, Scientific reports.

When to initiate immunoglobulin replacement therapy (IGRT) in antibody deficiency: a practical approach

J. Litzman, H. Chapel, S. Jolles, 2017, Clinical and experimental immunology.

Chronic immune activation in common variable immunodeficiency (CVID) is associated with elevated serum levels of soluble CD14 and CD25 but not endotoxaemia

M. Vlková, J. Litzman, O. Tichá, 2012, Clinical and experimental immunology.

Mapping susceptibility gene locus for IgA deficiency at del(18)(q22.3–q23); report of familial cryptic chromosome t(18q; 10p) translocations

J. Litzman, P. Tienari, M. Kähkönen, 2007, International Journal of Immunogenetics.

Clinical picture and treatment of 2212 patients with common variable immunodeficiency.

É. Oksenhendler, P. Soler-Palacín, A. Šedivá, 2014, The Journal of allergy and clinical immunology.

Reduced memory B cells in patients with hyper IgE syndrome.

A. Plebani, J. Franco, J. Litzman, 2008, Clinical immunology.

Terminally differentiated memory T cells are increased in patients with common variable immunodeficiency and selective IgA deficiency

M. Vlková, J. Litzman, T. Pavlík, 2017, Central-European journal of immunology.

Defective integration of activating signals derived from the T cell receptor (TCR) and costimulatory molecules in both CD4+ and CD8+ T lymphocytes of common variable immunodeficiency (CVID) patients

J. Litzman, H. Wolf, I. Hauber, 1997, Clinical and experimental immunology.

A defect in the early phase of T-cell receptor-mediated T-cell activation in patients with common variable immunodeficiency.

J. Litzman, H. Wolf, I. Hauber, 1994, Blood.

Expression of BAFF Receptors with Peripheral B Cell Numbers and the Soluble BAFF Levels Inversely Correlate

V. Lougaris, A. Plebani, J. Litzman, 2011 .

The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and function

A. Schulz, C. Cancrini, J. Litzman, 2009, The Journal of experimental medicine.

Association of FcRn expression with lung abnormalities and IVIG catabolism in patients with common variable immunodeficiency.

J. Litzman, B. Ravčuková, Jirí Jarkovský, 2010, Clinical immunology.

Antibody forming cells and plasmablasts in peripheral blood in CVID patients after vaccination.

M. Vlková, J. Litzman, V. Thon, 2011, Vaccine.

Neurological manifestation of immune system dysregulation resulting from CTLA-4 receptor mutation: a case report.

J. Litzman, J. Bednařík, P. Štourač, 2020, Multiple sclerosis and related disorders.

Successful renal transplantation in a patient with a Wiskott–Aldrich syndrome protein (WASP) gene mutation

M. Vlková, J. Litzman, Z. Chovancova, 2015, Transplant international : official journal of the European Society for Organ Transplantation.

Selective IgM Deficiency: Clinical and Laboratory Features of 17 Patients and a Review of the Literature

M. Vlková, P. Kralickova, J. Litzman, 2017, Journal of Clinical Immunology.

Regulatory B cells in CVID patients fail to suppress multifunctional IFN-γ+ TNF-α+ CD4+ T cells differentiation.

T. Kalina, M. Vlková, J. Litzman, 2015, Clinical immunology.

Impaired Toll-like receptor 8-mediated IL-6 and TNF-alpha production in antigen-presenting cells from patients with X-linked agammaglobulinemia.

A. Šedivá, J. Litzman, R. Spíšek, 2007, Blood.

Title: Impaired Toll-like receptor 8-mediated IL-6 and TNF-α production in antigen presenting cells from patients with X-linked agammaglobulinaemia Running title: Defective TLR-8 signaling in XLA

A. Šedivá, J. Litzman, R. Spíšek, 2006 .

The costimulatory signal CD28 is fully functional but cannot correct the impaired antigen response in T cells of patients with common variable immunodeficiency

J. Litzman, H. Wolf, J. Mannhalter, 1994, Clinical and experimental immunology.

Prognosis of Good syndrome: mortality and morbidity of thymoma associated immunode ﬁ ciency in perspective Clinical Immunology

Smita Y. Patel, J. Litzman, Smita Y Patel, 2016 .

Change in Referral Diagnoses and Diagnostic Delay in Hypogammaglobulinaemic Patients during 28 Years in a Single Referral Centre

J. Litzman, T. Pavlík, V. Thon, 2010, International Archives of Allergy and Immunology.

Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients

R. Schmidt, A. Plebani, J. Litzman, 2013, Clinical and experimental immunology.

Common variable immunodeficiency and malignancy: a report of two cases and possible explanation for the association

J. Litzman, I. Vořechovský, P. Hausner, 2005, Cancer Immunology, Immunotherapy.

Antigen presentation by common variable immunodeficiency (CVID) B cells and monocytes is unimpaired

J. Litzman, H. Wolf, M. Eibl, 1997, Clinical and experimental immunology.

Flow Based Enumeration of Plasmablasts in Peripheral Blood After Vaccination as a Novel Diagnostic Marker for Assessing Antibody Responses in Patients with Hypogammaglobulinaemia

M. Vlková, J. Litzman, V. Thon, 2012 .

Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations.

J. Litzman, B. Ravčuková, Jirí Jarkovský, 2012, Human immunology.

Therapeutic options for CTLA-4 Insufficiency.

V. Lougaris, T. Morio, K. Sullivan, 2021, The Journal of allergy and clinical immunology.

Neutrophils Are Dysregulated in Patients with Hereditary Angioedema Types I and II in a Symptom-Free Period

M. Vlková, J. Litzman, P. Souček, 2019, Mediators of inflammation.

Long‐term outcomes of 176 patients with X‐linked hyper‐IgM syndrome treated with or without hematopoietic cell transplantation

L. Notarangelo, J. Chou, C. Cunningham-Rundles, 2017, The Journal of allergy and clinical immunology.

Cytomegalovirus Disease in Patients with Common Variable Immunodeficiency: Three Case Reports

P. Kralickova, J. Litzman, J. Bureš, 2013, International Archives of Allergy and Immunology.

B-lymphocyte Subpopulations in Patients with Selective IgA Deficiency

M. Vlková, J. Litzman, J. Nechvatalova, 2012, Journal of Clinical Immunology.

T-LYMPHOCYTES IN IgA DEFICIENCY

J. Litzman, V. Thon, J. Lokaj, 2001 .

The mechanism of erythrocyte sedimentation in Westergren's examination.

J. Litzman, Z. Pospíšil, J. Mayer, 1992, Biorheology.

Wegener's granulomatosis: ischemic stroke as the first clinical manifestation (case study)

I. Rektor, J. Litzman, M. Bareš, 2002, Journal of Neurology.

Recurrent laryngeal papillomatosis: successful treatment with human papillomavirus vaccination

J. Litzman, J. Štěrba, P. Mudry, 2011, Archives of Disease in Childhood.

Altered Serum Cytokine Signature in Common Variable Immunodeficiency

M. Vlková, J. Litzman, Z. Hel, 2014, Journal of Clinical Immunology.

Isoprinosine does not protect against frequent respiratory tract infections in childhood

J. Litzman, G. Morgan, J. Lokaj, 1999, European Journal of Pediatrics.

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.

A. Schäffer, E. Gertz, A. Plebani, 2010, The Journal of allergy and clinical immunology.

Hyper‐IgE in the allergy clinic––when is it primary immunodeficiency?

Mark J. Ponsford, A. Šedivá, J. Litzman, 2018, Allergy.

Adverse effects of immunoglobulin therapy.

J. Litzman, Z. Chovancova, Iva Šutová, 2019, Vnitrni lekarstvi.

Subcutaneous immunoglobulin 16.5% for the treatment of pediatric patients with primary antibody immunodeficiency

R. Kobayashi, J. Litzman, Sudhir Gupta, 2022, Expert review of clinical immunology.

Characterization of Lymphocyte Subsets in Patients with Common Variable Immunodeficiency Reveals Subsets of Naive Human B Cells Marked by CD24 Expression

T. Kalina, M. Vlková, V. Kanderova, 2010, The Journal of Immunology.

Initial presenting manifestations in 16,486 patients with Inborn Errors of Immunity include infections and non-infectious manifestations.

Nurit Assia Batzir, K. Schwarz, D. Foell, 2021, The Journal of allergy and clinical immunology.

Profiling of polychromatic flow cytometry data on B‐cells reveals patients' clusters in common variable immunodeficiency

Tomáš Kalina, Anna Šedivá, Jiří Litzman, 2009, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

Age dependency and mutual relations in T and B lymphocyte abnormalities in common variable immunodeficiency patients

M. Vlková, J. Litzman, L. Bláha, 2006, Clinical and experimental immunology.

Monitoring of CD38high expression in peripheral blood CD8+ lymphocytes in patients after kidney transplantation as a marker of cytomegalovirus infection.

J. Litzman, O. Tichá, T. Freiberger, 2010, Transplant immunology.

Common variants at PVT1, ATG13–AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency

V. Lougaris, A. Plebani, J. Litzman, 2016, Nature Genetics.

Bacterial but Not Fungal Gut Microbiota Alterations Are Associated With Common Variable Immunodeficiency (CVID) Phenotype

P. Kralickova, J. Litzman, Juraj Bosák, 2019, Front. Immunol..

CEBPE-Mutant Specific Granule Deficiency Correlates With Aberrant Granule Organization and Substantial Proteome Alterations in Neutrophils

K. Bennett, E. Mejstrikova, J. Litzman, 2018, Front. Immunol..

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency.

A. Fischer, A. Plebani, J. Litzman, 2004, Clinical immunology.

IgA Deficiency in Czech Healthy Individuals and Selected Patient Groups

J. Litzman, J. Lokaj, I. Ševčíková, 2000, International Archives of Allergy and Immunology.

Soluble BAFF Levels Inversely Correlate with Peripheral B Cell Numbers and the Expression of BAFF Receptors

V. Lougaris, A. Plebani, J. Litzman, 2012, The Journal of Immunology.

European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management

K. Sullivan, J. Litzman, M. Seppänen, 2020, Journal of Clinical Immunology.

Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome.

J. Litzman, S. Strobel, H. Chapel, 1996, Archives of disease in childhood.

Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy

M. Vlková, P. Kralickova, J. Litzman, 2018, Journal of Clinical Immunology.

Clinical Efficacy, Safety and Tolerability of a New Subcutaneous Immunoglobulin 16.5% (Octanorm [Cutaquig®]) in the Treatment of Patients With Primary Immunodeficiencies

R. Kobayashi, J. Litzman, Sudhir Gupta, 2019, Front. Immunol..

Immunoglobulin D enhances immune surveillance by activating antimicrobial, pro-inflammatory and B cell-stimulating programs in basophils

Melanie Wilson, Poonam Rath, Marco Cattalini, 2009, Nature Immunology.

Pregnancy Outcome in Patients with Common Variable Immunodeficiency

M. Vlková, D. Jílek, P. Kralickova, 2015, Journal of Clinical Immunology.

Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy

M. Vlková, P. Kralickova, J. Litzman, 2018, Journal of Clinical Immunology.

Hereditary angio-oedema with C1 inhibitor deficiency: Characteristics and diagnostic delay of Czech patients from one centre.

J. Litzman, P. Kadlecová, P. Kuklínek, 2016, Allergologia et immunopathologia.

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.

Exon 1 polymorphism of the B2BKR gene does not influence the clinical status of patients with hereditary angioedema.

J. Litzman, L. Kolářová, T. Freiberger, 2002, Human immunology.

Registry‐based analysis of Icatibant and C1‐inhibitor use in treatment of laryngeal attacks of hereditary angioedema

P. Kralickova, J. Litzman, M. Svoboda, 2022, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema

J. Litzman, P. Mejstrik, L. Kolářová, 2002, Human mutation.

Gross deletions involving IGHM, BTK, or Artemis: a model for genomic lesions mediated by transposable elements.

M. van der Burg, M. V. van Zelm, J. V. van Dongen, 2008, American journal of human genetics.

Abstracts from the 10th C1-inhibitor deficiency workshop

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

Deep Intronic Mutation in SERPING1 Caused Hereditary Angioedema Through Pseudoexon Activation

J. Litzman, B. Ravčuková, P. Souček, 2020, Journal of Clinical Immunology.

Erratum: Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia

T. Kalina, M. Vlková, J. Stuchly, 2017, Scientific Reports.

B-lymphocyte Subpopulations in Patients with Selective IgA Deficiency

M. Vlková, J. Litzman, J. Nechvatalova, 2012, Journal of Clinical Immunology.

Human B Cells Marked by CD24 Expression Immunodeficiency Reveals Subsets of Naive Patients with Common Variable Characterization of Lymphocyte Subsets in

T. Kalina, M. Vlková, V. Kanderova, 2010 .

Patients With Common Variable Immunodeficiency (CVID) Show Higher Gut Bacterial Diversity and Levels of Low-Abundance Genes Than the Healthy Housemates

J. Litzman, Juraj Bosák, M. Lexa, 2021, Frontiers in Immunology.

Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement

T. Kalina, M. Vlková, E. Mejstrikova, 2019, Front. Immunol..

Selective IgM Deficiency: Clinical and Laboratory Features of 17 Patients and a Review of the Literature

M. Vlková, P. Kralickova, J. Litzman, 2017, Journal of Clinical Immunology.

Immune deficiencies , infection , and systemic immune disorders Mutations in STAT 3 and diagnostic guidelines for hyper-IgE syndrome

A. Schäffer, A. Plebani, C. Pignata, 2010 .

Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience

J. Litzman, C. Deswarte, B. Ravčuková, 2016, Journal of Clinical Immunology.

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders

E. López-Granados, J. Litzman, B. Ferry, 2010, Clinical and experimental immunology.

Gastrointestinal Complications in Primary Immunoglobulin Deficiencies

J. Litzman, 2018, Humoral Primary Immunodeficiencies.

Neutrophil and Granulocytic Myeloid-Derived Suppressor Cell–Mediated T Cell Suppression Significantly Contributes to Immune Dysregulation in Common Variable Immunodeficiency Disorders

M. Vlková, J. Litzman, Z. Hel, 2018, The Journal of Immunology.

T and B lymphocyte subpopulations and activation/differentiation markers in patients with selective IgA deficiency

M. Vlková, J. Litzman, J. Lokaj, 2006, Clinical and experimental immunology.

Altered Serum Cytokine Signature in Common Variable Immunodeficiency

M. Vlková, J. Litzman, Z. Hel, 2014, Journal of Clinical Immunology.

Czech Hizentra Noninterventional Study With Rapid Push: Efficacy, Safety, Tolerability, and Convenience of Therapy With 20% Subcutaneous Immunoglobulin.

D. Jílek, P. Kralickova, A. Šedivá, 2019, Clinical therapeutics.

Primary immunodeficiencies in adults.

J. Litzman, 2019, Vnitrni lekarstvi.

CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID

T. Kalina, V. Kanderova, D. Jílek, 2019, Front. Immunol..

Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?

J. Litzman, Hanns-Martin Lorenz, G. Häcker, 2022, Frontiers in Immunology.

[IgG subclasses and autoantibodies in adult patients with selective IgA deficiency].

J. Litzman, J. Lokaj, I. Ševčíková, 2000, Vnitrni lekarstvi.

Detection of Impaired IgG Antibody Formation Facilitates the Decision on Early Immunoglobulin Replacement in Hypogammaglobulinemic Patients

J. Litzman, M. Eibl, H. Wolf, 2015, Front. Immunol..

Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe

P. Kralickova, J. Litzman, A. Turley, 2015, Journal of Clinical Immunology.

Fifteen Years of the J Project

A. Šedivá, J. Litzman, I. Tuzankina, 2019, Journal of Clinical Immunology.

Infectious Complications and Immune/Inflammatory Response in Cardiogenic Shock Patients: A Prospective Observational Study

A. Mebazaa, J. Litzman, M. Legrand, 2017, Shock.

Treatment of antibody immunodeficiency.

J. Litzman, 2019, Vnitrni lekarstvi.

Long-term efficacy, safety, and tolerability of a subcutaneous immunoglobulin 16.5% (cutaquig®) in the treatment of patients with primary immunodeficiencies

R. Kobayashi, J. Litzman, Sudhir Gupta, 2022, Clinical and experimental immunology.

A concurrent occurrence of cutis laxa, Dandy‐Walker syndrome and immunodeficiency in a girl

J. Litzman, H. Bučková, J. Ventruba, 2003, Acta paediatrica.

Corrigendum to “Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency” [Clin. Immunol. 110 (2004) 22–29]

A. Plebani, J. Litzman, O. Sanal, 2004 .

Complement activation products in patients with common variable immunodeficiency

J. Litzman, J. Trávník, D. Bartoňková, 2006 .

[Personal experience with replacement therapy with intravenous gamma globulin].

J. Litzman, M. Eibl, V. Thon, 1995, Vnitrni lekarstvi.

Early manifestation and recognition of C2 complement deficiency in the form of pyogenic infection in infancy

M. Vlková, J. Litzman, V. Thon, 2003, Journal of paediatrics and child health.

Low ficolin‐2 levels in common variable immunodeficiency patients with bronchiectasis

J. Litzman, B. Grimbacher, U. Salzer, 2015, Clinical and experimental immunology.

Influence of FCRN expression on lung decline and intravenous immunoglobulin catabolism in common variable immunodeficiency patients

J. Litzman, 2014, Clinical and experimental immunology.

Toll-Like Receptor Stimulation Induces Higher TNF-α Secretion in Peripheral Blood Mononuclear Cells from Patients with Hyper IgE Syndrome

A. Plebani, J. Franco, J. Litzman, 2008, International Archives of Allergy and Immunology.

Spectrum and Management of Complement Immunodeficiencies (Excluding Hereditary Angioedema) Across Europe

P. Kralickova, J. Litzman, N. Kutukculer, 2015, Journal of Clinical Immunology.

Matrix metalloproteinase-9 and matrix metalloproteinase-2 as biomarkers of various courses in multiple sclerosis

J. Litzman, J. Bednařík, H. Novotná, 2009, Multiple sclerosis.

Secondary Combined Immunodeficiency in Pediatric Patients after the Fontan Operation: Three Case Reports

J. Litzman, E. Hlavackova, H. Jicinska, 2016, International Archives of Allergy and Immunology.

Incidence of primary immunodeficiencies in a population of south Moravia, Czechoslovakia.

J. Litzman, J. Lokaj, P. Kuklínek, 1995, Advances in Experimental Medicine and Biology.

Progression of selective IgA deficiency to common variable immunodeficiency in a 16 year old boy.

J. Litzman, V. Thon, J. Lokaj, 1996, Allergologia et Immunopathologia.

The Expression of Fc gamma Receptors on Leukocytes and Clinical Course of Common Variable Imminodeficiency (CVID)

M. Vlková, J. Litzman, V. Thon, 2005 .

Medical algorithm: Diagnosis and management of antibody immunodeficiencies

A. Šedivá, J. Litzman, S. Burns, 2021, Allergy.

Risk Factors for Severe COVID-19 and Hospital Admission in Patients With Inborn Errors of Immunity - Results From a Multicenter Nationwide Study

D. Jílek, P. Kralickova, A. Šedivá, 2022, Frontiers in Immunology.

Agammaglobulinaemia in a girl with a mosaic of ring 18 chromosome

J. Litzman, R. Gaillyová, Z. Zemanová, 1998, Journal of paediatrics and child health.

IgG4 immunoglobulin subclass and related pathological conditions or how to effectively imitate cancer disease

P. Filipensky, J. Litzman, Klára Novosádová, 2022, Klinicka onkologie.

A Rose Amongst the Thorns: the Mission of the J Project in a Conflictual World

A. Šedivá, J. Litzman, I. Tuzankina, 2022, Journal of Clinical Immunology.

Common variable immunodeficiency patients display elevated plasma levels of granulocyte activation markers elastase and myeloperoxidase

M. Vlková, J. Litzman, Z. Hel, 2019, International journal of immunopathology and pharmacology.

Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group

V. Lougaris, A. Plebani, G. Driessen, 2018, Journal of Clinical Immunology.

Staphylococcal food poisoning.

A. L. Wong, J. Gécz, M. Rietschel, 2002 .

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.

Regulation and Function of Human Immunoglobulin D

Bihui Huang, J. Litzman, K. Riesbeck, 2010 .

Soluble ST2 levels in patients with cardiogenic and septic shock are not predictors of mortality.

J. Litzman, J. Ševčíková, M. Dastych, 2012, Experimental and clinical cardiology.

PLAUR splicing pattern in hereditary angioedema patients’ monocytes and macrophages

M. Vlková, J. Litzman, P. Souček, 2023, Molecular Biology Reports.

Soluble BAFF Levels Inversely Correlate with Peripheral B Cell Numbers and the Expression of BAFF Receptors

V. Lougaris, A. Plebani, J. Litzman, 2012, The Journal of Immunology.

Toll-Like Receptor Stimulation Induces Higher TNF-α Secretion in Peripheral Blood Mononuclear Cells from Patients with Hyper IgE Syndrome

A. Plebani, J. Franco, J. Litzman, 2008, International Archives of Allergy and Immunology.

Pregnancy Outcome in Patients with Common Variable Immunodeficiency

M. Vlková, D. Jílek, P. Kralickova, 2015, Journal of Clinical Immunology.

New and recurrent gain-of-function STAT1 mutations in patients with chronic mucocutaneous candidiasis from Eastern and Central Europe

J. Casanova, A. Šedivá, J. Litzman, 2013, Journal of Medical Genetics.

Prognosis of Good syndrome: mortality and morbidity of thymoma associated immunodeficiency in perspective.

Smita Y. Patel, J. Litzman, M. van Deuren, 2016, Clinical immunology.

Overview of subcutaneous immunoglobulin 16.5% in primary and secondary immunodeficiency diseases.

R. Kobayashi, J. Litzman, Sudhir Gupta, 2022, Immunotherapy.

Erratum: Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia

T. Kalina, M. Vlková, Ondřej Pelák, 2017, Scientific Reports.

Common Variable Immunodeficiency patients with a phenotypic profile of immunosenescence present with thrombocytopenia

T. Kalina, M. Vlková, Ondřej Pelák, 2017, Scientific Reports.

Regulatory B cells in CVID patients fail to suppress multifunctional IFN-γ+ TNF-α+ CD4+ T cells differentiation.

T. Kalina, M. Vlková, J. Litzman, 2015, Clinical immunology.

CEBPE-Mutant Specific Granule Deficiency Correlates With Aberrant Granule Organization and Substantial Proteome Alterations in Neutrophils

K. Bennett, E. Mejstrikova, J. Litzman, 2018, Front. Immunol..

Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients

R. Schmidt, A. Plebani, J. Litzman, 2013, Clinical and experimental immunology.

Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group

V. Lougaris, A. Plebani, G. Driessen, 2018, Journal of Clinical Immunology.