Lista de obras - Jiri Litzman - Dominio Público Uruguay

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

artículo científico publicado en 2003

Agammaglobulinaemia in a girl with a mosaic of ring 18 chromosome

artículo científico publicado en 1998

Altered serum cytokine signature in common variable immunodeficiency

artículo científico publicado en 2014

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

artículo científico publicado en 2011

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

artículo científico publicado en 1997

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

artículo científico publicado en 2010

B-lymphocyte subpopulations in patients with selective IgA deficiency.

artículo científico publicado en 2012

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

scientific article published on 13 August 2019

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

artículo científico publicado en 2018

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

artículo científico publicado en 2018

Change in referral diagnoses and diagnostic delay in hypogammaglobulinaemic patients during 28 years in a single referral centre

scientific article published on 01 April 2010

Characterization of lymphocyte subsets in patients with common variable immunodeficiency reveals subsets of naive human B cells marked by CD24 expression.

artículo científico publicado en 2010

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

Clinical picture and treatment of 2212 patients with common variable immunodeficiency

artículo científico publicado en 2014

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

artículo científico publicado en 2004

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

artículo científico publicado en 2017

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

artículo científico publicado en 1990

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

artículo científico publicado en 2019

Common variable immunodeficiency: A defect at the level of T cells

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

artículo científico publicado en 2016

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]

scholarly article published in Clinical Immunology

Cytomegalovirus disease in patients with common variable immunodeficiency: three case reports

artículo científico publicado en 2013

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

artículo científico publicado en 2019

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 ⬇️

artículo científico publicado el 1 de noviembre de 1997

Detection of impaired IgG antibody formation facilitates the decision on early immunoglobulin replacement in hypogammaglobulinemic patients

artículo científico publicado en 2015

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

artículo científico publicado en 2003

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

artículo científico publicado en 2017

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

artículo científico publicado en 2002

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

artículo científico publicado en 2008

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

artículo científico publicado en 2016

ICOS deficiency in patients with common variable immunodeficiency.

artículo científico publicado en 2004

IgA deficiency in Czech healthy individuals and selected patient groups

scientific article published on 01 October 2000

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

artículo científico publicado en 2009

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

scientific article published on 07 November 2006

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

artículo científico publicado en 2016

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

artículo científico publicado en 2014

Isoprinosine does not protect against frequent respiratory tract infections in childhood

artículo científico publicado en 1999

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

scientific article published on 11 July 2008

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

artículo científico publicado en 2007

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

artículo científico publicado en 2010

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

artículo científico publicado en 2010

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders.

artículo científico publicado en 2010

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

scientific article published on 19 May 2019

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

artículo científico publicado en 2013

No association of FCRN promoter VNTR polymorphism with the rate of maternal-fetal IgG transfer

artículo científico publicado en 2010

No evidence for linkage between the hereditary angiooedema clinical phenotype and the BDKR1, BDKR2, ACE or MBL2 gene

artículo científico publicado en 2011

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

scientific article published on 18 September 2019

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

artículo científico publicado en 2013

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

artículo científico publicado en 2018

Pregnancy Outcome in Patients with Common Variable Immunodeficiency.

artículo científico publicado en 2015

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

artículo científico publicado en 2009

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

artículo científico publicado en 2016

Recurrent laryngeal papillomatosis: successful treatment with human papillomavirus vaccination

artículo científico publicado en 2011

Reduced memory B cells in patients with hyper IgE syndrome

artículo científico publicado en 2008

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

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Serum IgD levels in children under investigation for and with defined immunodeficiency.

artículo científico publicado en 1997

Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors

artículo científico publicado en 2012

Spectrum and management of complement immunodeficiencies (excluding hereditary angioedema) across Europe

artículo científico publicado en 2015

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

artículo científico publicado en 2015

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

artículo científico publicado en 2007

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

artículo científico publicado en 2017

The EUROclass trial: defining subgroups in common variable immunodeficiency.

artículo científico publicado en 2007

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

artículo científico publicado en 2009

The mechanism of erythrocyte sedimentation in Westergren's examination

artículo científico publicado el 1 de marzo de 1992

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

artículo científico publicado en 2008

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

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Základy vyšetření v klinické imunologii ⬇️

2007 Czech book edition

Lista de obras de Jiri Litzman

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

Agammaglobulinaemia in a girl with a mosaic of ring 18 chromosome

Altered serum cytokine signature in common variable immunodeficiency

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

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

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

B-lymphocyte subpopulations in patients with selective IgA deficiency.

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

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

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

Change in referral diagnoses and diagnostic delay in hypogammaglobulinaemic patients during 28 years in a single referral centre

Characterization of lymphocyte subsets in patients with common variable immunodeficiency reveals subsets of naive human B cells marked by CD24 expression.

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

Clinical picture and treatment of 2212 patients with common variable immunodeficiency

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

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

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

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

Common variable immunodeficiency: A defect at the level of T cells

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

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]

Cytomegalovirus disease in patients with common variable immunodeficiency: three case reports

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

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 ⬇️

Detection of impaired IgG antibody formation facilitates the decision on early immunoglobulin replacement in hypogammaglobulinemic patients

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

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

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

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

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

ICOS deficiency in patients with common variable immunodeficiency.

IgA deficiency in Czech healthy individuals and selected patient groups

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

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

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

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

Isoprinosine does not protect against frequent respiratory tract infections in childhood

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

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

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

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

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

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders.

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

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

No association of FCRN promoter VNTR polymorphism with the rate of maternal-fetal IgG transfer

No evidence for linkage between the hereditary angiooedema clinical phenotype and the BDKR1, BDKR2, ACE or MBL2 gene

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

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

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

Pregnancy Outcome in Patients with Common Variable Immunodeficiency.

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

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

Recurrent laryngeal papillomatosis: successful treatment with human papillomavirus vaccination

Reduced memory B cells in patients with hyper IgE syndrome

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

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

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

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

Serum IgD levels in children under investigation for and with defined immunodeficiency.

Soluble BAFF levels inversely correlate with peripheral B cell numbers and the expression of BAFF receptors

Spectrum and management of complement immunodeficiencies (excluding hereditary angioedema) across Europe

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

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

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

The EUROclass trial: defining subgroups in common variable immunodeficiency.

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

The mechanism of erythrocyte sedimentation in Westergren's examination

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

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

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

Základy vyšetření v klinické imunologii ⬇️