Lista de obras - Anna Sediva - Dominio Público Uruguay

AIRE deficiency in thymus of 2 patients with Omenn syndrome

artículo científico publicado en 2005

AIRE deficiency in thymus of 2 patients with Omenn syndrome

article

Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors.

artículo científico publicado en 2018

Alteration of B cell subsets and the receptor for B cell activating factor (BAFF) in paediatric patients with type 1 diabetes.

artículo científico publicado en 2017

Anti-CD20 (rituximab) treatment for atopic eczema

artículo científico publicado en 2008

Anti-IL6 Autoantibodies in an Infant With CRP-Less Septic Shock

scientific article published on 08 November 2019

Anti-N-methyl-D-aspartate receptor encephalitis: the clinical course in light of the chemokine and cytokine levels in cerebrospinal fluid.

artículo científico publicado en 2016

Antineutrophil cytoplasmic antibodies directed against bactericidal/permeability-increasing protein detected in children with cystic fibrosis inhibit neutrophil-mediated killing of Pseudomonas aeruginosa

artículo científico publicado en 2003

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

Case report: type 1 diabetes in monozygotic quadruplets

artículo científico publicado en 2011

Changes in innate and adaptive immunity over the first year after the onset of type 1 diabetes

artículo científico publicado en 2019

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

Characterization of the B-cell compartment in a patient with Schnitzler syndrome

artículo científico publicado en 2010

Clinical picture and treatment of 2212 patients with common variable immunodeficiency

artículo científico publicado en 2014

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study ⬇️

artículo científico publicado en 2016

Cluster of patients with Familial Mediterranean fever and heterozygous carriers of mutations in MEFV gene in the Czech Republic.

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes

artículo científico publicado en 2007

Cost-effective genotyping of human MBL2 gene mutations using multiplex PCR.

artículo científico publicado en 2004

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

artículo científico publicado en 2019

Decreased dendritic cell numbers but increased TLR9-mediated interferon-alpha production in first degree relatives of type 1 diabetes patients

artículo científico publicado en 2014

Diagnostic and pathogenetic role of antineutrophil cytoplasmic autoantibodies

artículo científico publicado en 2003

Differential cytokine profile in children with cystic fibrosis

artículo científico publicado en 2005

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

artículo científico publicado en 2018

Early development of immunity in diGeorge syndrome.

artículo científico publicado en 2005

Effective "activated PI3Kδ syndrome"-targeted therapy with the PI3Kδ inhibitor leniolisib.

artículo científico publicado en 2017

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

artículo científico publicado en 2017

Europe immunoglobulin map

artículo científico publicado en 2014

Exhausted phenotype of follicular CD8 T cells in CVID

artículo científico publicado en 2020

Expansion of T helper type 17 lymphocytes in patients with chronic granulomatous disease

scientific article published on 01 October 2011

Exposure to silica and risk of ANCA-associated vasculitis

artículo científico publicado en 2006

FOCUS on FOCIS: combined chemo-immunotherapy for the treatment of hormone-refractory metastatic prostate cancer.

scientific article published on 08 February 2009

Familiar Mediterranean fever in Czech Republic

artículo científico publicado en 2014

Follicular Helper T Cells in DiGeorge Syndrome

scientific article published on 23 July 2018

Generation of functional dendritic cells for potential use in the treatment of acute lymphoblastic leukemia

artículo científico publicado en 2002

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

artículo científico publicado en 2017

Gliadin fragments induce phenotypic and functional maturation of human dendritic cells

scientific article published on 01 November 2005

Helios expression in T-regulatory cells in patients with di George Syndrome

artículo científico publicado en 2014

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

artículo científico publicado en 2018

Immunological findings in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) and their family members: are heterozygotes subclinically affected?

artículo científico publicado en 2002

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

Kinetics of Toll-like receptor-4 splice variants expression in lipopolysaccharide-stimulated antigen presenting cells of healthy donors and patients with cystic fibrosis

artículo científico publicado en 2007

Long-term follow-up of Czech children with D+ hemolytic-uremic syndrome

artículo científico publicado en 2002

Low marginal zone-like B lymphocytes and natural antibodies characterize skewed B-lymphocyte subpopulations in del22q11 DiGeorge patients

artículo científico publicado en 2015

Lymphoproliferation, immunodeficiency and early-onset inflammatory bowel disease associated with a novel mutation in Caspase 8

artículo científico publicado en 2018

Maturation of dendritic cells by bacterial immunomodulators

artículo científico publicado en 2004

Mitochondrial uncoupling protein 2 gene transcript levels are elevated in maturating erythroid cells

artículo científico publicado en 2007

Mutual alteration of NOD2-associated Blau syndrome and IFNγR1 deficiency

artículo científico publicado en 2019

NF-κB, p38 MAPK, ERK1/2, mTOR, STAT3 and increased glycolysis regulate stability of paricalcitol/dexamethasone-generated tolerogenic dendritic cells in the inflammatory environment

artículo científico publicado en 2015

Negativity for Specific Autoantibodies in Patients with Type 1 Diabetes That Developed on a Background of Common Variable Immunodeficiency.

artículo científico publicado en 2016

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

artículo científico publicado en 2013

Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome

artículo científico publicado en 2014

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

artículo científico publicado en 2018

Plasmacytoid DCs, exposed to TSLP in synergy with TLR ligands, acquire significant potential towards Th2 polarization.

artículo científico publicado en 2013

Polymorphisms of TGF-beta1 in cystic fibrosis patients

artículo científico publicado en 2006

Prevalence and treatment of anti-NMDA receptor encephalitis

artículo científico publicado en 2013

Primary Sjögren syndrome in the paediatric age: a multicentre survey

artículo científico publicado en 2003

Primary immunodeficiencies in Central and Eastern Europe-the power of networking Report on the activity of the Jeffrey Modell Foundation Centers Network in Central and Eastern Europe

artículo científico publicado en 2019

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

artículo científico publicado en 2009

Schnitzlers SyndromeDifferential diagnostics, an overview of therapeutic options and description of 5 cases treated with anakinra

artículo científico publicado en 2016

Selective increase in blood dendritic cell antigen-3-positive dendritic cells in bronchoalveolar lavage fluid in allergic patients

scientific article published on 01 March 2012

Serum immunoglobulin free light chains in severe forms of atopic dermatitis

artículo científico publicado en 2010

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

Skin lesions in a boy with X-linked lymphoproliferative disorder: comparison of 5 SH2D1A deletion cases

artículo científico publicado en 2012

T regulatory lymphocytes in type 1 diabetes: Impaired CD25 expression and IL-2 induced STAT5 phosphorylation in pediatric patients

artículo científico publicado en 2016

TRNT1 missense mutations define an autoinflammatory disease characterized by recurrent fever, severe anemia, and b-cell immunodeficiency

artículo científico publicado en 2014

The TREC/KREC assay for the diagnosis and monitoring of patients with DiGeorge syndrome.

artículo científico publicado en 2014

Tolerogenic Dendritic Cells from Poorly Compensated Type 1 Diabetes Patients Have Decreased Ability To Induce Stable Antigen-Specific T Cell Hyporesponsiveness and Generation of Suppressive Regulatory T Cells.

artículo científico publicado en 2016

Unrelated partially matched lymphocyte infusions in a patient with complete DiGeorge/CHARGE syndrome

artículo científico publicado en 2007

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

scientific article published on 22 June 2018

X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world

scientific article published on 22 March 2019

Lista de obras de Anna Sediva

AIRE deficiency in thymus of 2 patients with Omenn syndrome

AIRE deficiency in thymus of 2 patients with Omenn syndrome

Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors.

Alteration of B cell subsets and the receptor for B cell activating factor (BAFF) in paediatric patients with type 1 diabetes.

Anti-CD20 (rituximab) treatment for atopic eczema

Anti-IL6 Autoantibodies in an Infant With CRP-Less Septic Shock

Anti-N-methyl-D-aspartate receptor encephalitis: the clinical course in light of the chemokine and cytokine levels in cerebrospinal fluid.

Antineutrophil cytoplasmic antibodies directed against bactericidal/permeability-increasing protein detected in children with cystic fibrosis inhibit neutrophil-mediated killing of Pseudomonas aeruginosa

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

Case report: type 1 diabetes in monozygotic quadruplets

Changes in innate and adaptive immunity over the first year after the onset of type 1 diabetes

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

Characterization of the B-cell compartment in a patient with Schnitzler syndrome

Clinical picture and treatment of 2212 patients with common variable immunodeficiency

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study ⬇️

Cluster of patients with Familial Mediterranean fever and heterozygous carriers of mutations in MEFV gene in the Czech Republic.

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

Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes

Cost-effective genotyping of human MBL2 gene mutations using multiplex PCR.

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

Decreased dendritic cell numbers but increased TLR9-mediated interferon-alpha production in first degree relatives of type 1 diabetes patients

Diagnostic and pathogenetic role of antineutrophil cytoplasmic autoantibodies

Differential cytokine profile in children with cystic fibrosis

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

Early development of immunity in diGeorge syndrome.

Effective "activated PI3Kδ syndrome"-targeted therapy with the PI3Kδ inhibitor leniolisib.

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

Europe immunoglobulin map

Exhausted phenotype of follicular CD8 T cells in CVID

Expansion of T helper type 17 lymphocytes in patients with chronic granulomatous disease

Exposure to silica and risk of ANCA-associated vasculitis

FOCUS on FOCIS: combined chemo-immunotherapy for the treatment of hormone-refractory metastatic prostate cancer.

Familiar Mediterranean fever in Czech Republic

Follicular Helper T Cells in DiGeorge Syndrome

Generation of functional dendritic cells for potential use in the treatment of acute lymphoblastic leukemia

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

Gliadin fragments induce phenotypic and functional maturation of human dendritic cells

Helios expression in T-regulatory cells in patients with di George Syndrome

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

Immunological findings in patients with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) and their family members: are heterozygotes subclinically affected?

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

Kinetics of Toll-like receptor-4 splice variants expression in lipopolysaccharide-stimulated antigen presenting cells of healthy donors and patients with cystic fibrosis

Long-term follow-up of Czech children with D+ hemolytic-uremic syndrome

Low marginal zone-like B lymphocytes and natural antibodies characterize skewed B-lymphocyte subpopulations in del22q11 DiGeorge patients

Lymphoproliferation, immunodeficiency and early-onset inflammatory bowel disease associated with a novel mutation in Caspase 8

Maturation of dendritic cells by bacterial immunomodulators

Mitochondrial uncoupling protein 2 gene transcript levels are elevated in maturating erythroid cells

Mutual alteration of NOD2-associated Blau syndrome and IFNγR1 deficiency

NF-κB, p38 MAPK, ERK1/2, mTOR, STAT3 and increased glycolysis regulate stability of paricalcitol/dexamethasone-generated tolerogenic dendritic cells in the inflammatory environment

Negativity for Specific Autoantibodies in Patients with Type 1 Diabetes That Developed on a Background of Common Variable Immunodeficiency.

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

Occurrence of B-cell lymphomas in patients with activated phosphoinositide 3-kinase δ syndrome

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

Plasmacytoid DCs, exposed to TSLP in synergy with TLR ligands, acquire significant potential towards Th2 polarization.

Polymorphisms of TGF-beta1 in cystic fibrosis patients

Prevalence and treatment of anti-NMDA receptor encephalitis

Primary Sjögren syndrome in the paediatric age: a multicentre survey

Primary immunodeficiencies in Central and Eastern Europe-the power of networking Report on the activity of the Jeffrey Modell Foundation Centers Network in Central and Eastern Europe

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

Schnitzlers SyndromeDifferential diagnostics, an overview of therapeutic options and description of 5 cases treated with anakinra

Selective increase in blood dendritic cell antigen-3-positive dendritic cells in bronchoalveolar lavage fluid in allergic patients

Serum immunoglobulin free light chains in severe forms of atopic dermatitis

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

Skin lesions in a boy with X-linked lymphoproliferative disorder: comparison of 5 SH2D1A deletion cases

T regulatory lymphocytes in type 1 diabetes: Impaired CD25 expression and IL-2 induced STAT5 phosphorylation in pediatric patients

TRNT1 missense mutations define an autoinflammatory disease characterized by recurrent fever, severe anemia, and b-cell immunodeficiency

The TREC/KREC assay for the diagnosis and monitoring of patients with DiGeorge syndrome.

Tolerogenic Dendritic Cells from Poorly Compensated Type 1 Diabetes Patients Have Decreased Ability To Induce Stable Antigen-Specific T Cell Hyporesponsiveness and Generation of Suppressive Regulatory T Cells.

Unrelated partially matched lymphocyte infusions in a patient with complete DiGeorge/CHARGE syndrome

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

X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world