Lista de obras - Eric Jeziorski - Dominio Público Uruguay

A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency

artículo científico publicado en 2019

A new autoinflammatory and autoimmune syndrome associated with NLRP1 mutations: NAIAD (NLRP1-associated autoinflammation with arthritis and dyskeratosis).

artículo científico publicado en 2016

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

artículo científico publicado en 2011

Atypical pneumonia linked to community-acquired staphylococcus aureus cross-transmission in the nursery.

artículo científico publicado en 2013

B-cell polyclonal activation and Epstein-Barr viral abortive lytic cycle are two key features in acute infectious mononucleosis

artículo científico publicado en 2011

BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy

artículo científico publicado en 2016

Benefits of rituximab as a second-line treatment for autoimmune haemolytic anaemia in children: a prospective French cohort study

artículo científico publicado en 2017

Bronchopulmonary squamous cell carcinoma associated with HPV 11 in a 15-year-old girl with a history of severe recurrent respiratory papillomatosis: a case report ⬇️

artículo científico publicado el 18 de mayo de 2011

Burden of Poor Health Conditions and Quality of Life in 656 Children with Primary Immunodeficiency

artículo científico publicado en 2017

Circulating cell-free BRAFV600E as a biomarker in children with Langerhans cell histiocytosis.

artículo científico publicado en 2017

Cladribine and cytarabine in refractory multisystem Langerhans cell histiocytosis: results of an international phase 2 study.

artículo científico publicado en 2015

Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia Registry

artículo científico publicado en 2014

Complications in the subacute phase of invasive Streptococcus pyogenes infections in pediatrics: two case reports and review of the literature.

artículo científico

Current insights in invasive group A streptococcal infections in pediatrics.

artículo científico

Diagnostic Yield of Next-generation Sequencing in Very Early-onset Inflammatory Bowel Diseases: A Multicentre Study

artículo científico publicado en 2018

Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children.

artículo científico publicado en 2016

Eruptive diseases of the children

artículo científico publicado en 2013

Evans Syndrome in Children: Long-Term Outcome in a Prospective French National Observational Cohort

artículo científico publicado en 2015

Expansion of regulatory T cells in patients with Langerhans cell histiocytosis

artículo científico publicado en 2007

Herpes-virus infection in patients with Langerhans cell histiocytosis: a case-controlled sero-epidemiological study, and in situ analysis.

artículo científico publicado en 2008

Implementation of an organizational infrastructure paediatric plan adapted to bronchiolitis epidemics

artículo científico publicado en 2019

Intravenous immunoglobulins for neonatal alloimmune neutropenia refractory to recombinant human granulocyte colony-stimulating factor

artículo científico publicado en 2010

Invasive pneumococcal disease in children can reveal a primary immunodeficiency

artículo científico publicado en 2014

KI and WU polyomaviruses in children, France

artículo científico publicado en 2008

Langerhans cell histiocytosis: therapeutic strategy and outcome in a 30-year nationwide cohort of 1478 patients under 18 years of age.

artículo científico publicado en 2016

Lymphoma-Like Syndrome: 4 Case Reports About Atypical Presentation of Primary Cytomegalovirus Infection in Immunocompetent Children

artículo científico publicado en 2015

Medical management of langerhans cell histiocytosis from diagnosis to treatment

artículo científico

No evidence for XMRV association in pediatric idiopathic diseases in France

artículo científico publicado en 2010

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

artículo científico publicado en 2018

Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) study

artículo científico publicado en 2016

Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part one

article

Relevance of human parechovirus detection in cerebrospinal fluid samples from young infants with sepsis-like illness.

artículo científico publicado en 2014

Searching for Common Mammalian Retroviruses in Pediatric Idiopathic Diseases.

artículo científico publicado en 2016

Second-line treatment trends and long-term outcomes of 392 children with chronic immune thrombocytopenic purpura: the French experience over the past 25 years

artículo científico publicado en 2020

Survey of Staphylococcus aureus in a general pediatric population and focus on isolates with three clinically relevant toxin-encoding genes

artículo científico publicado en 2018

Synovial-Fluid miRNA Signature for Diagnosis of Juvenile Idiopathic Arthritis

scientific article published on 26 November 2019

The French paediatric cohort of Castleman disease: a retrospective report of 23 patients

scientific article published on 17 April 2020

Thymus and mediastinal node involvement in childhood Langerhans cell histiocytosis: long-term follow-up from the French national cohort

artículo científico publicado en 2013

Torticollis in Children: A Challenging Diagnosis of C1-C2 Septic Arthritis.

artículo científico publicado en 2015

Treatment with cyclosporin in auto-immune cytopenias in children: The experience from the French cohort OBS'CEREVANCE

artículo científico publicado en 2018

What to expect from molecular tools for non-documented pediatric infectious diseases

artículo científico publicado en 2015

When Familial Hearing Loss Means Genetic Heterogeneity: A Model Case Report

artículo científico publicado en 2021

[DRESS syndrome]

scientific article published on 02 October 2014

Lista de obras de Eric Jeziorski

A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency

A new autoinflammatory and autoimmune syndrome associated with NLRP1 mutations: NAIAD (NLRP1-associated autoinflammation with arthritis and dyskeratosis).

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

Atypical pneumonia linked to community-acquired staphylococcus aureus cross-transmission in the nursery.

B-cell polyclonal activation and Epstein-Barr viral abortive lytic cycle are two key features in acute infectious mononucleosis

BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy

Benefits of rituximab as a second-line treatment for autoimmune haemolytic anaemia in children: a prospective French cohort study

Bronchopulmonary squamous cell carcinoma associated with HPV 11 in a 15-year-old girl with a history of severe recurrent respiratory papillomatosis: a case report ⬇️

Burden of Poor Health Conditions and Quality of Life in 656 Children with Primary Immunodeficiency

Circulating cell-free BRAFV600E as a biomarker in children with Langerhans cell histiocytosis.

Cladribine and cytarabine in refractory multisystem Langerhans cell histiocytosis: results of an international phase 2 study.

Clinical spectrum and long-term follow-up of 14 cases with G6PC3 mutations from the French Severe Congenital Neutropenia Registry

Complications in the subacute phase of invasive Streptococcus pyogenes infections in pediatrics: two case reports and review of the literature.

Current insights in invasive group A streptococcal infections in pediatrics.

Diagnostic Yield of Next-generation Sequencing in Very Early-onset Inflammatory Bowel Diseases: A Multicentre Study

Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children.

Eruptive diseases of the children

Evans Syndrome in Children: Long-Term Outcome in a Prospective French National Observational Cohort

Expansion of regulatory T cells in patients with Langerhans cell histiocytosis

Herpes-virus infection in patients with Langerhans cell histiocytosis: a case-controlled sero-epidemiological study, and in situ analysis.

Implementation of an organizational infrastructure paediatric plan adapted to bronchiolitis epidemics

Intravenous immunoglobulins for neonatal alloimmune neutropenia refractory to recombinant human granulocyte colony-stimulating factor

Invasive pneumococcal disease in children can reveal a primary immunodeficiency

KI and WU polyomaviruses in children, France

Langerhans cell histiocytosis: therapeutic strategy and outcome in a 30-year nationwide cohort of 1478 patients under 18 years of age.

Lymphoma-Like Syndrome: 4 Case Reports About Atypical Presentation of Primary Cytomegalovirus Infection in Immunocompetent Children

Medical management of langerhans cell histiocytosis from diagnosis to treatment

No evidence for XMRV association in pediatric idiopathic diseases in France

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) study

Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part one

Relevance of human parechovirus detection in cerebrospinal fluid samples from young infants with sepsis-like illness.

Searching for Common Mammalian Retroviruses in Pediatric Idiopathic Diseases.

Second-line treatment trends and long-term outcomes of 392 children with chronic immune thrombocytopenic purpura: the French experience over the past 25 years

Survey of Staphylococcus aureus in a general pediatric population and focus on isolates with three clinically relevant toxin-encoding genes

Synovial-Fluid miRNA Signature for Diagnosis of Juvenile Idiopathic Arthritis

The French paediatric cohort of Castleman disease: a retrospective report of 23 patients

Thymus and mediastinal node involvement in childhood Langerhans cell histiocytosis: long-term follow-up from the French national cohort

Torticollis in Children: A Challenging Diagnosis of C1-C2 Septic Arthritis.

Treatment with cyclosporin in auto-immune cytopenias in children: The experience from the French cohort OBS'CEREVANCE

What to expect from molecular tools for non-documented pediatric infectious diseases

When Familial Hearing Loss Means Genetic Heterogeneity: A Model Case Report

[DRESS syndrome]