Invasive pneumococcal disease in children can reveal a primary immunodeficiency. - Wikidata - wikimedia - TriplyDB

Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

http://www.wikidata.org/entity/Q33917973

about

Severe infectious diseases of childhood as monogenic inborn errors of immunity Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity The Antibody-Secreting Cell Response to Infection: Kinetics and Clinical Applications.Recurrent invasive pneumococcal disease in children: underlying clinical conditions, and immunological and microbiological characteristics.Clinical features and outcomes of invasive pneumococcal disease in a pediatric intensive care unit.Naturally Acquired Human Immunity to Pneumococcus Is Dependent on Antibody to Protein Antigens.Genetic Variation in NFKBIE Is Associated With Increased Risk of Pneumococcal Meningitis in Children.Exome Sequencing Reveals Primary Immunodeficiencies in Children with Community-Acquired Pseudomonas aeruginosa Sepsis.Rationale and prospects for novel pneumococcal vaccines.Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation.Spectrum and management of complement immunodeficiencies (excluding hereditary angioedema) across Europe.Is Pneumonia a Risk Factor or a Risk Marker for Long-Term Mortality?Characteristics and Serotype Distribution of Childhood Cases of Invasive Pneumococcal Disease Following Pneumococcal Conjugate Vaccination in England and Wales, 2006-2014.The Clinical Utility of Measuring IgG Subclass Immunoglobulins During Immunological Investigation for Suspected Primary Antibody Deficiencies.Evaluation of the role of stat3 in antibody and TH17-mediated responses to pneumococcal immunization and infection using a mouse model of Autosomal Dominant Hyper IgE Syndrome.Prevalence of Hypogammaglobulinemia in Adult Invasive Pneumococcal Disease.Mondini dysplasia with recurrent bacterial meningitis caused by three different pathogens.Mortality and morbidity in community-acquired sepsis in European pediatric intensive care units: a prospective cohort study from the European Childhood Life-threatening Infectious Disease Study (EUCLIDS).

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P2860

Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

http://www.wikidata.org/entity/Q33917973

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2014 nî lūn-bûn

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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2014 թվականի ապրիլին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

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Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

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Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

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Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

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Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

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Clinical Infectious Diseases

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Invasive pneumococcal disease in children can reveal a primary immunodeficiency.

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Caroline Thomas

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Catherine Jeudy

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Christèle Gras Le Guen

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Corinne Levy

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Cécile Bost-Bru

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Dominique Gendrel

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Emmanuel Grimprel

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Emmanuelle Varon

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Eric Jeziorski

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P2860

Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency

Whole-exome-sequencing-based discovery of human FADD deficiency

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

Pyogenic bacterial infections in humans with MyD88 deficiency

Pyogenic bacterial infections in humans with IRAK-4 deficiency

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

Burden of disease caused by Streptococcus pneumoniae in children younger than 5 years: global estimates

Isolated congenital asplenia: a French nationwide retrospective survey of 20 cases.

Diagnosis, microbial epidemiology, and antibiotic treatment of acute otitis media in children: a systematic review.

Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma

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Jean-Laurent Casanova

Véronique Frémeaux-Bacchi

Capucine Picard

Pierre-Louis Léger

Bertrand Boisson

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2014-04-23T00:00:00Z

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