Artigos
Indicações do uso de imunoglobulina intravenosa Consulta pública ANVISA - imunoglobulinas Consulta pública imunoglobulinas - Diário Oficial da União Germes associados com as principais categorias de imunodeficiências Algumas imunodeficiências primárias associadas a alterações genéticas Angioedema Hereditário Avaliação Laboratorial do Sistema Imunológico Classificação das Imunodeficiências Características das clínicas das PID Datas de descoberta de algumas imunodeficiências primárias (1926-1965) Os 10 Sinais de Alerta para Imunodeficiência Primária na Criança adaptados para o nosso meio
Artigos em inglês
Complement Levels in Brazilian Children During and After Meningococcal Meningitis Griscelli Syndrome: Characterization of a New Mutation and Rescue of T-Cytotoxic Activity by Retroviral Transfer of RAB27A Gene Genetic Linkage of Hyper-IgE Syndrome to Chromosome 4 Primary immunodeficiency diseases: An update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005 Cytokines and Immunodeficiency Diseases The X-Linked Hyper-IgM Syndrome Lymphocyte subsets in healthy children from birth through 18 years of age Primary Immune Deficiency Diseases in America Primary immunodeficiency diseases: An update Applying Public Health Strategies to Primary Immunodeficiency Diseases Day Care Centers and Respiratory Health Have We Seen the Last Variant of Severe Combined Immunodeficiency? The 10 Warning Signs© of Primary Immunodeficiency Imunodeficiência
Artigos do Summer School
Congenital neutropenia: advances in diagnosis and treatment Molecular Defects in Human Severe Combined Immunodeficiency and Approaches to Immune Reconstitution Search for polio virus carriers among people with primary immune deficiency diseases in the United States, Mexico, Brazil, and the United Kingdom Female agammaglobulinemia due to the Bruton tyrosine kinase deficiency caused by extremely skewed X-chromosome inactivation The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy Genotype/phenotype correlations in X-linked agammaglobulinemia Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group Hyper-IgE syndromes Hyper-IgE Syndrome Is Not Associated With Defects in Several Candidate Toll-Like Receptor Pathway Genes Severe combined immunodeficiency. A model disease for molecular immunology and therapy CXCR4 mutations in WHIM syndrome: a misguided immune system? Effects of Absorption with Pneumococcal Type 22F Polysaccharide on Maternal, Cord Blood, and Infant Immunoglobulin G Antipneumococcal Polysaccharide Antibodies Bone Marrow Transplantation for Severe Combined Immune Deficiencys Characteristics of mycobacterial infection in patients with immunodeficiency and nuclear factorekB essential modulator mutation, with or without ectodermal dysplasia Finding NEMO: genetic disorders of NF-êB activation The presentation and natural history of immunodeficiency caused by nuclear factor kB essential modulator mutation Human nuclear factor kB essential modulator mutation can result in immunodeficiency without ectodermal dysplasia Human disease resulting from gene mutations that interfere with appropriate nuclear factor-kB activation No Indication for a Defect in Toll-Like Receptor Signaling in Patients with Hyper-IgE Syndrome Paralytic Poliomyelitis Caused by a Vaccine-derived Polio Virus in an Antibody-deficient Argentinean Child Disabled Receptor Signaling and New Primary Immunodeficiency Disorders Practice parameter for the diagnosis and management of primary immunodeficiency Chronic and Recurrent Pneumonias in Children Tuberculosis in children and adults: two distinct genetic diseases Biomedicine and Diseases: Review The health status and quality of life of adults with X-linked agammaglobulinemia
