Produção Nacional
Revisado por pares
A proposal of warning signs for primary immunodeficiencies in the first year of life
2011; Wiley; Volume: 22; Issue: 3 Linguagem: Inglês
10.1111/j.1399-3038.2010.01084.x
ISSN1399-3038
AutoresMagda Carneiro‐Sampaio, Cristina Miuki Abe Jacob, Cléa Rodrigues Leone,
Tópico(s)Pediatric health and respiratory diseases
ResumoPediatric Allergy and ImmunologyVolume 22, Issue 3 p. 345-346 LETTER TO THE EDITOR A proposal of warning signs for primary immunodeficiencies in the first year of life Magda Carneiro-Sampaio, Magda Carneiro-Sampaio Department of Pediatrics, Faculdade de Medicina daUniversidade de São Paulo, São Paulo, Brazil E-mail: [email protected]Search for more papers by this authorCristina Miuki Abe Jacob, Cristina Miuki Abe Jacob Department of Pediatrics, Faculdade de Medicina daUniversidade de São Paulo, São Paulo, Brazil E-mail: [email protected]Search for more papers by this authorCléa Rodrigues Leone, Cléa Rodrigues Leone Department of Pediatrics, Faculdade de Medicina daUniversidade de São Paulo, São Paulo, Brazil E-mail: [email protected]Search for more papers by this author Magda Carneiro-Sampaio, Magda Carneiro-Sampaio Department of Pediatrics, Faculdade de Medicina daUniversidade de São Paulo, São Paulo, Brazil E-mail: [email protected]Search for more papers by this authorCristina Miuki Abe Jacob, Cristina Miuki Abe Jacob Department of Pediatrics, Faculdade de Medicina daUniversidade de São Paulo, São Paulo, Brazil E-mail: [email protected]Search for more papers by this authorCléa Rodrigues Leone, Cléa Rodrigues Leone Department of Pediatrics, Faculdade de Medicina daUniversidade de São Paulo, São Paulo, Brazil E-mail: [email protected]Search for more papers by this author First published: 04 April 2011 https://doi.org/10.1111/j.1399-3038.2010.01084.xCitations: 21Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1 Notarangelo LD, Fischer A, Geha RS, et al. Primary immunodeficiency diseases: 2009 update. J Allergy Clin Immunol 2009: 124: 1161–78. 2 Buckley RH. The multiple causes of human SCID. J Clin Invest 2004: 114: 1409–11. 3 Pessach I, Walter J, Notarangelo LD. Recent advances in Primary Imunodeficiencies: identification of novel genetic defects and unanticipated phenotypes. Pediatr Res 2009: 65 (5 Pt 2): 3R–12R. 4 Puck JM. Population-based newborn screening for severe combined immune deficiency: steps towards implementation. J Allergy Clin Immunol 2007: 120: 760–8. 5 Janka GE. Hemophagocytic syndromes. Blood Rev 2007: 21: 245–53. 6 Gambineri E, Perroni L, Passerini L, et al. Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity. J Allergy Clin Immunol 2008: 122: 1105–1112. 7 Kobrynski LJ, Sullivan KE. Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes. Lancet 2007: 370: 1443–52. 8 Routes JM, Grossman WJ, Verbsky J, et al. Statewide newborn screening for severe T-cell lymphopenia. JAMA 2009: 302: 2465–70. Citing Literature Volume22, Issue3May 2011Pages 345-346 ReferencesRelatedInformation
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