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Outcome of SARS-CoV-2 Infection in 121 Patients With Inborn Errors of Immunity: A Cross-sectional Study

Autor: Gisele Loth, Fernanda Casares Marcelino, Irma Cecília Douglas Paes Barreto, Carolina Sanchez Aranda, Sérgio Duarte Dortas Junior, Laire Schidlowski, Juliana Folloni Fernandes, Simone Pestana, Eli Mansour, Maria Luiza Oliva Alonso, Almerinda Rego Silva, Gustavo Soldateli, Raisa G. Ulaf, Priscila Fillipo, Olga Akiko Takano, Pérsio Roxo-Junior, Rafaela Guimarães, Janaíra Fernandes Ferreira, Cristina M. Kokron, Ekaterini Goudouris, Solange Oliveira Rodrigues Valle, Carmem Bonfim, Danielli Christinni Bichuetti-Silva, Eliana C. Toledo, Antonio Condino-Neto, Luciana Araújo Oliveira Cunha, Anete Sevciovic Grumach, Fernanda Pinto-Mariz, Regina Sumiko Watanabe Di Gesu, Natasha Rebouças Ferraroni, Maria Isabel Valdomir Nadaf, Julia Lopes Garcia, Leonardo Oliveira Mendonça, Ellen de Oliveira Dantas, Fernanda Lugão Campinhos, Flavia Anisio, Myrthes Toledo Barros, Albertina Varandas Capelo, Carolina Prando

Publikováno v: Journal of Clinical Immunology
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

Purpose: There is still scarce data on SARS-CoV-2 infection in patients with Inborn Errors of Immunity (IEI) and many questions. We aimed to describe the clinical outcome of SARS-CoV-2 infection in Brazilian IEI patients and to identify factors influ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdf3aa282d5ebcf5a075aab4f86697aa
https://doi.org/10.21203/rs.3.rs-286146/v1

Clinical and genetic findings in two siblings with X-Linked agammaglobulinemia and bronchiolitis obliterans: a case report

Autor: Ronaldo da Silva Francisco Junior, Guilherme Loss de Morais, Joseane Biso de Carvalho, Cristina dos Santos Ferreira, Alexandra Lehmkuhl Gerber, Ana Paula de C Guimarães, Flávia Anisio Amendola, Fernanda Pinto-Mariz, Zilton Farias Meira de Vasconcelos, Ekaterini Simões Goudouris, Ana Tereza Ribeiro de Vasconcelos

Publikováno v: BMC Pediatrics, Vol 22, Iss 1, Pp 1-5 (2022)

Abstract Background X-linked agammaglobulinemia (XLA) is an Inborn Errors of Immunity (IEI) characterized by pan-hypogammaglobulinemia and low numbers of B lymphocytes due to mutations in BTK gene. Usually, XLA patients are not susceptible to respira

Externí odkaz: https://doaj.org/article/e303b09fe71d48cfb4d2b1d34c0b19a9

Severe combined imunodeficiency caused by defect of the common gamma chain of the interleukin 2 receptor

Autor: Livia Lucas Lima, Paula Lauria, Anna Luiza Paola Martins, Sandra Bastos, Celso Ungier, Abelardo Neto, Liziane Nunes, Luanda De Alleluia, Flavia Anisio

Publikováno v: The World Allergy Organization Journal

Results The mutation detected was a defect of the common gamma chain of the interleukin 2 receptor (IL2Rg). Even though genetic counseling advised otherwise the patient’s mother got pregnant during follow-up and as no compatible donor was found we

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e700156cb5e1206f207a7f6eec6cc9