Zobrazeno 1 - 10
of 213
pro vyhledávání: '"Anete Sevciovic Grumach"'
Autor:
Francisca Jacinta Feitoza de Oliveira, Maria Aparecida Alves de Oliveira Serra, Leonardo Hunaldo dos Santos, Márcio Flávio Moura de Araújo, Rosemeire Navickas Constantino da Silva, Anete Sevciovic Grumach
Publikováno v:
Tropical Medicine and Infectious Disease, Vol 7, Iss 5, p 71 (2022)
The present study aimed at analyzing the serum levels of mannose-binding lectin (MBL) and ficolin-3 (FCN3) in leprosy patients and their healthy family contacts in a hyperendemic region in northeastern Brazil. A cross-sectional study was carried out
Externí odkaz:
https://doaj.org/article/37cb99df6fc5405db16a3336663aff21
Publikováno v:
Jornal de Pediatria, Vol 97, Iss , Pp S75-S83 (2021)
Objectives: The aim of the report is to describe the main immunodeficiencies with syndromic characteristics according to the new classification of Inborn Errors of Immunity. Data source: The data search was centered on the PubMed platform on review s
Externí odkaz:
https://doaj.org/article/3d72352effad49b3ab812bae8b2ca6a3
Publikováno v:
Jornal de Pediatria, Vol 97, Iss , Pp S84-S90 (2021)
Objectives: Inborn Errors of Immunity are characterized by infectious conditions and manifestations of immune dysregulation. The diversity of clinical phenotypes can make it difficult to direct the laboratory investigation. This article aims to updat
Externí odkaz:
https://doaj.org/article/21f2f1246ad64440be8fe185d5d7be96
Autor:
Camila Lopes Veronez, Régis Albuquerque Campos, Rosemeire Navickas Constantino-Silva, Priscila Nicolicht, João Bosco Pesquero, Anete Sevciovic Grumach
Publikováno v:
Frontiers in Medicine, Vol 6 (2019)
Abdominal pain due to intestinal swellings is one of the most common manifestations in hereditary angioedema (HAE). Bowel swellings can cause severe abdominal pain, nausea, vomiting, and diarrhea, which may lead to misdiagnosis of gastrointestinal di
Externí odkaz:
https://doaj.org/article/f15f112d33b245b584b2bae9abd391f7
Autor:
Camila Lopes Veronez, Anne Aabom, Renan Paulo Martin, Rafael Filippelli-Silva, Rozana Fátima Gonçalves, Priscila Nicolicht, Agatha Ribeiro Mendes, Jane Da Silva, Mar Guilarte, Anete Sevciovic Grumach, Eli Mansour, Anette Bygum, João Bosco Pesquero
Publikováno v:
Frontiers in Medicine, Vol 6 (2019)
Hereditary angioedema (HAE) is an autosomal dominant disease caused by C1-INH deficiency due to mutations in SERPING1 (C1-INH-HAE) in most of the cases, or by specific mutations in factor XII gene, F12 (F12-HAE). Identification of polymorphisms in th
Externí odkaz:
https://doaj.org/article/11f2c8ef89a14a6c8e850219d5e9c290
Autor:
Aleena Banerji M.D., Murat Baş M.D., Jonathan A. Bernstein M.D., Isabelle Boccon-Gibod M.D., Maria Bova M.D., Ph.D., John Dempster, Anete Sevciovic Grumach M.D., Ph.D., Markus Magerl M.D., Kimberly Poarch PA-C, Manuel Branco Ferreira M.D., Ph.D.
Publikováno v:
Allergy & Rhinology, Vol 7 (2016)
Background Published literature documents the substantial burden of hereditary angioedema (HAE) with C1 inhibitor deficiency on the quality of life and work productivity of patients. However, despite advances in the field and the availability of guid
Externí odkaz:
https://doaj.org/article/b30aaad2889d4d5094757a7b59114f5f
Autor:
Solange Oliveira Rodrigues Valle, Alfeu Tavares França, Regis A. Campos, Anete Sevciovic Grumach
Publikováno v:
Clinical Medicine Insights: Blood Disorders, Vol 2011, Iss 4, Pp 21-30 (2011)
Externí odkaz:
https://doaj.org/article/36bcbda536a04d529414a9228c6c27a8
Publikováno v:
Jornal de Pediatria, Vol 82, Iss 5, Pp S181-S188 (2006)
OBJETIVO: Apresentar uma abordagem prática ao diagnóstico e conduta na alergia a antibióticos beta-lactâmicos. FONTES DOS DADOS: Periódicos da área de alergia indexados nas bases MEDLINE e LILACS, além de estudos e textos clássicos que tratam
Externí odkaz:
https://doaj.org/article/3e669df88a7f45e2b42e3952c5dff5cb
Autor:
Anete Sevciovic Grumach, Ângela Tayra, Heloisa Helena Souza Marques, Luiza Harunari Matida, Maria Gomes Valente
Publikováno v:
DST, Vol 10, Iss 1 (1998)
Externí odkaz:
https://doaj.org/article/686fa215ffdc45ee8a06bbf289d43eec
Autor:
Regis Albuquerque Campos, Solange Oliveira Rodrigues Valle, Alfeu Tavares França, Elisabete Cordeiro, Faradiba Sarquis Serpa, Yara Ferreira Mello, Teresinha Malheiros, Eliana Toledo, Elie Mansour, Gustavo Fusaro, Anete Sevciovic Grumach
Publikováno v:
São Paulo Medical Journal, Vol 132, Iss 5, Pp 261-265
CONTEXT AND OBJECTIVE: Hereditary angioedema (HAE) with C1 inhibitor deficiency manifests as recurrent episodes of edema involving the skin, upper respiratory tract and gastrointestinal tract. It can be lethal due to asphyxia. The aim here was to eva
Externí odkaz:
https://doaj.org/article/1c7386cc49c74213bf79c369e4cf400f