Reply to 'House dust mite liquid SLIT effective in atopic dermatitis, even with suboptimal dosing'

Autor: Edine Coelho, Pimentel, Maria Eduarda T, Zanetti, Sarah Sella, Langer, Janaina Michelle L, Melo, Mariana P L, Ferriani, Orlando, Trevisan Neto, Marina Mendonça, Dias, Pérsio, Roxo-Junior, Jorgete, Silva, Davi Casale, Aragon, L Karla, Arruda

Publikováno v: The Journal of Allergy and Clinical Immunology: In Practice. 10:1937-1939

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3e9cd26bb36cfb193c7396fcabdb8a2
https://doi.org/10.1016/j.jaip.2022.04.022

Study of angiopoietin and plasminogen genes in hereditary angioedema

Autor: Tatielly Kruk, Liya Regina Mikami, Nelson Augusto Rosário Filho, Lilian Pereira Ferrari, Marina Mendonça Dias, Luisa Karla de Paula Arruda, Adriana S. Moreno, Herberto José Chong-Neto, Wagner Narciso de Campos

Publikováno v: Revista da Associação Médica Brasileira, Vol 66, Iss 4, Pp 502-506 (2020)
Revista da Associação Médica Brasileira v.66 n.4 2020
Revista da Associação Médica Brasileira
Associação Médica Brasileira (AMB)
instacron:AMB

SUMMARY OBJECTIVE To investigate the presence of the Angiopoietin 1 (ANGPT1) and Plasminogen (PLG) mutations in patients with Hereditary Angioedema (HAE) and normal C1 esterase inhibitor (C1-INH) levels, who do not harbor the F12 gene mutation. METHO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30b4b496fa9a144dbf026e1dd9ace1cd
https://pubmed.ncbi.nlm.nih.gov/32578786

Serum baseline tryptase level as a marker for the severity of anaphylaxis

Autor: Janaina Michelle Lima Melo, Marina Mendonça Dias, Davi Casale Aragon, Luana S.M. Maia, Orlando Trevisan-Neto, Vinicius Aniceto, Adriana S. Moreno, Luisa Karla de Paula Arruda

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

Background: Anaphylaxis is a severe and potentially fatal allergic disease or hypersensitivity reaction with variable clinical presentation. Biomarkers in anaphylaxis could be useful to improve diagnosis, to allow endotyping of patients, and to predi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55e3f3ac75b07934ed874874e3d32fbc

University and public health system partnership: A real-life intervention to improve asthma management

Autor: Elcio Oliveira Vianna, Virgínia Paes Leme Ferriani, Ana Carla S. Araujo, Pérsio Roxo, Jorgete Maria e Silva, Luana Queiroz, Nelio Domingos, Rosângela Araujo, Adriana S. Moreno, Janaina Michelle Lima Melo, Marcos Brown Gonçalves, Marina Mendonça Dias, Larissa Panazolo, L. Karla Arruda, Rosa Parreira, Davi Casale Aragon, Andrea Cetlin, Patricia Stefanelli, Luane Marques de Mello, Marcos C. Borges

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

Asthma is under-diagnosed in many parts of the world. We aimed to assess the outcome of a capacitating program on asthma for non-specialist physicians and other healthcare professionals working in the public system in Ribeirão Preto, Brazil.A group

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d34ed77eca5da6573a511552c9dd5dcd
https://pubmed.ncbi.nlm.nih.gov/27715349

Coagulation Factor XII Gene Mutation in Brazilian Families with Hereditary Angioedema with Normal C1 Inhibitor

Autor: L. Karla Arruda, Wagner Narciso de Campos, Joël Lunardi, Faradiba Sarquis Serpa, Denise Ponard, Wilson A. Silva, Marina Mendonça Dias, Alfeu Tavares França, Soloni Afra Pires Levy, Solange Oliveira Rodrigues Valle, Helen Andrade Arcuri, Adriana S. Moreno, Nicole Monnier, Mario Sergio Palma, Konrad Bork

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

Background: Hereditary angioedema (HAE) with normal C1 inhibitor (C1-INH) is a rare disorder. Mutations of the gene encoding coagulation factor XII have been identified in a subset of patients with this condition. Our aim was to investigate mutations

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4d93f582202d28713aaa6fa9a6ac8f1
https://pubmed.ncbi.nlm.nih.gov/25790805