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1
Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]
Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]

Luana Sella Motta Maia Adriana Santos Moreno; Mariana Paes Leme Ferriani; Fernanda Leonel Nunes; Maria Fernanda Ferraro; Marina Mendonça Dias; Pérsio Roxo-Junior; Fabrício Moura Dias; Solange Oliveira Rodrigues Valle; Soloni  Levy; Maria Luiza Oliva Alonso; Alfeu Tavares França; Faradiba Sarquis Serpa; Antônio Abílio Motta; Felipe Gonçalves Motta Maia; Davi Casale Aragon; Willy Sarti; Wilson Araújo da Silva Junior; Konrad  Bork; Sven Cichon; Luisa Karla de Paula Arruda

Allergy West Sussex v. 74, n. 5, p. 1013-1016, 2019

West Sussex 2019

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2978935 Estantes Deslizantes )(Acessar)

2
Gender Influence on Hereditary Angioedema with C1-inhibitor Deficiency
Gender Influence on Hereditary Angioedema with C1-inhibitor Deficiency
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Gender Influence on Hereditary Angioedema with C1-inhibitor Deficiency

Priscila Takejima Juliana F. B Garcia; Marcelo V Aun; Jorge Kalil; Antonio Abilio Motta; Pedro Giavina-Bianchi; Annual Meeting of the AAAAI (2017 Atlanta, Georgia)

Journal of Allergy and Clinical Immunology Philadelphia v. 139, n. suppl. 2, p. AB237, abst. 743, 2017

Philadelphia 2017

Acesso online. A biblioteca também possui exemplares impressos.

3
Hereditary angioedema with normal C1 inhibitor prevalence, clinical features and treatment of patients in a University Hospital in Brazil
Hereditary angioedema with normal C1 inhibitor prevalence, clinical features and treatment of patients in a University Hospital in Brazil
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Hereditary angioedema with normal C1 inhibitor prevalence, clinical features and treatment of patients in a University Hospital in Brazil

M. V. Aun E Longen; N. C Portilho; R. C Agondi; J Kalil; A. A Motta; P Giavina-Bianchi; Congress of the European Academy of Allergy and clinical Immunology (2015 Barcelona, Spain)

Allergy Copenhagen v. 70, suppl. 101, p. 255, abstr. 593, 2015

Copenhagen 2015

Acesso online. A biblioteca também possui exemplares impressos.

4
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema insights from a Brazilian family
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema insights from a Brazilian family
Material Type:
Artigo 		Adicionar ao Meu Espaço

A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema insights from a Brazilian family

M. F. Ferraro A. S Moreno; E. C Castelli; Eduardo Antônio Donadi; M. S Palma; H. A Arcuri; A. P Lange; K Bork; Willy Sarti; Luisa Karla de Paula Arruda

Allergy Oxford v. 66, n. 10, p. 1384-1390, 2011

Oxford 2011

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2193334 Estantes Deslizantes )(Acessar)

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Deste Autor:

  1. Motta, A
  2. Kalil, J
  3. Arruda, L
  4. Bork, K
  5. Moreno, A

Neste Assunto:

  1. Angioedema
  2. Doenças Hereditárias
  3. Bradicinina
  4. Doenças Genéticas
  5. Brasil

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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