Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Vania Oliveira Carvalho"'
Autor:
Cristina Rodrigues Cruz, Vania Oliveira Carvalho, Rosaly Vieira Santos, Tony Tannous Tahan, Andrea Maciel Oliveira Rossoni, Hermenio Cavalcante Lima
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 105, Iss 3, Pp 293-298 (2010)
Changes in immune system functions are one of the most important consequences of human immunodeficiency virus (HIV) infection. Studies have reported a higher prevalence of disease mediated by immunological hypersensitivity mechanisms in HIV-positive
Externí odkaz:
https://doaj.org/article/71d4130d179748fe9d2728a7725b21ea
Autor:
Rafaela Moura de Oliveira, Vania Oliveira Carvalho, Guilherme Moreno, Gustavo de Oliveira Gamo, Guilherme Rocha, Jhenyffer Leriano, João Pedro Giacomet
Publikováno v:
Jornal Paranaense de Pediatria. 23
Autor:
Jean Carlos Pereira da Luz, Paula Adriele dos Santos, Priscila Vernizi Roth, Bianca Manfroi da Silva, Ramon Eduardo Szymczak Conde, Vania Oliveira Carvalho, Júlia Macedo de Britto, Fernanda Laís Soares de Lima, Camilli Martins
Publikováno v:
Jornal Paranaense de Pediatria. 22
Autor:
Danielle Arake Zanatta, Matheus N Jamur, Renata Robl Imoto, Vania Oliveira Carvalho, Mateus P Breziniscki, Priscila Vernizi Roth, Paula R Szyhta, Ricardo Zimmermann, Marcio Y Katayama
Publikováno v:
Jornal Paranaense de Pediatria. 21
Autor:
Danielle Arake Zanatta, Vânia Oliveira Carvalho, Regina Paula Guimarães Vieira Cavalcante da Silva
Publikováno v:
Jornal de Pediatria, Vol 99, Iss 6, Pp 582-587 (2023)
Objectives: Determine the frequency of dermatological diagnoses in preterm newborns up to 28 days of life and associated perinatal factors. Method: a cross-sectional analytical study with a convenience sample and prospective data collection, was cond
Externí odkaz:
https://doaj.org/article/9ab90b7af6ba4004addd86411b7e8d6f
Autor:
Patricia F. Herkert, Renata Robl, Ricardo H Camiña, Betina Werner, Cristina de Oliveira Rodrigues, Gheniffer Fornari, Vania Oliveira Carvalho, Renata R. Gomes, Kerstin Taniguchi Abagge, Vania A. Vicente
Publikováno v:
Medical Mycology Case Reports, Vol 6, Iss C, Pp 58-61 (2014)
Medical Mycology Case Reports
Medical Mycology Case Reports
Fusarium oxysporum has been described as a pathogen causing onychomycosis, its incidence has been increasing in immunocompetent and disseminated infection can occur in immunosuppressed individuals. We describe the first case of congenital onychomycos
Autor:
Guilherme Santos Piedade, Bruno Leonardo Bancke Laverde, Vania Oliveira Carvalho, Paulo Sergio Beirao Junior, Caroline Cunico, Adriane Celli, Manuela Lucas de Mello
Publikováno v:
Carvalho, Vania O; Celli, Adriane; Bancke Laverde, Bruno Leonardo; Cunico, Caroline; Santos Piedade, Guilherme; Lucas de Mello, Manuela; et al.(2016). Progeria and the early aging in children: a case report. Dermatology Online Journal, 22(2). Retrieved from: http://www.escholarship.org/uc/item/7kt4f85m
The Hutchinson-Gilford syndrome or progeria is a rare autosomal dominant syndrome characterized by premature aging and involvement of internal systems, such as the circulatory and locomotor. The diagnosis is essentially clinical and the manifestation
Publikováno v:
Jornal de Pediatria, Vol 98, Iss 2, Pp 204-211 (2022)
Objective: Evaluate the effectiveness of a children's soap with physiological pH in maintaining cutaneous pH and moisture of the newborn (NB)’s skin after the first bath. Methods: Randomized, controlled and double-blind clinical trial in a rooming-
Externí odkaz:
https://doaj.org/article/ff8f04d1fbb64714a240096ab578d906
Autor:
Marjorie Uber, Renata Robl, Vania Oliveira Carvalho, Kerstin Taniguchi Abagge, Talita Sana Valério, Leide Parolin Marinoni, Mayara Schulze Cosechen Rosvailer
Publikováno v:
Archives of disease in childhood - Education & practice edition. 100:278-279
Autor:
Juliana Gomes Loyola Presa, Laura Rogers Morrisey, Angélica Vasselai, Kerstin Taniguchi Abagge, Leide Parolin Marinoni, Vania Oliveira Carvalho, Carmem Bonfim
Publikováno v:
Archives of disease in childhood. 98(4)
Introduction Wiskott–Aldrich syndrome (WAS) is an X-linked primary immunodeficiency caused by a mutation of the WAS protein gene. This protein actively participates in important cellular processes, and its presence is related to diverse clinical ma