Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jose D Ribeiro"'
Autor:
Katia CA Aguiar, Nely AG Nucci, Fernando AL Marson, Tais DR Hortencio, Antonio F Ribeiro, Jose D Ribeiro
Publikováno v:
Psicologia em Estudo, Vol 21, Iss 2 (2016)
O presente estudo examinou os desafios psicológicos de adolescentes com fibrose cística (FC) no Brasil, por meio de uma entrevista semiestruturada com perguntas abertas: [(i) Como é ter FC para você?; (ii) Você tem necessidades especiais por ter
Externí odkaz:
https://doaj.org/article/aa9df900a5cd4ec6bf3de26056164612
Prevalence of constipation in cystic fibrosis patients: a systematic review of observational studies
Autor:
Marina A. Stefano, Rosana E. Poderoso, Jochen G. Mainz, Jose D. Ribeiro, Antonio F. Ribeiro, Elizete Aparecida Lomazi
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 96, Iss 6, Pp 686-692 (2020)
Objective: To systematically revise the literature in search of data about the prevalence of constipation in patients with cystic fibrosis according to the publications in this field, which partly refer to guidelines defined in 2010 by the European S
Externí odkaz:
https://doaj.org/article/08a676d69bfe4228931ce2640290193f
Autor:
Natascha S. Sandy, Lilian H.P. Massabki, Aline C. Gonçalves, Antonio F. Ribeiro, Jose D. Ribeiro, Maria de Fátima C.P. Servidoni, Elizete A. Lomazi
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 96, Iss 6, Pp 732-740 (2020)
Objective: To evaluate the demographics, genotype, and clinical presentation of pediatric patients presenting with distal intestinal obstruction syndrome (DIOS), and factors associated with DIOS recurrence. Methods: Case series of ten patients (media
Externí odkaz:
https://doaj.org/article/05b31bf62f3a46a89786734a44d5d66e
Akademický článek
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Autor:
Katia CA Aguiar, Nely AG Nucci, Fernando AL Marson, Tais DR Hortencio, Antonio F Ribeiro, Jose D Ribeiro
Publikováno v:
Psicologia em Estudo, Vol 21, Iss 2, Pp 211-222 (2016)
The present study examined the psychological challenges of adolescents with cystic fibrosis (CF) in Brazil. A semi-structured interview with open-ended questions [(i) What is it like for you to have CF?; (ii) Do you have any special needs because you
Autor:
Marisa Sousa, Maria F Servidoni, Adriana M Vinagre, Anabela S Ramalho, Luciana C Bonadia, Verónica Felício, Maria A Ribeiro, Inna Uliyakina, Fernando A Marson, Arthur Kmit, Silvia R Cardoso, José D Ribeiro, Carmen S Bertuzzo, Lisete Sousa, Karl Kunzelmann, Antônio F Ribeiro, Margarida D Amaral
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e47708 (2012)
BackgroundCystic Fibrosis (CF) is caused by ∼1,900 mutations in the CF transmembrane conductance regulator (CFTR) gene encoding for a cAMP-regulated chloride (Cl(-)) channel expressed in several epithelia. Clinical features are dominated by respira
Externí odkaz:
https://doaj.org/article/2860c930e59242669d87fa4093d5ef95
Autor:
Carvalho IA; Departamento de Veterinária, Universidade Federal de Viçosa , Viçosa, MG , Brasil., Campos VE, Souza IM, Zanardo LG, Filho JD, Gomes MJ, Moreira MA
Publikováno v:
Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] [Braz J Microbiol] 2012 Apr; Vol. 43 (2), pp. 581-5. Date of Electronic Publication: 2012 Jun 01.