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Items: 4

1.

Chloride Conductance, Nasal Potential Difference and Cystic Fibrosis Pathophysiology.

Procianoy EDFA, de Abreu E Silva FA, Maróstica PJC, Quinton PM.

Lung. 2019 Nov 16. doi: 10.1007/s00408-019-00293-6. [Epub ahead of print]

PMID:
31734731
2.

Low-level resistance and clonal diversity of Pseudomonas aeruginosa among chronically colonized cystic fibrosis patients.

Ferreira AG, Leão RS, Carvalho-Assef AP, da Silva ÉA, Firmida Mde C, Folescu TW, Paixão VA, Santana MA, de Abreu e Silva FA, Barth AL, Marques EA.

APMIS. 2015 Dec;123(12):1061-8. doi: 10.1111/apm.12463. Epub 2015 Nov 2.

PMID:
26522829
3.

Association of nutritional status, plasma, albumin levels and pulmonary function in cystic fibrosis.

Souza dos Santos Simon MI, Drehmer M, de Abreu E Silva FA, Hoffmann A, Druck Ricachinewsky C, de Fonseca Andrade Procianoy E, Scattolin I, Saldanha Menna Barreto S.

Nutr Hosp. 2011 Nov-Dec;26(6):1322-7. doi: 10.1590/S0212-16112011000600019.

PMID:
22411378
4.

Cystic fibrosis patient with Burkholderia pseudomallei infection acquired in Brazil.

Barth AL, de Abreu E Silva FA, Hoffmann A, Vieira MI, Zavascki AP, Ferreira AG, da Cunha LG Jr, Albano RM, de Andrade Marques E.

J Clin Microbiol. 2007 Dec;45(12):4077-80. Epub 2007 Oct 17.

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