Monica De Cassia Firmida
Overview
Explore the profile of Monica De Cassia Firmida including associated specialties, affiliations and a list of published articles.
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7
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78
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Recent Articles
1.
Abelenda V, Costa C, De Cassia Firmida M, De Oliveira R, Rufino R, Lopes A
Monaldi Arch Chest Dis
. 2025 Jan;
PMID: 39783834
With the increasing use of highly effective modulator therapy (HEMT) in adults with cystic fibrosis (awCF), it is necessary to determine the evolution of the most dynamic physiological markers of...
2.
Abelenda V, Costa C, De Cassia Firmida M, Lopes A
Physiother Res Int
. 2024 Mar;
29(2):e2087.
PMID: 38551092
Background And Objectives: Cardiopulmonary and skeletal muscle impairment and poor physical activity are potential contributors to reduced functional capacity in cystic fibrosis (CF). The Glittre-ADL test (TGlittre) has great potential...
3.
Athanazio R, Tanni S, Ferreira J, Dalcin P, Fuccio M, Esposito C, et al.
J Bras Pneumol
. 2023 May;
49(2):e20230040.
PMID: 37194817
Cystic fibrosis (CF) is a genetic disease that results in dysfunction of the CF transmembrane conductance regulator (CFTR) protein, which is a chloride and bicarbonate channel expressed in the apical...
4.
Lopes A, Mafort T, Costa C, Rufino R, De Cassia Firmida M, Kirk K, et al.
J Ultrasound Med
. 2020 Sep;
40(7):1391-1399.
PMID: 32996607
Objectives: The aim of this study was to describe findings from lung ultrasound (LUS) and computed tomography (CT) in health professionals with coronavirus disease 2019 pneumonia and to evaluate the...
5.
Leite C, de Freitas F, De Cassia Firmida M, Leao R, Albano R, Marques E
Braz J Microbiol
. 2020 Sep;
51(4):1747-1755.
PMID: 32944872
The application of next-generation sequencing tools revealed that the cystic fibrosis respiratory tract is a polymicrobial environment. We have characterized the airway bacterial microbiota of five adult patients with cystic...
6.
Athanazio R, Silva Filho L, Vergara A, Ribeiro A, Riedi C, Procianoy E, et al.
J Bras Pneumol
. 2017 Jul;
43(3):219-245.
PMID: 28746534
Cystic fibrosis (CF) is an autosomal recessive genetic disorder characterized by dysfunction of the CFTR gene. It is a multisystem disease that most often affects White individuals. In recent decades,...
7.
da Costa Ferreira Leite C, Folescu T, De Cassia Firmida M, Cohen R, Leao R, de Freitas F, et al.
BMC Pulm Med
. 2017 Jul;
17(1):100.
PMID: 28705217
Background: Burkholderia cepacia complex is a group of opportunistic pathogens in cystic fibrosis (CF) patients believed to be associated with poor prognosis and patient-to-patient transmissibility. Little is known about clinical...
8.
Ferreira A, Leao R, DAlincourt Carvalho-Assef A, Dos Santos Ribeiro da Silva E, De Cassia Firmida M, Folescu T, et al.
APMIS
. 2015 Nov;
123(12):1061-8.
PMID: 26522829
A prospective study was conducted in Brazil to evaluate antimicrobial resistance patterns and molecular epidemiology of Pseudomonas aeruginosa isolates from cystic fibrosis (CF) patients with chronic lung infection. All isolates...