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Items: 1 to 50 of 75

1.

A negative screening of rare genetic variants in the ADIPOQ and STATH genes in cystic fibrosis.

Coutinho CAAC, Marson FAL, Ribeiro JD, Bertuzzo CS.

Pulmonology. 2019 Oct 9. pii: S2531-0437(19)30171-0. doi: 10.1016/j.pulmoe.2019.09.003. [Epub ahead of print]

2.

The Use of Ultrasound as a Tool to Evaluate Pulmonary Disease in Cystic Fibrosis.

Peixoto AO, Marson FA, Dertkigil SS, Dertkigil RP, Souza TH, Fraga AM, Ribeiro AF, Toro AA, Ribeiro JD.

Respir Care. 2019 Oct 8. pii: respcare.07038. doi: 10.4187/respcare.07038. [Epub ahead of print]

PMID:
31594833
3.

The applicability of gene sequencing and MALDI-TOF to identify less common gram-negative rods (Advenella, Castellaniella, Kaistia, Pusillimonas and Sphingobacterium) from environmental isolates.

Sant' Anna D, Sampaio JLM, Sommaggio LRD, Mazzeo DEC, Marin-Morales MA, Marson FAL, Levy CE.

Antonie Van Leeuwenhoek. 2019 Sep 27. doi: 10.1007/s10482-019-01333-0. [Epub ahead of print]

PMID:
31560092
4.

Concordance between whole- and half-body scans to evaluate body composition in dual-energy X-ray absorptiometry in children and adolescents with different nutritional and pubertal conditions.

Ferreira MS, Marson FAL, Wolf VLW, da Silva MTN, Zambon MP, Antonio MÂRGM, Ribeiro JD, Mendes RT.

Nutrition. 2019 Oct;66:78-86. doi: 10.1016/j.nut.2019.03.018. Epub 2019 Apr 26.

PMID:
31247496
5.

Severe pulmonary disease in an adult primary ciliary dyskinesia population in Brazil.

Olm MAK, Marson FAL, Athanazio RA, Nakagawa NK, Macchione M, Loges NT, Omran H, Rached SZ, Bertuzzo CS, Stelmach R, Saldiva PHN, Ribeiro JD, Jones MH, Mauad T.

Sci Rep. 2019 Jun 18;9(1):8693. doi: 10.1038/s41598-019-45017-1.

6.

Lactulose Breath Testing Can Be a Positive Predictor Before Weight Gain in Participants with Obesity Submitted to Roux-en-Y Gastric Bypass.

Coelho LK, Carvalho NS, Navarro-Rodriguez T, Marson FAL, Carvalho PJPC.

Obes Surg. 2019 Jun 11. doi: 10.1007/s11695-019-04006-z. [Epub ahead of print]

PMID:
31187458
7.

Novel, rare and common pathogenic variants in the CFTR gene screened by high-throughput sequencing technology and predicted by in silico tools.

Pereira SV, Ribeiro JD, Ribeiro AF, Bertuzzo CS, Marson FAL.

Sci Rep. 2019 Apr 17;9(1):6234. doi: 10.1038/s41598-019-42404-6.

8.

Extent of rescue of F508del-CFTR function by VX-809 and VX-770 in human nasal epithelial cells correlates with SNP rs7512462 in SLC26A9 gene in F508del/F508del Cystic Fibrosis patients.

Kmit A, Marson FAL, Pereira SV, Vinagre AM, Leite GS, Servidoni MF, Ribeiro JD, Ribeiro AF, Bertuzzo CS, Amaral MD.

Biochim Biophys Acta Mol Basis Dis. 2019 Jun 1;1865(6):1323-1331. doi: 10.1016/j.bbadis.2019.01.029. Epub 2019 Feb 1.

PMID:
30716472
9.

Analysis of motor and respiratory function in Duchenne muscular dystrophy patients.

Luiz LC, Marson FAL, Bresciani Almeida CC, Toro AADC, Nucci A, Ribeiro JD.

Respir Physiol Neurobiol. 2019 Apr;262:1-11. doi: 10.1016/j.resp.2019.01.009. Epub 2019 Jan 17.

PMID:
30660861
10.

Volumetric capnography versus spirometry for the evaluation of pulmonary function in cystic fibrosis and allergic asthma.

Almeida-Junior A, Marson FAL, Almeida CCB, Ribeiro MÂGO, Paschoal IA, Moreira MM, Ribeiro JD.

J Pediatr (Rio J). 2018 Dec 7. pii: S0021-7557(18)30909-4. doi: 10.1016/j.jped.2018.10.008. [Epub ahead of print]

11.

Evaluation of continuous constant current and continuous pulsed current in sweat induction for cystic fibrosis diagnosis.

Gomez CCS, Marson FAL, Servidoni MF, Ribeiro AF, Ribeiro MÂGO, Gama VAL, Costa ET, Ribeiro JD, Vieira Junior FU.

BMC Pulm Med. 2018 Sep 14;18(1):153. doi: 10.1186/s12890-018-0696-3.

12.

Mineral Disorders in Adult Inpatients Receiving Parenteral Nutrition. Is Older Age a Contributory Factor?

Hortencio TDR, Golucci APBS, Marson FAL, Ribeiro AF, Nogueira RJ.

J Nutr Health Aging. 2018;22(7):811-818. doi: 10.1007/s12603-018-1035-3.

PMID:
30080225
13.

Femoral-facial syndrome: A review of the literature and 14 additional patients including a monozygotic discordant twin pair.

Lacarrubba-Flores MDJ, Carvalho DR, Ribeiro EM, Moreno CA, Esposito AC, Marson FAL, Loureiro T, Cavalcanti DP.

Am J Med Genet A. 2018 Sep;176(9):1917-1928. doi: 10.1002/ajmg.a.40425. Epub 2018 Aug 2. Review.

PMID:
30070764
14.

Lipid profile associated with the systemic inflammatory response syndrome and sepsis in critically ill patients.

Golucci APBS, Marson FAL, Ribeiro AF, Nogueira RJN.

Nutrition. 2018 Nov;55-56:7-14. doi: 10.1016/j.nut.2018.04.007. Epub 2018 May 9.

PMID:
29960160
15.

Correlation between parameters of volumetric capnography and spirometry during a submaximal exercise protocol on a treadmill in patients with cystic fibrosis and healthy controls.

Parazzi PLF, Marson FAL, Ribeiro MAGO, Schivinski CIS, Ribeiro JD.

Pulmonology. 2019 Jan - Feb;25(1):21-31. doi: 10.1016/j.pulmoe.2018.04.006. Epub 2018 Jun 25.

16.

Chloride and sodium ion concentrations in saliva and sweat as a method to diagnose cystic fibrosis.

Gonçalves AC, Marson FAL, Mendonça RMH, Bertuzzo CS, Paschoal IA, Ribeiro JD, Ribeiro AF, Levy CE.

J Pediatr (Rio J). 2019 Jul - Aug;95(4):443-450. doi: 10.1016/j.jped.2018.04.005. Epub 2018 May 19.

17.

Influence of AIDS antiretroviral therapy on the growth pattern.

Golucci APBS, Marson FAL, Valente MFF, Branco MM, Prado CC, Nogueira RJN.

J Pediatr (Rio J). 2019 Jan - Feb;95(1):7-17. doi: 10.1016/j.jped.2018.02.006. Epub 2018 Apr 13.

18.

Interaction among variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1, and SLC9A3) and CFTR mutations with clinical markers of cystic fibrosis.

Pereira SVN, Ribeiro JD, Bertuzzo CS, Marson FAL.

Pediatr Pulmonol. 2018 Jul;53(7):888-900. doi: 10.1002/ppul.24005. Epub 2018 Apr 10.

PMID:
29635781
19.

Disease-modifying genetic factors in cystic fibrosis.

Marson FAL.

Curr Opin Pulm Med. 2018 May;24(3):296-308. doi: 10.1097/MCP.0000000000000479. Review.

PMID:
29517584
20.

Association between oxygenation and ventilation indices with the time on invasive mechanical ventilation in infants.

Camargo Barros Rocha DA, Marson FAL, Almeida CCB, Almeida Junior AA, Ribeiro JD.

Pulmonology. 2018 Feb 2. pii: S2173-5115(17)30180-X. doi: 10.1016/j.rppnen.2017.10.010. [Epub ahead of print]

21.

Association between single nucleotide polymorphisms in TLR4, TLR2, TLR9, VDR, NOS2 and CCL5 genes with acute viral bronchiolitis.

Alvarez AE, Marson FAL, Bertuzzo CS, Bastos JCS, Baracat ECE, Brandão MB, Tresoldi AT, das Neves Romaneli MT, Almeida CCB, de Oliveira T, Schlodtmann PG, Corrêa E, de Miranda MLF, Dos Reis MC, De Pieri JV, Arns CW, Ribeiro JD.

Gene. 2018 Mar 1;645:7-17. doi: 10.1016/j.gene.2017.12.022. Epub 2017 Dec 15.

PMID:
29253610
22.

Respiratory syncytial virus in Brazilian infants - Ten years, two cohorts.

Wollmeister E, Alvarez AE, Bastos JCS, Marson FAL, Ribeiro JD, Baracat ECE, Arns CW, Riccetto AGL.

J Clin Virol. 2018 Jan;98:33-36. doi: 10.1016/j.jcv.2017.12.002. Epub 2017 Dec 6.

PMID:
29227860
23.

Pancreatic Insufficiency in Cystic Fibrosis: Influence of Inflammatory Response Genes.

Marson FAL, Bertuzzo CS, de Araujo TK, Hortencio TDR, Ribeiro AF, Ribeiro JD.

Pancreas. 2018 Jan;47(1):99-109. doi: 10.1097/MPA.0000000000000963.

PMID:
29215541
24.

Evaluation of respiratory dynamics by volumetric capnography during submaximal exercise protocol of six minutes on treadmill in cystic fibrosis patients.

Parazzi PLF, Marson FAL, Ribeiro MAGO, Schivinski CIS, Ribeiro JD.

J Pediatr (Rio J). 2019 Jan - Feb;95(1):76-86. doi: 10.1016/j.jped.2017.10.007. Epub 2017 Nov 29.

25.

Thirty Years of Sweat Chloride Testing at One Referral Center.

Faria AG, Marson FAL, Gomez CCS, Servidoni MF, Ribeiro AF, Ribeiro JD.

Front Pediatr. 2017 Oct 26;5:222. doi: 10.3389/fped.2017.00222. eCollection 2017.

26.

Challenges in the identification of Chryseobacterium indologenes and Elizabethkingia meningoseptica in cases of nosocomial infections and patients with cystic fibrosis.

de Carvalho Filho ÉB, Marson FAL, Levy CE.

New Microbes New Infect. 2017 Sep 13;20:27-33. doi: 10.1016/j.nmni.2017.09.002. eCollection 2017 Nov.

27.

Cystic fibrosis transmembrane regulator haplotypes in households of patients with cystic fibrosis.

Furgeri DT, Marson FAL, Correia CAA, Ribeiro JD, Bertuzzo CS.

Gene. 2018 Jan 30;641:137-143. doi: 10.1016/j.gene.2017.10.052. Epub 2017 Oct 18.

PMID:
29054758
28.

Burkholderia cepacia complex in cystic fibrosis in a Brazilian reference center.

Dentini P, Marson FAL, Bonadia LC, Bertuzzo CS, Ribeiro AF, Levy CE, Ribeiro JD.

Med Microbiol Immunol. 2017 Dec;206(6):447-461. doi: 10.1007/s00430-017-0521-2. Epub 2017 Sep 30.

PMID:
28965239
29.

Association of clinical severity of cystic fibrosis with variants in the SLC gene family (SLC6A14, SLC26A9, SLC11A1 and SLC9A3).

Pereira SV, Ribeiro JD, Bertuzzo CS, Marson FAL.

Gene. 2017 Sep 20;629:117-126. doi: 10.1016/j.gene.2017.07.068. Epub 2017 Jul 27.

PMID:
28756021
30.

Variants in the interleukin 8 gene and the response to inhaled bronchodilators in cystic fibrosis.

Furlan LL, Ribeiro JD, Bertuzzo CS, Salomão Junior JB, Souza DRS, Marson FAL.

J Pediatr (Rio J). 2017 Nov - Dec;93(6):639-648. doi: 10.1016/j.jped.2017.03.005. Epub 2017 Jul 15.

31.

Personalized or Precision Medicine? The Example of Cystic Fibrosis.

Marson FAL, Bertuzzo CS, Ribeiro JD.

Front Pharmacol. 2017 Jun 20;8:390. doi: 10.3389/fphar.2017.00390. eCollection 2017. Review.

32.

Sweat test and cystic fibrosis: overview of test performance at public and private centers in the state of São Paulo, Brazil.

Servidoni MF, Gomez CCS, Marson FAL, Toro AADC, Ribeiro MÂGO, Ribeiro JD, Ribeiro AF; Grupo Colaborativo de Estudos em Fibrose Cística.

J Bras Pneumol. 2017 Mar-Apr;43(2):121-128. doi: 10.1590/S1806-37562016000000076. English, Portuguese.

33.

Hypertonic Saline as a Useful Tool for Sputum Induction and Pathogen Detection in Cystic Fibrosis.

Ferreira ACM, Marson FAL, Cohen MA, Bertuzzo CS, Levy CE, Ribeiro AF, Ribeiro JD.

Lung. 2017 Aug;195(4):431-439. doi: 10.1007/s00408-017-0008-3. Epub 2017 Apr 28.

PMID:
28455785
34.

Physical performance, quality of life and sexual satisfaction evaluation in adults with cystic fibrosis: An unexplored correlation.

Aguiar KCA, Marson FAL, Gomez CCS, Pereira MC, Paschoal IA, Ribeiro AF, Ribeiro JD.

Rev Port Pneumol (2006). 2017 Jul - Aug;23(4):179-192. doi: 10.1016/j.rppnen.2017.02.009. Epub 2017 Apr 21.

35.

Spirometry and volumetric capnography in lung function assessment of obese and normal-weight individuals without asthma.

Ferreira MS, Mendes RT, Marson FAL, Zambon MP, Antonio MARGM, Paschoal IA, Toro AADC, Severino SD, Ribeiro MAGO, Ribeiro JD.

J Pediatr (Rio J). 2017 Jul - Aug;93(4):398-405. doi: 10.1016/j.jped.2016.10.007. Epub 2017 Apr 19.

36.

Corrigendum to "Variants of estrogen receptor alpha and beta genes modify the severity of sporadic breast cancer" [Gene 608C (2017) 73-78].

Rezende LM, Marson FAL, Lima CSP, Bertuzzo CS.

Gene. 2017 Jul 1;619:76. doi: 10.1016/j.gene.2017.03.031. Epub 2017 Apr 7. No abstract available.

PMID:
28363082
37.

Can MTHFR C677T and A1298C Polymorphisms Alter the Risk and Severity of Sporadic Breast Cancer in Brazilian Women?

Rezende LM, Marson FAL, Lima CSP, Bertuzzo CS.

Clin Breast Cancer. 2017 Jul;17(4):e199-e208. doi: 10.1016/j.clbc.2017.02.004. Epub 2017 Feb 16.

PMID:
28330681
38.

Erratum to: Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?

Faria AG, Marson FA, de Souza Gomez CC, Ribeiro MÂ, Morais LB, de Fátima Servidoni M, Bertuzzo CS, Sakano E, Goto M, Paschoal IA, Pereira MC, Hessel G, Levy CE, Toro AA, Peixoto AO, Simões MC, Lomazi EA, Nogueira RJ, Ribeiro AF, Ribeiro JD.

Diagn Pathol. 2017 Feb 27;12(1):22. doi: 10.1186/s13000-017-0611-x. No abstract available.

39.

Erratum to: IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability.

Furlan LL, Marson FA, Ribeiro JD, Bertuzzo CS, Salomão Junior JB, Souza DR.

Hum Genet. 2017 Mar;136(3):347-348. doi: 10.1007/s00439-017-1761-3. No abstract available.

PMID:
28160095
40.

Variants of estrogen receptor alpha and beta genes modify the severity of sporadic breast cancer.

Rezende LM, Marson FA, Lima CS, Bertuzzo CS.

Gene. 2017 Apr 15;608:73-78. doi: 10.1016/j.gene.2017.01.010. Epub 2017 Jan 18. Erratum in: Gene. 2017 Jul 1;619:76.

PMID:
28109853
41.

The correlation between age and sweat chloride levels in sweat tests.

Faria AG, Marson FAL, Ribeiro AF, Ribeiro JD.

Rev Port Pneumol (2006). 2017 Jul - Aug;23(4):227-230. doi: 10.1016/j.rppnen.2016.11.001. Epub 2016 Dec 27. No abstract available.

42.

Correlation between acoustic rhinometry, computed rhinomanometry and cone-beam computed tomography in mouth breathers with transverse maxillary deficiency.

Sakai RHUS, Marson FAL, Sakuma ETI, Ribeiro JD, Sakano E.

Braz J Otorhinolaryngol. 2016 Nov 25. pii: S1808-8694(16)30234-8. doi: 10.1016/j.bjorl.2016.10.015. [Epub ahead of print]

43.

Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?

Faria AG, Marson FA, Gomez CC, Ribeiro MÂ, Morais LB, Servidoni MF, Bertuzzo CS, Sakano E, Goto M, Paschoal IA, Pereira MC, Hessel G, Levy CE, Toro AA, Peixoto AO, Simões MC, Lomazi EA, Nogueira RJ, Ribeiro AF, Ribeiro JD.

Diagn Pathol. 2016 Oct 26;11(1):103. Erratum in: Diagn Pathol. 2017 Feb 27;12 (1):22.

44.

Classification of CFTR mutation classes.

Marson FAL, Bertuzzo CS, Ribeiro JD.

Lancet Respir Med. 2016 Aug;4(8):e37-e38. doi: 10.1016/S2213-2600(16)30188-6. Epub 2016 Jul 1. No abstract available.

PMID:
27377414
45.

IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability.

Furlan LL, Marson FA, Ribeiro JD, Bertuzzo CS, Salomão Junior JB, Souza DR.

Hum Genet. 2016 Aug;135(8):881-94. doi: 10.1007/s00439-016-1684-4. Epub 2016 May 21. Erratum in: Hum Genet. 2017 Mar;136(3):347-348.

PMID:
27209008
46.

Association of growth and nutritional parameters with pulmonary function in cystic fibrosis: a literature review.

Mauch RM, Kmit AH, Marson FA, Levy CE, Barros-Filho AA, Ribeiro JD.

Rev Paul Pediatr. 2016 Dec;34(4):503-509. doi: 10.1016/j.rpped.2015.12.002. Epub 2016 Apr 16. Review. English, Portuguese.

47.

Association between clinical variables related to asthma in schoolchildren born with very low birth weight with and without bronchopulmonary dysplasia.

Gonçalves Eda S, Mezzacappa-Filho F, Severino SD, Ribeiro MÂ, Marson FA, Morcilo AM, Toro AA, Ribeiro JD.

Rev Paul Pediatr. 2016 Sep;34(3):271-80. doi: 10.1016/j.rpped.2015.12.005. Epub 2016 Feb 17. English, Portuguese.

48.

Ventilatory Efficiency in Children and Adolescents: A Systematic Review.

Parazzi PL, Marson FA, Ribeiro MA, Schivinski CI, Ribeiro JD.

Dis Markers. 2015;2015:546891. doi: 10.1155/2015/546891. Epub 2015 May 3. Review.

49.

Ventilatory abnormalities in patients with cystic fibrosis undergoing the submaximal treadmill exercise test.

Parazzi PL, Marson FA, Ribeiro MA, de Almeida CC, Martins LC, Paschoal IA, Toro AA, Schivinski CI, Ribeiro JD.

BMC Pulm Med. 2015 May 19;15:63. doi: 10.1186/s12890-015-0056-5.

50.

Microbiological characteristics of sepsis in a University hospital.

Vendemiato AV, von Nowakonski A, Marson FA, Levy CE.

BMC Infect Dis. 2015 Feb 14;15:58. doi: 10.1186/s12879-015-0798-y.

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