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Prevalence and factors associated with nontuberculous mycobacteria in non-cystic fibrosis bronchiectasis: a multicenter observational study

BMC infectious diseases, 2016-08, Vol.16 (1), p.437-437, Article 437

2016

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Acute exacerbation of idiopathic pulmonary fibrosis: an algorithmic approach to diagnosis and management

Journal of internal medicine, 2021-06, Vol.289 (6), p.930-932

2021

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The Relation of CFTR-Genotype and Associated Comorbidities to Development of Pulmonary Atelectasis in Cystic Fibrosis Patients

Archivos de bronconeumología (English ed.), 2022-09, Vol.58 (9), p.666-668

2022

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Reliability of blood eosinophil count in steady-state bronchiectasis

Pulmonology, 2024-01

2024

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Predicting high risk of exacerbations in bronchiectasis: the E-FACED score

International journal of chronic obstructive pulmonary disease, 2017-01, Vol.12, p.275-284

2017

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In vivo attenuation and genetic evolution of a ST247-SCCmecI MRSA clone after 13 years of pathogenic bronchopulmonary colonization in a patient with cystic fibrosis: implications of the innate immune response

Mucosal immunology, 2015-03, Vol.8 (2), p.362-371

2015

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WS03.7 Coexistence of prey and predator bacteria in cystic fibrosis lung microbiota

Journal of cystic fibrosis, 2017-06, Vol.16, p.S6-S6

2017

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240 Descriptive analysis of atelectasis as a pulmonary complication in cystic fibrosis

Journal of cystic fibrosis, 2017-06, Vol.16, p.S124-S124

2017

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41 Impact of treatment with ivacaftor on Spanish cystic fibrosis patients with gating mutations

Journal of cystic fibrosis, 2017-06, Vol.16, p.S74-S74

2017

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Pseudomonas aeruginosa and lung function decline in patients with bronchiectasis

Clinical microbiology and infection, 2021-03, Vol.27 (3), p.428-434

2021

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Clinical and Microbiological Features of a Cystic Fibrosis Patient Chronically Colonized with Pandoraea sputorum Identified by Combining 16S rRNA Sequencing and Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry

Journal of Clinical Microbiology, 2012-03, Vol.50 (3), p.1096-1098

2012

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87 Metagenomic approach to bacterial identification in induced sputum from cystic fibrosis subjects

Journal of cystic fibrosis, 2014-06, Vol.13, p.S68-S68

2014

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How are the ancient cystic fibrosis patients? Cystic fibrosis diagnosed over 60 years-old

Respiratory medicine case reports, 2017-01, Vol.21 (C), p.49-51

2017

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122 A one-year experience of routine identification by MALDI-TOF MS of non-fermenting Gram-negative rods recovered from respiratory samples from cystic fibrosis patients

Journal of cystic fibrosis, 2011, Vol.10, p.S31-S31

2011

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188 Association of lung function with adherence to inhaled antibiotic treatment in patients with cystic fibrosis (CF)

Journal of cystic fibrosis, 2013-06, Vol.12, p.S96-S96

2013

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WS13.04 Shotgun metagenomic for cystic fibrosis gut-lung microbiome and antibiotic resistant genes characterisation

Journal of cystic fibrosis, 2023-06, Vol.22, p.S27-S27

2023

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128 Population structure of Pseudomonas aeruginosa from cystic fibrosis patients

Journal of cystic fibrosis, 2011, Vol.10, p.S33-S33

2011

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216 Long-term inhaled ampicillin for the treatment of methicillin-susceptible Staphylococcus aureus bronchopulmonary infection in cystic fibrosis patients

Journal of cystic fibrosis, 2011, Vol.10, p.S55-S55

2011

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Evaluation of the MALDI-TOF system in the identification of non-fermenting Gram-negative rods recovered from sputum samples from cystic fibrosis patients

Journal of cystic fibrosis, 2010, Vol.9, p.S26-S26

2010

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Bronchial colonization features of cystic fibrosis patients over two different periods in a single CF unit in Madrid (Spain), 1995–97 vs 2006–08

Journal of cystic fibrosis, 2010, Vol.9, p.S25-S25

2010

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Clinical features of a cystic fibrosis patient chronically colonized with Pandoraea pnomenusa identified using MALDI-TOF mass spectrometry

Journal of cystic fibrosis, 2010, Vol.9, p.S121-S121

2010

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178 Assessment of pulmonary inflammation in cystic fibrosis patients by calprotectin determination in induced sputum

Journal of cystic fibrosis, 2011, Vol.10, p.S45-S45

2011

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High prevalence in cystic fibrosis patients of multiresistant hospital-acquired methicillin-resistant Staphylococcus aureus ST228-SCCmecI capable of biofilm formation

Journal of antimicrobial chemotherapy, 2008-11, Vol.62 (5), p.961-967

2008

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Response to "In vivo attenuation and genetic evolution of a ST247-SCCmecI MRSA clone after 13 years of pathogenic bronchopulmonary colonization in a patient with cystic fibrosis: implications of the innate immune response"

Mucosal immunology, 2015-05, Vol.8 (3), p.697-698

2015

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Clonal structure, genetic diversity and dynamic population of Staphylococcus aureus in cystic fibrosis patients

Journal of cystic fibrosis, 2010, Vol.9, p.S33-S33

2010

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Prevalence and factors associated with nontuberculous mycobacteria in non-cystic fibrosis bronchiectasis: a multicenter observational study

Acute exacerbation of idiopathic pulmonary fibrosis: an algorithmic approach to diagnosis and management

The Relation of CFTR-Genotype and Associated Comorbidities to Development of Pulmonary Atelectasis in Cystic Fibrosis Patients

Reliability of blood eosinophil count in steady-state bronchiectasis

Predicting high risk of exacerbations in bronchiectasis: the E-FACED score

In vivo attenuation and genetic evolution of a ST247-SCCmecI MRSA clone after 13 years of pathogenic bronchopulmonary colonization in a patient with cystic fibrosis: implications of the innate immune response

WS03.7 Coexistence of prey and predator bacteria in cystic fibrosis lung microbiota

240 Descriptive analysis of atelectasis as a pulmonary complication in cystic fibrosis

41 Impact of treatment with ivacaftor on Spanish cystic fibrosis patients with gating mutations

Pseudomonas aeruginosa and lung function decline in patients with bronchiectasis

Clinical and Microbiological Features of a Cystic Fibrosis Patient Chronically Colonized with Pandoraea sputorum Identified by Combining 16S rRNA Sequencing and Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry

87 Metagenomic approach to bacterial identification in induced sputum from cystic fibrosis subjects

How are the ancient cystic fibrosis patients? Cystic fibrosis diagnosed over 60 years-old

122 A one-year experience of routine identification by MALDI-TOF MS of non-fermenting Gram-negative rods recovered from respiratory samples from cystic fibrosis patients

188 Association of lung function with adherence to inhaled antibiotic treatment in patients with cystic fibrosis (CF)

WS13.04 Shotgun metagenomic for cystic fibrosis gut-lung microbiome and antibiotic resistant genes characterisation

128 Population structure of Pseudomonas aeruginosa from cystic fibrosis patients

216 Long-term inhaled ampicillin for the treatment of methicillin-susceptible Staphylococcus aureus bronchopulmonary infection in cystic fibrosis patients

Evaluation of the MALDI-TOF system in the identification of non-fermenting Gram-negative rods recovered from sputum samples from cystic fibrosis patients

Bronchial colonization features of cystic fibrosis patients over two different periods in a single CF unit in Madrid (Spain), 1995–97 vs 2006–08

Clinical features of a cystic fibrosis patient chronically colonized with Pandoraea pnomenusa identified using MALDI-TOF mass spectrometry

178 Assessment of pulmonary inflammation in cystic fibrosis patients by calprotectin determination in induced sputum

High prevalence in cystic fibrosis patients of multiresistant hospital-acquired methicillin-resistant Staphylococcus aureus ST228-SCCmecI capable of biofilm formation

Response to "In vivo attenuation and genetic evolution of a ST247-SCCmecI MRSA clone after 13 years of pathogenic bronchopulmonary colonization in a patient with cystic fibrosis: implications of the innate immune response"

Clonal structure, genetic diversity and dynamic population of Staphylococcus aureus in cystic fibrosis patients

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