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Mireille van Westreenen

Researcher at Erasmus University Rotterdam

Publications -  29
Citations -  488

Mireille van Westreenen is an academic researcher from Erasmus University Rotterdam. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 9, co-authored 23 publications receiving 324 citations. Previous affiliations of Mireille van Westreenen include Erasmus University Medical Center.

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Development of the Nasopharyngeal Microbiota in Infants with Cystic Fibrosis

TL;DR: From diagnosis onward, distinct patterns of nasopharyngeal microbiota development in infants with CF under 6 months of age compared with control subjects are observed and a marked effect of antibiotic therapy leading toward a gram-negative microbial composition is observed.
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Concordance between upper and lower airway microbiota in infants with cystic fibrosis.

TL;DR: The inconsistent intra-individual concordance between microbiota of the upper and lower respiratory niches suggests that the lungs of infants with CF may have their own microbiome that seems seeded by, but is not identical to, the upper respiratory tract microbiome.
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Diagnosis of invasive pulmonary aspergillosis in children with bronchoalveolar lavage galactomannan.

TL;DR: Assessment of galactomannan in bronchoalveolar lavage fluid is a proposed tool to diagnose invasive pulmonary aspergillosis in children.
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An Update on Eight "New" Antibiotics against Multidrug-Resistant Gram-Negative Bacteria.

TL;DR: In this article, the authors reviewed the in vitro activities of these new antibiotics, especially against ESBL and CPE microorganisms, potential side effects, and clinical studies in complicated urinary tract infection (cUTI), intra-abdominal infections (cIAI), and hospital-acquired pneumonia/ventilator-associatedpneumonia (HAP/VAP).
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Patient-Specific Modeling of Regional Antibiotic Concentration Levels in Airways of Patients with Cystic Fibrosis: Are We Dosing High Enough?

TL;DR: CFD modeling showed that concentrations of inhaled antibiotic delivered to the small airways are highly patient specific and vary throughout the bronchial tree, suggesting that anti-Pa treatment of especially the smallAirway treatment of patients with CF can be improved.