Search Results - "Rubbo, Bruna"
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Clinical care for primary ciliary dyskinesia: current challenges and future directions
Published in European respiratory review (30-09-2017)“…Primary ciliary dyskinesia (PCD) is a rare genetic disease that affects the motility of cilia, leading to impaired mucociliary clearance. It is estimated that…”
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2
Accuracy of High-Speed Video Analysis to Diagnose Primary Ciliary Dyskinesia
Published in Chest (01-05-2019)“…Diagnosis of primary ciliary dyskinesia (PCD) relies on a combination of tests. High-speed video microscopy analysis (HSVA) is widely used to contribute to the…”
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3
Diagnosing primary ciliary dyskinesia: an international patient perspective
Published in The European respiratory journal (01-10-2016)“…Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sino-pulmonary disease, with symptoms starting soon after birth. A…”
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The association between multi-disciplinary staffing levels and mortality in acute hospitals: a systematic review
Published in Human resources for health (20-04-2023)“…Health systems worldwide are faced with the challenge of adequately staffing their hospital services. Much of the current research and subsequent policy has…”
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Staffing levels and hospital mortality in England: a national panel study using routinely collected data
Published in BMJ open (17-05-2023)“…ObjectivesExamine the association between multiple clinical staff levels and case-mix adjusted patient mortality in English hospitals. Most studies…”
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Ear and upper airway clinical outcome measures for use in primary ciliary dyskinesia research: a scoping review
Published in European respiratory review (30-09-2023)“…Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by pulmonary, otological and sino-nasal manifestations. Well-defined clinical outcome…”
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The effects of methionine acquisition and synthesis on Streptococcus pneumoniae growth and virulence
Published in PloS one (22-01-2013)“…Bacterial pathogens need to acquire nutrients from the host, but for many nutrients their importance during infection remain poorly understood. We have…”
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Priorities and barriers for research related to primary ciliary dyskinesia
Published in ERJ open research (01-09-2024)“…Despite advances in primary ciliary dyskinesia (PCD) research, many questions remain; diagnosis is complex and no disease-specific therapies exist. Using a…”
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Associations between respiratory pathogens and lung function in primary ciliary dyskinesia: cross-sectional analysis from the PROVALF-PCD cohort
Published in ERJ open research (01-09-2024)“…Respiratory pathogens are frequently isolated from airway samples in primary ciliary dyskinesia (PCD) patients. Few studies have investigated associations…”
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Standardised clinical data from patients with primary ciliary dyskinesia: FOLLOW-PCD
Published in ERJ open research (01-01-2020)“…Clinical data on primary ciliary dyskinesia (PCD) are limited, heterogeneous and mostly derived from retrospective chart reviews, leading to missing data and…”
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The Palestinian primary ciliary dyskinesia population: first results of the diagnostic and genetic spectrum
Published in ERJ open research (01-03-2023)“…Diagnostic testing for primary ciliary dyskinesia (PCD) started in 2013 in Palestine. We aimed to describe the diagnostic, genetic and clinical spectrum of the…”
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Translation of the quality-of-life measure for adults with primary ciliary dyskinesia and its application in patients in Brazil
Published in Jornal brasileiro de pneumologia (2019)“…Primary ciliary dyskinesia (PCD) is a genetic disorder that is typically inherited in an autosomal recessive manner. It is clinically characterized by…”
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Lower airway clinical outcome measures for use in primary ciliary dyskinesia research: a scoping review
Published in ERJ open research (01-10-2021)“…Disease-specific, well-defined and validated clinical outcome measures are essential in designing research studies. Poorly defined outcome measures hamper…”
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Proceedings of the 3rd BEAT-PCD Conference and 4th PCD Training School
Published in BMC proceedings (18-12-2018)“…Primary ciliary dyskinesia (PCD) is a chronic suppurative airways disease that is usually recessively inherited and has marked clinical phenotypic…”
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Proceedings of the 4th BEAT-PCD Conference and 5th PCD Training School
Published in BMC proceedings (19-06-2020)“…Abstract Primary ciliary dyskinesia (PCD) is an inherited ciliopathy leading to chronic suppurative lung disease, chronic rhinosinusitis, middle ear disease,…”
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Proceedings of the 2nd BEAT-PCD conference and 3rd PCD training school: part 1
Published in BMC proceedings (05-03-2018)“…Primary ciliary dyskinesia (PCD) is a rare heterogenous condition that causes progressive suppurative lung disease, chronic rhinosinusitis, chronic otitis…”
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Key paediatric messages from the 2018 European Respiratory Society International Congress
Published in ERJ open research (01-04-2019)“…In this article, the Group Chairs and early career members of the European Respiratory Society (ERS) Paediatric Assembly highlight some of the most interesting…”
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Nurse staffing levels and patient outcomes: A systematic review of longitudinal studies
Published in International journal of nursing studies (01-10-2022)“…BACKGROUNDThe contribution of registered nurses towards safe patient care has been demonstrated in many studies. However, most of the evidence linking staffing…”
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The patient's experience of primary ciliary dyskinesia: a systematic review
Published in Quality of life research (01-09-2017)“…Background Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmonary disease, with symptoms starting soon after…”
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Topological data analysis reveals genotype-phenotype relationships in primary ciliary dyskinesia
Published in The European respiratory journal (01-08-2021)“…Primary ciliary dyskinesia (PCD) is a heterogeneous inherited disorder caused by mutations in approximately 50 cilia-related genes. PCD genotype-phenotype…”
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