Search Results - "Frachon, I."
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Mediator (benfluorex), a french and worldwide public health disaster
Published in Clinical therapeutics (01-08-2013)Get full text
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Follow-up strategies for lung transplant recipients in France
Published in Revue des maladies respiratoires (01-04-2023)“…Lung transplantation (LT) requires sustained care for a frequently polypathological condition. Follow-up is focused on three main issues: 1/stability of…”
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Pulmonary siderosis in a welder, diagnosis on unusual pneumopathy
Published in Revue des maladies respiratoires (01-02-2022)“…Pulmonary siderosis or welder's lung is an occupational lung disease that is usually observed after chronic exposure to iron dust. A 55-years-old welder…”
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Evaluation of quantitative PCR for early diagnosis of Pseudomonas aeruginosa infection in cystic fibrosis: a prospective cohort study
Published in Clinical microbiology and infection (01-03-2017)“…Early detection of Pseudomonas aeruginosa lung positivity is a key element in cystic fibrosis (CF) management. PCR has increased the accuracy of detection of…”
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Characterisation of severe obliterative bronchiolitis in rheumatoid arthritis
Published in The European respiratory journal (01-05-2009)“…The characteristics of patients with rheumatoid arthritis (RA) who develop obliterative bronchiolitis characterised by severe airflow obstruction have been…”
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Fenfluramine-like cardiovascular side-effects of benfluorex
Published in The European respiratory journal (01-03-2009)“…Since 1976, benfluorex has been approved in Europe as a hypolipidemic and hypoglycemic drug, and is commonly used in the treatment of the metabolic syndrome…”
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Update on the roles of distal airways in asthma
Published in European respiratory review (01-06-2009)“…For affiliations, please see the Acknowledgements section CORRESPONDENCE: D. Dusser, Service de Pneumologie, Hôpital Cochin, 27 rue du Faubourg, St Jacques…”
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ePS01.3 Cascade carrier testing within CF-affected families: who makes the test and when?
Published in Journal of cystic fibrosis (01-06-2016)Get full text
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Chronic thromboembolic pulmonary hypertension: a tribute to pulmonary endarterectomy
Published in The European respiratory journal (01-02-2009)Get full text
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Improvement of HIV-related pulmonary hypertension after the introduction of an antiretroviral therapy
Published in The European respiratory journal (01-07-2009)Get full text
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Treatments targeting distal airways in asthma: update on clinical studies
Published in Revue des maladies respiratoires (01-10-2009)“…Two strategies are possible for targeting distal airways in asthma. The first one is systemic, with the delivery of medications either orally or intravenously…”
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Pulmonary arterial hypertension in the elderly subject
Published in Revue des maladies respiratoires (2010)“…To describe the features of pulmonary arterial hypertension (PAH) in elderly patients. A single centre, descriptive study of PAH patients consecutively…”
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Transforming growth factor beta in normal human lung: preferential location in bronchial epithelial cells
Published in Thorax (01-08-1994)“…BACKGROUND--Transforming growth factor beta (TGF-beta) is an immunomodulatory cytokine regulating the proliferation and differentiation of various cell types…”
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Pulmonary toxicity of chemotherapy and G/GM-CSF: a report of five cases
Published in Respiratory medicine (1999)Get full text
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Education and Self-Management: A One-Year Randomized Trial in Stable Adult Asthmatic Patients
Published in The Journal of asthma (01-01-2002)“…Objective: to assess the effects of an educational program in asthmatic patients, following treatment readjustment. Methods: moderate to severe asthmatic…”
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P102 Clear illustration of improved survival in cystic fibrosis using the Kaplan-Meier method: the 50-year experience of Brittany, France
Published in Journal of cystic fibrosis (01-06-2023)Get full text
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Cftr transgene expression in primary ΔF508 epithelial cell cultures from human nasal polyps following gene transfer with cationic phosphonolipids
Published in Molecular biotechnology (01-03-2004)“…Cystic fibrosis (CF) is the most common autosomal lethal recessive disorder in the Caucasian population. The major cause of mortality is lung disease, owing to…”
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Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system
Published in Clinical genetics (01-07-2002)“…Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with different related disorders such as congenital bilateral…”
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