Search Results - "Blanchon, S."
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Long term NIV in an infant with Hallermann-Streiff syndrome: A case report and overview of respiratory morbidity
Published in Frontiers in pediatrics (03-11-2022)“…Hallermann-Streiff syndrome (HSS) is a rare congenital syndrome with different anomalies including midface hypoplasia, beak nose and micrognathia. The upper…”
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Remodelling and inflammation in preschoolers with severe recurrent wheeze and asthma outcome at school age
Published in Clinical and experimental allergy (01-07-2018)“…Summary Background The influence of airway remodelling and inflammation in preschoolers with severe recurrent wheeze on asthma outcomes is poorly understood…”
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Treatment Decisions in Children With Asthma in a Real-Life Clinical Setting: The Swiss Paediatric Airway Cohort
Published in The journal of allergy and clinical immunology in practice (Cambridge, MA) (01-04-2022)“…Asthma treatment should be modified according to symptom control and future risk, but there are scarce data on what drives treatment adjustments in routine…”
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Recombination of Nanometric Vesicles during Freeze-Drying
Published in Langmuir (28-02-2006)“…Concentrated dispersions of nanometric lipid vesicles (mean diameter 20 nm) in water/maltose solutions have been freeze-dried and then redispersed in water,…”
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Characterization of upper airway ciliary beat by coupling isolated and collective cilia motion analysis
Published in Cilia (London) (13-07-2015)Get full text
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6
Hardness of moist agglomerates in relation to interparticle friction, granule liquid content and nature
Published in Powder technology (04-06-2001)“…Wet agglomerates deform plastically until they break through crack propagation. On the particulate level, liquid bridges are responsible for the strength of…”
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Interest of CT scan for the follow up of primary ciliary diskinesia
Published in Paediatric respiratory reviews (2010)Get full text
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P373 Impact of elexacaftor/tezacaftor/ivacaftor on quality of life in children with cystic fibrosis
Published in Journal of cystic fibrosis (01-06-2024)Get full text
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P046 Early parameters to predict long-term efficacy of CFTR modulators in patients with cystic fibrosis
Published in Journal of cystic fibrosis (01-06-2023)Get full text
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A new approach for determination of powder wettability
Published in International journal of pharmaceutics (13-06-1997)“…Based on the work initiated by Shanker, R.M., Baltusis, P.J. and Hruska, R.M. (Development of a new technique for the assessment of wettability of powders…”
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Phenotype-endotype in very severe preschool wheezers: The P'titAsthme cohort: Eur Respir J
Published in The European respiratory journal (01-09-2018)Get full text
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Congenital ciliary dyskinesia. Focus
Published in Revue de pneumologie clinique (01-08-2013)“…Primary ciliary dyskinesia (PCD) is a rare autosomal recessive disease, caused by specific primary structural and/or functional abnormalities of the motile…”
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115 Home-based non attended respiratory polygraphy in children: feasibility and accuracy for interpretation
Published in Chest (01-05-2017)Get full text
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P018 Follow-up of children with Cystic Fibrosis Screen Positive, Inconclusive Diagnosis (CFSPID) in Switzerland
Published in Journal of cystic fibrosis (2021)Get full text
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15
Dyskinésies ciliaires primitives de l’enfant
Published in Journal de pédiatrie et de puériculture (01-06-2020)“…Les dyskinésies ciliaires primitives (DCP) sont des maladies génétiques rares dues à des anomalies de structure et/ou de fonction des cils mobiles,…”
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Dyskinésies ciliaires primitives : actualités diagnostiques
Published in Revue française d'allergologie (2009) (01-04-2016)“…Les dyskinésies ciliaires primitives (DCP) sont des affections génétiques rares, liées à une anomalie de structure et/ou de fonction des cils. Il existe 2…”
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Pneumocystis jiroveci pneumonia during prolonged corticosteroid therapy in an immunocompetent infant
Published in Revue de pneumologie clinique (01-10-2008)“…Pneumocystis jiroveci (PJ) infection is rare in infants and is suggestive of primary or secondary immunodeficiency. We report on a case of severe PJ pneumonia…”
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Diagnostic of Primary Ciliary Dyskinesia: guidelines to obtain appropriate ciliate cell samples
Published in Cilia (London) (16-11-2012)Get full text
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Diagnostic algorithm for Primary Ciliary Dyskinesia: recommendations of the French National Centre for Rare Respiratory Diseases
Published in Cilia (London) (16-11-2012)Get full text
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Évolution nutritionnelle au cours de la première année de vie des enfants dépistés pour la mucoviscidose
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-05-2016)“…Évaluer l’impact du dépistage néonatal de la mucoviscidose sur l’évolution nutritionnelle précoce. Étude rétrospective monocentrique réalisée du 1/10/02 au…”
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