Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Laurence S. Hanssens"'
Publikováno v:
Immunity, Inflammation and Disease, Vol 9, Iss 2, Pp 608-614 (2021)
Abstract Background and Methods Hypergammaglobulinemia (hyper‐IgG) and hypogammaglobulinemia (hypo‐IgG) have been reported in patients with cystic fibrosis (CF). Although the clinical respiratory course is paradoxically different, depending on th
Externí odkaz:
https://doaj.org/article/ae652be88bae484882093b1a6cde3d60
Publikováno v:
Cells, Vol 10, Iss 11, p 2844 (2021)
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein called Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). The CFTR protein is known to acts as a chloride (Cl−) channel expressed in the e
Externí odkaz:
https://doaj.org/article/d265e9e8330342e58ed891de8c5be39f
Autor:
Kristine Desager, Eva J. Peirsman, Kate Sauer, Marc Raes, Luc Pattyn, Thierry J. Carvelli, Françoise Vermeulen, Laurence S. Hanssens, Pierre Y. Hage
Publikováno v:
Pediatric Pulmonology. 49:624-631
exacerbations were registered in the FeNO group. 24% of the children in the FeNO group experienced one or more exacerbations per year, compared with 48% in the clinical group (P ¼0.017). The proportion of symptom-free days did not differ between gro
Autor:
Laurence S, Hanssens, Sandra F, Mulier
Publikováno v:
Journal de pharmacie de Belgique. 62(1)
Asthma is a chronic inflammatory disorder of the airways with an impact on the life of the patient, his family and the society. Asthma is the most common chronic disease of the childhood. Consequently, prevention and treatment of asthma are real chal