Zobrazeno 1 - 10
of 126
pro vyhledávání: '"F, Pennaforte"'
Autor:
F Pennaforte, B Capy, F Lavaud, D. Sabouraud-Leclerc, J.-F. Fontaine, V Sulmont, S Menu-Guillemin
Publikováno v:
Archives de Pédiatrie. 3:861-865
Resume L'allergie au latex est de plus en plus frequente, tant chez l'adulte que l'enfant. Elle est potentiellement grave puisque c'est en pediatrie la premiere cause de choc anaphylactique peroperatoire. Population. — Un diagnostic d'allergie au l
Autor:
Catherine Perrot-Minot, Sophie de Bentzmann, Christine Clavel, Michel Roussey, Edith Puchelle, Jean-Marie Zahm, Eric Deneuville, F. Pennaforte
Publikováno v:
American journal of respiratory and critical care medicine. 156(1)
We investigated the physicochemical and transport properties of sputum samples collected in physiotherapy from a well-documented group of 27 cystic fibrosis (CF) patients with identified CF genotypes. Sputum samples were characterized ex vivo for the
Publikováno v:
Human mutation. 9(4)
Autor:
D, Sabouraud-Leclerc, J F, Fontaine, F, Lavaud, S, Menu-Guillemin, B, Capy, V, Sulmont, F, Pennaforte
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 3(9)
Latex allergy is now well-known in adults and children. It represents the first cause of anaphylactic operating shock in pediatrics.A diagnosis of latex allergy was made in 16 children (five girls and 11 boys), aged 2 to 15 years, because of evoking
Autor:
C, Clavel, F, Pennaforte, F, Pigeon, M, Mozelle, M C, Boutterin, I, Duval-Binninger, C, F-erec, P, Birembaut
Publikováno v:
Annales de biologie clinique. 54(2)
Cystic fibrosis (CF) is the most common lethal autosomal recessive disorder among Caucasians and is caused by abnormalities in the cystic fibrosis transmembrane conductance regulator gene (CFTR). CFTR gene encodes a chloride channel that regulates se
Autor:
A. Dabadie, Michel Roussey, S Shak, E. Deneuville, F. Pennaforte, J. M. Zahm, S Girod de Bentzmann, C. Perrot-Minnot, E. Puchelle
Publikováno v:
The European respiratory journal. 8(3)
Recombinant human deoxyribonuclease (rhDNase) has been demonstrated to reduce the viscosity of purulent cystic fibrosis (CF) respiratory mucus, to improve pulmonary function and to reduce the risk of respiratory tract infectious exacerbations, but it
Publikováno v:
Archives de Pédiatrie. 5:819-820
Autor:
Frédérique Pigeon, Claude Férec, Christine Clavel, F. Pennaforte, C. Verlingue, Philippe Birembaut
Publikováno v:
Human Mutation. 9:368-369
Autor:
Jacques Motte, J.L. Pennaforte, A.S. Trentesaux, F. Pennaforte, Pascal Sabouraud, Nathalie Bednarek
Publikováno v:
Archives de Pédiatrie. 3:936
Publikováno v:
Pediatrie. 36(8)