Zobrazeno 1 - 10
of 48
pro vyhledávání: '"J P, Chazalette"'
Autor:
J. P. Chazalette, Dominique Chabasse, Jean-Philippe Bouchara, B. Cimon, J. F. Vinatier, Jacqueline Carrère
Publikováno v:
Medical Mycology. 37:291-293
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72135bd6b12653ef7fc22570712e6a42
https://doi.org/10.1111/j.1365-280x.1999.00232.x
https://doi.org/10.1111/j.1365-280x.1999.00232.x
Publikováno v:
Journal of Clinical Microbiology. 33:924-929
Secretion of Pseudomonas aeruginosa elastase, exotoxin A, and alkaline protease in sputum during bronchopulmonary exacerbations was examined in 18 cystic fibrosis patients chronically infected with this microorganism. The patients were studied during
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f57ee5b67139047ecd8c7592168a2fec
https://doi.org/10.1128/jcm.33.4.924-929.1995
https://doi.org/10.1128/jcm.33.4.924-929.1995
Publikováno v:
Journal of Medical Genetics. 31:541-544
The cystic fibrosis transmembrane conductance regulator (CFTR) gene of 600 unrelated cystic fibrosis (CF) patients living in France (excluding Brittany) was screened for 105 different mutations. This analysis resulted in the identification of 86% of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::724a6c9b2c5dc9f5bd6d4018465ec9b9
https://doi.org/10.1136/jmg.31.7.541
https://doi.org/10.1136/jmg.31.7.541
Autor:
J. P. Chazalette
Publikováno v:
Drug Investigation. 5:274-280
In 15 children (mean age 12 years) with proven cystic fibrosis and a lipid absorption coefficient (LAC) < 90%, the efficacy of a pancreatic enzyme formulation (Panzytrat® 25 000) was compared with placebo in a randomised double-blind parallel group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::652edbb568341012852becd7b4ec32c2
https://doi.org/10.1007/bf03259592
https://doi.org/10.1007/bf03259592
Autor:
I. Ounis, G. Lenoir, J. P. Chazalette, F. Douchain, D. Sommelet Olive, J. Derelle, M. Loeuil, M. Jehanne
Publikováno v:
Drug Investigation. 3:76-81
This study was designed to evaluate the prophylactic action of RU-41740 (‘Biostim’) on upper respiratory tract (URT) infections in a group of children with mild cystic fibrosis. RU-41740 is an immunomodulator of biological origin used against rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87d0c58d5e7477497eb945ed83df7bd5
https://doi.org/10.1007/bf03259545
https://doi.org/10.1007/bf03259545
Publikováno v:
Medical Mycology. 37:291-293
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6ccf513f4cd49c34fd0ee2af2ffe177
https://doi.org/10.1046/j.1365-280x.1999.00232.x
https://doi.org/10.1046/j.1365-280x.1999.00232.x
Autor:
Jacqueline Carrère, Jean-Philippe Bouchara, J. F. Vinatier, J. P. Chazalette, B. Cimon, Dominique Chabasse
Publikováno v:
Medical Mycology. 37:291-293
Penicillium emersonii Stolk, the conidial state of Talaromyces emersoniii Stolk, is a heat-resistant fungus usually isolated from soil. In this paper the authors report, to our knowledge, the first human case in which P. emersonii chronically coloniz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e8abf4e33024221cf833ad1a7e9aa48
https://doi.org/10.1080/j.1365-280x.1999.00232.x
https://doi.org/10.1080/j.1365-280x.1999.00232.x
Autor:
Laurent Viard, J. P. Chazalette, Bernard Kreitmann, Alberto Riberi, J. Camboulives, Dominique Metras
Publikováno v:
Lung Transplantation ISBN: 9783662046791
Until 1984, cystic fibrosis (CF) was considered as a contra-indication to lung transplantation for the following reasons: 1) The importance of the bronchopulmonary sepsis with polyresistant organisms inducing an increased post-operative risk. 2) The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::268c36a893d180eb2b34ea9772582f6e
https://doi.org/10.1007/978-3-662-04677-7_4
https://doi.org/10.1007/978-3-662-04677-7_4
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3fab3ef416a21141b363357c2dc0b4b
https://pubmed.ncbi.nlm.nih.gov/11811057
https://pubmed.ncbi.nlm.nih.gov/11811057
Autor:
T, Merrot, A, Delarue, K, Chaumoitre, M, Panuel, S, Sigaudy, J P, Chazalette, P, Alessandrini
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 8(7)
Epididymal and ductal anomalies can be discovered incidentally during inguinal herniorraphy in children. The congenital bilateral absence of vas deferens is frequently associated with cystic fibrosis.This agenesia of vas deferens was detected in a 5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dfb44e7e27232c8afbd29862cc635e2f
https://pubmed.ncbi.nlm.nih.gov/11484456
https://pubmed.ncbi.nlm.nih.gov/11484456