Zobrazeno 1 - 10
of 43
pro vyhledávání: '"F. Bey-Omar"'
Autor:
F. Magne, Raphaele Nove-Josserand, Isabelle Durieu, Quitterie Reynaud, V. Cottin, F. Bey-Omar, L. Laoust, Stéphane Durupt
Publikováno v:
Journal of Cystic Fibrosis. 16:89-90
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d032be94bafdf6cdcf648c805dd743d
https://doi.org/10.1016/j.jcf.2016.10.008
https://doi.org/10.1016/j.jcf.2016.10.008
Publikováno v:
Fertility and Sterility. 77:889-896
Objective: To study the correlation between genital phenotype and cystic fibrosis genotype in men lacking at least one vas deferens. Design: Prospective study. Setting: Institut Rhonalpin pour la Reproduction Humaine, Lyon-Bron, France. Patient(s): F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd8677fd48de678028ad78dfc9cff19e
https://doi.org/10.1016/s0015-0282(02)02954-0
https://doi.org/10.1016/s0015-0282(02)02954-0
Publikováno v:
Andrologie. 11:21-32
L’absence des canaux deferents est une cause rare d’infertilite masculine associee dans 80% des cas a des mutations sur le gene de la mucoviscidose. Cependant, les correlations entre le genotype et le phenotype anatomique des voies excretrices du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a48c4ecb62790fd04888220c70a2921
https://doi.org/10.1007/bf03034392
https://doi.org/10.1007/bf03034392
Autor:
D. Vital Durand, Isabelle Durieu, Yves Morel, G. Bellon, J. Rollet, Dominique Boggio, F. Bey-Omar
Publikováno v:
La Revue de Médecine Interne. 18:114-118
Resume L'agenesie bilaterale des canaux deferents est responsable d'une sterilite masculine par azoospermie excretoire et represente 1de l'ensemble des sterilites masculines. Cette forme de sterilite peut beneficier maintenant d'un programme de fecon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7522fa2b058863d325a78c5eef650094
https://doi.org/10.1016/s0248-8663(97)84676-0
https://doi.org/10.1016/s0248-8663(97)84676-0
Autor:
Hervé Lejeune, Dominique Boggio, Denis Vital Durand, Raphaele Nove Josserand, Isabelle Durieu, F. Bey-Omar, J. Rollet
Publikováno v:
Human Reproduction
Human Reproduction, Oxford University Press (OUP), 2001, 16 (10), pp.2093-2097
Human Reproduction, Oxford University Press (OUP), 2001, 16 (10), pp.2093-2097
BACKGROUND: Most infertile males with congenital bilateral absence of vas deferens (CBAVD) carry mutations on the cystic fibrosis transmembrane conductance regulator gene and may express mild cystic fibrosis (CF) symptoms. Barriers to paternity for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7c320321130dc708613fa2e559806e3
https://pubmed.ncbi.nlm.nih.gov/11574497
https://pubmed.ncbi.nlm.nih.gov/11574497
Publikováno v:
La Revue de medecine interne. 18(2)
Congenital bilateral absence of vas deferens causes male excretory infertility and represents 1 to 2% of male infertility. Because of a genotypic similarity with cystic fibrosis, the possible in vitro fertilization with epididymal sperm requires care
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2db31d9b7d915f5b9b36af50052d6cd1
https://pubmed.ncbi.nlm.nih.gov/9092029
https://pubmed.ncbi.nlm.nih.gov/9092029
Publikováno v:
Thorax
Thorax, BMJ Publishing Group, 2005, 60 (11), pp.974-975. ⟨10.1136/thx.2005.048207⟩
Thorax, BMJ Publishing Group, 2005, 60 (11), pp.974-975. ⟨10.1136/thx.2005.048207⟩
The distribution of cystic fibrosis (CF) transmembrane conductance regulator (CFTR) genotypes is not well characterised in patients with CF diagnosed after childhood, the majority of whom are compound heterozygotes for ΔF508.1 We describe such a pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::725ee1784fad53f0657b4936be6a8cda
https://doi.org/10.1136/thx.2005.048207
https://doi.org/10.1136/thx.2005.048207
Publikováno v:
Bulletin de l'Academie nationale de medecine. 178(2)
Therapeutical solutions now can be proposed to some excretory azoospermia, using in vitro-fertilization with epididymal sperm. The encouraging results obtained with this new approach should be analyzed with the genetic risk, sometimes encountered in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a37a2f17787853bbaacc13bcb55c351f
https://pubmed.ncbi.nlm.nih.gov/8039006
https://pubmed.ncbi.nlm.nih.gov/8039006
Publikováno v:
La Revue de Médecine Interne. 14:981
We investigated clinical data, sweat electrolytes and cystic fibrosis (CF) mutations in twelve patients with congenital bilateral aplasia of vasa deferentia (CBAVD) to debate arguments for diagnosing CF. Sweat chloride concentration was definitely ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::442f824729561159e8f61dfa0df49d9e
https://doi.org/10.1016/s0248-8663(05)80099-2
https://doi.org/10.1016/s0248-8663(05)80099-2
Publikováno v:
Pediatrie. 38(2)
The longitudinal study of five infants affected with congenital hyperplasia (CAH) due to 21-hydroxylase deficiency illustrate the aggravation of the salt losing syndrome during the initial period of replacement therapy with hydrocortisone alone, asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::592f82bcf314676f652ca4438ea81ff3
https://pubmed.ncbi.nlm.nih.gov/6622141
https://pubmed.ncbi.nlm.nih.gov/6622141