Authors:
Merrot, T
Delarue, A
Chaumoitre, K
Panuel, M
Sigaudy, S
Chazalette, JP
Alessandrini, P
Citation: T. Merrot et al., Congenital bilateral absence of vas deferens and inguinal herniorrhaphy inan infant: an early and rare presentation of cystic fibrosis, ARCH PED, 8(7), 2001, pp. 728-730
Authors:
Cimon, B
Carrere, J
Chazalette, JP
Ginies, JL
Chabasse, D
Bouchara, JP
Citation: B. Cimon et al., Bronchopulmonary mycoses in cystic fibrosis. Results of a five-year longitudinal study, J MYCOL MED, 10(3), 2000, pp. 128-135
Authors:
Feigelson, J
Pecau, Y
Poquet, M
Terdjman, P
Carrere, J
Chazalette, JP
Ferec, C
Citation: J. Feigelson et al., Imaging changes in the pancreas in cystic fibrosis: A retrospective evaluation of 55 cases seen over a period of 9 years, J PED GASTR, 30(2), 2000, pp. 145-151
Authors:
Romey, MC
Guittard, C
Chazalette, JP
Frossard, P
Dawson, KP
Patton, MA
Casals, T
Bazarbachi, T
Girodon, E
Rault, G
Bozon, D
Seguret, F
Demaille, J
Claustres, M
Citation: Mc. Romey et al., Complex allele [-102T > A+S549R(T > G)] is associated with milder forms ofcystic fibrosis than allele S549R[T > G) alone, HUM GENET, 105(1-2), 1999, pp. 145-150