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Results: 1-9 |
Results: 9
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus
Authors: Verpy, E Masmoudi, S Zwaenepoel, I Leibovici, M Hutchin, TP Del Castillo, I Nouaille, S Blanchard, S Laine, S Popot, JL Moreno, F Mueller, RF Petit, C
Citation: E. Verpy et al., Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus, NAT GENET, 29(3), 2001, pp. 345-349
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness
Authors: Masmoudi, S Antonarakis, SE Schwede, T Ghorbel, AM Gratri, M Pappasavas, MP Drira, M Elgaied-Boutila, A Wattenhofer, M Rossier, C Scott, HS Ayadi, H Guipponi, M
Citation: S. Masmoudi et al., Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness, HUM MUTAT, 18(2), 2001, pp. 101-108
On the existence of positive solutions of nonlinear elliptic equations
Authors: Maatoug, L Masmoudi, S
Citation: L. Maatoug et S. Masmoudi, On the existence of positive solutions of nonlinear elliptic equations, POTENT ANAL, 15(3), 2001, pp. 187-197
Existence theorem of nonlinear singular boundary value problem
Authors: Maagli, H Masmoudi, S
Citation: H. Maagli et S. Masmoudi, Existence theorem of nonlinear singular boundary value problem, NONLIN ANAL, 46(4), 2001, pp. 465-473
From DFNB2 to Usher syndrome: Variable expressivity of the same disease
Authors: Ben Zina, Z Masmoudi, S Ayadi, H Chaker, F Ghorbel, AM Drira, M Petit, C
Citation: Z. Ben Zina et al., From DFNB2 to Usher syndrome: Variable expressivity of the same disease, AM J MED G, 101(2), 2001, pp. 181-183
Positive solutions of a singular nonlinear differential operator of fourthorder
Authors: Masmoudi, S Zribi, M
Citation: S. Masmoudi et M. Zribi, Positive solutions of a singular nonlinear differential operator of fourthorder, NONLIN ANAL, 42(8), 2000, pp. 1365-1376
Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation
Authors: Masmoudi, S Charfedine, I Hmani, M Grati, M Ghorbel, AM Elgaied-Boulila, A Drira, M Hardelin, JP Ayadi, H
Citation: S. Masmoudi et al., Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation, AM J MED G, 90(1), 2000, pp. 38-44
Aneurysm of the thoracic aorta complicating pseudo-coarctation.
Authors: Frikha, I Masmoudi, S Hadjkacem, A Ghemissou, N Kolsi, K Khannous, M Karoui, A Sahnoun, Y
Citation: I. Frikha et al., Aneurysm of the thoracic aorta complicating pseudo-coarctation., ARCH MAL C, 93(2), 2000, pp. 195-198
On the solutions of a semilinear singular differential operator
Authors: Maagli, H Masmoudi, S
Citation: H. Maagli et S. Masmoudi, On the solutions of a semilinear singular differential operator, POTENT ANAL, 10(3), 1999, pp. 289-304
Risultati: 1-9 |