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Results: 1-15 |
Results: 15
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
Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family (vol 72, pg 43, 2001)
Authors: Waldegger, S Moschen, I Ramirez, A Smith, RJH Ayadi, H Lang, F Kubisch, C
Citation: S. Waldegger et al., Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family (vol 72, pg 43, 2001), GENOMICS, 77(1-2), 2001, pp. 115-115
Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family
Authors: Waldegger, S Moschen, I Ramirez, A Smith, RJH Ayadi, H Lang, F Kubisch, C
Citation: S. Waldegger et al., Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family, GENOMICS, 72(1), 2001, pp. 43-50
Inhibition of potato virus Y NIa activity: preparation of monoclonal antibody directed against PVY NI protein that inhibits cleavage of PVY polyprotein
Authors: Rouis, S Traincard, F Gargouri, R Dartevelle, S Jeannequin, O Mazie, JC Ayadi, H
Citation: S. Rouis et al., Inhibition of potato virus Y NIa activity: preparation of monoclonal antibody directed against PVY NI protein that inhibits cleavage of PVY polyprotein, ARCH VIROL, 146(7), 2001, pp. 1297-1306
HLA class I and II polymorphisms in a large multiplex family with autoimmune thyroid diseases
Authors: Elleuch-Bougacha, N Maalej, A Makni, H Bellassouad, M Abid, M Jouida, J Ayed, K Charron, D Tamouza, R Ayadi, H
Citation: N. Elleuch-bougacha et al., HLA class I and II polymorphisms in a large multiplex family with autoimmune thyroid diseases, CLIN ENDOCR, 55(4), 2001, pp. 557-558
Lack of linkage and association between autoimmune thyroid diseases and the CTLA-4 gene in a large Tunisian family
Authors: Maalej, A Bougacha, N Rebai, A Bellassouad, M Ayadi-Makni, F Abid, M Jouida, J Makni, H Ayadi, H
Citation: A. Maalej et al., Lack of linkage and association between autoimmune thyroid diseases and the CTLA-4 gene in a large Tunisian family, HUMAN IMMUN, 62(11), 2001, pp. 1245-1250
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
Polymorphisms of HLA DQB1 CAR1/CAR2 and TNF alpha IR2/IR4 microsatellite markers in patients affected with Graves disease
Authors: Maalej, A Kacem, HH Bellassoued, M Abid, M Makni, H Ayadi, H
Citation: A. Maalej et al., Polymorphisms of HLA DQB1 CAR1/CAR2 and TNF alpha IR2/IR4 microsatellite markers in patients affected with Graves disease, CLIN IMMUNO, 96(2), 2000, pp. 91-93
Dry cough in a 17-year-old patient: mediastinal ganglioneuroma
Authors: Ayadi, H Gargouri, O Ayoub, A
Citation: H. Ayadi et al., Dry cough in a 17-year-old patient: mediastinal ganglioneuroma, REV MAL RES, 17(6), 2000, pp. 1101-1102
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
Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates
Authors: Ben Arab, S Hmani, M Denoyelle, F Boulila-Elgaied, A Chardenoux, S Hachicha, S Petit, C Ayadi, H
Citation: S. Ben Arab et al., Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates, CLIN GENET, 57(6), 2000, pp. 439-443
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2
Authors: Hmani, M Ghorbel, A Boulila-Elgaied, A Ben Zina, Z Kammoun, W Drira, M Chaabouni, M Petit, C Ayadi, H
Citation: M. Hmani et al., A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2, EUR J HUM G, 7(3), 1999, pp. 363-367
Analysis of immunoglobulin VH and TCR C beta polymorphisms in a large family with thyroid autoimmune disorder
Authors: Fakhfakh, F Maalej, A Makni, H Abid, M Jouida, J Zouali, M Ayadi, H
Citation: F. Fakhfakh et al., Analysis of immunoglobulin VH and TCR C beta polymorphisms in a large family with thyroid autoimmune disorder, EXP CLIN IM, 16(4), 1999, pp. 185-191
Genetic heterogeneity in familial nonmedullary thyroid carcinoma: Exclusion of linkage to RET, MNG1, and TCO in 56 families
Authors: Lesueur, F Stark, M Tocco, T Ayadi, H Delisle, MJ Goldgar, DE Schlumberger, M Romeo, G Canzian, F
Citation: F. Lesueur et al., Genetic heterogeneity in familial nonmedullary thyroid carcinoma: Exclusion of linkage to RET, MNG1, and TCO in 56 families, J CLIN END, 84(6), 1999, pp. 2157-2162
Poisoning evidence and clinical symptoms in Tunisian agricultural workers exposed to insecticides
Authors: Hadidane, R Ayachi, S Ayadi, H Masmoudi, AS Hammami, M Hammami, S Akrout, M Brahem, Y
Citation: R. Hadidane et al., Poisoning evidence and clinical symptoms in Tunisian agricultural workers exposed to insecticides, HUMAN AND ENVIRONMENTAL EXPOSURE TO XENOBIOTICS, 1999, pp. 715-720
Risultati: 1-15 |