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Hammadi Ayadi

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Tunisia

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Sandra A Rebuffat; Hammadi Ayadi; Noura Bougacha-Elleuch; Ilhem Charfeddine; Maha Kammoun-Krichen; Sylvie Peraldi-Roux
IL-1β and TSH disturb thyroid epithelium integrity in autoimmune thyroid diseases.
Salima Belguith-Maalej; Rihab Kallel; Mouna Mnif; Mohamed Abid; Hammadi Ayadi; Hassen Hadj Kacem
Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis disease.
Ghada Ben Salah; Emna Mkaouar-Rebai; Hammadi Ayadi; Imen Ayadi; Faiza Fakhfakh; Nourhene Fendri-Kriaa; Amine Fourati; Fakhri Kallabi; Hassen Kamoun
DNA repair gene polymorphisms at XRCC1 (Arg194Trp, Arg280His, and Arg399Gln) in a healthy Tunisian population: interethnic variation and functional prediction.

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2013: Sandra A Rebuffat; Hammadi Ayadi; Noura Bougacha-Elleuch; Ilhem Charfeddine; Maha Kammoun-Krichen; Sylvie Peraldi-Roux
IL-1β and TSH disturb thyroid epithelium integrity in autoimmune thyroid diseases.
Immunobiology 2013;218(3):285-91.
2013: Salima Belguith-Maalej; Rihab Kallel; Mouna Mnif; Mohamed Abid; Hammadi Ayadi; Hassen Hadj Kacem
Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis disease.
Genetics research 2013;95(1):38-44.
2012: Ghada Ben Salah; Emna Mkaouar-Rebai; Hammadi Ayadi; Imen Ayadi; Faiza Fakhfakh; Nourhene Fendri-Kriaa; Amine Fourati; Fakhri Kallabi; Hassen Kamoun
DNA repair gene polymorphisms at XRCC1 (Arg194Trp, Arg280His, and Arg399Gln) in a healthy Tunisian population: interethnic variation and functional prediction.
Genetic testing and molecular biomarkers 2012;16(10):1218-25.
2012: Ghada Ben Salah; Hammadi Ayadi; Nourhene Fendri-Kriaa; Amine Fourati; Fakhri Kallabi; Hassen Kamoun; Emna Mkaouar-Rebai; Faiza Fakhfakh
An interethnic variability and a functional prediction of DNA repair gene polymorphisms: the example of XRCC3 (p.Thr241>Met) and XPD (p.Lys751>Gln) in a healthy Tunisian population.
Molecular biology reports 2012;39(10):9639-47.
2012: Maha Kammoun-Krichen; Mouna Mnif; Sylvie Péraldi-Roux; Ahmed Rebai; Sandra Rebuffat; Fadia Bougacha; Noura Bougacha-Elleuch; Ilhem Charffedine; Emilie Glasson; Mohamed Abid; Fatma Ayadi; Hammadi Ayadi
IL-1β a potential factor for discriminating between thyroid carcinoma and atrophic thyroiditis.
European cytokine network 2012;23(3):101-6.
2012: Mariem Ben Said; Saber Masmoudi; Felipe Moreno; Hammadi Ayadi; Zeineb Benzina; Houria Dhouib; Abdelmoneem Ghorbel; Mounira Hmani-Aifa
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.
International journal of pediatric otorhinolaryngology 2012;76(6):832-6.
2012: M Ben Hamad; G Chabchoub; François Cornelis; F Fakhfakh; Hammadi Ayadi; Zouhir Bahloul; S Marzouk; Elisabeth Petit-Teixeira; Ahmed Rebai; Abdellatif Maalej
Association study of CARD8 (p.C10X) and NLRP3 (p.Q705K) variants with rheumatoid arthritis in French and Tunisian populations.
International journal of immunogenetics 2012;39(2):131-6.
2011: Laurence Molina; Sabine Peres; Nicolas Salvetat; Nicolas Sommerer; Randa Ben Ameur; Hammadi Ayadi; Fayçal Jarraya; Franck Molina; Claude Granier
Analysis of the variability of human normal urine by 2D-GE reveals a "public" and a "private" proteome.
Journal of proteomics 2011;75(1):70-80.
2011: Mariem Bensaïd; Ignacio Del Castillo; Ilhem Charfeddine; Abdelmonem Ghorbel; Bochra Hakim; Boutheina Hammami; Mounira Hmani-Aifa; Hammadi Ayadi; Abdelaziz Tlili; Saber Masmoudi
DFNB66 and DFNB67 loci are non allelic and rarely contribute to autosomal recessive nonsyndromic hearing loss.
European journal of medical genetics 2011;54(6):e565-9.
2011: Mariem Ben Saïd; Zeineb Benzina; Ignacio Del Castillo; Ilhem Charfeddine; Abdelmonem Ghorbel; Bochra Hakim; Ayda Khalfallah; Chamseddine Khifagi; Saber Masmoudi; Melek Mnejja; Khalil Turki; Hammadi Ayadi; Leila Ayedi; Mounira Hmani- Aifa
A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family.
European journal of medical genetics 2011;54(6):e535-41.
2011: Ayda Khalfallah; Imed Lahmar; Hammadi Ayadi; Ilhem Charfeddine; Leila Dhouib; Nabil Driss; Abdelmonem Ghorbel; Hassen HadjKacem; Bochra Hakim; Malek Mnejja; Mohamed Ali Mosrati; Isabelle Schrauwen; Guy Van Camp; Saber Masmoudi
Association of COL1A1 and TGFB1 polymorphisms with otosclerosis in a Tunisian population.
Annals of human genetics 2011;75(5):598-604.
2011: Noura Bougacha-Elleuch; N Charfi; Jomaa Jouida; Abdellatif Maalej; Mouna Mnif; Ahmed Rebai; Saida Ben Arab; Mohamed Ben Lassouad; Mohamed Abid; Hammadi Ayadi
No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree.
Journal of genetics 2011;90(2):333-7.
2011: K Saidas Nair; Mounira Hmani-Aifa; Zain Ali; Alison L Kearney; Danilo G Macalinao; Ioan M Cosma; Walid Bouassida; Bochra Hakim; Zeineb Benzina; Ileana Soto; Peter Söderkvist; Gareth R Howell; Richard S Smith; Hammadi Ayadi; Salma Ben Salem; Simon W M John
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice.
Nature genetics 2011;43(6):579-84.
2011: Chamseddine Kifagi; Kaouthar Makni; Mouhamed Boudawara; Fatma Mnif; Naziha Hamza; Mouhamed Abid; Claude Granier; Hammadi Ayadi
Association of genetic variations in TCF7L2, SLC30A8, HHEX, LOC387761, and EXT2 with Type 2 diabetes mellitus in Tunisia.
Genetic testing and molecular biomarkers 2011;15(6):399-405.
2011: Salima Belguith-Maalej; Sandra A Rebuffat; Ilhem Charfeddine; Mouna Mnif; R Farid Nadir; Mohamed Abid; Ali Ghorbel; Sylvie Peraldi-Roux; Hammadi Ayadi; Hassen Hadj Kacem
SLC26A4 expression among autoimmune thyroid tissues.
Immunobiology 2011;216(5):571-8.
2011: M Ben Hamad; F Cornelis; H Mbarek; G Chabchoub; S Marzouk; Zouhir Bahloul; Ahmed Rebai; F Fakhfakh; Hammadi Ayadi; Elisabeth Petit-Teixeira; Abdellatif Maalej
Signal transducer and activator of transcription and the risk of rheumatoid arthritis and thyroid autoimmune disorders.
Clinical and experimental rheumatology 2011;29(2):269-74.
2010: Soumaya Triki-Fendri; Suad Alfadhli; Imen Ayadi; Najla Kharrat; Hammadi Ayadi; Ahmed Rebai
Genetic structure of Kuwaiti population revealed by Y-STR diversity.
Annals of human biology 2010;37(6):827-35.
2010: Lobna Hadjkacem-Loukil; Leila Keskes; Ikhlass Hadj Salem; Ali Bahloul; Faiza Fakhfakh; Hassen Hadj Kacem; Hammadi Ayadi
Analysis of azoospermia factor loci polymorphisms among Tunisian infertile men with varicocele.
Genetic testing and molecular biomarkers 2010;():.
2010: Ayda Khalfallah; Isabelle Schrauwen; Malek Mnaja; Erik Fransen; Imed Lahmar; Megan Ealy; Leila Dhouib; Hammadi Ayadi; Ilhem Charfedine; Nabil Driss; Ali Ghorbel; Richard J H Smith; Saber Masmoudi; Guy Van Camp
Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia.
Annals of human genetics 2010;74(5):399-405.
2010: Randa Ben Ameur; Laurence Molina; Capucine Bolvin; Chamseddine Kifagi; Fayçal Jarraya; Hammadi Ayadi; Franck Molina; Claude Granier
Proteomic approaches for discovering biomarkers of diabetic nephropathy.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010;25(9):2866-75.
2010: I Ben Rebeh; N Yoshimi; Hassen Hadj Kacem; S Yanohco; B Hammami; M Mnif; M Araki; Ali Ghorbel; Hammadi Ayadi; Saber Masmoudi; H Miyazaki
Two missense mutations in SLC26A4 gene: a molecular and functional study.
Clinical genetics 2010;78(1):74-80.
2010: Mariem Ben Saïd; Mounira Hmani-Aifa; Imen Amar; Shahid Mahmood Baig; Mirna Mustapha; Sedigheh Delmaghani; Abdelaziz Tlili; Abdelmonem Ghorbel; Hammadi Ayadi; Guy Van Camp; Richard J H Smith; Mustafa Tekin; Saber Masmoudi
High frequency of the p.R34X mutation in the TMC1 gene associated with nonsyndromic hearing loss is due to founder effects.
Genetic testing and molecular biomarkers 2010;14(3):307-11.
2010: Rihab Kallel; Ricard Marcos; Mouna Mnif; Antonia Velázquez; Mohamed Abid; Abdelmounaim Akdi; Hammadi Ayadi; Salima Belguith-Maalej; Ilhem Charfeddine; Pere Galofré; Abdelmonaim Ghorbel; Hassen Hadj Kacem
Genetic investigation of FOXE1 polyalanine tract in thyroid diseases: new insight on the role of FOXE1 in thyroid carcinoma.
Cancer biomarkers : section A of Disease markers 2010;8(1):43-51.
2010: Hassen Hadj Kacem; Rihab Kallel; Salima Belguith-Maalej; Mouna Mnif; Ilhem Charfeddine; Ali Ghorbel; Mohamed Abid; Hammadi Ayadi; Saber Masmoudi
SLC26A4 variations among Graves' hyper-functioning thyroid gland.
Disease markers 2010;29(2):63-9.
2010: Imen Ben Rebeh; Madeleine Morinière; Leila Ayadi; Zeineb Benzina; Ilhem Charfedine; Jamel Feki; Hammadi Ayadi; Abdelmonem Ghorbel; Faouzi Baklouti; Saber Masmoudi
Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.
Molecular vision 2010;16():1898-906.
2010: Salima Belguith-Maalej; Hassen Hadj Kacem; Sandra A Rebuffat; Mouna Mnif-Feki; Brigitte Nguyen; Mohamed Abid; René Gross; Hammadi Ayadi; Sylvie Peraldi-Roux
Absence of anti-pendrin auto-antibodies in the sera of Tunisian patients with autoimmune thyroid diseases.
Clinical laboratory 2010;56(7-8):335-43.
2009: Salima Belguith-Maalej; Hassen Hadj Kacem; Neila Kaddour; Zouhir Bahloul; Hammadi Ayadi
DNase1 exon2 analysis in Tunisian patients with rheumatoid arthritis, systemic lupus erythematosus and Sjögren syndrome and healthy subjects.
Rheumatology international 2009;30(1):69-74.
2009: Lobna Hadjkacem-Loukil; Myriam Ghorbel; Ali Bahloul; Hammadi Ayadi; Leila Ammar-Keskes
Genetic association between AZF region polymorphism and Klinefelter syndrome.
Reproductive biomedicine online 2009;19(4):547-51.
2009: Mounira Hmani-Aifa; Salma Ben Salem; Zeineb Benzina; Walid Bouassida; Riadh Messaoud; Khalil Turki; Moncef Khairallah; Ahmed Rebaï; Faïza Fakhfekh; Peter Söderkvist; Hammadi Ayadi
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.
Human genetics 2009;126(4):575-87.
2009: Kaouthar Makni; Faïçal Jarraya; Abdelmajid Khabir; Basma Hentati; Mohamed Ben Hmida; Hafedh Makni; Tahia Boudawara; Rchid Jlidi; Jamil Hachicha; Hammadi Ayadi
Renal alpha-smooth muscle actin: a new prognostic factor for lupus nephritis.
Nephrology (Carlton, Vic.) 2009;14(5):499-505.
2009: Hanen Belguith; Abedelaziz Tlili; Houria Dhouib; Imen Ben Rebeh; Imed Lahmar; Ilhem Charfeddine; Nabil Driss; Abdelmonem Ghorbel; Hammadi Ayadi; Saber Masmoudi
Mutation in gap and tight junctions in patients with non-syndromic hearing loss.
Biochemical and biophysical research communications 2009;385(1):1-5.
2009: Ghazi Chabchoub; Elisabeth Petit Teixiera; Abdellatif Maalej; Mariem Ben Hamad; Zouheir Bahloul; Francois Cornelis; Hammadi Ayadi
The R620W polymorphism of the protein tyrosine phosphatase 22 gene in autoimmune thyroid diseases and rheumatoid arthritis in the Tunisian population.
Annals of human biology 2009;36(3):342-9.
2009: Hassen Hadj Kacem; S Rebuffat; M Mnif-Féki; S Belguith-Maalej; Hammadi Ayadi; S Péraldi-Roux
Autoimmune thyroid diseases: genetic susceptibility of thyroid-specific genes and thyroid autoantigens contributions.
International journal of immunogenetics 2009;36(2):85-96.
2009: Mounira Hmani-Aifa; Zeineb Benzina; Fareeha Zulfiqar; Houria Dhouib; Amber Shahzadi; Ali Ghorbel; Ahmed Rebaï; Peter Söderkvist; Sheikh Amer Riazuddin; William J Kimberling; Hammadi Ayadi
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
European journal of human genetics : EJHG 2009;17(4):474-82.
2009: Hanen Belguith; Mounira Aifa-Hmani; Houria Dhouib; Mariem Ben Said; Mohamed Ali Mosrati; Imed Lahmar; Jihen Moalla; Ilhem Charfeddine; Nabil Driss; Saida Ben Arab; Abdelmonem Ghorbel; Hammadi Ayadi; Saber Masmoudi
Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus.
Genetic testing and molecular biomarkers 2009;13(1):147-51.
2009: G Chabchoub; Elif Uz; Abdellatif Maalej; Chigdem A Mustafa; Ahmed Rebai; Mouna Mnif; Zouheir Bahloul; Nadir R Farid; Tayfun Ozcelik; Hammadi Ayadi
Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases.
Arthritis research & therapy 2009;11(4):R106.
2008: N Bougacha-Elleuch; M Ben Lassoued; Laboratoire Biochimie et Genie Enzymatique des Lipases; S Zouari; Hammadi Ayadi
Characterization of V71M mutation in the aquaporin-2 gene causing nephrogenic diabetes insipidus.
Journal of genetics 2008;87(3):279-82.
2008: Maha Kammoun-Krichen; Noura Bougacha-Elleuch; Ahmed Rebai; Mouna Mnif; Mohamed Abid; Hammadi Ayadi
TNF gene polymorphisms in Graves' disease: TNF-308 A/G meta-analysis.
Annals of human biology 2008;35(6):656-61.
2008: Zubair M Ahmed; Saber Masmoudi; Ersan Kalay; Inna A Belyantseva; Mohamed Ali Mosrati; Rob W J Collin; Saima Riazuddin; Mounira Hmani-Aifa; Hanka Venselaar; Mayya N Kawar; Abdelaziz Tlili; Bert van der Zwaag; Shahid Y Khan; Leila Ayadi; Sheikh Amer Riazuddin; Robert J Morell; Andrew J Griffith; Ilhem Charfedine; Refik Caylan; Jaap Oostrik; Ahmet Karaguzel; Abdelmonem Ghorbel; Sheikh Riazuddin; Thomas B Friedman; Hammadi Ayadi; Hannie Kremer
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
Nature genetics 2008;40(11):1335-40.
2008: Abdellatif Maalej; M Ben Hamad; A Rebaï; V H Teixeira; Z Bahloul; S Marzouk; N R Farid; Hammadi Ayadi; François Cornelis; Elisabeth Petit-Teixeira
Association of IRF5 gene polymorphisms with rheumatoid arthritis in a Tunisian population.
Scandinavian journal of rheumatology 2008;37(6):414-8.
2008: Maha Kammoun-Krichen; Noura Bougacha-Elleuch; Kaouthar Makni; Mouna Mnif; Joumaa Jouida; Mohamed Abid; Ahmed Rebai; Hammadi Ayadi
A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian population.
Cytokine 2008;43(2):110-3.
2008: Claude Granier; Kaouthar Makni; Laurence Molina; Benedicte Jardin-Watelet; Hammadi Ayadi; Faiçal Jarraya
Gene and protein markers of diabetic nephropathy.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2008;23(3):792-9.
2008: Imen Ben Rebeh; Zeineb Benzina; Houria Dhouib; Imen Hadjamor; Mustapha Amyere; Leila Ayadi; Khalil Turki; Bouthaina Hammami; Noureddine Kmiha; Hassen Kammoun; Bochra Hakim; Ilhem Charfedine; Miikka Vikkula; Abdelmonem Ghorbel; Hammadi Ayadi; Saber Masmoudi
Identification of candidate regions for a novel Usher syndrome type II locus.
Molecular vision 2008;14():1719-26.
2008: Salima Belguith-Maalej; Hassen Hadj Kacem; Ahmed Rebai; Mouna Mnif; Mohamed Abid; Hammadi Ayadi
Thyroglobulin polymorphisms in Tunisian patients with autoimmune thyroid diseases (AITD).
Immunobiology 2008;213(7):577-83.
2008: Abdelaziz Tlili; Imen Ben Rebeh; Mounira Aifa-Hmani; Houria Dhouib; Jihen Moalla; Jihen Tlili-Chouchène; Mariem Ben Said; Imed Lahmar; Zeineb Benzina; Ilhem Charfedine; Nabil Driss; Ali Ghorbel; Hammadi Ayadi; Saber Masmoudi
TMC1 but not TMC2 is responsible for autosomal recessive nonsyndromic hearing impairment in Tunisian families.
Audiology & neuro-otology 2008;13(4):213-8.
2008: Abdellatif Maalej; Elisabeth Petit-Teixeira; G Chabchoub; Mariam Ben Hamad; Ahmed Rebai; Nadir R Farid; François Cornelis; Hammadi Ayadi
Lack of association of VDR gene polymorphisms with thyroid autoimmune disorders: familial and case/control studies.
Journal of clinical immunology 2008;28(1):21-5.
2007: Maha Kammoun-Krichen; Noura Bougacha-Elleuch; Kaouthar Makni; Maha Rebai; Sylvie Peraldi-Roux; Ahmed Rebai; Mouna Mnif; Mohamed Abid; Jomaa Jouida; Hammadi Ayadi
Association analysis of interleukin gene polymorphisms in autoimmune thyroid diseases in the Tunisian population.
European cytokine network 2007;18(4):196-200.
2007: Kaouthar Makni; Hassen Hadj Kacem; Ahmed Rebaï; Mohamed Abid; Hammadi Ayadi
Association and linkage studies of the 20q11.2 region (GRD-2 locus) with Graves' disease in the Tunisian population.
Annals of human biology 2007;34(5):566-72.
2007: Lobna Hadjkacem-Loukil; Imen Ayadi; Ali Bahloul; Hammadi Ayadi; Leila Ammar-Keskes
Tag STS in the AZF region associated with azoospermia in a Tunisian population.
Journal of andrology 2007;28(5):652-8.
2007: Abdelaziz Tlili; Saber Masmoudi; H Dhouib; S Bouaziz; I Ben Rebeh; J Chouchen; K Turki; Zeineb Benzina; Ilhem Charfedine; Mohamed Drira; Hammadi Ayadi
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.
Annals of human genetics 2007;71(Pt 2):271-5.
2006: G Chabchoub; Mouna Mnif; Abdellatif Maalej; N Charfi; Hammadi Ayadi; Mohamed Abid
[Epidemiologic study of autoimmune thyroid disease in south Tunisia].
Annales d'endocrinologie 2006;67(6):591-5.
2006: Dorra Sellami; Kaouthar Makni; Hanene Chaker; Madiha Kharrat; N Hentati; Khaoula Kammoun; F Chabouni; M Ben Hamida; Jamil Hachicha; R Salomon; C Antignac; Hammadi Ayadi; Jamel Feki
[Ocular manifestations associated with nephronophthisis and genetic study in three Tunisian families].
Journal français d'ophtalmologie 2006;29(9):1019-23.
2006: G Chabchoub; Elisabeth Petit-Teixeira; Abdellatif Maalej; Céline Pierlot; Zouhir Bahloul; François Cornélis; Hammadi Ayadi
Lack of association between signaling lymphocytic activation molecule family member 1 gene and rheumatoid arthritis in the French and Tunisian populations.
Annals of the rheumatic diseases 2006;65(11):1538-9.
2006: Souad Rouis; Pierre Lafaye; Leila Jaoua-Aydi; Zidani Sghaier; Hammadi Ayadi; Radhia Gargouri-Bouzid
Cloning and expression of functional single-chain Fv antibodies directed against NIa and coat proteins of potato virus Y.
Journal of virological methods 2006;137(1):1-6.
2006: Madiha Kharrat; Saloua Makni; Kaouthar Makni; Khaoula Kammoun; Khaled Charfeddine; H Azaeiz; Faiçal Jarraya; Mohamed Ben Hmida; Marie-Claire Gubler; Hammadi Ayadi; Jamil Hachicha
Autosomal dominant Alport's syndrome: study of a large Tunisian family.
Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 2006;17(3):320-5.
2006: G Chabchoub; Abdellatif Maalej; Elisabeth Petit-Teixeira; Elodie Glikmans; Ahmed Rebai; N R Farid; François Cornelis; Hammadi Ayadi
Polymorphisms in the protein tyrosine phosphatase (PTPN22) gene is not associated with autoimmune thyroid in a large affected Tunisian family.
Clinical immunology (Orlando, Fla.) 2006;120(2):235-6.
2006: L Hadj-Kacem; Hassen Hadj Kacem; Hammadi Ayadi; Leila Ammar-Keskes; N Chakroun-Fki; Tarek Rebai; Ali Bahloul; Mohamed Nabil Mhiri
Screening of Y chromosome microdeletions in Tunisian infertile men.
Archives of andrology 2006;52(3):169-74.
2006: Emna Mkaouar-Rebai; Abdelaziz Tlili; Saber Masmoudi; Nacim Louhichi; Ilhem Charfeddine; Mohamed Ben Amor; Imed Lahmar; Nabil Driss; Mohamed Drira; Hammadi Ayadi; Faiza Fakhfakh
Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss.
Biochemical and biophysical research communications 2006;340(4):1251-8.
2006: Hassen Hadj Kacem; Ahmed Rebai; Noureddine Kaffel; Mohamed Abid; Hammadi Ayadi
Evidence for linkage and association between autoimmune thyroid diseases and the 18q12-q21 region in a large Tunisian family.
International journal of immunogenetics 2006;33(1):25-32.
2006: Nacim Louhichi; Pascale Richard; C H Triki; M Meziou; Hammadi Ayadi; Pascale Guicheney; Faiza Fakhfakh
Novel mutations in LAMA2 gene responsible for a severe phenotype of congenital muscular dystrophy in two Tunisian families.
Archives de l'Institut Pasteur de Tunis 2006;83(1-4):19-23.
2005: Abdellatif Maalej; Elisabeth Petit-Teixeira; Laëtitia Michou; Ahmed Rebai; François Cornelis; Hammadi Ayadi
Association study of VDR gene with rheumatoid arthritis in the French population.
Genes and immunity 2005;6(8):707-11.
2005: Hanen Belguith; S Hajji; N Salem; Ilhem Charfeddine; Imed Lahmar; M B Amor; Karim Ouldim; Eliane Chouery; Nabil Driss; Mohamed Drira; André Mégarbané; Ahmed Rebai; abdelaziz sefiani; Saber Masmoudi; Hammadi Ayadi
Analysis of GJB2 mutation: evidence for a Mediterranean ancestor for the 35delG mutation.
Clinical genetics 2005;68(2):188-9.
2005: Abdelaziz Tlili; Ilhem Charfedine; Imed Lahmar; Zeineb Benzina; Ben Amor Mohamed; Dominique Weil; Nabil Idriss; Mohamed Drira; Saber Masmoudi; Hammadi Ayadi
Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss.
Human mutation 2005;25(5):503.
2005: L Hadjkacem Loukil; Tahia Boudawara; Imen Ayadi; Ali Bahloul; Rachid Jlidi; Hammadi Ayadi; Leila Keskes
High androgen receptor immunoexpression in human "Sertoli cell only" testis.
Archives de l'Institut Pasteur de Tunis 2005;82(1-4):47-51.
2005: Abdelaziz Tlili; Minna Männikkö; Ilhem Charfedine; Imed Lahmar; Zeineb Benzina; Mohamed Ben Amor; Nabil Driss; Leena Ala-Kokko; Mohamed Drira; Saber Masmoudi; Hammadi Ayadi
A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family.
Human heredity 2005;60(3):123-8.
2004: Nacim Louhichi; Mariem Meziou; Souad Rouis; Chahnez Triki; Hammadi Ayadi; Faiza Fakhfakh
Contribution of immunological and genetic investigations to improve classification of patients with congenital muscular dystrophy.
Neurosciences (Riyadh, Saudi Arabia) 2004;9(4):247-53.
2004: Saber Masmoudi; Ilhem Charfedine; I B Rebeh; Ahmed Rebai; Abdelaziz Tlili; Ali Ghorbel; Hanen Belguith; Christine Petit; Mohamed Drira; Hammadi Ayadi
Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
Clinical genetics 2004;66(4):358-64.
2004: Lobna Hadjkacem; Hassen Hadj Kacem; Amel Boulila; Ali Bahloul; Hammadi Ayadi; Leila Ammar-Keskes
Androgen receptor gene CAG repeats length in fertile and infertile Tunisian men.
Annales de génétique 2004;47(3):217-24.
2004: Hammadi Ayadi; Hassen Hadj Kacem; Ahmed Rebai; Nadir R Farid
The genetics of autoimmune thyroid disease.
Trends in endocrinology and metabolism: TEM 2004;15(5):234-9.
2004: Saida Ben Arab; Saber Masmoudi; Najeh Beltaief; Slah Hachicha; Hammadi Ayadi
Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness.
Genetic epidemiology 2004;27(1):74-9.
2004: Abdellatif Maalej; Fadhila Mbarki; Ahmed Rebai; Foued Karray; Jomaa Jouida; Mohamed Abid; Hammadi Ayadi
Evidence of association between FKBP1B and thyroid autoimmune disorders in a large Tunisian family.
Autoimmunity 2004;37(3):237-9.
2004: Abdellatif Maalej; Ahmed Rebai; Adnen Ayadi; Jomaa Jouida; Hafedh Makni; Hammadi Ayadi
Allelic structure and distribution of 103 STR loci in a Southern Tunisian population.
Journal of genetics 2004;83(1):65-71.
2004: Nacim Louhichi; Chahnez Triki; Susana Quijano-Roy; Pascale Richard; Samira Makri; Mériem Méziou; Brigitte Estournet; Slah Mrad; Norma B Romero; Hammadi Ayadi; Pascale Guicheney; Faiza Fakhfakh
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families.
Neurogenetics 2004;5(1):27-34.
2003: Pampa Chakraborty; Hassen Hadj Kacem; Kauothar Makni-Karray; Faiçal Jarraya; Jamil Hachicha; Hammadi Ayadi
The A/T mutation in exon 2 of the DNASE1 gene is not present in Tunisian patients with systemic lupus erythematosus or in healthy subjects.
Arthritis and rheumatism 2003;48(11):3297-8.
2003: Hassen Hadj Kacem; Ahmed Rebai; Noureddine Kaffel; Saber Masmoudi; Mohamed Abid; Hammadi Ayadi
PDS is a new susceptibility gene to autoimmune thyroid diseases: association and linkage study.
The Journal of clinical endocrinology and metabolism 2003;88(5):2274-80.
2003: Dominique Weil; Aziz El-Amraoui; Saber Masmoudi; Mirna Mustapha; Yoshiaki Kikkawa; Sophie Lainé; Sedigheh Delmaghani; Avital Adato; Sellama Nadifi; Zeineb Ben Zina; Christian Hamel; Andreas Gal; Hammadi Ayadi; Hiromichi Yonekawa; Christine Petit
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.
Human molecular genetics 2003;12(5):463-71.
2003: Saber Masmoudi; Abdelaziz Tlili; Marja Majava; Ali Ghorbel; Sébastien Chardenoux; Arnaud Lemainque; Zeineb Ben Zina; Jihene Moala; Minna Männikkö; Dominique Weil; Mark Lathrop; Leena Ala-Kokko; Mohamed Drira; Christine Petit; Hammadi Ayadi
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.
European journal of human genetics : EJHG 2003;11(2):185-8.
2003: Chiraz Bouchlaka; Sonia Abdelhak; Ahlem Amouri; Hela Ben Abid; Sondes Hadiji; Mounir Frikha; Tarek Ben Othman; Fethi Amri; Hammadi Ayadi; Mongia Hachicha; Ahmed Rebaï; Ali Saad; Koussay Dellagi
Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.
Journal of human genetics 2003;48(7):352-61.
2003: Chahnez Triki; Nacim Louhichi; Mériam Méziou; Fakher Choyakh; Mohamed Salah Kéchaou; Rachid Jlidi; Chokri Mhiri; Faiza Fakhfakh; Hammadi Ayadi
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts, unlinked to the LAMA2, FCMD, MEB and CMD1B loci, in three Tunisian patients.
Neuromuscular disorders : NMD 2003;13(1):4-12.
2002: Souad Rouis; Hammadi Ayadi; S Bouaziz; L Lakhoua; R Gargouri
In situ immunocytochemical detection of potyviral proteins in plant cells.
Biotechnic & histochemistry : official publication of the Biological Stain Commission 2002;77(3):111-5.
2002: M Hmani-Aifa; Saida Ben Arab; K Kharrat; Dana J Orten; A Boulila-Elgaied; Mohamed Drira; Slah Hachicha; William J Kimberling; Hammadi Ayadi
Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome.
Journal of medical genetics 2002;39(4):281-3.
2001: Hassen Hadj Kacem; N Kaddour; F Z Adyel; Zouhir Bahloul; Hammadi Ayadi
HLA-DQB1 CAR1/CAR2, TNFa IR2/IR4 and CTLA-4 polymorphisms in Tunisian patients with rheumatoid arthritis and Sjögren's syndrome.
Rheumatology (Oxford, England) 2001;40(12):1370-4.
2001: Hassen Hadj Kacem; M Bellassoued; Noura Bougacha-Elleuch; Mohamed Abid; Hammadi Ayadi
CTLA-4 gene polymorphisms in Tunisian patients with Graves' disease.
Clinical immunology (Orlando, Fla.) 2001;101(3):361-5.
2001: Abdellatif Maalej; N Bougacha; Ahmed Rebai; Mohamed Bellassouad; F Ayadi-Makni; Mohamed Abid; Jomaa Jouida; Hafedh Makni; Hammadi Ayadi
Lack of linkage and association between autoimmune thyroid diseases and the CTLA-4 gene in a large Tunisian family.
Human immunology 2001;62(11):1245-50.
2001: N Elleuch-Bougacha; Abdellatif Maalej; Hafedh Makni; Mohamed Bellassouad; Mohamed Abid; Jomaa Jouida; Khaled Ayed; D Charron; R Tamouza; Hammadi Ayadi
HLA class I and II polymorphisms in a large multiplex family with autoimmune thyroid diseases.
Clinical endocrinology 2001;55(4):557-8.
2001: Saber Masmoudi; Stylianos E Antonarakis; Torsten Schwede; Ali Ghorbel; M Gratri; M P Pappasavas; Mohamed Drira; A Elgaied-Boulila; Marie Wattenhofer; Colette Rossier; Hamish Scott; Hammadi Ayadi; Michel Guipponi
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness.
Human mutation 2001;18(2):101-8.
2001: Souad Rouis; F Traincard; R Gargouri; S Dartevelle; O Jeannequin; JC Mazié; Hammadi Ayadi
Inhibition of potato virus Y NIa activity: preparation of monoclonal antibody directed against PVY NI protein that inhibits cleavage of PVY polyprotein.
Archives of virology 2001;146(7):1297-306.
2001: Zeineb Ben Zina; Saber Masmoudi; Hammadi Ayadi; F Chaker; Ali Ghorbel; Mohamed Drira; Christine Petit
From DFNB2 to Usher syndrome: variable expressivity of the same disease.
American journal of medical genetics 2001;101(2):181-3.
2001: Abdellatif Maalej; Hafedh Makni; F Ayadi; M Bellassoued; Jomaa Jouida; N Bouguacha; Mohamed Abid; Hammadi Ayadi
A full genome screening in a large Tunisian family affected with thyroid autoimmune disorders.
Genes and immunity 2001;2(2):71-5.
2000: Saber Masmoudi; A Elgaied-Boulila; I Kassab; Saida Ben Arab; S Blanchard; J E Bouzouita; Mohamed Drira; A Kassab; Slah Hachicha; Christine Petit; Hammadi Ayadi
Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE.
Journal of medical genetics 2000;37(11):E39.
2000: Abdellatif Maalej; Hassen Hadj Kacem; M Bellassoued; Mohamed Abid; Hafedh Makni; Hammadi Ayadi
Polymorphisms of HLA DQB1 CAR1/CAR2 and TNFalpha IR2/IR4 microsatellite markers in patients affected with Graves disease.
Clinical immunology (Orlando, Fla.) 2000;96(2):91-3.
2000: Saida Ben Arab; M Hmani; F Denoyelle; A Boulila-Elgaied; Sébastien Chardenoux; Slah Hachicha; Christine Petit; Hammadi Ayadi
Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates.
Clinical genetics 2000;57(6):439-43.
2000: Saber Masmoudi; Ilhem Charfedine; M Hmani; M'hamed Grati; Ali Ghorbel; A Elgaied-Boulila; Mohamed Drira; J P Hardelin; Hammadi Ayadi
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation.
American journal of medical genetics 2000;90(1):38-44.
2000: Noura Bougacha-Elleuch; R Tamouza; Mohamed Bellassouad; Jomaa Jouida; Mohamed Abid; Abdellatif Maalej; Hafedh Makni; Hammadi Ayadi
Analysis of heat shock protein polymorphisms in a large family with autoimmune thyroid diseases.
Archives de l'Institut Pasteur de Tunis 2000;77(1-4):23-4.
2000: M Aifa-Hmani; Hammadi Ayadi
Deafness genes and the mechanism of hearing.
Archives de l'Institut Pasteur de Tunis 2000;77(1-4):17-21.
1999: M Hmani; Ali Ghorbel; A Boulila-Elgaied; Zeineb Ben Zina; W Kammoun; Mohamed Drira; Mohamed Chaabouni; Christine Petit; Hammadi Ayadi
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.
European journal of human genetics : EJHG 1999;7(3):363-7.
1999: Faiza Fakhfakh; Abdellatif Maalej; Hafedh Makni; Mohamed Abid; Jomaa Jouida; M Zouali; Hammadi Ayadi
Analysis of immunoglobulin VH and TCR cbeta polymorphisms in a large family with thyroid autoimmune disorder.
Experimental and clinical immunogenetics 1999;16(4):185-91.
1998: Saber Masmoudi; Leila Keskes; Imed Feki; Faiza Fakhfakh; Chahnez Triki; F Ghribi; Chokri Mhiri; Hammadi Ayadi
[Detection of fragile X syndrome by molecular hybridization in 29 families affected by hereditary mental retardation].
La Tunisie médicale 1998;76(8-9):244-9.
1998: Mounir Frikha; Faiza Fakhfakh; Sondes Mseddi; Jalel Gargouri; L Ghali; Z Labiadh; M Harrabi; Taoufik Souissi; Hammadi Ayadi
[Hemoglobin beta S haplotype in the Kebili region (southern Tunisia)].
Transfusion clinique et biologique : journal de la Société française de transfusion sanguine 1998;5(2):166-72.
1998: F Z Adyel; Hafedh Makni; Jamil Hachicha; Rachid Jlidi; N Trigui; Hammadi Ayadi
Deposition of IgG anti-actin antibodies on kidneys of glomerular nephropathy patients with an enhanced glomerular alpha smooth muscle actin expression.
Nephron 1998;78(4):410-5.
1997: Françoise Denoyelle; Dominique Weil; Marion A Maw; SA Wilcox; NJ Lench; DR Allen-Powell; AH Osborn; Hans-Henrik M Dahl; A Middleton; MJ Houseman; Catherine Dodé; Sandrine Marlin; A Boulila-ElGaïed; M'hamed Grati; Hammadi Ayadi; S BenArab; Pierre Bitoun; Geneviève Lina-Granade; Jacqueline Godet; Mirna Mustapha; Jacques Loiselet; E El-Zir; A Aubois; Alain Joannard; E N Garabédian; R J Gardner; J Levilliers; R F Mueller; Christine Petit
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.
Human molecular genetics 1997;6(12):2173-7.
1997: Avital Adato; Dominique Weil; H Kalinski; Y Pel-Or; Hammadi Ayadi; Christine Petit; Michael Korostishevsky; Batsheva Bonne-Tamir
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.
American journal of human genetics 1997;61(4):813-21.
1997: Hafedh Makni; S Makni-Krichene; Mohamed Abid; Jomaa Jouida; A Jarraya; J Charreire; Hammadi Ayadi
[Predisposition to thyroid autoimmune diseases].
Presse médicale (Paris, France : 1983) 1997;26(25):1181-5.
1997: Dominique Weil; P Küssel; Stéphane Blanchard; G Lévy; F Levi-Acobas; Mohamed Drira; Hammadi Ayadi; Christine Petit
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene.
Nature genetics 1997;16(2):191-3.
1997: A Boulila-Elgaïed; Saber Masmoudi; Mohamed Drira; M Gouia; Hassan Chaib; Christine Petit; Hammadi Ayadi
Contribution of DFNB1 and DFNB2 loci to neurosensory deafness in affected Tunisian families.
Archives de l'Institut Pasteur de Tunis 1997;74(1-2):5-8.
1997: Faiza Fakhfakh; Hammadi Ayadi; Abdellatif Maalej; Zouhir Bahloul; A Jarraya; M Zouali
Polymorphism of the human immunoglobulin heavy chain locus in rheumatoid arthritis.
Autoimmunity 1997;25(2):109-16.
1997: H Chaïb; J Kaplan; S Gerber; C Vincent; Hammadi Ayadi; R Slim; Arnold Munnich; Jean Weissenbach; Christine Petit
A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21.
Human molecular genetics 1997;6(1):27-31.
1996: A Boulila; Jamil Hachicha; F Z Adyel; Rachid Jlidi; Stratis Avrameas; Therese Ternynck; Hammadi Ayadi
Deposition of anti-actin antibodies in the kidney of a patient with systemic lupus erythematosus under immunosuppressive treatment.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1996;11(12):2478-81.
1996: Faiza Fakhfakh; Hammadi Ayadi; Zouhir Bahloul; A Jarraya; M Sioud; M Zouali
Antibody epitopes probed by immunoselected phage-display library peptides in members of a family with various rheumatic manifestations.
Clinical and experimental rheumatology 1996;14(6):607-11.
1996: Hafedh Makni; Abdellatif Maalej; F Ayadi; Mohamed Abid; Jomaa Jouida; Hammadi Ayadi
[Clinical and biological follow up of a family with high prevalence of thyroid autoimmune disease].
La Tunisie médicale 1996;74(10):433-8.
1996: I Chabchoub; Hafedh Makni; A Boulila-el Gaied; Abdellatif Maalej; Mohamed Abid; Jomaa Jouida; Hammadi Ayadi
Expression of the autoreactive Ig repertoire in a large family, with high prevalence of thyroid autoimmune diseases.
Archives de l'Institut Pasteur de Tunis 1996;73(3-4):163-6.
1996: Faiza Fakhfakh; Chokri Mhiri; Chahnez Triki; Hammadi Ayadi
[Molecular analysis of ten families with Duchenne muscular atrophy].
La Tunisie médicale 1996;74(3):113-8.
1996: Chokri Mhiri; Chahnez Triki; Faiza Fakhfakh; F Chouayakh; I Fki; Rachid Jlidi; Hammadi Ayadi; Nouri Zouari
[Duchenne muscular dystrophy: clinico-pathologic study of 10 families from South Tunisia].
La Tunisie médicale 1996;74(2):85-92.
1996: Jamil Hachicha; M Kharrat; Mohamed Ben Hmida; J Mnif; Mongia Hachicha; Hammadi Ayadi; Rachid Jlidi; MS Kechaou; Ali Triki; A Jarraya
[Renal needle biopsy in children. Technical aspects and results].
Annales de radiologie 1996;39(4-5):204-7.
1996: F Z Adyel; B Hentati; A Boulila; Jamil Hachicha; Therese Ternynck; Stratis Avrameas; Hammadi Ayadi
Characterization of autoantibody activities in sera anti-DNA antibody and circulating immune complexes from 12 systemic lupus erythematosus patients.
Journal of clinical laboratory analysis 1996;10(6):451-7.
1995: L H Noel; Jamil Hachicha; Hammadi Ayadi; Mohamed Ben Hmida; Rachid Jlidi; A Jarraya
[Polynuclear neutrophil anti-cytoplasmic antibodies or ANCA: current aspects].
La Tunisie médicale 1995;73(6-7):229-34.
1994: Hafedh Makni; Jalel Gargouri; Mounir Frikha; Faiza Fakhfakh; A Mziou; Hammadi Ayadi; Taoufik Souissi
[Cytological and immunochemical analysis of forty cases of multiple myeloma].
La Tunisie médicale 1994;72(12):707-12.
1994: P Guilford; Hammadi Ayadi; Stéphane Blanchard; Hassan Chaib; D Le Paslier; Jean Weissenbach; Mohamed Drira; Christine Petit
A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.
Human molecular genetics 1994;3(6):989-93.
1993: Faiza Fakhfakh; E Mihaesco; Hammadi Ayadi; Jean-Claude Brouet; A Tsapis
[Alpha heavy chain disease. Molecular analysis of a new case].
Presse médicale (Paris, France : 1983) 1993;22(22):1047-51.
1993: A Boulila Elgaied; B Hintati; Faiza Fakhfakh; H Karray; Jamil Hachicha; A Jarraya; Hammadi Ayadi
[Immunological analysis of 16 antinuclear antibodies in disseminated lupus erythematosus].
La Tunisie médicale 1993;71(2):91-5.
1992: Hafedh Makni; Mohamed Abid; Jomaa Jouida; A Jarraya; Hammadi Ayadi
[Autoimmune dysthyroidisms with autosomal recessive transmission: 25 cases].
La Tunisie médicale 1992;70(12):579-82.
1992: Jamil Hachicha; A Bellaj; F Sellami; T Rebai; Hammadi Ayadi; K Charfeddine; A Jarraya
[Primary glomerular nephropathies in southern Tunisia].
Presse médicale (Paris, France : 1983) 1992;21(40):1914.
1992: Faiza Fakhfakh; Koussay Dellagi; Hammadi Ayadi; A Bouguerra; R Fourati; Farhat Ben Ayed; Jean-Claude Brouet; A Tsapis
Alpha heavy chain disease alpha mRNA contain nucleotide sequences of unknown origins.
European journal of immunology 1992;22(11):3037-40.
1992: Hammadi Ayadi; E Mihaesco; N Congy; J P Roy; M C Gendron; J Laperriere; F Prelli; Blas Frangione; Jean-Claude Brouet
H chain V region sequences of three human monoclonal IgM with anti-myelin-associated glycoprotein activity.
Journal of immunology (Baltimore, Md. : 1950) 1992;148(9):2812-6.
1991: Faiza Fakhfakh; S Rouis; Hafedh Makni; Hammadi Ayadi
[Determination of the frequency of the A2m (2) allele of immunoglobin A in the Tunisian population by RFLP analysis].
Revue française de transfusion et d'hémobiologie : bulletin de la Société nationale de transfusion sanguine 1991;34(6):441-7.
1991: Faiza Fakhfakh; Hammadi Ayadi; A Bouguerra; R Fourati; Farhat Ben Ayed; A Tsapis; Koussay Dellagi
[Rearrangement of immunoglobulin genes in alpha heavy chain disease: a criterion of monoclonality].
Archives de l'Institut Pasteur de Tunis 1991;68(3-4):251-9.
1991: Hammadi Ayadi; Patrice N Marche; A el Gaaied; C Liebe-Gris; Pierre-André Cazenave
Organization and structure of wild rabbit kappa2 genes: implications for regulation of kappa expression.
Research in immunology 1991;142(3):191-7.
1991: Hammadi Ayadi; Patrice N Marche; Pierre-André Cazenave
Evolution of the rabbit immunoglobulin kappa chain genes.
Immunogenetics 1991;34(3):201-7.
1990: Hammadi Ayadi; Pierre-André Cazenave; Patrice N Marche
Structure of rearranged and germ-line rabbit V kappa genes indicated that the CDR3 is encoded by the V kappa gene.
European journal of immunology 1990;20(2):259-64.
1989: E Mihaesco; Hammadi Ayadi; N Congy; M C Gendron; J P Roy; H Heyermann; Blas Frangione; Jean-Claude Brouet
Multiple mutations in the variable region of the kappa light chains of three monoclonal human IgM with anti-myelin-associated glycoprotein activity.
The Journal of biological chemistry 1989;264(36):21481-5.
1989: Jalel Gargouri; Hammadi Ayadi; Taoufik Souissi
[Electrophoresis and immunoelectrophoresis. A biochemical study: apropos of 188 cases].
La Tunisie médicale 1989;67(4):263-9.
1989: Jalel Gargouri; Hammadi Ayadi; F Ben Aissa; A Bouguerra; Taoufik Souissi
[Protein electrophoresis and the quantitative determination of immunoglobulins: Tunisian standards].
La Tunisie médicale 1989;67(1):47-52.
1988: Jalel Gargouri; Hammadi Ayadi; Taoufik Souissi; K Ayed
[Monoclonal antibodies. Acquisition and use in medicine].
La Tunisie médicale 1988;66(1):5-12.