Relationship between genetic polymorphisms of angiotensin-converting enzyme and methylenetetrahydrofolate reductase as risk factors for type 2 diabetes in Tunisian patients
Mehri, Sounira, Koubaa, Nadia, Nakbi, Amel, Hammami, Sonia, Chaaba, Raja, Mahjoub, Sinda, Zouari, Bechir, Abid, Mohamed, Arab, Saida Ben, Baudin, Bruno, Hammami, Mohamed
Published in Clinical biochemistry (01.02.2010)
Published in Clinical biochemistry (01.02.2010)
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Angiotensin-converting enzyme insertion/deletion gene polymorphism in a Tunisian healthy and acute myocardial infarction population
Mehri, Sounira, Baudin, Bruno, Mahjoub, Sinda, Zaroui, Amira, Bénéteau-Burnat, Bénédicte, Mechmeche, Rachid, Hammami, Mohamed, Ben Arab, Saïda
Published in Genetic testing and molecular biomarkers (01.02.2010)
Published in Genetic testing and molecular biomarkers (01.02.2010)
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Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness
Ben Arab, Saida, Masmoudi, Saber, Beltaief, Najeh, Hachicha, Slah, Ayadi, Hammadi
Published in Genetic epidemiology (01.07.2004)
Published in Genetic epidemiology (01.07.2004)
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Clinical and genetic analysis of two Tunisian otosclerosis families
Ali, Insaf Bel Hadj, Thys, Melissa, Beltaief, Najeh, Schrauwen, Isabelle, Dieltjens, Nele, Vanderstraeten, Kathleen, Besbes, Ghazi, Mnif, Emna, Hachicha, Slah, Arab, Saïda Ben, Camp, Guy Van
Published in American journal of medical genetics. Part A (15.07.2007)
Published in American journal of medical genetics. Part A (15.07.2007)
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Journal Article
Dilated Cardiomyopathy due to the Novel MT-CYB Missense Mutation m.14757T>C
Zarrouk, Sinda, Finsterer, Josef, Mehri, Sounira, Ourda, Fatma, Ben Arab, Saida, Boussada, Raafik
Published in Journal of medical cases (01.11.2021)
Published in Journal of medical cases (01.11.2021)
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Genotypic interactions of renin–angiotensin system genes with diabetes type 2 in a Tunisian population
Mehri, Sounira, Koubaa, Nadia, Hammami, Sonia, Mahjoub, Sinda, Chaaba, Raja, Nakbi, Amel, Zouari, Bechir, Abid, Mohamed, Arab, Saida Ben, Baudin, Bruno, Hammami, Mohamed
Published in Life sciences (1973) (03.07.2010)
Published in Life sciences (1973) (03.07.2010)
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A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9
Bel Hadj Ali, Insaf, Thys, Melissa, Beltaief, Najeh, Schrauwen, Isabelle, Hilgert, Nele, Vanderstraeten, Kathleen, Dieltjens, Nele, Mnif, Emna, Hachicha, Slah, Besbes, Ghazi, Ben Arab, Saïda, Van Camp, Guy
Published in Human genetics (01.04.2008)
Published in Human genetics (01.04.2008)
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Journal Article
Angiotensinogen gene polymorphism in acute myocardial infarction patients
Mehri, Sounira, Mahjoub, Sinda, Farhati, Abdeljelil, Bousaada, Rafik, Ben Arab, Saïda, Baudin, Bruno, Hammami, Mohamed
Published in Journal of the renin-angiotensin-aldosterone system (01.03.2011)
Published in Journal of the renin-angiotensin-aldosterone system (01.03.2011)
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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
Belguith, Hanen, Aifa-Hmani, Mounira, Dhouib, Houria, Said, Mariem Ben, Mosrati, Mohamed Ali, Lahmar, Imed, Moalla, Jihen, Charfeddine, Ilhem, Driss, Nabil, Arab, Saida Ben, Ghorbel, Abdelmonem, Ayadi, Hammadi, Masmoudi, Saber
Published in Genetic testing and molecular biomarkers (01.02.2009)
Published in Genetic testing and molecular biomarkers (01.02.2009)
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Markers of subtypes in inflammatory breast cancer studied by immunohistochemistry: prominent expression of P-cadherin
Ben Hamida, Azza, Labidi, Intidhar S, Mrad, Karima, Charafe-Jauffret, Emmanuelle, Ben Arab, Saïda, Esterni, Benjamin, Xerri, Luc, Viens, Patrice, Bertucci, François, Birnbaum, Daniel, Jacquemier, Jocelyne
Published in BMC cancer (29.01.2008)
Published in BMC cancer (29.01.2008)
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A non-syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q
Weissenbach, Jean, Arab, Saida Ben, Belkahia, Ali, Guilford, Parry, Blanchard, Stéphane, Levilliers, Jacqueline, Petit, Christine
Published in Nature genetics (01.01.1994)
Published in Nature genetics (01.01.1994)
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Journal Article
No major genes in autoimmune thyroid diseases: complex segregation and epidemiological studies in a large Tunisian pedigree
BOUGACHA-ELLEUCH, NOURA, ARAB, SAIDA BEN, REBAI, AHMED, MNIF, MOUNA, MAALEJ, ABDELLATIF, CHARFI, NADIA, LASSOUAD, MOHAMED BEN, JOUIDA, JOMAA, ABID, MOHAMED, AYADI, HAMMADI
Published in Journal of genetics (01.08.2011)
Published in Journal of genetics (01.08.2011)
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Journal Article
Consanguinity, endogamy, and genetic disorders in Tunisia
Ben Halim, Nizar, Ben Alaya Bouafif, Nissaf, Romdhane, Lilia, Kefi Ben Atig, Rym, Chouchane, Ibtissem, Bouyacoub, Yosra, Arfa, Imen, Cherif, Wafa, Nouira, Sonia, Talmoudi, Faten, Lasram, Khaled, Hsouna, Sana, Ghazouani, Welid, Azaiez, Hela, El Matri, Leila, Abid, Abdelmajid, Tebib, Neji, Ben Dridi, Marie-Françoise, Kachboura, Salem, Amouri, Ahlem, Mokni, Mourad, Ben Arab, Saida, Dellagi, Koussay, Abdelhak, Sonia
Published in Journal of community genetics (01.04.2013)
Published in Journal of community genetics (01.04.2013)
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Journal Article
Association of ACE I/D polymorphism in Tunisian patients with dilated cardiomyopathy
Mahjoub, Sinda, Mehri, Sounira, Bousaada, Rafik, Ouarda, Fatma, Zaroui, Amira, Zouari, Bechir, Mechmeche, Rachid, Hammami, Mohamed, Ben Arab, Saida
Published in Journal of the renin-angiotensin-aldosterone system (01.09.2010)
Published in Journal of the renin-angiotensin-aldosterone system (01.09.2010)
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Journal Article
HLA class I polymorphisms in Tunisian patients with otosclerosis
Bel Hadj Ali, Insaf, Ben Saida, Asma, Beltaief, Najeh, Namouchi, Imen, Besbes, Ghazi, Ghazoueni, Ezzeddine, Ben Arab, Saida
Published in Annals of human biology (01.05.2012)
Published in Annals of human biology (01.05.2012)
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Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates
Ben Arab, Saïda, Hmani, Mounira, Denoyelle, Françoise, Boulila-Elgaied, Amel, Chardenoux, Sebastien, Hachicha, Slah, Petit, Christine, Ayadi, Hammadi
Published in Clinical genetics (01.06.2000)
Published in Clinical genetics (01.06.2000)
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Journal Article
Clinical and genetic analysis of two tunisian otosclerosis families: Special issue: The genetic basis of deafness
INSAF BEL HADJ ALI, THYS, Melissa, VAN CAMP, Guy, BELTAIEF, Najeh, SCHRAUWEN, Isabelle, DIELTJENS, Nele, VANDERSTRAETEN, Kathleen, BESBES, Ghazi, MNIF, Emna, HACHICHA, Slah, BEN ARAB, Saida
Published in American journal of medical genetics. Part A (2007)
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Published in American journal of medical genetics. Part A (2007)
Journal Article
Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE
MASMOUDI, SABER, ELGAIED-BOULILA, AMEL, KASSAB, ILYES, ARAB, SAIDA BEN, BLANCHARD, STEPHANE, BOUZOUITA, JA-EL, DRIRA, MOHAMED, KASSAB, AICHA, HACHICHA, SLAH, PETIT, CHRISTINE, AYADI, HAMMADI
Published in Journal of medical genetics (01.11.2000)
Published in Journal of medical genetics (01.11.2000)
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