Mandibuloacral dysplasia type A in five tunisian patients
R, Sakka, H, Marmouch, M, Trabelsi, A, Achour, M, Golli, I, Hannachi, E, Kerkeni, K, Monastiri, F, Maazoul, R, M'rad
Published in European journal of medical genetics (01.02.2021)
Published in European journal of medical genetics (01.02.2021)
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Journal Article
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis
M'hamdi, O., Redin, C., Stoetzel, C., Ouertani, I., Chaabouni, M., Maazoul, F., M'rad, R., Mandel, J.L., Dollfus, H., Muller, J., Chaabouni, H.
Published in Clinical genetics (01.02.2014)
Published in Clinical genetics (01.02.2014)
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Journal Article
Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V
Kharrat, M, Trabelsi, S, Chaabouni, M, Maazoul, F, Kraoua, L, Ben Jemaa, L, Gandoura, N, Barsaoui, S, Morel, Y, M'rad, R, Chaabouni, H
Published in Clinical genetics (01.10.2010)
Published in Clinical genetics (01.10.2010)
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Journal Article
Both cIAP1 and cIAP2 regulate TNFα-mediated NF-κB activation
Mahoney, D.J, Cheung, H.H, Mrad, R. Lejmi, Plenchette, S, Simard, C, Enwere, E, Arora, V, Mak, T.W, Lacasse, E.C, Waring, J, Korneluk, R.G
Published in Proceedings of the National Academy of Sciences - PNAS (19.08.2008)
Published in Proceedings of the National Academy of Sciences - PNAS (19.08.2008)
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Journal Article
FOXL2 mutations in Tunisian patients with blepharophimosis-ptosis-epicanthus inversus syndrome
Kraoua, L, Chaabouni, M, Trabelsi, M, Chelly, I, Maazoul, F, Ben Abdallah, N, Boukthir, S, Barsaoui, S, Chaabouni, H, M'rad, R
Published in Clinical genetics (01.06.2010)
Published in Clinical genetics (01.06.2010)
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Journal Article
Repulsive-force out-of-plane large stroke translation micro electrostatic actuator
He, S, Ben Mrad, R, Chong, J
Published in Journal of micromechanics and microengineering (01.07.2011)
Published in Journal of micromechanics and microengineering (01.07.2011)
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Journal Article
Neuropsychiatric manifestations in Cornelia de Lange syndrome
Majdoub, F, Souissi, A, Trabelsi, M, Ziadi, A, Belguith, N, Maazoul, F, Guirat, M, Boujelbene, I, Kamoun, H, Mrad, R, Masmoudi, S, I Ben Ayed
Published in European psychiatry (01.03.2023)
Published in European psychiatry (01.03.2023)
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Journal Article
A novel UBE3A truncating mutation in large Tunisian Angelman syndrome pedigree
Abaied, L., Trabelsi, M., Chaabouni, M., Kharrat, M., Kraoua, L., M'rad, R., Tebib, N., Maazoul, F., Chaabouni, H.
Published in American journal of medical genetics. Part A (01.01.2010)
Published in American journal of medical genetics. Part A (01.01.2010)
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Journal Article
Epigenetics' implication in autism spectrum disorders: A review
Hamza, M, Halayem, S, Mrad, R, Bourgou, S, Charfi, F, Belhadj, A
Published in Encéphale (01.08.2017)
Published in Encéphale (01.08.2017)
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Journal Article
Genetic analysis of Turner syndrome: 89 cases in Tunisia
Kammoun, I, Chaabouni, M, Trabelsi, M, Ouertani, I, Kraoua, L, Chelly, I, M'rad, R, Ben Jemaa, L, Maâzoul, F, Chaabouni, H
Published in Annales d'endocrinologie (01.11.2008)
Published in Annales d'endocrinologie (01.11.2008)
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Journal Article
Using capacitance measurements in EWOD devices to identify fluid composition and control droplet mixing
Schertzer, M.J., Ben-Mrad, R., Sullivan, P.E.
Published in Sensors and actuators. B, Chemical (04.03.2010)
Published in Sensors and actuators. B, Chemical (04.03.2010)
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Journal Article
Automated detection of particle concentration and chemical reactions in EWOD devices
Schertzer, M.J., Ben Mrad, R., Sullivan, P.E.
Published in Sensors and actuators. B, Chemical (31.03.2012)
Published in Sensors and actuators. B, Chemical (31.03.2012)
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Journal Article
Myalgia in familial Mediterranean fever
B'chir Hamzaoui, S, Bouslama, K, Abdallah, M, M'rad, R, M'rad, S, Ben Dridi, M
Published in Revue neurologique (01.01.2007)
Published in Revue neurologique (01.01.2007)
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Journal Article
The modern bowel preparation in colonoscopy
Sharara, Ala I, Abou Mrad, Rachel R
Published in Gastroenterology clinics of North America (01.09.2013)
Published in Gastroenterology clinics of North America (01.09.2013)
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Journal Article
Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia
Jerbi, M., Ben Rekaya, M., Naouali, C., Jones, M., Messaoud, O., Tounsi, H., Nagara, M., Chargui, M., Kefi, R., Boussen, H., Mokni, M., Mrad, R., Boubaker, M.S., Abdelhak, S., Khaled, A., Zghal, M., Yacoub-Youssef, H.
Published in British journal of dermatology (1951) (01.02.2016)
Published in British journal of dermatology (1951) (01.02.2016)
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