Search Results - "Mrad, Ridha"

A MEMS Optical Phased Array Based on Pitch Tunable Silicon Micromirrors for LiDAR Scanners by Mohammad, Tarek, He, Siyuan, Mrad, Ridha Ben

“…This paper presents the design, modeling, fabrication, and testing of an optical phased array (OPA) based scanner utilizing microelectromechanical system…”
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Review of Zinc Oxide Piezoelectric Nanogenerators: Piezoelectric Properties, Composite Structures and Power Output by Bhadwal, Neelesh, Ben Mrad, Ridha, Behdinan, Kamran

“…Lead-containing piezoelectric materials typically show the highest energy conversion efficiencies, but due to their toxicity they will be limited in future…”
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Analysis of Optical Diffraction Profiles Created by Phase-Modulating MEMS Micromirror Arrays by Mohammad, Tarek, He, Siyuan, Mrad, Ridha Ben

“…This paper presents modeling and analysis of light diffraction and light-intensity modulation performed by an optical phased array (OPA) system based on…”
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Design, Modeling, and Demonstration of a MEMS Repulsive-Force Out-of-Plane Electrostatic Micro Actuator by Siyuan He, Ben Mrad, R.

“…An analytical model is developed for a two-layer repulsive-force out-of-plane micro electrostatic actuator by using conformal mapping techniques. The model…”
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Phenotype Spectrum in Tunisian Population with NPHP1 Deletion by Hammi, Yousra, Ferjani, Maryem, Meddeb, Rym, Kacem, Rania, Sayari, Taha, Mrad, Ridha, Gargah, Tahar

“…Nephronophthisis (NPHP) is a tubulointerstitial kidney disorder with an autosomal recessive inheritance pattern. Its genetic heterogeneity contributes to…”
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A rare cause of hypertension in an 11-year-old boy: Answers by Boussetta, Abir, Jellouli, Manel, Meddeb, Rim, Mrad, Ridha, Jouini, Riadh, Karray, Amina, Jlidi, Said, Gargah, Tahar

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A rare cause of hypertension in an 11-year-old boy: Questions by Boussetta, Abir, Jellouli, Manel, Meddeb, Rim, Mrad, Ridha, Jouini, Riadh, Karray, Amina, Jlidi, Said, Gargah, Tahar

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Characterization of RF sputtered thin film potassium sodium niobate (KNN) with silicon and nickel electrodes by Madani, Ali, Mrad, Ridha Ben, Sinclair, Anthony N.

“…A low cost recipe for thin film deposition of Potassium Sodium Niobate, (Na,K)NbO 3 (KNN) is pursued. The use of expensive noble metals as electrodes was…”
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Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases by Hamdi, Yosr, Boujemaa, Maroua, Ben Rekaya, Mariem, Ben Hamda, Cherif, Mighri, Najah, El Benna, Houda, Mejri, Nesrine, Labidi, Soumaya, Daoud, Nouha, Naouali, Chokri, Messaoud, Olfa, Chargui, Mariem, Ghedira, Kais, Boubaker, Mohamed Samir, Mrad, Ridha, Boussen, Hamouda, Abdelhak, Sonia

“…A family history of breast cancer has long been thought to indicate the presence of inherited genetic events that predispose to this disease. In North Africa,…”
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Constitutional mismatch repair deficiency syndrome with atypical features caused by a homozygous MLH1 missense variant (c.1918C>A, p.(Pro640Thr)): a case report by Akrout, Firas, Achour, Ahlem, Tops, Carli M. J., Gallon, Richard, Meddeb, Rym, Achoura, Sameh, Ben Rekaya, Mariem, Hamdeni, Emna, Rammeh, Soumaya, Chkili, Ridha, Mansouri, Nada, Belguith, Neila, Mrad, Ridha

“…Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder caused by biallelic germline mutations in one of the…”
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A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci by Hamdi, Yosr, Ben Rekaya, Mariem, Jingxuan, Shan, Nagara, Majdi, Messaoud, Olfa, Benammar Elgaaied, Amel, Mrad, Ridha, Chouchane, Lotfi, Boubaker, Mohamed Samir, Abdelhak, Sonia, Boussen, Hamouda, Romdhane, Lilia

“…Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles…”
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Primary Hyperoxaluria Type 1: Clinical, Paraclinical, and Evolutionary Aspects in Adults from One Nephrology Center by Meriam, Hajji, Bettaieb, Asma, Kaaroud, Hayet, Ben Hamida, Fethi, Gargeh, Taher, Mrad, Ridha, Bouzid, Kahena, Abderrahim, Ezzeddine

“…Introduction. Primary hyperoxaluria type 1 (PH1) is a rare and inherited condition of urolithiasis. The aim of our study was to analyze clinical, paraclinical,…”
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Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment by Mkaouar, Rahma, Riahi, Zied, Charfeddine, Cherine, Chelly, Imen, Boudabbous, Hela, Dallali, Hamza, Bonnet, Crystel, Hechmi, Meriem, Bekri, Soumeya, Zitouna, Nadia, Zekri, Lotfi, Tounsi, Amel, Kefi, Rym, Marrakchi, Jihene, Messaoud, Olfa, Kraoua, Ichraf, Maalej, Sonia, Turki Ben Youssef, Ilhem, Ben Hmid, Ahlem, Giraudet, Fabrice, Bouchoucha, Sami, Tebib, Neji, Besbes, Ghazi, Petit, Christine, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha

“…Alpha-Mannosidosis (AM) is an ultra-rare storage disorder caused by a deficiency of lysosomal alpha-mannosidase encoded by the MAN2B1 gene. Clinical…”
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Novel ALPK3 mutation in a Tunisian patient with pediatric cardiomyopathy and facio-thoraco-skeletal features by Jaouadi, Hager, Kraoua, Lilia, Chaker, Lilia, Atkinson, Alexandre, Delague, Valérie, Levy, Nicolas, Benkhalifa, Rym, Mrad, Ridha, Abdelhak, Sonia, Zaffran, Stéphane

“…Pediatric cardiomyopathy is a complex disease with clinical and genetic heterogeneity. Recently, the ALPK3 gene was described as a new hereditary…”
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Introduction to the Special Section on Microelectromechanical Systems in Industrial Environments by Luque, Antonio, Mrad, Ridha Ben

“…The 11 papers in this special section provide a comprehensive review of the industrial applications of microelectromechanical systems (MEMS)…”
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Genome Tunisia Project: paving the way for precision medicine in North Africa by Hamdi, Yosr, Trabelsi, Mediha, Ghedira, Kais, Boujemaa, Maroua, Ben Ayed, Ikhlas, Charfeddine, Cherine, Souissi, Amal, Rejeb, Imen, Kammoun Rebai, Wafa, Hkimi, Chaima, Neifar, Fadoua, Jandoubi, Nouha, Mkaouar, Rahma, Chaouch, Melek, Bennour, Ayda, Kamoun, Selim, Chaker Masmoudi, Hend, Abid, Nabil, Mezghani Khemakhem, Maha, Masmoudi, Saber, Saad, Ali, BenJemaa, Lamia, BenKahla, Alia, Boubaker, Samir, Mrad, Ridha, Kamoun, Hassen, Abdelhak, Sonia, Gribaa, Moez, Belguith, Neila, Kharrat, Najla, Hmida, Dorra, Rebai, Ahmed

“…Key discoveries and innovations in the field of human genetics have led to the foundation of molecular and personalized medicine. Here, we present the Genome…”
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Genetic testing for hereditary cancer syndromes in Tunisian patients: Impact on health system by Jandoubi, Nouha, Boujemaa, Maroua, Mighri, Najah, Mejri, Nesrine, Ben Nasr, Sonia, Bouaziz, Hanen, Berrazega, Yosra, Rachdi, Haifa, Daoud, Nouha, Zribi, Aref, Ayari, Jihene, El Benna, Houda, Labidi, Soumaya, Haddaoui, Abderazzek, Mrad, Ridha, Ben Ahmed, Slim, Boussen, Hamouda, Abdelhak, Sonia, Boubaker, Samir, Hamdi, Yosr

“…•A phenotypic overlap between cancer syndromes was observed which may cause clinical misdiagnosis. This underscores the crucial role of genetic testing and the…”
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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health by Mkaouar, Rahma, Riahi, Zied, Marrakchi, Jihene, Mezzi, Nessrine, Romdhane, Lilia, Boujemaa, Maroua, Dallali, Hamza, Sayeb, Marwa, Lahbib, Saida, Jaouadi, Hajer, Boudabbous, Hela, Zekri, Lotfi, Chargui, Mariem, Messaoud, Olfa, Elyounsi, Meriem, Kraoua, Ichraf, Zaouak, Anissa, Turki, Ilhem, Mokni, Mourad, Boucher, Sophie, Petit, Christine, Giraudet, Fabrice, Mbarek, Chiraz, Besbes, Ghazi, Halayem, Soumeyya, Zainine, Rim, Turki, Hamida, Tounsi, Amel, Bonnet, Crystel, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha, Charfeddine, Cherine

“…[This corrects the article DOI: 10.3389/fgene.2024.1384094.]…”
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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health by Mkaouar, Rahma, Riahi, Zied, Marrakchi, Jihene, Mezzi, Nessrine, Romdhane, Lilia, Boujemaa, Maroua, Dallali, Hamza, Sayeb, Marwa, Lahbib, Saida, Jaouadi, Hager, Boudabbous, Hela, Zekri, Lotfi, Chargui, Mariem, Messaoud, Olfa, Elyounsi, Meriem, Kraoua, Ichraf, Zaouak, Anissa, Turki, Ilhem, Mokni, Mourad, Boucher, Sophie, Petit, Christine, Giraudet, Fabrice, Mbarek, Chiraz, Besbes, Ghazi, Halayem, Soumeyya, Zainine, Rim, Turki, Hamida, Tounsi, Amel, Bonnet, Crystel, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha, Charfeddine, Cherine

“…Hearing impairment (HI) is a prevalent neurosensory condition globally, impacting 5% of the population, with over 50% of congenital cases attributed to genetic…”
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An Overview of Electrospray Applications in MEMS and Microfluidic Systems by Chiarot, P. R., Sullivan, P., Ben Mrad, R.

“…Integrating electrospray into microelectromechanical systems (MEMS) and microfluidic systems supports applications in diverse fields from biotechnology to…”
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