Carrier Frequency Offset Estimation in OFDM systems as a Quadratic Eigenvalue Problem von Eslahi, A., Mahmoudi, A., Kaabi, H.

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P04.20 Analysis of HORMAD1, FTHL17 and ADAM29 Cancer/testis specific genes expression in Glioblastoma von Anvari, K, Mojarrad, M, Gholamin, M, Fathi, M, Tabatabaii, A, Eslahi, A

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Evaluation of the Sympathetic Skin Response in Men with Chronic Prostatitis: A Case-Control Study von Eslahi, Ali, Farpour, Hamidreza, Hosseini, Azar, Ahmed, Faisal, Chowdhury, Umayir, Nikbakht, Hossein-Ali

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Catastrophic Complications of Circumcision by Traditional Circumcisers von Ahmed, Faisal, Al Wageeh, Saleh, Ghabisha, Saif, Al Shami, Ebrahim, Al Naggar, Khalil, Obaid, Ghamdan, Eslahi, Ali, Alfaragi, Mohammed

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The role of ultrasonography in detecting urinary tract calculi compared to CT scan von Ahmed, Fisal, Askarpour, Mohammad-Reza, Eslahi, Ali, Nikbakht, Hossein-Ali, Jafari, Seyed-Hamed, Hassanpour, Abbas, Makarem, Alireza, Salama, Hussein, Ayoub, Abbas

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11 Results and complications of percutaneous nephrolithotomy (PCNL): Report of over 12,000 cases in Southern Iran von Hosseini, M.M, Aminsharifi, A, Irani, D, Haghpanah, R, Eslahi, A, Yousefi, A, Inaloo, R, Zaki-Abbasi, M

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S233 Tubeless Mini-Perc Percutaneous Nephrolithotomy (MPCNL) in preschool children von Hosseini, M.M, Aminsharifi, A, Shakeri, S, Eslahi, A, Basiratnia, M, Derakhshan, A, Fallahzadeh, M.H

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S235 Outcome of percutaneous nephrolithotomy in high volume, training center: Results and complications of the 8375 cases von Hosseini, M.M, Aminsharifi, A.R, Irani, D, Hassanpour, A, Eslahi, A, Yousefi, A.R, Inaloo, R, Hakimelahi, H, Zaki-Abbasi, M

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Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome von Salpietro, V, Maroofian, R, Zaki, MS, Wangen, J, Ciolfi, A, Barresi, S, Efthymiou, S, Lamaze, A, Aughey, GN, Al Mutairi, F, Rad, A, Rocca, C, Calì, E, Accogli, A, Zara, F, Striano, P, Mojarrad, M, Tariq, H, Giacopuzzi, E, Taylor, JC, Oprea, G, Skrahina, V, Rehman, KU, Abd Elmaksoud, M, Bassiony, M, El Said, HG, Abdel-Hamid, MS, Al Shalan, M, Seo, G, Kim, S, Lee, H, Khang, R, Issa, MY, Elbendary, HM, Rafat, K, Marinakis, NM, Traeger-Synodinos, J, Ververi, A, Sourmpi, M, Eslahi, A, Khadivi Zand, F, Beiraghi Toosi, M, Babaei, M, Jackson, A, Hannah, MG, Bugiardini, E, Bertini, E, Kriouile, Y, El-Khorassani, M, Aguennouz, M, Groppa, S, Karashova, BM, Goraya, JS, Sultan, T, Avdjieva, D, Kathom, H, Tincheva, R, Banu, S, Veggiotti, P, Verrotti, A, Lanari, M, Savasta, S, Macaya, A, Garavaglia, B, Borgione, E, Papacostas, S, Vikelis, M, Chelban, V, Kaiyrzhanov, R, Cortese, A, Sullivan, R, Papanicolaou, EZ, Dardiotis, E, Maqbool, S, Ibrahim, S, Kirmani, S, Rana, NN, Atawneh, O, Lim, SY, Zuccotti, GV, Marseglia, GL, Esposito, S, Shaikh, F, Cogo, P, Corsello, G, Mangano, S, Nardello, R, Mangano, D, Scardamaglia, A, Koutsis, G, Scuderi, C, Ferrara, P, Morello, G, Zollo, M, Berni-Canani, R, Terracciano, LM, Sisto, A, Di Fabio, S, Strano, F, Scorrano, G

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TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes von Van De Weghe, JC, Giordano, JL, Mathijssen, IB, Mojarrad, M, Lugtenberg, D, Miller, CV, Dempsey, JC, Mohajeri, MSA, van Leeuwen, E, Pajkrt, E, Klaver, CCW, Houlden, H, Eslahi, A, Waters, AM, University of Washington Center for Mendelian Genomics, Bamshad, MJ, Nickerson, DA, Aggarwal, VS, de Vries, BBA, Maroofian, R, Doherty, D

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Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants von Neuray, C, Maroofian, R, Scala, M, Sultan, T, Pai, GS, Mojarrad, M, El Khashab, H, DeHoll, L, Yue, W, Alsaif, HS, Zanetti, MN, Bello, O, Person, R, Eslahi, A, Khazaei, Z, Feizabadi, MH, Efthymiou, S, SYNaPS Study Group, El-Bassyouni, HT, Soliman, DR, Tekes, S, Ozer, L, Baltaci, V, Khan, S, Beetz, C, Amr, KS, Salpietro, V, Jamshidi, Y, Alkuraya, FS, Houlden, H

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RSRC1 loss-of-function variants cause mild to moderate autosomal recessive intellectual disability von Scala, M, Mojarrad, M, Riazuddin, S, Brigatti, KW, Ammous, Z, Cohen, JS, Hosny, H, Usmani, MA, Shahzad, M, Stanley, V, Eslahi, A, Person, RE, Elbendary, HM, Comi, AM, Poskitt, L, Salpietro, V, Genomics, QS, Rosenfeld, JA, Williams, KB, Marafi, D, Xia, F, Biderman Waberski, M, Zaki, MS, Gleeson, J, Puffenberger, E, Houlden, H, Maroofian, R

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Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases von Perenthaler, E, Nikoncuk, A, Yousefi, S, Berdowski, WM, Alsagob, M, Capo, I, van der Linde, HC, van den Berg, P, Jacobs, EH, Putar, D, Ghazvini, M, Aronica, E, van IJcken, WFJ, de Valk, WG, Medici-van den Herik, E, van Slegtenhorst, M, Brick, L, Kozenko, M, Kohler, JN, Bernstein, JA, Monaghan, KG, Begtrup, A, Torene, R, Al Futaisi, A, Al Murshedi, F, Mani, R, Al Azri, F, Kamsteeg, E-J, Mojarrad, M, Eslahi, A, Khazaei, Z, Darmiyan, FM, Doosti, M, Karimiani, EG, Vandrovcova, J, Zafar, F, Rana, N, Kandaswamy, KK, Hertecant, J, Bauer, P, AlMuhaizea, MA, Salih, MA, Aldosary, M, Almass, R, Al-Quait, L, Qubbaj, W, Coskun, S, Alahmadi, KO, Hamad, MHA, Alwadaee, S, Awartani, K, Dababo, AM, Almohanna, F, Colak, D, Dehghani, M, Mehrjardi, MYV, Gunel, M, Ercan-Sencicek, AG, Passi, GR, Cheema, HA, Efthymiou, S, Houlden, H, Bertoli-Avella, AM, Brooks, AS, Retterer, K, Maroofian, R, Kaya, N, van Ham, TJ, Barakat, TS

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Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease von Rice, GI, Kitabayashi, N, Barth, M, Briggs, TA, Burton, ACE, Carpanelli, ML, Cerisola, AM, Colson, C, Dale, RC, Danti, FR, Darin, N, De Azua, B, De Giorgis, V, De Goede, CGL, Desguerre, I, De laet, C, Eslahi, A, Fahey, MC, Fallon, P, Fay, A, Fazzi, E, Gorman, MP, Gowrinathan, NR, Hully, M, Kurian, MA, Leboucq, N, Lin, J-PS-M, Lines, MA, Mar, SS, Maroofian, R, Marti-Sanchez, L, McCullagh, G, Mojarrad, M, Narayanan, V, Orcesi, S, Ortigoza-Escobar, JD, Perez-Duenas, B, Petit, F, Ramsey, KM, Rasmussen, M, Rivier, F, Rodriguez-Pombo, P, Roubertie, A, Stodberg, TI, Toosi, MB, Toutain, A, Uettwiller, F, Ulrick, N, Vanderver, A, Waldman, A, Livingston, JH, Crow, YJ

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PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment von Zollo, M, Ahmed, M, Ferrucci, V, Salpietro, V, Asadzadeh, F, Carotenuto, M, Maroofian, R, Al-Amri, A, Singh, R, Scognamiglio, I, Mojarrad, M, Musella, L, Duilio, A, Di Somma, A, Karaca, E, Rajab, A, Al-Khayat, A, Mohapatra, TM, Eslahi, A, Ashrafzadeh, F, Rawlins, LE, Prasad, R, Gupta, R, Kumari, P, Srivastava, M, Cozzolino, F, Rai, SK, Monti, M, Harlalka, GV, Simpson, MA, Rich, P, Al-Salmi, F, Patton, MA, Chioza, BA, Efthymiou, S, Granata, F, Di Rosa, G, Wiethoff, S, Borgione, E, Scuderi, C, Mankad, K, Hanna, MG, Pucci, P, Houlden, H, Lupski, JR, Crosby, AH, Baple, EL

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Can weather variables and electricity demand predict carbon emissions allowances prices? Evidence from the first three phases of the EU ETS von Eslahi, Mohammadehsan, Mazza, Paolo

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Compressive Sensing Image Restoration Using Adaptive Curvelet Thresholding and Nonlocal Sparse Regularization von Eslahi, Nasser, Aghagolzadeh, Ali

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Smart Polymeric Hydrogels for Cartilage Tissue Engineering: A Review on the Chemistry and Biological Functions von Eslahi, Niloofar, Abdorahim, Marjan, Simchi, Abdolreza

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Synthesis, characterization and antibacterial properties of a novel nanocomposite based on polyaniline/polyvinyl alcohol/Ag von Ghaffari-Moghaddam, Mansour, Eslahi, Hassan

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Resiliency Enhancement and Power Quality Optimization of Converter-Based Renewable Energy Microgrids von Eslahi, Mohammad Sadegh, Vaez-Zadeh, Sadegh, Rodriguez, Jose

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