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Prevalence of congenital heart disease among neonates in Fayoum district
Amin, Sayed Ali, Elfakhrany, Sumer Nady Mohamed, Abd Elmoktader, Ahmed Mahmoud
Published in Progress in pediatric cardiology (01.09.2025)
Published in Progress in pediatric cardiology (01.09.2025)
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6-Pyruvoyltetrahydropterin Synthase Deficiency: Review and Report of 28 Arab Subjects
Almannai, Mohammed, Felemban, Rana, Saleh, Mohammed A., Faqeih, Eissa A., Alasmari, Ali, AlHashem, Amal, Mohamed, Sarar, Sunbul, Rawda, Al-Murshedi, Fathiya, AlThihli, Khalid, Eyaid, Wafaa, Ali, Rehab, Ben-Omran, Tawfeg, Blau, Nenad, El-Hattab, Ayman W., Alfadhel, Majid
Published in Pediatric neurology (01.07.2019)
Published in Pediatric neurology (01.07.2019)
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Consanguineous marriage among familial multiple sclerosis subjects: A national registry-based study
Salehi, Zahra, Naghizadeh, Mohammad Mehdi, Ezabadi, Sajjad Ghane, Ebrahimitirtashi, Azadeh, Abbasi Kasbi, Naghmeh, Khodaie, Faezeh, Aliyari, Shahram, Ashtari, Fereshteh, Baghbanian, Seyed Mohammad, Nabavi, Seyed Massood, Hosseini, Samaneh, Razazian, Nazanin, Shaygannejad, Vahid, Majdi-Nasab, Nastaran, Harirchian, Mohammad Hossein, Bayati, Asghar, Kamali, Hoda, Hosseni Nejad Mir, Nahid, Beladi Moghadam, Nahid, Poursadeghfard, Maryam, Mozhdehipanah, Hossein, Jalali, Nazanin, Nahayati, Mohammad Ali, Faraji, Fardin, Kamyari, Naser, Sahraian, Mohammad Ali, Maghbooli, Zhila, Eskandarieh, Sharareh
Published in Heliyon (30.06.2024)
Published in Heliyon (30.06.2024)
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Association of R1939W and P1987R variants of Otoferlin (OTOF) gene with severe to profound nonsyndromic sensorineural hearing loss in Pakistani subjects
Naseer, Hammael, Rasid, Amir, Majeed, Asifa, Ali Baig, Zunaira
Published in Pakistan journal of medical sciences (01.09.2023)
Published in Pakistan journal of medical sciences (01.09.2023)
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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.
Published in American journal of human genetics (03.03.2016)
Published in American journal of human genetics (03.03.2016)
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A Study of Effect of Consanguinity on Cochlear Morphology in Patients with Congenital Bilateral Profound Sensorineural Hearing Loss
Kavitha, Y., Sabarigirish, K., Joish, Upendra Kumar, Saxena, Sanjeev, Dutta, Angshuman
Published in Indian journal of otolaryngology, and head, and neck surgery (01.12.2017)
Published in Indian journal of otolaryngology, and head, and neck surgery (01.12.2017)
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A two fold risk of metabolic syndrome in a sample of patients with schizophrenia: Do consanguinity and family history increase risk?
Bener, Abdulbari, Al-Hamaq, Abdulla O.A.A., Dafeeah, Elnour E.
Published in Diabetes & metabolic syndrome clinical research & reviews (01.01.2014)
Published in Diabetes & metabolic syndrome clinical research & reviews (01.01.2014)
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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
Scott, Eric M, Halees, Anason, Itan, Yuval, Spencer, Emily G, He, Yupeng, Azab, Mostafa Abdellateef, Gabriel, Stacey B, Belkadi, Aziz, Boisson, Bertrand, Abel, Laurent, Clark, Andrew G, Alkuraya, Fowzan S, Casanova, Jean-Laurent, Gleeson, Joseph G
Published in Nature genetics (01.09.2016)
Published in Nature genetics (01.09.2016)
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Genome-Wide Association Study Identifies a Novel Locus Contributing to Type 2 Diabetes Susceptibility in Sikhs of Punjabi Origin From India
Saxena, Richa, Saleheen, Danish, Been, Latonya F., Garavito, Martha L., Braun, Timothy, Bjonnes, Andrew, Young, Robin, Ho, Weang Kee, Rasheed, Asif, Frossard, Philippe, Sim, Xueling, Hassanali, Neelam, Radha, Venkatesan, Chidambaram, Manickam, Liju, Samuel, Rees, Simon D., Ng, Daniel Peng-Keat, Wong, Tien-Yin, Yamauchi, Toshimasa, Hara, Kazuo, Tanaka, Yasushi, Hirose, Hiroshi, McCarthy, Mark I., Morris, Andrew P., Basit, Abdul, Barnett, Anthony H., Katulanda, Prasad, Matthews, David, Mohan, Viswanathan, Wander, Gurpreet S., Singh, Jai Rup, Mehra, Narinder K., Ralhan, Sarju, Kamboh, M. Ilyas, Mulvihill, John J., Maegawa, Hiroshi, Tobe, Kazuyuki, Maeda, Shiro, Cho, Yoon S., Tai, E. Shyong, Kelly, M. Ann, Chambers, John C., Kooner, Jaspal S., Kadowaki, Takashi, Deloukas, Panos, Rader, Daniel J., Danesh, John, Sanghera, Dharambir K.
Published in Diabetes (New York, N.Y.) (01.05.2013)
Published in Diabetes (New York, N.Y.) (01.05.2013)
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ASSOCIATION OF PARENTAL SOCIOECONOMIC STATUS AND AGE WITH CONSANGUINITY- A SYSTEMATIC REVIEW
Hemant, Charmode Sundip
Published in Journal of evolution of medical and dental sciences (20.08.2018)
Published in Journal of evolution of medical and dental sciences (20.08.2018)
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Demographic features of subjects with congenital glaucoma
Tamçelik, Nevbahar, Atalay, Eray, Bolukbasi, Selim, Çapar, Olgu, Ozkok, Ahmet
Published in Indian journal of ophthalmology (01.05.2014)
Published in Indian journal of ophthalmology (01.05.2014)
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