المؤلفون: IŞIKAY, Sedat, HIZLI, Şamil, ÇOŞKUN, Serkan, YILMAZ, Kutluhan

المصدر: Arquivos de Gastroenterologia. December 2015 52(4)

مصطلحات موضوعية: Celiac disease, Electroencephalography, Transglutaminases, Epilepsy, Child

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032015000400272

المؤلفون: IŞIKAY, Sedat, KOCAMAZ, Halil

المصدر: Arquivos de Gastroenterologia. September 2015 52(3)

مصطلحات موضوعية: Celiac disease, Neurologic manifestations, Child

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032015000300167

المؤلفون: IŞIKAY, Şedat, IŞIKAY, Nurgül, KOCAMAZ, Halil, HIZLI, Şamil

المصدر: Arquivos de Gastroenterologia. June 2015 52(2)

مصطلحات موضوعية: Celiac disease, Peripheral nervous system diseases, Electrophysiological phenomena, Child

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032015000200134

المؤلفون: IŞIKAY, Sedat, IŞIKAY, Nurgül, KOCAMAZ, Halil

المصدر: Arquivos de Gastroenterologia. March 2015 52(1)

مصطلحات موضوعية: Familial Mediterranean Fever, Celiac disease, Child

وصف الملف: text/html

URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-28032015000100012

المؤلفون: Deb, Wallid, Rosenfelt, Cory, Vignard, Virginie, Papendorf, Jonas Johannes, Möller, Sophie, Wendlandt, Martin, Studencka-Turski, Maja, Cogné, Benjamin, Besnard, Thomas, Ruffier, Léa, Toutain, Bérénice, Poirier, Léa, Cuinat, Silvestre, Kritzer, Amy, Crunk, Amy, diMonda, Janette, Vengoechea, Jaime, Mercier, Sandra, Kleinendorst, Lotte, van Haelst, Mieke M., Zuurbier, Linda, Sulem, Telma, Katrínardóttir, Hildigunnur, Friðriksdóttir, Rún, Sulem, Patrick, Stefansson, Kari, Jonsdottir, Berglind, Zeidler, Shimriet, Sinnema, Margje, Stegmann, Alexander P.A., Naveh, Natali, Skraban, Cara M., Gray, Christopher, Murrell, Jill R., Isikay, Sedat, Pehlivan, Davut, Calame, Daniel G., Posey, Jennifer E., Nizon, Mathilde, McWalter, Kirsty, Lupski, James R., Isidor, Bertrand, Bolduc, François V., Bézieau, Stéphane, Krüger, Elke, Küry, Sébastien, Ebstein, Frédéric

المصدر: Deb , W , Rosenfelt , C , Vignard , V , Papendorf , J J , Möller , S , Wendlandt , M , Studencka-Turski , M , Cogné , B , Besnard , T , Ruffier , L , Toutain , B , Poirier , L , Cuinat , S , Kritzer , A , Crunk , A , diMonda , J , Vengoechea , J , Mercier , S , Kleinendorst , L , van Haelst , M M , Zuurbier , L , Sulem , T , Katrínardóttir , H , Friðriksdóttir , R , ....

مصطلحات موضوعية: /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being, name=SDG 3 - Good Health and Well-being

الاتاحة: https://pure.eur.nl/en/publications/4e964dd7-36f5-4fb9-8bc4-c94d13f4d3b7
https://doi.org/10.1016/j.ajhg.2024.05.016
http://www.scopus.com/inward/record.url?scp=85197070758&partnerID=8YFLogxK

المؤلفون: Işıkay, Sedat

المصدر: Annals of Indian Academy of Neurology ; volume 25, issue 5, page 928-930 ; ISSN 0972-2327

الاتاحة: https://doi.org/10.4103/aian.aian_293_22
https://journals.lww.com/10.4103/aian.aian_293_22

المؤلفون: Duan, Ruizhi, Hijazi, Hadia, Gulec, Elif Yilmaz, Eker, Hatice Koçak, Costa, Silvia R., Sahin, Yavuz, Ocak, Zeynep, Isikay, Sedat, Ozalp, Ozge, Bozdogan, Sevcan, Aslan, Huseyin, Elcioglu, Nursel, Bertola, Débora R., Gezdirici, Alper, Du, Haowei, Fatih, Jawid M., Grochowski, Christopher M., Akay, Gulsen, Jhangiani, Shalini N., Karaca, Ender, Gu, Shen, Coban-Akdemir, Zeynep, Posey, Jennifer E., Bayram, Yavuz, Sutton, V. Reid, Carvalho, Claudia M.B., Pehlivan, Davut, Gibbs, Richard A., Lupski, James R.

المصدر: Human Genetics and Genomics Advances ; volume 3, issue 4, page 100132 ; ISSN 2666-2477

الاتاحة: http://dx.doi.org/10.1016/j.xhgg.2022.100132
https://api.elsevier.com/content/article/PII:S2666247722000483?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2666247722000483?httpAccept=text/plain

المؤلفون: Calame, Daniel G, Wong, Jovi Huixin, Panda, Puravi, Nguyen, Dat Tuan, Leong, Nancy C P, Sangermano, Riccardo, Patankar, Sohil G, Abdel-Hamid, Mohamed S, AlAbdi, Lama, Safwat, Sylvia, Flannery, Kyle P, Dardas, Zain, Fatih, Jawid M, Murali, Chaya, Kannan, Varun, Lotze, Timothy E, Herman, Isabella, Ammouri, Farah, Rezich, Brianna, Efthymiou, Stephanie, Alavi, Shahryar, Murphy, David, Firoozfar, Zahra, Nasab, Mahya Ebrahimi, Bahreini, Amir, Ghasemi, Majid, Haridy, Nourelhoda A, Goldouzi, Hamid Reza, Eghbal, Fatemeh, Karimiani, Ehsan Ghayoor, Begtrup, Amber, Elloumi, Houda, Srinivasan, Varunvenkat M, Gowda, Vykuntaraju K, Du, Haowei, Jhangiani, Shalini N, Coban-Akdemir, Zeynep, Marafi, Dana, Rodan, Lance, Isikay, Sedat, Rosenfeld, Jill A, Ramanathan, Subhadra, Staton, Michael, Oberg, Kerby C, Clark, Robin D, Wenman, Catharina, Loughlin, Sam, Saad, Ramy, Ashraf, Tazeen, Male, Alison, Tadros, Shereen, Boostani, Reza, Abdel-Salam, Ghada M H, Zaki, Maha, Mardi, Ali, Hashemi-Gorji, Farzad, Abdalla, Ebtesam, Manzini, M Chiara, Pehlivan, Davut, Posey, Jennifer E, Gibbs, Richard A, Houlden, Henry, Alkuraya, Fowzan S, Bujakowska, Kinga, Maroofian, Reza, Lupski, James R, Nguyen, Long N

المصدر: Genet Med ; ISSN:1530-0366

مصطلحات موضوعية: Choline, Diamond-Blackfan anemia, FLVCR1, Neurodegeneration, Neurodevelopmental disorders

Relation: https://doi.org/10.1016/j.gim.2024.101273; https://pubmed.ncbi.nlm.nih.gov/39306721

الاتاحة: https://doi.org/10.1016/j.gim.2024.101273
https://pubmed.ncbi.nlm.nih.gov/39306721

المؤلفون: TALİM, BERİL, ÇETİNKAYA, ARDA, Akarsu, Nurten A., GÜREL, AYŞE, Gumruk, Fatma, Houlden, Henry, Pagliarini, David J., Casanova, Jean-Laurent, Lupski, James R., Gleeson, Joseph G., Isikay, Sedat, Eyaid, Wafaa, Alsubhi, Afaf, Chaabouni, Myriam, Maroofian, Reza, Bascom, Charles C., Khotaei, Ghamar Taj, Seyedpour, Simin, Rezaei, Nima, Bauer, Peter, Tripolszki, Kornelia, Ordonez, Natalia, Isfort, Robert J., Zaki, Maha S., Kayserili, Hulya, Hasbini, Dana, Gilani, Naser, Ly, Thanh Thao Nguyen, Coon, Joshua J., Xue, Shifeng, Yilmaz, Elanur, Boisson, Bertrand, Keng, Soh Sok, Choo, Siew Chin, Ali, Nur Ain, Chai, Guoliang, Laine, Candice, Pehlivan, Davut, Paul, Franziska, Sotiropoulou, Kortessa, Georgiadou, Danai, Cimen, Deniz Ugurlu, Efthymiou, Stephanie, Mbarek, Hamdi, Arman-Bilir, Ozlem, Ceylaner, Serdar, Mitani, Tadahiro, Simsek-Kiper, Pelin O., Yarali, Nese, Liang, Chao, Sirota, Fernanda L., Nathan, Fatima M., Cepni, Ece, Shishkova, Evgenia, Unal, Sule, Rensvold, Jarred, Sng, Danielle, Teoh, Tze Shin, Chia, Crystal Y., Loh, Abigail Y. T., Zhang, Shan, Reversade, Bruno, Bard, Frederic A., Ho, Lena, Mathuru, Ajay S., Bertoli-Avella, Aida, Maurer-Stroh, Sebastian, Lee, Cheryl, Traspas, Ricardo Moreno, Maier, Michael, Seet, Sze Hwee, Wong, Hui Hui

الاتاحة: https://doi.org/10.1016/j.ajhg.2021.05.003
https://avesis.hacettepe.edu.tr/publication/details/f907748c-dfad-40eb-985e-fa4fc9b47100/oai

المؤلفون: Işıkay, Sedat

المصدر: Annals of Indian Academy of Neurology ; volume 24, issue 5, page 770-771 ; ISSN 0972-2327

الاتاحة: https://doi.org/10.4103/aian.aian_1282_20
https://journals.lww.com/10.4103/aian.AIAN_1282_20

المؤلفون: Mitani, Tadahiro, Isikay, Sedat, Gezdirici, Alper, Gulec, Elif Yilmaz, Punetha, Jaya, Fatih, Jawid M., Herman, Isabella, Akay, Gulsen, Du, Haowei, Calame, Daniel G., Ayaz, Akif, Tos, Tulay, Yesil, Gozde, Aydin, Hatip, Geckinli, Bilgen, Elcioglu, Nursel, Candan, Sukru, Sezer, Ozlem, Erdem, Haktan Bagis, Gul, Davut, Demiral, Emine, Elmas, Muhsin, Yesilbas, Osman, Kilic, Betul, Gungor, Serdal, Ceylan, Ahmet C., Bozdogan, Sevcan, Ozalp, Ozge, Cicek, Salih, Aslan, Huseyin, Yalcintepe, Sinem, Topcu, Vehap, Bayram, Yavuz, Grochowski, Christopher M., Jolly, Angad, Dawood, Moez, Duan, Ruizhi, Jhangiani, Shalini N., Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Marafi, Dana, Akdemir, Zeynep Coban, Karaca, Ender, Carvalho, Claudia M.B., Gibbs, Richard A., Posey, Jennifer E., Lupski, James R., Pehlivan, Davut

المصدر: The American Journal of Human Genetics ; volume 108, issue 10, page 1981-2005 ; ISSN 0002-9297

الاتاحة: http://dx.doi.org/10.1016/j.ajhg.2021.08.009
https://api.elsevier.com/content/article/PII:S0002929721003086?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0002929721003086?httpAccept=text/plain

المؤلفون: Kocamaz, Halil, Işıkay, Sedat

المصدر: https://www.intechopen.com/books/7860.

مصطلحات موضوعية: Epilepsy - Advances in Diagnosis and Therapy

Relation: https://mts.intechopen.com/articles/show/title/epilepsy-and-gi-disorders

الاتاحة: https://mts.intechopen.com/articles/show/title/epilepsy-and-gi-disorders
https://doi.org/10.5772/intechopen.85813

المؤلفون: Işıkay, Şedat

المساهمون: HKÜ, Sağlık Bilimleri Fakültesi, Fizyoterapi ve Rehabilitasyon Bölümü, orcid:0000-0002-8208-509X

مصطلحات موضوعية: botulinum toxin, case report, child, chin, chinclinical article

Relation: Journal of Pediatric Neurosciences; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Isikay, S. (January 01, 2020). Hereditary chin trembling. Journal of Pediatric Neurosciences, 15, 1, 66.; https://doi.org/10.4103/jpn.JPN_140_18; https://hdl.handle.net/20.500.11782/2243; 15; 66

الاتاحة: https://hdl.handle.net/20.500.11782/2243
https://doi.org/10.4103/jpn.JPN_140_18

المؤلفون: Marafi, Dana, Mitani, Tadahiro, Isikay, Sedat, Hertecant, Jozef, Almannai, Mohammed, Manickam, Kandamurugu, Abou Jamra, Rami, El‐Hattab, Ayman W., Rajah, Jaishen, Fatih, Jawid M., Du, Haowei, Karaca, Ender, Bayram, Yavuz, Punetha, Jaya, Rosenfeld, Jill A., Jhangiani, Shalini N., Boerwinkle, Eric, Akdemir, Zeynep C., Erdin, Serkan, Hunter, Jill V., Gibbs, Richard A., Pehlivan, Davut, Posey, Jennifer E., Lupski, James R.

المساهمون: Deutsche Forschungsgemeinschaft, National Heart, Lung, and Blood Institute, Muscular Dystrophy Association, National Institute of Neurological Disorders and Stroke, Uehara Memorial Foundation, National Human Genome Research Institute, American Academy of Neurology, National Institutes of Health, American Brain Foundation, International Rett Syndrome Foundation

المصدر: Annals of Clinical and Translational Neurology ; volume 7, issue 5, page 610-627 ; ISSN 2328-9503 2328-9503

الاتاحة: http://dx.doi.org/10.1002/acn3.51003
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Facn3.51003
https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.51003
https://onlinelibrary.wiley.com/doi/full-xml/10.1002/acn3.51003

المؤلفون: Isikay, Sedat

المصدر: Journal of Pediatric Neurosciences ; volume 15, issue 1, page 66 ; ISSN 1817-1745

الاتاحة: https://doi.org/10.4103/jpn.jpn_140_18

المؤلفون: ISIKAY, Sedat, SIRIKCI, Akif

المصدر: Journal of Pediatric Neurosciences ; volume 15, issue 2, page 105 ; ISSN 1817-1745

الاتاحة: https://doi.org/10.4103/jpn.jpn_143_18

المؤلفون: Kocamaz, Halil, Işıkay, Sedat

المساهمون: HKÜ, Sağlık Bilimleri Fakültesi, Fizyoterapi ve Rehabilitasyon Bölümü, Işıkay, Sedat

مصطلحات موضوعية: down, sendrom, çölyak

وصف الملف: application/pdf

Relation: Archives of Clinical and Experimental Medicine; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Kocamaz, H., Işıkay, S. (2018). Gastrointestinal findings in children with Down syndrome: Is there an early sign for Celiac disease?. Archives of Clinical and Experimental Medicine: Cilt, 3, s. 195-197.; https://hdl.handle.net/20.500.11782/2684; 195; 197

الاتاحة: https://hdl.handle.net/20.500.11782/2684

المؤلفون: Siekierska, Aleksandra, Stamberger, Hannah, Deconinck, Tine, Oprescu, Stephanie N., Partoens, Michèle, Zhang, Yifan, Sourbron, Jo, Adriaenssens, Elias, Mullen, Patrick, Wiencek, Patrick, Hardies, Katia, Lee, Jeong-Soo, Giong, Hoi-Khoanh, Distelmaier, Felix, Elpeleg, Orly, Helbig, Katherine L., Hersh, Joseph, Isikay, Sedat, Jordan, Elizabeth, Karaca, Ender, Kecskes, Angela, Lupski, James R., Kovacs-Nagy, Reka, May, Patrick, Narayanan, Vinodh, Pendziwiat, Manuela, Ramsey, Keri, Rangasamy, Sampathkumar, Shinde, Deepali N., Spiegel, Ronen, Timmerman, Vincent, von Spiczak, Sarah, Helbig, Ingo, Weckhuysen, Sarah, Francklyn, Christopher, Antonellis, Anthony, de Witte, Peter, Partoens, Michele, Balak, Chris, Belnap, Newell, Claasen, Ana, Courtright, Amanda, de Both, Matt, Huentelman, Matthew J., Naymik, Marcus, Richholt, Ryan, Siniard, Ashley L., Szelinger, Szabolcs, Craig, David W., Schrauwen, Isabelle, Afawi, Zaid, Balling, Rudi, Baulac, Stephanie, Barisic, Nina, Caglayan, Hande S., Craiu, Dana, Guerrero-Lopez, Rosa, Guerrini, Renzo, Hjalgrim, Helle, Jahn, Johanna, Klein, Karl Martin, Leguern, Eric, Lemke, Johannes R., Lerche, Holger, Marini, Carla, Moller, Rikke S., Muhle, Hiltrud, Rosenow, Felix, Serratosa, Jose, Suls, Arvid, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Zara, Federico, De Jonghe, Peter

المساهمون: C4RCD Research Group, AR working group of the EuroEPINOMICS RES Consortium

المصدر: 2041-1723 ; Nature communications

مصطلحات موضوعية: Biology, Human medicine, Engineering sciences. Technology

وصف الملف: pdf

Relation: info:eu-repo/semantics/altIdentifier/isi/000458398900002

الاتاحة: https://hdl.handle.net/10067/1570980151162165141
https://repository.uantwerpen.be/docman/irua/7d3ab9/157098.pdf

المؤلفون: Link, Nichole, Chung, Hyunglok, Jolly, Angad, Withers, Marjorie, Tepe, Burak, Arenkiel, Benjamin R, Shah, Priya S, Krogan, Nevan J, Aydin, Hatip, Geckinli, Bilgen B, Tos, Tulay, Isikay, Sedat, Tuysuz, Beyhan, Mochida, Ganesh H, Thomas, Ajay X, Clark, Robin D, Mirzaa, Ghayda M, Lupski, James R, Bellen, Hugo J

المصدر: Developmental Cell, vol 51, iss 6

مصطلحات موضوعية: Genetics, Rare Diseases, Pediatric, Stem Cell Research, Congenital Structural Anomalies, Neurological, Good Health and Well Being, Animals, Asymmetric Cell Division, Cell Division, Cell Polarity, Drosophila melanogaster, Humans, Membrane Proteins, Microcephaly, Mutation, Neural Stem Cells, Neurons, Nuclear Proteins, Zika Virus, Ballchen, Bazooka, L(2)gl, MCPH16, Miranda, NS4A, VRK1, aPKC, brain development, congenital infection

جغرافية الموضوع: 713 - 729.e6

وصف الملف: application/pdf

Relation: qt4np6183x; https://escholarship.org/uc/item/4np6183x

الاتاحة: https://escholarship.org/uc/item/4np6183x

المؤلفون: Pehlivan, Davut, Bayram, Yavuz, Gunes, Nilay, Akdemir, Zeynep Coban, Shukla, Anju, Bierhals, Tatjana, TABAKCI, BURCU, Sahin, Yavuz, Gezdirici, Alper, Fatih, Jawid M., Gulec, Elif Yilmaz, YEŞİL, GÖZDE, Punetha, Jaya, Ocak, Zeynep, Grochowski, Christopher M., Karaca, Ender, Albayrak, Hatice Mutlu, Radhakrishnan, Periyasamy, Erdem, Haktan Bagis, Sahin, Ibrahim, Yildirim, Timur, Bayhan, Ilhan A., Bursali, Aysegul, Elmas, Muhsin, Yuksel, Zafer, Ozdemir, Ozturk, Silan, Fatma, Yildiz, Onur, Yesilbas, Osman, Isikay, Sedat, Balta, Burhan, Gu, Shen, Jhangiani, Shalini N., Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Boerwinkle, Eric, Gibbs, Richard A., Tsiakas, Konstantinos, Hempel, Maja, Girisha, Katta Mohan, Gul, Davut, Posey, Jennifer E., Elcioglu, Nursel H., Tuysuz, Beyhan, Lupski, James R.

المساهمون: YEŞİL, Gözde

مصطلحات موضوعية: Pehlivan D., Bayram Y., Gunes N., Akdemir Z. C., Shukla A., Bierhals T., TABAKCI B., Sahin Y., Gezdirici A., Fatih J. M., et al., The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance-, AMERICAN JOURNAL OF HUMAN GENETICS, cilt.105, ss.132-150

Time: 2019

وصف الملف: application/pdf

Relation: https://hdl.handle.net/20.500.12645/10311; WOS:000473723000011; 85068067184

الاتاحة: https://hdl.handle.net/20.500.12645/10311
https://doi.org/10.1016/j.ajhg.2019.05.015