Zobrazeno 1 - 10
of 410
pro vyhledávání: '"S. Karadimas"'
Publikováno v:
Brain and Spine, Vol 2, Iss , Pp 101401- (2022)
Externí odkaz:
https://doaj.org/article/304bd43dc98043b589ded2c12f3454a1
Autor:
Konstantinidou, Anastasia E., Fryssira, Helen, Sifakis, Stavros, Karadimas, Charalampos, Kaminopetros, Petros, Agrogiannis, Georgios, Velonis, Stylianos, Nikkels, Peter G.J., Patsouris, Efstratios
Publikováno v:
American Journal of Medical Genetics. Part A; October 2009, Vol. 149 Issue: 10 p2206-2211, 6p
Autor:
E. Huang, B. Kwon, A. Kim, C. Lin, R. Schouten, N. Egge, R. El-Hawary, J. Street, V.K. Noonan, R. Lewis, J. Wilson, A. Santos, K. Rajamanickam, S. Casha, Y. Zhang, A. Ranganathan, N. Dea, A. Quateen, D. Arora, A. Melnyk, A. Kelly, S. Ferrara, M. Nadeau, M. McCabe, Z. Wang, C. Goldstein, S. Choi, M. Shamji, E. Abraham, J. Gill, S.A. Harris, S. Kim, M. Fehlings, A. Fichadi, D. Hartig, K. Lundine, Drew Bednar, A. Kesani, N.A Manson, J. Norton, D. Whitehurst, S. Karadimas, C.S. Bailey, S. Jones, A. Dold, M. Hashem, E. Dodwell, A. Simmonds, A. Soroceanu, R.A. Glennie, E. Su Moon, P. Hwang, K. Allen, L. Jing, B. Mata, M. Gabr, W. Richardson, L. Setton, J. Fleming, K. Gurr, S. Bailey, F. Siddiqi, A. Lawendy, D. Sanders, M. Staudt, E. Canacari, E. Brown, A. Robinson, K. McGuire, C. Chrysostoum, Y. Raja Rampersaud, M.F. Dvorak, K.C. Thomas, M.C. Boyd, K.R. Gurr, S.I. Bailey, C.G Fisher, J. Batke, M. Boyd, M. Dvorak, C. Fisher, S. Paquette, A. Vaccaro, J. Chapman, P. Arnold, C. Shaffrey, B. Kopjar, B. Snyder, J. Wright, S. Lewis, R. Zeller, P. Moroz, S. Bacon, P. Jarzem, D. Hedden, J. Howard, P. Sturm, P. Cahill, A. Samdani, M. Vitale, P. Gabos, N. Bodin, C. d’Amato, C. Harris, J. Smith, E. Parent, D. Hill, M. Moreau, J. Mahood, A. Bodrogi, H. Abbas, S. Goldstein, Y. Bronstein, S. Chua, S. Magana, A. Van Houwelingen, E. Halpern, S. Jhaveri, A. Lim, P. Leelapattana, F. Siddiqqi, K. Satkunendrarajah, V. Noonan, S. Bryan, K. Aronyk, R. Fox, A. Nataraj, J. Pugh, R. Elliott, M. McKeon, E.P. Abraham, G. Davis, M. Rogers, M. Staples, G. Quan, R.J. Hurlbert, W.B. Jacobs, S. Duplessis, N. Jha, S. Hewson, E. Massicotte, S. Mortaz, P. Coyte, Y.R. Rampersaud, B. Andrew, H. Modi, D. Roffey, I. Miles, E. Wai, N. Manson, D. Eastwood, R. Elliot, I. Bains, E. Yong, G. Sutherland, V.W.S. Chan, O. Persaud, A. Koshkin, R. Brull, N. Hassan, S. Petis, M. Kowalczuk, B. Petrisor, B. Drew, M. Bhandari, C. DiPaola, S. McLachlin, C. Bailey, C. Dunning, M.G. Fehlings, P. Wing, E. Itshayek, F. Biering-Sorensen, A. Bradi, R. Pokrupa, T. Wen, S. Kingwell, J. Chak, V. Singh, P. Cripton, T. Oxland, Z. Wali, D. Yen, A. Alfllouse, A. Alzahrani, H. Jiang, F. Kortbeek, R. Reddy, R. Rampersaud, J. Hurlbert, W. Yong, D. Zygun, D. McGowan, V.W. Yong, B. Mendis, S. Chakraborty, T. Nguyen, E. Tsai, A. Chen, D. Atkins, D. Tsui, A. Townson, C. Craven, M. Ford, H. Ahn, A. Kiss, J. Harrop, R. Grossman, R. Frankowski, J. Guest, B. Aarabi, A. Cheung, B. Sun, L. Marais, M. Queyranne, D. Fourney, M. Johnson, A. Yee, J. Finkelstein, J. Paquet, S. Parent, S. Christie, J. Lange, A. Lapinsky, P. Connolly, J. Eck, D. Rabin, R. Lee, M. Sofia, J. Shin, K. Tung, R. Ghag, T. Goyal, J. Littlewood, R. Cho, K. Thomas, G. Swamy
Publikováno v:
Canadian Journal of Surgery. 55:S35-S58
Akademický článek
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Publikováno v:
Journal of Orthopaedic Surgery & Research. 9/4/2024, Vol. 19 Issue 1, p1-9. 9p.
Autor:
Qu, Ruomu1,2,3,4 (AUTHOR), Wang, Ben1,2,3 (AUTHOR), Yang, Yiyuan1,4 (AUTHOR), Liu, Zexiang1,4 (AUTHOR), Chen, Zhuo1,4 (AUTHOR), Wu, Yunxia1,2,3 (AUTHOR), Li, Xiumao5 (AUTHOR), Jiang, Liang1,2,3 (AUTHOR) jiangliang@bjmu.edu.cn, Liu, Xiaoguang1,2,3 (AUTHOR), Liu, Zhongjun1,2,3 (AUTHOR)
Publikováno v:
BMC Musculoskeletal Disorders. 6/6/2024, Vol. 25 Issue 1, p1-9. 9p.
Cranioectodermal dysplasia (CED), also known as Sensenbrenner syndrome, is a rare autosomal recessive genetic disorder characterized by typical craniofacial, skeletal and ectodermal defects, and tubulointerstitial nephritis leading to early end-stage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6e901edf128bc73c4e89cd3e7d81f44a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3089989
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3089989
Klinefelter syndrome represents the most commonly found human sex chromosomal abnormality. It is characterized by small, firm testes with hyalinization of the seminiferous tubules, elevated gonadotropins and azoospermia. Males with Klinefelter syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::33b83c7c47abd705419317768af24ac7
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3095247
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3095247
PURPOSE. To report a case of retinopathy associated with the longterm intake of the antiepileptic drug clonazepam. METHODS. Case report. RESULTS. A 36-year-old woman, with a history of long-term use of the antiepileptic drug clonazepam developed subt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::02c5fc5172bbf778d01f47d3f59c72d5
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084539
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084539
Autor:
Pota, Vincenzo1 (AUTHOR), Sansone, Pasquale1 (AUTHOR), De Sarno, Sara1 (AUTHOR), Aurilio, Caterina1 (AUTHOR), Coppolino, Francesco1 (AUTHOR), Barbarisi, Manlio2 (AUTHOR), Barbato, Francesco3 (AUTHOR), Fiore, Marco1 (AUTHOR), Cosenza, Gianluigi1 (AUTHOR), Passavanti, Maria Beatrice1 (AUTHOR), Pace, Maria Caterina1 (AUTHOR)
Publikováno v:
Behavioural Neurology. 3/16/2024, Vol. 2024, p1-23. 23p.