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Özgür Duman

Istanbul University

18H指数
95论文数
843被引数
收录论文 13
发表时间
Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohortnusinersen治疗I型脊髓性肌萎缩症患儿:土耳其队列4年临床经验
err2025-03-27
err0
errOAAI
errBektas, Omer; Gulsen, Murat; Dursun, Onur Burak; Tekin, Ahmet; Yuksel, Deniz; Demir, Ercan; Ozturk, Gulten; Saltik, Sema; Herguler, Ozlem; Ozcelik, Ayse Aysima; Tan, Huseyin; Ozgor, Bilge; Ekici, Arzu; Yuksel, Merve Feyza; Sahin, Suleyman; Duman, Ozgur; Komur, Mustafa; Baydan, Figen; Yildiz, Edibe Pembeguel; Kara, Bulent; Yis, Uluc; Kanmaz, Seda; Carman, Kuersat Bora; Arslan, Elif Acar; Canpolat, Mehmet; Guven, Ahmet Sami; Oztuncer, Gokcen; Unalp, Aycan; Ardicli, Didem; Karaduman, Aynur Ayse; Zararsiz, Gokmen; Deda, Gulhis
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Course of patients with Ulcerative colitis who have achieved disease clearance from the moment of diagnosis
err2025-01-22
err0
PREAI
errRustamzade, A.; Hacialioglu, C.; Duman, O.; Topuz, S.; Uzun, Z.; Telli, P.; Gurbanov, A.; Yagli, M. A.; Dagci, G.; Genc, S.; Cavus, B.; Ormeci, A. CIfcibasi; Akyuz, F.; Demir, K.; Besisik, S. F.; Kaymakoglu, S.
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Clinical and Laboratory Features in Anti-NF155 Autoimmune Nodopathy
err2022-01-01
err43
errOAAI
errMartin-Aguilar, Lorena; Lleixa, Cinta; Pascual-Goni, Elba; Caballero-Avila, Marta; Martinez-Martinez, Laura; Diaz-Manera, Jordi; Rojas-Garcia, Ricard; Cortes-Vicente, Elena; Turon-Sans, Janina; de Luna, Noemi; Suarez-Calvet, Xavier; Gallardo, Eduard; Rajabally, Yusuf; Scotton, Sangeeta; Jacobs, Bart C.; Baars, Adaja; Cortese, Andrea; Vegezzi, Elisa; Hoftberger, Romana; Zimprich, Fritz; Roesler, Cornelia; Nobile-Orazio, Eduardo; Liberatore, Giuseppe; Hiew, Fu Liong; Martinez-Pineiro, Alicia; Carvajal, Alejandra; Pinar-Morales, Raquel; Uson-Martin, Mercedes; Alberti, Olalla; Lopez-Perez, Maria Angeles; Marquez, Fabian; Pardo-Fernandez, Julio; Munoz-Delgado, Laura; Cabrera-Serrano, Macarena; Ortiz, Nicolau; Bartolome, Manuel; Duman, Ozgur; Bril, Vera; Segura-Chavez, Darwin; Pitarokoili, Kalliopi; Steen, Claudia; Illa, Isabel; Querol, Luis
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Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia (vol 144, pg 1422, 2021)
errBRAIN
IF11.7
err2021-08-31
err2
errOAAI
errWiessner, Manuela; Maroofian, Reza; Ni, Meng-Yuan; Pedroni, Andrea; Muller, Juliane S.; Stucka, Rolf; Beetz, Christian; Efthymiou, Stephanie; Santorelli, Filippo M.; Alfares, Ahmed A.; Zhu, Changlian; Meszarosova, Anna Uhrova; Alehabib, Elham; Bakhtiari, Somayeh; Janecke, Andreas R.; Otero, Maria Gabriela; Chen, Jin Yun Helen; Peterson, James T.; Strom, Tim M.; De Jonghe, Peter; Deconinck, Tine; De Ridder, Willem; De Winter, Jonathan; Pasquariello, Rossella; Ricca, Ivana; Alfadhel, Majid; van de Warrenburg, Bart P.; Portier, Ruben; Bergmann, Carsten; Firouzabadi, Saghar Ghasemi; Jin, Sheng Chih; Bilguvar, Kaya; Hamed, Sherifa; Abdelhameed, Mohammed; Haridy, Nourelhoda A.; Maqbool, Shazia; Rahman, Fatima; Anwar, Najwa; Carmichael, Jenny; Pagnamenta, Alistair T.; Wood, Nick W.; Mau-Them, Frederic Tran; Haack, Tobias; Di Rocco, Maja; Ceccherini, Isabella; Iacomino, Michele; Zara, Federico; Salpietro, Vincenzo; Scala, Marcello; Rusmini, Marta; Xu, Yiran; Wang, Yinghong; Suzuki, Yasuhiro; Koh, Kishin; Nan, Haitian; Ishiura, Hiroyuki; Tsuji, Shoji; Lambert, Laetitia; Schmitt, Emmanuelle; Lacaze, Elodie; Kuepper, Hanna; Dredge, David; Skraban, Cara; Goldstein, Amy; Willis, Mary J. H.; Grand, Katheryn; Graham, John M., Jr.; Lewis, Richard A.; Millan, Francisca; Duman, Ozguer; Dundar, Nihal Olgac; Uyanik, Goekhan; Schoels, Ludger; Nuernberg, Peter; Nuernberg, Gudrun; Catala-Bordes, Andrea; Seeman, Pavel; Kuchar, Martin; Darvish, Hossein; Rebelo, Adriana; Boucanova, Filipa; Medard, Jean-Jacques; Chrast, Roman; Auer-Grumbach, Michaela; Alkuraya, Fowzan S.; Shamseldin, Hanan; Al Tala, Saeed; Varaghchi, Jamileh Rezazadeh; Najafi, Maryam; Deschner, Selina; Glaeser, Dieter; Huettel, Wolfgang; Kruer, Michael C.; Kamsteeg, Erik-Jan; Takiyama, Yoshihisa; Zuechner, Stephan; Baets, Jonathan; Synofzik, Matthis; Schuele, Rebecca; Horvath, Rita; Houlden, Henry; Bartesaghi, Luca; Lee, Hwei-Jen; Ampatzis, Konstantinos; Pierson, Tyler Mark; Senderek, Jan
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Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegiaHPDL中的双等位基因变体导致纯的和复杂的遗传性痉挛性截瘫
errBRAIN
IF11.7
err2021-05-10
err29
errOAAI
errWiessner, Manuela; Maroofian, Reza; Ni, Meng-Yuan; Pedroni, Andrea; Muller, Juliane S.; Stucka, Rolf; Beetz, Christian; Efthymiou, Stephanie; Santorelli, Filippo M.; Alfares, Ahmed A.; Zhu, Changlian; Meszarosova, Anna Uhrova; Alehabib, Elham; Bakhtiari, Somayeh; Janecke, Andreas R.; Otero, Maria Gabriela; Chen, Jin Yun Helen; Peterson, James T.; Strom, Tim M.; De Jonghe, Peter; Deconinck, Tine; De Ridder, Willem; De Winter, Jonathan; Pasquariello, Rossella; Ricca, Ivana; Alfadhel, Majid; van de Warrenburg, Bart P.; Portier, Ruben; Bergmann, Carsten; Firouzabadi, Saghar Ghasemi; Jin, Sheng Chih; Bilguvar, Kaya; Hamed, Sherifa; Abdelhameed, Mohammed; Haridy, Nourelhoda A.; Maqbool, Shazia; Rahman, Fatima; Anwar, Najwa; Carmichael, Jenny; Pagnamenta, Alistair; Wood, Nick W.; Mau-Them, Frederic Tran; Haack, Tobias; Di Rocco, Maja; Ceccherini, Isabella; Iacomino, Michele; Zara, Federico; Salpietro, Vincenzo; Scala, Marcello; Rusmini, Marta; Xu, Yiran; Wang, Yinghong; Suzuki, Yasuhiro; Koh, Kishin; Nan, Haitian; Ishiura, Hiroyuki; Tsuji, Shoji; Lambert, Laetitia; Schmitt, Emmanuelle; Lacaze, Elodie; Kuepper, Hanna; Dredge, David; Skraban, Cara; Goldstein, Amy; Willis, Mary J. H.; Grand, Katheryn; Graham, John M., Jr.; Lewis, Richard A.; Millan, Francisca; Duman, Ozgur; Dundar, Nihal; Uyanik, Gokhan; Schols, Ludger; Nuernberg, Peter; Nuernberg, Gudrun; Bordes, Andrea Catala; Seeman, Pavel; Kuchar, Martin; Darvish, Hossein; Rebelo, Adriana; Boucanova, Filipa; Medard, Jean-Jacques; Chrast, Roman; Auer-Grumbach, Michaela; Alkuraya, Fowzan S.; Shamseldin, Hanan; Al Tala, Saeed; Varaghchi, Jamileh Rezazadeh; Najafi, Maryam; Deschner, Selina; Glaeser, Dieter; Huettel, Wolfgang; Kruer, Michael C.; Kamsteeg, Erik-Jan; Takiyama, Yoshihisa; Zuchner, Stephan; Baets, Jonathan; Synofzik, Matthis; Schuele, Rebecca; Horvath, Rita; Houlden, Henry; Bartesaghi, Luca; Lee, Hwei-Jen; Ampatzis, Konstantinos; Pierson, Tyler Mark; Senderek, Jan
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err收藏
The genomic and clinical landscape of fetal akinesia (vol 22, pg 511, 2020)
err2020-08-01
err0
errOAAI
errPergande, Matthias; Motameny, Susanne; Ozdemir, Ozkan; Kreutzer, Mona; Wang, Haicui; Daimaguler, Huelya-Sevcan; Becker, Kerstin; Karakaya, Mert; Ehrhardt, Harald; Elcioglu, Nursel; Ostojic, Slavica; Chao, Cho-Ming; Kawalia, Amit; Duman, Ozgur; Koy, Anne; Hahn, Andreas; Reimann, Jens; Schoner, Katharina; Schanzer, Anne; Westhoff, Jens H.; Schwaibold, Eva Maria Christina; Cossee, Mireille; Imbert-Bouteille, Marion; von Pein, Harald; Haliloglu, Goknur; Topaloglu, Haluk; Altmuller, Janine; Nurnberg, Peter; Thiele, Holger; Heller, Raoul; Cirak, Sebahattin
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err收藏
The genomic and clinical landscape of fetal akinesia
err2020-03-01
err41
errOAAI
errPergande, Matthias; Motameny, Susanne; Oezdemir, Oezkan; Kreutzer, Mona; Wang, Haicui; Daimagueler, Huelya-Sevcan; Becker, Kerstin; Karakaya, Mert; Ehrhardt, Harald; Elcioglu, Nursel; Ostojic, Slavica; Chao, Cho-Ming; Kawalia, Amit; Duman, Ozgur; Koy, Anne; Hahn, Andreas; Reimann, Jens; Schoner, Katharina; Schaenzer, Anne; Westhoff, Jens H.; Schwaibold, Eva Maria Christina; Cossee, Mireille; Imbert-Bouteille, Marion; von Pein, Harald; Haliloglu, Goknur; Topaloglu, Haluk; Altmueller, Janine; Nuernberg, Peter; Thiele, Holger; Heller, Raoul; Cirak, Sebahattin
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Interleukin-6 Gene Polymorphism in Febrile Seizures
err2012-01-01
err28
PREAI
errNur, Banu Guzel; Kahramaner, Zelal; Duman, Ozgur; Dundar, Nihal Olgac; Sallakci, Nilgun; Yavuzer, Ugur; Haspolat, Senay
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Authors reply: New clues on the path of understanding unilateral naevoid telangiectasia
err2011-12-21
err1
PREAI
errAkman-Karakas, A.; Kandemir, H.; Senol, U.; Unal, A.; Duman, O.; Ciftcioglu, M. A.; Haspolat, S.; Alpsoy, E.
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Unilateral nevoid telangiectasia accompanied by neurological disorders
err2011-01-17
err8
PREAI
errAkman-Karakas, A.; Kandemir, H.; Senol, U.; Unal, A.; Duman, O.; Ciftcioglu, M. A.; Haspolat, S.; Alpsoy, E.
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Spontaneous Periodic Hypothermia and Hyperhidrosis
err2008-12-01
err21
PREAI
errDundar, Nihal Olgac; Boz, Adil; Duman, Ozgur; Aydin, Funda; Haspolat, Senay
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Brain stem lipoma presenting as paroxysmal headache with autonomic features
err2004-01-06
err6
PREAI
errDuman, O; Goksu, E; Akyuz, M; Haspolat, S; Senol, U
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