A Multidisciplinary Approach to Opportunistic Infections in a Late-presenter Person Living with HIV von Bahar, Abdul Rasheed, Ekim, Yasemin, Uysal, Serkan, Sönmezer, Meli̇ha Çağla, Gülmez, Dolunay, Çeli̇k Önder, Sevgen, Onur, Mehmet Ruhi̇, Arıkan Akdağlı, Sevtap, Inkaya, Ahmet Çağkan, Inan, Dilara, Ünal, Serhat

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Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience von Simsek-Kiper, Pelin Ozlem, Urel-Demir, Gizem, Taskiran, Ekim Z., Arslan, Umut Ece, Nur, Banu, Mihci, Ercan, Haliloglu, Mithat, Alanay, Yasemin, Utine, Gulen Eda, Boduroglu, Koray

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Investigation of Genetic Causes in a Developmental Disorder: Oculoauriculovertebral Spectrum von Güleray, Naz, Koşukcu, Can, Oğuz, Sümeyra, Ürel Demir, Gizem, Taşkıran, Ekim Z., Kiper, Pelin Özlem Şimşek, Utine, Gülen Eda, Alanay, Yasemin, Boduroğlu, Koray, Alikaşifoğlu, Mehmet

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Spondyloepimetaphyseal dysplasia EXTL3‐deficient type: Long‐term follow‐up and review of the literature von Akalın, Akçahan, Taskiran, Ekim Z., Şimşek‐Kiper, Pelin Özlem, Utine, Eda, Alanay, Yasemin, Özçelik, Uğur, Boduroğlu, Koray

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Management of children with congenital nephrotic syndrome: challenging treatment paradigms von Dufek, Stephanie, Holtta, Tuula, Trautmann, Agnes, Ylinen, Elisa, Alpay, Harika, Ariceta, Gema, Aufricht, Christoph, Bacchetta, Justine, Bakkaloglu, Sevcan A, Bayazit, Aysun, Cicek, Rumeysa Yasemin, Dursun, Ismail, Duzova, Ali, Ekim, Mesiha, Iancu, Daniela, Jankauskiene, Augustina, Klaus, Günter, Paglialonga, Fabio, Pasini, Andrea, Printza, Nikoleta, Said Conti, Valerie, do Sameiro Faria, Maria, Schmitt, Claus Peter, Stefanidis, Constantinos J, Verrina, Enrico, Vidal, Enrico, Vondrak, Karel, Webb, Hazel, Zampetoglou, Argyroula, Bockenhauer, Detlef, Edefonti, Alberto, Shroff, Rukshana

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Familial Mediterranean Fever (FMF) in Turkey: Results of a Nationwide Multicenter Study

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Further expanding the mutational spectrum and investigation of genotype–phenotype correlation in 3M syndrome von Simsek‐Kiper, Pelin Ozlem, Taskiran, Ekim, Kosukcu, Can, Arslan, Umut Ece, Cormier‐Daire, Valérie, Gonc, Nazlı, Ozon, Alev, Alikasifoglu, Ayfer, Kandemir, Nurgun, Utine, Gulen Eda, Alanay, Yasemin, Alikasifoglu, Mehmet, Boduroglu, Koray

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TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia von Alanay, Yasemin, Ergüner, Bekir, Utine, Eda, Haçarız, Orçun, Kiper, Pelin Ozlem Simsek, Taşkıran, Ekim Zihni, Perçin, Ferda, Uz, Elif, Sağıroğlu, Mahmut Şamil, Yuksel, Bayram, Boduroglu, Koray, Akarsu, Nurten Ayse

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Epigenotype and phenotype correlations in patients with Beckwith-Wiedemann syndrome von Bilgin, Burçak, Kabaçam, Serkan, Taşkıran, Ekim, Şimşek-Kiper, Pelin Özlem, Alanay, Yasemin, Boduroğlu, Koray, Utine, Gülen Eda

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Otoantikorları Negatif Sneddon Sendromu: Olgu Sunumu ve Literatürün Gözden Geçirilmesi von ARSLAN, Ekim, CEYHAN DİRİCAN, Ayten, ERTEM, Devrimsel Harika, ALTUNKAYNAK, Yavuz, BAYBAŞ, Sevim, ÖZKAN, Yasemin

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Antiphospholipid-antibody-negative Sneddon's Syndrome: a case report and review of the literature/Otoantikorlari negatif Sneddon Sendromu: olgu sunumu ve literaturun gozden geciril... von Arslan, Ekim, Dirican, Ayten Ceyhan, Ertem, Devrimsel Harika, Altunkaynak, Yavuz, Baybas, Sevim, Ozkan, Yasemin

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Otoantikorlari Negatif Sneddon Sendromu: Olgu Sunumu ve Literatürün Gözden Geçirilmesi/Antiphospholipid-Antibody-Negative Sneddon's Syndrome: A Case Report and Review of the Litera... von Arslan, Ekim, Dirican, Ayten Ceyhan, Ertem, Devrimsel Harika, Altunkaynak, Yavuz, Baybas, Sevim, Özkan, Yasemin

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Spondyloepimetaphyseal dysplasia EXTL3-deficient type: Long-term follow-up and review of the literature von Akalın, Akçahan, Taskiran, Ekim Z, Şimşek-Kiper, Pelin Özlem, Utine, Eda, Alanay, Yasemin, Özçelik, Uğur, Boduroğlu, Koray

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