Stress-induced Childhood Onset Neurodegeneration with Ataxia and Seizures (CONDSIAS) presenting with torticollis attacks: Phenotypic variability of the same mutation in two Turkish... von Ozturk, Gulten, Ayaz, Akif, Topcu, Yasemin, Akyuz, Gülcan, Unver, Olcay, Akbeyaz, Ismail, Ekinci, Gazanfer, Turkdogan, Dilsad

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Knowledge, attitudes, and practice of general pediatricians and pediatric subspecialists towards oral health in children: a survey in Turkey von Akbeyaz Sivet, Ecem, Yilmazkasapoglu Turkay, Ece, Akbeyaz, Ismail Hakki, Kargul, Betul

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Spontaneously Resolving Hyperreninemic Hypertension Caused by Accessory Renal Artery Stenosis in a 13‐Year‐Old Girl: A Case Report von Akbeyaz, Ismail Hakki, Tirosh, Amit, Robinson, Cemre, Broadney, Miranda M., Papadakis, Georgios Z., Belyavskaya, Elena, Lyssikatos, Charalampos, Lodish, Maya B., Stratakis, Constantine A.

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Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations von Chundru, V. Kartik, Zhang, Zhancheng, Walter, Klaudia, Lindsay, Sarah J., Danecek, Petr, Eberhardt, Ruth Y., Gardner, Eugene J., Malawsky, Daniel S., Wigdor, Emilie M., Torene, Rebecca, Retterer, Kyle, Wright, Caroline F., Ólafsdóttir, Hildur, Guillen Sacoto, Maria J., Ayaz, Akif, Akbeyaz, Ismail Hakki, Türkdoğan, Dilşad, Al Balushi, Aaisha Ibrahim, Bertoli-Avella, Aida, Bauer, Peter, Szenker-Ravi, Emmanuelle, Reversade, Bruno, McWalter, Kirsty, Sheridan, Eamonn, Firth, Helen V., Hurles, Matthew E., Samocha, Kaitlin E., Ustach, Vincent D., Martin, Hilary C.

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Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes von Yılmaz, Ünsal, Gücüyener, Kıvılcım, Yavuz, Merve, Öncel, İbrahim, Saltık, Sema, Ünver, Olcay, Yılmaz, Sanem, Erol, İlknur, Öztoprak, Ülkühan, Elitez, Duygu Aykol, Direk, Meltem Çobanoğulları, Bodur, Muhittin, Teber, Serap, Yılmaz, Ünsal, Anlar, Banu, Gücüyener, Kıvılcım, Ünver, Olcay, Çıtak Kurt, Ayşegül Neşe, Tosun, Ayşe, Yılmaz, Sanem, Özgör, Bilge, Öztoprak, Ülkühan, Aykol, Duygu, Yıldız, Edibe Pembegül, Yarar, Coşkun, Haspolat, Şenay, İncecik, Faruk, Kutluk, Gültekin, Dundar, Nihal Olgac, Öncel, İbrahim, Demir, Ercan, Türkdoğan, Dilşad, Yalnızoğlu, Dilek, Akbaş, Salih, Güleç, Ayten, Yılmaz, Deniz, Ayanoğlu, Müge, Kanmaz, Seda, Beşen, Şeyda, Öztürk, Selcan, Yüksel, Deniz, Gürkaş, Esra, Oktay, Seçil, Serin, Hepsen Mine, Karadağ, Meral, Hakkı Akbeyaz, İsmail, Yiş, Uluç, Polat, Burçin Gönüllü, Okan, Mehmet Sait, Bektaş, Ömer, Orgun, Leman Tekin, Günbey, Ceren, Gültutan, Pembe, Aksoy, Erhan, Akyüz, Gülcan, Tekgül, Hasan, Kürekçi, Fulya, Kurul, A. Semra Hız, Çarman, Kürşat Bora, Duman, Özgür, Kömür, Mustafa, Yıldırım, Miraç, Alıcı, Nurettin, Gümüş, Hakan, Polat, Muzaffer, Konuşkan, Bahadır, Güngör, Olcay, Mert, Gülen Gül, Edizer, Selvinaz, Mıhçı, Filiz, Yavuz, Merve, Toker, Rabia Tütüncü, Şahin, Sevim, Gencpinar, Pinar, Yıldırım, Elif, Yüksel, Ersin, Ekici, Arzu, Deniz, Adnan, Yayici Köken, Özlem, Okuyaz, Çetin, Süt, Nurşah Yeniay, Atasoy, Ergin, Yetkin, Mehmet Fatih, Bilgin, Neslihan, Tekin, Hande Gazeteci, Özçelik, Aysima, Türköz, Ayşe Nur, Cavusoglu, Dilek, Özkan, Mehbare, Tekin, Emine, Koç, Habibe, Sarıgeçili, Esra, Sarıtaş, Serdar, Ayça, Senem, Şenoğlu, Mine Çiğdem, Kamaşak, Tülay, Keskin, Filiz, Karaoğlu, Pakize, İpek, Rojan, Acer, Hamit

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Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations von Chundru, V Kartik, Zhang, Zhancheng, Walter, Klaudia, Lindsay, Sarah J, Danecek, Petr, Eberhardt, Ruth Y, Gardner, Eugene J, Malawsky, Daniel S, Wigdor, Emilie M, Torene, Rebecca, Retterer, Kyle, Wright, Caroline F, Ólafsdóttir, Hildur, Guillen Sacoto, Maria J, Ayaz, Akif, Akbeyaz, Ismail Hakki, Türkdoğan, Dilşad, Al Balushi, Aaisha Ibrahim, Bertoli-Avella, Aida, Bauer, Peter, Szenker-Ravi, Emmanuelle, Reversade, Bruno, McWalter, Kirsty, Sheridan, Eamonn, Firth, Helen V, Hurles, Matthew E, Samocha, Kaitlin E, Ustach, Vincent D, Martin, Hilary C

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Spontaneously Resolving Hyperreninemic Hypertension Caused by Accessory Renal Artery Stenosis in a 13-Year-Old Girl: A Case Report von Akbeyaz, Ismail Hakki, Tirosh, Amit, Robinson, Cemre, Broadney, Miranda M, Papadakis, Georgios Z, Belyavskaya, Elena, Lyssikatos, Charalampos, Lodish, Maya B, Stratakis, Constantine A

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