Search Results - "Akbeyaz, Ismail Hakki"

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

“…The authors describe the clinical investigation and progress of a 13‐year‐old girl diagnosed with hypertension 4 years prior to her admission. A thorough…”
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Knowledge, attitudes, and practice of general pediatricians and pediatric subspecialists towards oral health in children: a survey in Turkey by Akbeyaz Sivet, Ecem, Yilmazkasapoglu Turkay, Ece, Akbeyaz, Ismail Hakki, Kargul, Betul

“…This study aimed to evaluate the level of knowledge, attitudes, and practices of general pediatricians (GPs) and pediatric subspecialists (PSs) practicing in…”
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Federated analysis of autosomal recessive coding variants in 29,745 developmental disorder patients from diverse populations by 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.

“…Autosomal recessive coding variants are well-known causes of rare disorders. We quantified the contribution of these variants to developmental disorders in a…”
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Spontaneously Resolving Hyperreninemic Hypertension Caused by Accessory Renal Artery Stenosis in a 13-Year-Old Girl: A Case Report by Akbeyaz, Ismail Hakki, Tirosh, Amit, Robinson, Cemre, Broadney, Miranda M, Papadakis, Georgios Z, Belyavskaya, Elena, Lyssikatos, Charalampos, Lodish, Maya B, Stratakis, Constantine A

“…The authors describe the clinical investigation and progress of a 13-year-old girl diagnosed with hypertension 4 years prior to her admission. A thorough…”
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Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes by 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

“…The discovery of anti-myelin oligodendrocyte glycoprotein (MOG)-IgG and anti-aquaporin 4 (AQP4)-IgG and the observation on certain patients previously…”
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