Vitamin D levels in children and adolescents with autism von Şengenç, Esma, Kıykım, Ertuğrul, Saltik, Sema

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Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum von Taylan, Fulya, Costantini, Alice, Coles, Nicole, Pekkinen, Minna, Héon, Elise, Şıklar, Zeynep, Berberoğlu, Merih, Kämpe, Anders, Kıykım, Ertuğrul, Grigelioniene, Giedre, Tüysüz, Beyhan, Mäkitie, Outi

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Analysis of Biotinidase Activity in Serum by Digital Imaging Colorimetry Detection von Destanoğlu, Orhan, Cansever, M. Şerif, İşat, Esra, Zübarioğlu, Tanyel, Aktuğlu Zeybek, A. Çiğdem, Kıykım, Ertuğrul

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Separation and quantification of the urinary enantiomers of 2‐hydroxyglutaric acid by capillary electrophoresis with capacitively coupled contactless conductivity detection: Applic... von Cansever, M. Şerif, Öztekin, Nevin, Kıykım, Ertuğrul, Zübarioğlu, Tanyel, Aktuğlu Zeybek, Ayşe Çiğdem

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Pteridine and tryptophan pathways in children with type 1 diabetes: Isoxanthopterin as an indicator of endothelial dysfunction von Özer, Yavuz, Cansever, Mehmet Şerif, Turan, Hande, Bayramoğlu, Elvan, Bingöl Aydın, Dilek, İşat, Esra, Ceyhun, Emre, Zubarioğlu, Tanyel, Aktuğlu Zeybek, Ayşe Çiğdem, Kıykım, Ertuğrul, Evliyaoğlu, Olcay

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Telemedicine Applications in a Tertiary Pediatric Hospital in Turkey During COVID-19 Pandemic von Aydemir, Sezin, Ocak, Suheyla, Saygılı, Seha, Hopurcuoğlu, Duhan, Haşlak, Fatih, Kıykım, Ertuğrul, Aktuğlu Zeybek, Çiğdem, Celkan, Tiraje, Demirgan, Ebru Burcu, Kasapçopur, Özgür, Çokuğraş, Haluk, Kıykım, Ayça, Canpolat, Nur

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Serum Neopterin, Biopterin, Tryptophan, and Kynurenine Levels in Patients with Fabry Disease von Uçar, Tuğçe, Cansever, Mehmet Şerif, Isat, Esra, Zubarioğlu, Tanyel, Aktuğlu Zeybek, Ayşe Çiğdem, Topçu, Birol, Seyahi, Nurhan, Kıykım, Ertuğrul

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Auto brewery syndrome from the perspective of the neurologist von Ser, Merve Hazal, Çalıkuşu, Fatma Zehra, Erener, Nursena, Destanoğlu, Orhan, Kıykım, Ertuğrul, Siva, Aksel

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Clinical, biochemical, and molecular insights into Cerebrotendinous Xanthomatosis: A nationwide study of 100 Turkish individuals von Zubarioglu, Tanyel, Kıykım, Ertuğrul, Köse, Engin, Eminoğlu, Fatma Tuba, Teke Kısa, Pelin, Balcı, Mehmet Cihan, Özer, Işıl, İnci, Aslı, Çilesiz, Kübra, Canda, Ebru, Yazıcı, Havva, Öztürk-Hişmi, Burcu, Bulut, Fatma Derya, Dorum, Sevil, Akgun, Abdurrahman, Yalçın-Çakmaklı, Gül, Kılıç-Yıldırım, Gonca, Soyuçen, Erdoğan, Akçalı, Aylin, Güneş, Dilek, Durmuş, Aslı, Gündüz, Ayşegül, Kasapkara, Çiğdem Seher, Göksoy, Emine, Akar, Halil Tuna, Ersoy, Melike, Erdöl, Şahin, Yıldız, Yılmaz, Hanağası, Haşmet Ayhan, Arslan, Nur, Aktuğlu-Zeybek, Çiğdem

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Capillary electrophoresis with capacitively coupled contactless conductivity detection for the determination of urinary ethylmalonic acid for the diagnosis of ethylmalonic aciduria von Özçelik, Sirun, Öztekin, Nevin, Kıykım, Ertuğrul, Cansever, Mehmet Şerif, Aktuğlu‐Zeybek, Ayşe Çiğdem

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Rapid determination of L-2-hydoxyglutaric acid in urine samples by capillary electrophoresis with indirect UV detection von Cansever,Mehmet Şerif, Kalaycıoğlu,Zeynep, Zübarioğlu,Tanyel, Kıykım,Ertuğrul, Aktuğlu Zeybek,Ayşe Çiğdem, Erim,Fatma Bedia

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Evaluation of clinical, neuroradiologic, and genotypic features of patients with L-2-hydroxyglutaric aciduria von Zübarioğlu, Tanyel, Yalçınkaya, Cengiz, Oruç, Çiğdem, Kıykım, Ertuğrul, Cansever, Mehmet Şerif, Gezdirici, Alper, Yeşil, Gözde, Enver, Ece Öge, Zeybek, Çiğdem Aktuğlu

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A Methionine-Portioning-Based Medical Nutrition Therapy with Relaxed Fruit and Vegetable Consumption in Patients with Pyridoxine-Nonresponsive Cystathionine-β-Synthase Deficiency von Uygur, Esma, Aktuglu-Zeybek, Cigdem, Aghalarov, Mirsaid, Cansever, Mehmet Serif, Kıykım, Ertugrul, Zubarioglu, Tanyel

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Comparison of Cost Analysis in Patients with Tetrahydrobiopterin-Responsive and Non-Responsive Phenylketonuria in Turkey von Karaca Sahin, Merve, Aktuglu Zeybek, Ayse Cigdem, Zubarioglu, Tanyel, Cansever, Mehmet Serif, Kıykım, Ertugrul

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İdrarda Orotik Asit’in Temassız İletkenlik Dedektörü Kullanılarak Kapiler Elektroforez Yöntemi İle Hızlı Tayini von CANSEVER, Mehmet Şerif, ÖZTEKİN, Nevin, ADIMCILAR, Veselina, ZÜBARİOĞLU, Tanyel, KIYKIM, Ertuğrul, AKTUĞLU, Ayşe

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Exploring congenital sucrase-isomaltase deficiency in autism spectrum disorder patients with irritable bowel syndrome symptoms: A prospective SI gene sequencing study von Zubarioglu, Tanyel, Ulgen, Dilara, Akca-Yesil, Sedanur, Akbulut, Selin, Onay, Huseyin, Uzunyayla-Inci, Gozde, Beser, Omer Faruk, Hatemi, Ali İbrahim, Aktuğlu-Zeybek, Çiğdem, Kiykim, Ertuğrul

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Evaluation of plasma carnitine status in patients diagnosed with juvenile idiopathic arthritis von ZEYBEK, AYŞE ÇİĞDEM AKTUĞLU, KIYKIM, ERTUĞRUL, BARUT, KENAN, ZÜBARİOĞLU, TANYEL, CANSEVER, MEHMET ŞERİF, KASAPÇOPUR, ÖZGÜR

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Cobalamin C defect‐hemolytic uremic syndrome caused by new mutation in MMACHC von Adrovic, Amra, Canpolat, Nur, Caliskan, Salim, Sever, Lale, Kıykım, Ertugrul, Agbas, Ayse, Baumgartner, Matthias R

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An Overview of Acute Hepatic Porphyrias: Clinical Implications, Diagnostic Approaches, and Management Strategies von Zübarioğlu, Tanyel, Kıykım, Ertuğrul, Aktuğlu-Zeybek, Çiğdem

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Maternal Inborn Errors of Metabolism Detected in Expanded Newborn Metabolic Screening von Tin, Oğuzhan, Zübarioğlu, Tanyel, Cansever, Mehmet Şerif, Kıykım, Ertuğrul, Aktuğlu-Zeybek, Çiğdem

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