Positive effects of ketogenic diet on weight control in children with obesity due to Prader–Willi syndrome von Teke Kısa, Pelin, Güzel, Orkide, Arslan, Nur, Demir, Korcan

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A Novel Homozygous GALK1 Variant Combined With Cataract and Prolonged Jaundice von Ozler, Oguz, Egeli, Bugra Han, Zeybek, Selcan, Eris, Erdem, Teke Kisa, Pelin

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Experience with cascade screening: A comprehensive family pedigree analysis of two index patients with Fabry disease von Kisa, Pelin Teke, Hismi, Burcu Ozturk, Kocabey, Mehmet, Gulten, Zumrut Arslan, Huddam, Bulent, Ekinci, Selim, Bozkaya, Evrim, Akar, Harun, Pekuz, Ozge K. Karalar, Aydogan, Ayca, Arslan, Nur

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Lipemia Retinalis Diagnosed Incidentally After Laser Photocoagulation Treatment for Retinopathy of Prematurity von Öztürk, Taylan, Karataş Yiğitaslan, Ezgi, Teke Kısa, Pelin, Onay, Hüseyin, Saatci, Ali Osman

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A challenging etiology of myopathy: The late-onset Pompe disease von Inel, Tuba Yuce, Avsar, Aydan Koken, Kisa, Pelin Teke, Ozer, Erdener, Sari, Ismail

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Inflammatory rheumatic diseases in patients with ochronotic arthropathy von Yuce Inel, Tuba, Kisa, Pelin Teke, Balci, Ali, Uslu, Sadettin, Arslan, Zumrut, Hismi, Burcu Ozturk, Ucar, Ulku, Arslan, Nur, Onen, Fatos, Sari, Ismail

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Role of surveillance screening in detecting tumor recurrence after treatment of childhood cancers von Teke Kısa, Pelin, Emir, Suna

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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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Evaluation of Demographic and Clinical Characteristics of Patients with Mucopolysaccharidosis von Teke Kısa, Pelin, Köse, Engin, Ateşoğlu, Merve, Arslan, Nur

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Fabry disease in familial Mediterranean fever according to the severity of the disease von Uslu, Sadettin, Kabadayi, Gökhan, Teke Kısa, Pelin, Yüce Inel, Tuba, Arslan, Zümrüt, Arslan, Nur, Akar, Servet, Onen, Fatos, Sari, Ismail

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Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement von Kısa, Pelin Teke, Yildirim, Gonca Kilic, Hismi, Burcu Ozturk, Dorum, Sevil, Kusbeci, Ozge Yilmaz, Topak, Ali, Baydan, Figen, Celik, Fatma Nazlı Durmaz, Gorukmez, Orhan, Gulten, Zumrut Arslan, Ekici, Arzu, Ozkan, Serhat, Yaman, Aylin, Arslan, Nur

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Could lysosomal acid lipase enzyme activity be used for clinical follow-up in cryptogenic cirrhosis? von KÖSE, ENGİN, ÇAĞATAY, ELÇİN, MERCAN, TUTKU YARAŞ, KISA, PELİN TEKE, GÜLER, SEMİNAY, GÜLTEN, ZÜMRÜT ARSLAN, AKARSU, MESUT, OKTAY, YAVUZ, KAYALI, HÜLYA AYAR, ARSLAN, NUR

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Evaluation of the Genetically Diagnosed Mitochondrial Disease Cases with Neuromuscular Involvement von Günay, Çağatay, Paketçi, Cem, Edem, Pınar, Sarıkaya Uzan, Gamze, Hız Kurul, Ayşe Semra, Arslan Gülten, Zümrüt, Teke Kısa, Pelin, Arslan, Nur, Yıs, Uluç

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Frequency and status of depression and anxiety in mothers of children with inborn errors of metabolism with restricted diet, with and without risk of metabolic crises von Kisa, Pelin Teke, Uzun, Ozlem Unal, Gunduz, Mehmet, Bulbul, Fatma Selda, Kose, Engin, Arslan, Nur

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A Novel PNPLA2 Variant in a Female Patient with Neutral Lipid Storage Disease with Myopathy and Hypogonadotropic Hypogonadism von Şenol, Hüseyin Bahadır, Kısa, Pelin Teke, Kulu, Bahar, Ören, Hale, Arslan, Nur, Yiş, Uluç

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Functional vitamin B12 deficiency in phenylketonuria patients and healthy controls: An evaluation with combined indicator of vitamin B12 status as a biochemical index von Akış, Merve, Kant, Melis, Işık, İshak, Kısa, Pelin Teke, Köse, Engin, Arslan, Nur, İşlekel, Hüray

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Investigating myelin oligodendrocyte glycoprotein antibodies in hereditary citrullinemia von Oncel, Ibrahim, Yousefi, Mohammadreza, Inci, Asli, Gulten, Zumrut Arslan, Kisa, Pelin Teke, Karaca, Meryem, Unal, Özlem, Gunduz, Mehmet, Kor, Deniz, Mungan, Neslihan Onenli, Arslan, Nur, Tumer, Leyla, Gucuyener, Kivilcim, Vural, Atay, Anlar, Banu

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Alkaptonuria in Turkey: Clinical and molecular characteristics of 66 patients von Kisa, Pelin Teke, Gunduz, Mehmet, Dorum, Sevil, Uzun, Ozlem Unal, Cakar, Nafiye Emel, Yildirim, Gonca Kilic, Erdol, Sahin, Hismi, Burcu Ozturk, Tugsal, Handan Yarkan, Ucar, Ulku, Gorukmez, Ozlem, Gulten, Zumrut Arslan, Kucukcongar, Aynur, Bulbul, Selda, Sari, Ismail, Arslan, Nur

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Serum Level of Biotin Rather than the Daily Dosage Is the Main Determinant of Interference on Thyroid Function Assays von Paketçi, Ahu, Köse, Engin, Gürsoy Çalan, Özlem, Acar, Sezer, Teke, Pelin, Demirci, Ferhat, Abacı, Ayhan, Demir, Korcan, Arslan, Nur, Böber, Ece

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Evaluation of the Genetically Diagnosed Mitochondrial Disease Cases with Neuromuscular Involvement/Noromuskuler Tutulum Gosteren Genetik Tanili Mitokondriyal Hastalik Tanili Olgula... von Gunay, Cagatay, Paketci, Cem, Edem, Pinar, Uzan, Gamze Sarikaya, Kurul, Ayse Semra Hiz, Gulten, Zumrut Arslan, Kisa, Pelin Teke, Arslan, Nur, Yis, Uluc

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