Reversible pulmonary arterial hypertension in cobalamin-dependent cobalamin C disease due to a novel mutation in the MMACHC gene von Gündüz, Mehmet, Ekici, Filiz, Özaydın, Eda, Ceylaner, Serdar, Perez, Belen

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Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow up von Gündüz, Mehmet, Özaydın, Eda, Atar, Müge Büyüktaşlı, Koç, Nevra, Kırsaçlıoğlu, Ceyda, Köse, Gülşen, Cefalù, Angelo Baldassare, Averna, Maurizio, Tarugi, Patrizia

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3-HMG Coenzyme A Lyase Deficiency: Macrocephaly and Left Ventricular Noncompaction with a Novel Mutation von Köksal, Tülin, Gündüz, Mehmet, Özaydın, Eda, Azak, Emine

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Differences in iron deficiency anemia and mean platelet volume between children with simple and complex febrile seizures von Özaydın, Eda, Arhan, Ebru, Cetinkaya, Bilge, Özdel, Semanur, Değerliyurt, Aydan, Güven, Alev, Köse, Gülsen

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The Association Between Vitamin D Status and Recurrent Wheezing von Özaydın, Eda, Bütün, Mehmet Fatih, Çakır, Bahar Çuhacı, Köse, Gülşen

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Hypertrophic Cardiomyopathy with Familial Chylomicronemia Syndrome: Is it an Incidental Finding or a New Association? von Gündüz, Mehmet, Koç, Nevra, Özaydın, Eda, Ekici, Filiz

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Viral etiology in infants hospitalized for acute bronchiolitis von Azkur, Dilek, Özaydın, Eda, Dibek-Mısırlıoğlu, Emine, Vezir, Emine, Tombuloğlu, Duygu, Köse, Gülşen, Kocabaş, Can N

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Stepwise diet management in pediatric gastrointestinal graft versus host disease von Koç, Nevra, Gündüz, Mehmet, Azık, M Fatih, Tavil, Betül, Gürlek-Gökçebay, Dilek, Özaydın, Eda, Tunç, Bahattin, Uçkan, Duygu

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Homozygous SLC20A2 mutations cause congenital CMV infection-like phenotype von Ceylan, Ahmet Cevdet, Kireker Köylü, Oya, Özyürek, Hamit, Özaydin, Eda, Yön, Mehmet İlker, Kasapkara, Çiğdem Seher

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Acute hemorrhagic pancreatitis due to the use of valproic acid in a child von Ozaydin, Eda, Yükselgüngör, Handan, Köse, Gülşen

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Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function von Walsh, Meghan T, Iqbal, Jahangir, Josekutty, Joby, Soh, James, Di Leo, Enza, Özaydin, Eda, Gündüz, Mehmet, Tarugi, Patrizia, Hussain, M Mahmood

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The Relationship between Vitamin D Receptor Gene Polymorphisms and Bone Density, Osteocalcin Level and Growth in Adolescents von zaydn, Eda, Dayangac-Erden, Didem, Erdem-Yurter, Hayat, Derman, Orhan, Cokun, Turgay

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PHACES syndrome presenting as hemangiomas, sternal clefting and congenital ulcerations on the helices von DURUSOY, Cicek, MIHCI, Ercan, TACOY, Sukran, OZAYDIN, Eda, ALPSOY, Erkan

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A newborn with pentalogy of Cantrell and pulmonary hypoplasia von Unal, Sevim, Cakmak Celik, Fatma, Ozaydin, Eda, Kaçar, Ayper, Günal, Nazlihan

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Management of central diabetes insipidus with oral desmopressin in a patient with ectrodactyly and cleft lip/palate (ECP) syndrome von Ozaydin, Eda, Aycan, Zehra, Yusufoğlu, Arzu Meltem, Cetinkaya, Ergun, Ergen, Saime, Unal, Sevim, Köse, Gülşen

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Abstract 232: A Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal ß-Sheet in the Lipid Transfer and ApoB Secretion Activities of Microsomal T... von Walsh, Meghan T, Di Leo, Enza, Ozaydin, Eda, Tarugi, Patrizia, Hussain, Mahmood

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Abstract 547: A Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of N-terminal β-barrel in Microsomal Triglyceride Transfer Protein Function von Walsh, Meghan, Iqbal, Jahangir, Josekutty, Joby, Soh, James, Di Leo, Enza, Ozaydin, Eda, Gunduz, Mehmet, Tarugi, Patrizia, Hussain, Mahmood

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Valproate-Associated Coagulopathies in Children During Short-Term Treatment von Köse, Gülsen, Arhan, Ebru, Unal, Bahadır, Ozaydın, Eda, Guven, Alev, Saylı, Tulin R.

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Mucocele of the anterior lingual salivary glands: from extravasation to an alarming mass with a benign course von Andıran, Nesibe, Sarıkayalar, Fikriye, Ünal, Ömer Faruk, Baydar, Dilek Ertoy, Özaydın, Eda

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İki Yaşındaki Kız Çocuğunda Levetirasetama Bağlı Akut Rabdomiyoliz von ÖZAYDIN, Eda, ATEŞ, Sema

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