Homozygous SLC20A2 mutations cause congenital CMV infection-like phenotype
Ceylan, Ahmet Cevdet, Kireker Köylü, Oya, Özyürek, Hamit, Özaydin, Eda, Yön, Mehmet İlker, Kasapkara, Çiğdem Seher
Published in Acta neurologica Belgica (01.10.2023)
Published in Acta neurologica Belgica (01.10.2023)
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Novel Abetalipoproteinemia Missense Mutation Highlights the Importance of the N-Terminal β-Barrel in Microsomal Triglyceride Transfer Protein Function
Walsh, Meghan T, Iqbal, Jahangir, Josekutty, Joby, Soh, James, Di Leo, Enza, Özaydin, Eda, Gündüz, Mehmet, Tarugi, Patrizia, Hussain, M Mahmood
Published in Circulation. Cardiovascular genetics (01.10.2015)
Published in Circulation. Cardiovascular genetics (01.10.2015)
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The Relationship between Vitamin D Receptor Gene Polymorphisms and Bone Density, Osteocalcin Level and Growth in Adolescents
zaydn, Eda, Dayangac-Erden, Didem, Erdem-Yurter, Hayat, Derman, Orhan, Cokun, Turgay
Published in Journal of Pediatric Endocrinology and Metabolism (01.05.2010)
Published in Journal of Pediatric Endocrinology and Metabolism (01.05.2010)
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PHACES syndrome presenting as hemangiomas, sternal clefting and congenital ulcerations on the helices
DURUSOY, Cicek, MIHCI, Ercan, TACOY, Sukran, OZAYDIN, Eda, ALPSOY, Erkan
Published in Journal of dermatology (01.03.2006)
Published in Journal of dermatology (01.03.2006)
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A newborn with pentalogy of Cantrell and pulmonary hypoplasia
Unal, Sevim, Cakmak Celik, Fatma, Ozaydin, Eda, Kaçar, Ayper, Günal, Nazlihan
Published in Anadolu kardiyoloji dergisi : AKD (01.12.2009)
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Published in Anadolu kardiyoloji dergisi : AKD (01.12.2009)
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Management of central diabetes insipidus with oral desmopressin in a patient with ectrodactyly and cleft lip/palate (ECP) syndrome
Ozaydin, Eda, Aycan, Zehra, Yusufoğlu, Arzu Meltem, Cetinkaya, Ergun, Ergen, Saime, Unal, Sevim, Köse, Gülşen
Published in Turkish journal of pediatrics (01.01.2009)
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Published in Turkish journal of pediatrics (01.01.2009)
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3-HMG Coenzyme A Lyase Deficiency: Macrocephaly and Left Ventricular Noncompaction with a Novel Mutation
Köksal, Tülin, Gündüz, Mehmet, Özaydın, Eda, Azak, Emine
Published in Indian journal of pediatrics (01.07.2015)
Published in Indian journal of pediatrics (01.07.2015)
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Differences in iron deficiency anemia and mean platelet volume between children with simple and complex febrile seizures
Özaydın, Eda, Arhan, Ebru, Cetinkaya, Bilge, Özdel, Semanur, Değerliyurt, Aydan, Güven, Alev, Köse, Gülsen
Published in Seizure (London, England) (01.04.2012)
Published in Seizure (London, England) (01.04.2012)
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Microsomal triglyceride transfer protein gene mutations in Turkish children: A novel mutation and clinical follow up
Gündüz, Mehmet, Özaydın, Eda, Atar, Müge Büyüktaşlı, Koç, Nevra, Kırsaçlıoğlu, Ceyda, Köse, Gülşen, Cefalù, Angelo Baldassare, Averna, Maurizio, Tarugi, Patrizia
Published in Indian journal of gastroenterology (01.05.2016)
Published in Indian journal of gastroenterology (01.05.2016)
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The Association Between Vitamin D Status and Recurrent Wheezing
Özaydın, Eda, Bütün, Mehmet Fatih, Çakır, Bahar Çuhacı, Köse, Gülşen
Published in Indian journal of pediatrics (01.11.2013)
Published in Indian journal of pediatrics (01.11.2013)
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Journal Article
Viral etiology in infants hospitalized for acute bronchiolitis
Azkur, Dilek, Özaydın, Eda, Dibek-Mısırlıoğlu, Emine, Vezir, Emine, Tombuloğlu, Duygu, Köse, Gülşen, Kocabaş, Can N
Published in Turkish journal of pediatrics (01.11.2014)
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Published in Turkish journal of pediatrics (01.11.2014)
Journal Article
A Rare Cause of Protein Losing Enteropathy: Collagenous Sprue
Karaku, Esra, Ekinci, Özgür, K rsaçl o lu, Ceyda Tuna, Özayd n, Eda, Atakan, Canan, Dursun, Ay e
Published in Fetal and pediatric pathology (01.04.2015)
Published in Fetal and pediatric pathology (01.04.2015)
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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 Triglyceride Transfer Protein
Walsh, Meghan T, Di Leo, Enza, Ozaydin, Eda, Tarugi, Patrizia, Hussain, Mahmood
Published in Arteriosclerosis, thrombosis, and vascular biology (01.05.2014)
Published in Arteriosclerosis, thrombosis, and vascular biology (01.05.2014)
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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
Walsh, Meghan, Iqbal, Jahangir, Josekutty, Joby, Soh, James, Di Leo, Enza, Ozaydin, Eda, Gunduz, Mehmet, Tarugi, Patrizia, Hussain, Mahmood
Published in Arteriosclerosis, thrombosis, and vascular biology (01.05.2015)
Published in Arteriosclerosis, thrombosis, and vascular biology (01.05.2015)
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Acute hemorrhagic pancreatitis due to the use of valproic acid in a child
Ozaydin, Eda, Yükselgüngör, Handan, Köse, Gülşen
Published in European journal of paediatric neurology (01.03.2008)
Published in European journal of paediatric neurology (01.03.2008)
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Journal Article
A new case of VACTERL association with congenital arachnoid cyst
Unal, Sevim, Kibar, Ayse Esin, Ozaydin, Eda, Karadag, Nilgün, Balci, Sevim
Published in Clinical dysmorphology (01.07.2008)
Published in Clinical dysmorphology (01.07.2008)
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