Search Results - Serdar Ceylaner

A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation by Fatma Dursun, Serdar Ceylaner

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Rodriguez lethal acrofacial dysostosis syndrome with ambiguous genitalia by Ulku Mete Ural, Serdar Ceylaner

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Central Precocious Puberty in an Infant with Sotos Syndrome and Response to Treatment by Tuğba Kontbay, Zeynep Şıklar, Serdar Ceylaner, Merih Berberoğlu

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Prenatal Diagnosis of Thoraco-Omphalopagus Conjoined Twins At 13+ Weeks of Pregnancy: A Case Report by Gürkan Kıran, Hakan Kıran, Serdar Ceylaner, Savaş Karakuş

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Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2 by Erdal Eren, Havva Tezcan Ünlü, Serdar Ceylaner, Ömer Tarım

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"Double Hit" Homozygous Mutations for Two Different Rare Inborn Errors of Metabolism: A Burden for Countries with High Prevalences of Consangineous Marriages by Asburçe Olgaç, Leyla Tümer, Serdar Ceylaner, Gürsel Biberoğlu, Alev Hasanoğlu

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Non-immune Hydrops Fetalis Secondary to Nuchal Cystic Hygroma: Prenatal Detection and Postnatal Evaluation of 5 Cases by Süleyman Eserdağ, Ebru Zülfikaroğlu, Görkem Tuncay, Serdar Ceylaner, Nuri Danışman

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Siblings with Ethylmalonic Encephalopathy: Case Report by Çiğdem Seher Kasapkara, Ayşe Aksoy, Emine Polat, Mustafa Kılıç, Serdar Ceylaner

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Coexistence of borderline ovarian epithelial tumor, primary pelvic hydatid cyst, and lymphoepithelioma-like gastric carcinoma by Tayfun Gungor, Sunduz Ozlem Altinkaya, Levent Sirvan, Roberto Alvarez Lafuente, Serdar Ceylaner

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Prenatal Diagnosis Of Catch22 Syndrome by Rana Karayalçın, Serdar Ceylaner, Feride İffet Şahin, Şebnem Özyer, Melike Doğanay, Nuri Danışman

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Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the <italic... by Meliha Demiral, Hüseyin Demirbilek, Edip Unal, Ceren Damla Durmaz, Serdar Ceylaner, Mehmet Nuri Özbek

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Is Bioavailable Vitamin D Better Than Total Vitamin D to Evaluate Vitamin D Status in Obese Children? by Gülin Karacan Küçükali, Özlem Gülbahar, Şervan Özalkak, Hasan Dağlı, Serdar Ceylaner, Zehra Aycan, Şenay Savaş Erdeve

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Mitotically Active Follicular Nodule in Early Childhood: A Case Report with a Novel Mutation in the Thyroglobulin Gene by Sirmen Kızılcan Çetin, Zehra Aycan, Zeynep Şıklar, Serpil Dizbay Sak, Serdar Ceylaner, Elif Özsu, Merih Berberoğlu

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A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report by İlknur Bağrul, Serdar Ceylaner, Yasemin Tasci Yildiz, Serife Tuncez, Elif Arslanoglu Aydin, Esra Bağlan, Semanur Ozdel, Mehmet Bülbül

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Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2 by Hande Turan, Aydilek Dağdeviren Çakır, Yavuz Özer, Gürkan Tarçın, Bahar Özcabi, Serdar Ceylaner, Oya Ercan, Saadet Olcay Evliyaoğlu

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Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency? by Gökcan Öztürk, Şule Haskoloğlu, Nazlı Deveci, Hasret Erkmen, Nur Ayça Çelik, Gülsan Sucak, Serdar Ceylaner, Aydan İkincioğulları, Figen Doğu

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A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care by Aslı Derya Kardelen, Esin Karakılıç Özturan, Şükran Poyrazoğlu, Firdevs Baş, Serdar Ceylaner, Sjoerd D. Joustra, Jan M. Wit, Feyza Darendeliler

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A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome by Fatma Derya Bulut, Deniz Kör, Berna Şeker Yılmaz, Mustafa Yılmaz, Derya Ufuk Altıntaş, Serdar Ceylaner, Sebile Kılavuz, Neslihan Önenli Mungan

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Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation by Hüsniye Yücel, Çiğdem Genç Sel, Çiğdem Seher Kasapkara, Gülin Karacan Küçükali, Senay Savas-Erdeve, Ülkühan Öztoprak, Serdar Ceylaner, Saliha Şenel, Meltem Akçaboy

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