Showing 1 - 19 results of 19 for search 'Serdar Ceylaner', query time: 0.09s Refine Results
  1. 1
    A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation

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

    Published 2019
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  2. 2
    Rodriguez lethal acrofacial dysostosis syndrome with ambiguous genitalia

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

    Published 2016
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  3. 3
    Central Precocious Puberty in an Infant with Sotos Syndrome and Response to Treatment

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

    Published 2022
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  4. 4
    Prenatal Diagnosis of Thoraco-Omphalopagus Conjoined Twins At 13+ Weeks of Pregnancy: A Case Report

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

    Published 2007
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  5. 5
    Compound Heterozygous Variants in FAM111A Cause Autosomal Recessive Kenny-Caffey Syndrome Type 2

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

    Published 2023
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  6. 6
    "Double Hit" Homozygous Mutations for Two Different Rare Inborn Errors of Metabolism: A Burden for Countries with High Prevalences of Consangineous Marriages

    "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

    Published 2018
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  7. 7
    Non-immune Hydrops Fetalis Secondary to Nuchal Cystic Hygroma: Prenatal Detection and Postnatal Evaluation of 5 Cases

    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

    Published 2006
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  8. 8
    Siblings with Ethylmalonic Encephalopathy: Case Report

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

    Published 2018
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  9. 9
    Coexistence of borderline ovarian epithelial tumor, primary pelvic hydatid cyst, and lymphoepithelioma-like gastric carcinoma

    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

    Published 2011
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  10. 10
    Prenatal Diagnosis Of Catch22 Syndrome

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

    Published 2010
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  11. 11
    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>GLI2</italic> Gene

    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

    Published 2020
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  12. 12
    Is Bioavailable Vitamin D Better Than Total Vitamin D to Evaluate Vitamin D Status in Obese Children?

    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

    Published 2021
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  13. 13
    Mitotically Active Follicular Nodule in Early Childhood: A Case Report with a Novel Mutation in the Thyroglobulin Gene

    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

    Published 2024
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  14. 14
    A novel mutation in the proteoglycan 4 gene causing CACP syndrome: two sisters report

    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

    Published 2023
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  15. 15
    Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2

    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

    Published 2021
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  16. 16
    Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency?

    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

    Published 2024
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  17. 17
    A Novel Pathogenic IGSF1 Variant in a Patient with GH and TSH Deficiency Diagnosed by High IGF-I Values at Transition to Adult Care

    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

    Published 2023
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  18. 18
    A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome

    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

    Published 2018
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  19. 19
    Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation

    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

    Published 2021
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