Serdar Ceylaner

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 21

Top Topics

Regulatory T Cells

Top Venues

Journal of clinical research in pediatric endocrinology

Journal of clinical immunology

Turkish journal of haematology : official journal of Turkish Society of Haematology

Hormones (Athens, Greece)

This page only lists publications with an associated author ORCID identifier.

Publications

Zehra Busra Azizoglu, Royala Babayeva, Zehra Şule Haskoloğlu, Mustafa Burak Acar, Serife Ayaz-Guner, Fatma Zehra Okus, Mohammad Bilal Alsavaf, Salim Can, Kemal Erdem Basaran, Mehmed Fatih Canatan, Alper Ozcan, Hasret Erkmen, Can Berk Leblebici, Ebru Yilmaz, Musa Karakukcu, Mehmet Köse, Özlem Canöz, Ahmet Ozen, Elif Karakoç Aydıner, Serdar Ceylaner, Gülsüm Gümüş, Huseyin Per, Hakan Gumus, Halit Canatan, Servet Ozcan, Figen Doğu, Aydan İkincioğulları, Ekrem Ünal, Safa Barış, Ahmet Eken
DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans. Journal of clinical immunology 44 (8) (2024)
Zehra Busra Azizoglu, Royala Babayeva, Zehra Şule Haskoloğlu, Mustafa Burak Acar, Serife Ayaz-Guner, Fatma Zehra Okus, Mohammad Bilal Alsavaf, Salim Can, Kemal Erdem Basaran, Mehmed Fatih Canatan, Alper Ozcan, Hasret Erkmen, Can Berk Leblebici, Ebru Yilmaz, Musa Karakukcu, Mehmet Köse, Özlem Canöz, Ahmet Ozen, Elif Karakoç Aydıner, Serdar Ceylaner, Gülsüm Gümüş, Huseyin Per, Hakan Gumus, Halit Canatan, Servet Ozcan, Figen Doğu, Aydan İkincioğulları, Ekrem Ünal, Safa Barış, Ahmet Eken
DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans. Journal of clinical immunology 44 (8) (2024)
Halil Korkut Daglar, Didem Kaymak, Serdar Ceylaner, Nihal Şahin Uysal, Cem Yaşar Sanhal
Prenatal diagnosis of pulmonary arteriovenous malformations with a postnatal diagnosis of Osler-Weber-Rendu syndrome. Journal of clinical ultrasound : JCU (2024)
Zehra Busra Azizoglu, Royala Babayeva, Zehra Şule Haskoloğlu, Mustafa Burak Acar, Serife Ayaz-Guner, Fatma Zehra Okus, Mohammad Bilal Alsavaf, Salim Can, Kemal Erdem Basaran, Mehmed Fatih Canatan, Alper Ozcan, Hasret Erkmen, Can Berk Leblebici, Ebru Yilmaz, Musa Karakukcu, Mehmet Köse, Özlem Canöz, Ahmet Ozen, Elif Karakoç Aydıner, Serdar Ceylaner, Gülsüm Gümüş, Huseyin Per, Hakan Gumus, Halit Canatan, Servet Ozcan, Figen Doğu, Aydan İkincioğulları, Ekrem Ünal, Safa Barış, Ahmet Eken
DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans. Journal of clinical immunology 44 (8) (2024)
Halil Korkut Daglar, Didem Kaymak, Serdar Ceylaner, Nihal Şahin Uysal, Cem Yaşar Sanhal
Prenatal diagnosis of pulmonary arteriovenous malformations with a postnatal diagnosis of Osler-Weber-Rendu syndrome. Journal of clinical ultrasound : JCU 52 (5) (2024)
Zehra Busra Azizoglu, Royala Babayeva, Zehra Şule Haskoloğlu, Mustafa Burak Acar, Serife Ayaz-Guner, Fatma Zehra Okus, Mohammad Bilal Alsavaf, Salim Can, Kemal Erdem Basaran, Mehmed Fatih Canatan, Alper Ozcan, Hasret Erkmen, Can Berk Leblebici, Ebru Yilmaz, Musa Karakukcu, Mehmet Köse, Özlem Canöz, Ahmet Ozen, Elif Karakoç Aydıner, Serdar Ceylaner, Gülsüm Gümüş, Huseyin Per, Hakan Gumus, Halit Canatan, Servet Ozcan, Figen Doğu, Aydan İkincioğulları, Ekrem Ünal, Safa Barış, Ahmet Eken
DIAPH1-Deficiency is Associated with Major T, NK and ILC Defects in Humans. Journal of clinical immunology 44 (8) (2024)
Seyda Erdoğan, Gül Yalçın Çakmaklı, Bülent Elibol, Serdar Ceylaner, Muhittin Cenk Akbostancı
Could miglustat be a potential candidate in the treatment of action myoclonus renal failure syndrome? Acta neurologica Belgica (2023)
Uğur Muşabak, Serdar Ceylaner, Tuba Erdogan, Ebru Sebnem Ayva
A Case of Common Variable Immunodeficiency with CREBP Gene Mutation without Rubinstein Taybi Syndrome Features. Case reports in immunology 2022 (2022)
Gülin Karacan Küçükali, Özlem Gülbahar, Şervan Özalkak, Hasan Dağlı, Serdar Ceylaner, Zehra Aycan, Senay Savas Erdeve
Is Bioavailable Vitamin D Better Than Total Vitamin D to Evaluate Vitamin D Status in Obese Children? Journal of clinical research in pediatric endocrinology 13 (4) (2021)
Tibbe Dhooge, Tim Van Damme, Delfien Syx, Laura Muiño Mosquera, Sheela Nampoothiri, Anil Radhakrishnan, Pelin Özlem Şimsek Kiper, Gülen Eda Utine, Maryse Bonduelle, Isabelle Migeotte, Osama Essawi, Serdar Ceylaner, Adila Al Kindy, Brad Tinkle, Sofie Symoens, Fransiska Malfait
More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome. Human mutation 42 (6) (2021)
Gonca Kilic Yildirim, Coskun Yarar, Berna Seker Yilmaz, Serdar Ceylaner
Niemann-Pick type C disease with a novel intronic mutation: three Turkish cases from the same family. Journal of pediatric endocrinology & metabolism : JPEM (2021)
Muhammed Yuksel, Ayşe Armutlu, Farinaz Nazmi, Serdar Ceylaner, Cigdem Arikan
A novel insight into the pathophysiology of autoimmune hepatitis: An immune activator mutation in the FLT3 receptor. Hepatology forum 2 (3) (2021)
Berna Seker Yilmaz, Deniz Kor, Fatma Derya Bulut, Sebile Kılavuz, Serdar Ceylaner, Halise Neslihan Onenli Mungan
Clinical and molecular findings in 37 Turkish patients with isolated methylmalonic acidemia Turkish journal of medical sciences 51 (3) (2021)
Hande Turan, Aydilek Dagdeviren Cakir, Yavuz Özer, Gurkan Tarcin, Mesut Dursun, Serdar Ceylaner, Oya Ercan, Saadet Olcay Evliyaoglu
Clinical and Genetic Characteristics of Patients with Corticosterone Methyloxidase Deficiency Type 2: Novel Mutations in CYP11B2 Journal of clinical research in pediatric endocrinology 13 (2) (2020)
Husniye Yucel, Çiğdem Genç Sel, Çiğdem Seher Kasapkara, Gülin Karacan Küçükali, Senay Savas Erdeve, Ülkühan Öztoprak, Serdar Ceylaner, Saliha Şenel, Meltem Akcaboy
Treatment Difficulties in Hypomagnesemia Secondary to the Transient Receptor Potential Melastatin 6 Gene: A Case Report with Novel Mutation Journal of clinical research in pediatric endocrinology 13 (1) (2020)
Edip Unal, Meliha Demiral, Ruken Yıldırım, Funda Feryal Taş, Serdar Ceylaner, Mehmet Nuri Özbek
Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review. Hormones (Athens, Greece) 20 (2) (2020)
Şule Haskoloğlu, Ayşenur Öztürk, Gökcan Öztürk, Sevgi Köstel Bal, Candan İslamoğlu, Kübra Baskın, Serdar Ceylaner, Lale Ş. Tufan, Figen Doğu, Aydan İkincioğulları
Clinical Features and Outcomes of 23 Patients with Wiskott-Aldrich Syndrome: A Single-Center Experience Turkish journal of haematology : official journal of Turkish Society of Haematology 37 (4) (2020)
Duran Canatan, Abdullah Çim, Serpil Delibaş, Emel Altunsoy, Serdar Ceylaner
Importance of DNA Sequencing for Abnormal Hemoglobins Detected by HPLC Screening Turkish journal of haematology : official journal of Turkish Society of Haematology 37 (2) (2020)
Asli Derya Kardelen Al, Manolya Kara, Dilek Güller, Esin Karakılıc Ozturan, Zehra Yavaş Abalı, Serdar Ceylaner, Ayça Kiykim, Serdar Cantez, Selda Hancerlı Torun, Şükran Poyrazoğlu, Firdevs Baş, Feyza Darendelıler
LRBA deficiency: a rare cause of type 1 diabetes, colitis, and severe immunodeficiency. Hormones (Athens, Greece) 20 (2) (2020)
Meliha Demiral, Hüseyin Demirbilek, Edip Unal, Ceren Damla Durmaz, Serdar Ceylaner, Mehmet Nuri Özbek
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 GLI2 Gene Journal of clinical research in pediatric endocrinology 12 (3) (2019)
Fatma Dursun, Serdar Ceylaner
A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation Journal of clinical research in pediatric endocrinology 11 (2) (2018)