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Serdar Ceylaner

Showing results (91-100 of 244) with videos related to

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Expert Review of Clinical Immunology|October 28, 2025
TBXAS1 deficiency: a novel monogenic cause of chronic nonbacterial osteomyelitis responsive to COX inhibitorsRabia Miray Kisla Ekinci, Serdar Ceylaner, Fatma Dereli Devrez, et al.
The Turkish Journal of Pediatrics|January 30, 2018
p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiencyBerna Şeker-Yılmaz, Deniz Kör, Gökhan Tümgör, et al.
European Journal of Medical Genetics|May 2, 2021
Isolated congenital diaphragm hernia associated with homozygous SLIT3 gene variant in dizygous twinsTugba Barsan Kaya, Ozge Aydemir, Serdar Ceylaner, et al.
JAAD Case Reports|June 14, 2019
A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the <i>PEPD</i> geneEsra Kiratli Nalbant, Nermin Karaosmanoglu, Omer Kutlu, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 1, 2013
Primary adrenal insufficiency caused by a novel mutation in DAX1 geneOlcay Evliyaoğlu, İpek Dokurel, Feride Bucak, et al.
Prenatal Diagnosis|June 22, 2007
Evaluation of 2407 fetuses in a Turkish populationGülay Ceylaner, Serdar Ceylaner, Ilker Günyeli, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 9, 2016
Cystinosis in Eastern TurkeyMurat Doğan, Keziban Bulan, Sultan Kaba, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 2, 2015
Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-upBerna Seker Yilmaz, Deniz Kor, Neslihan Onenli Mungan, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Coexistence of Kabuki Syndrome and Autoimmune ThyroiditisFatih Gürbüz, Özge Özalp Yüreğir, Serdar Ceylaner, et al.
The Turkish Journal of Pediatrics|May 18, 2016
Pyridoxine-dependent epilepsy in two Turkish patients in Turkey and review of the literatureGülen Gül-Mert, Faruk İncecik, M Özlem Hergüner, et al.
Pageof 25

Showing results (91-100 of 244) with videos related to

Sort By:
Pageof 25
Expert Review of Clinical Immunology|October 28, 2025
TBXAS1 deficiency: a novel monogenic cause of chronic nonbacterial osteomyelitis responsive to COX inhibitorsRabia Miray Kisla Ekinci, Serdar Ceylaner, Fatma Dereli Devrez, et al.
The Turkish Journal of Pediatrics|January 30, 2018
p.Val452Ile mutation of the SLC25A13 gene in a Turkish patient with citrin deficiencyBerna Şeker-Yılmaz, Deniz Kör, Gökhan Tümgör, et al.
European Journal of Medical Genetics|May 2, 2021
Isolated congenital diaphragm hernia associated with homozygous SLIT3 gene variant in dizygous twinsTugba Barsan Kaya, Ozge Aydemir, Serdar Ceylaner, et al.
JAAD Case Reports|June 14, 2019
A rare case of prolidase deficiency with situs inversus totalis, identified by a novel mutation in the <i>PEPD</i> geneEsra Kiratli Nalbant, Nermin Karaosmanoglu, Omer Kutlu, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 1, 2013
Primary adrenal insufficiency caused by a novel mutation in DAX1 geneOlcay Evliyaoğlu, İpek Dokurel, Feride Bucak, et al.
Prenatal Diagnosis|June 22, 2007
Evaluation of 2407 fetuses in a Turkish populationGülay Ceylaner, Serdar Ceylaner, Ilker Günyeli, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 9, 2016
Cystinosis in Eastern TurkeyMurat Doğan, Keziban Bulan, Sultan Kaba, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 2, 2015
Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-upBerna Seker Yilmaz, Deniz Kor, Neslihan Onenli Mungan, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 14, 2016
Coexistence of Kabuki Syndrome and Autoimmune ThyroiditisFatih Gürbüz, Özge Özalp Yüreğir, Serdar Ceylaner, et al.
The Turkish Journal of Pediatrics|May 18, 2016
Pyridoxine-dependent epilepsy in two Turkish patients in Turkey and review of the literatureGülen Gül-Mert, Faruk İncecik, M Özlem Hergüner, et al.
Pageof 25