Stimulus-induced myoclonus treated effectively with clonazepam in genetically confirmed Coffin–Lowry syndrome()

Por Arslan, Elif Acar, Ceylaner, Serdar, Turanlı, Güzide
Publicado no Epilepsy Behav Case Rep (2014)

Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1

Por Yalcin Celik, Cetin Okuyaz, Ali Ertug Arslankoylu, Serdar Ceylaner
Publicado em 2017-01-01

Merosin-negative congenital muscular dystrophy: Report of five cases

Por Incecik, Faruk, Herguner, Ozlem M., Ceylaner, Serdar, Altunbasak, Sakir
Publicado no J Pediatr Neurosci (2015)

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis

Por Gürbüz, Fatih, Ceylaner, Serdar, Topaloğlu, Ali Kemal, Yüksel, Bilgin
Publicado no J Clin Res Pediatr Endocrinol (2016)

Mitochondrial membrane protein-associated neurodegeneration in a Turkish patient

Por Incecik, Faruk, Hergüner, Ozlem M., Besen, Seyda, Ceylaner, Serdar
Publicado no J Pediatr Neurosci (2016)

Lethal neonatal rigidity and multifocal seizure syndrome with a new mutation in BRAT1

Por Celik, Yalcin, Okuyaz, Cetin, Arslankoylu, Ali Ertug, Ceylaner, Serdar
Publicado no Epilepsy Behav Case Rep (2017)

Histopathological analysis of the placental lesions in pregnancies complicated with IUGR and stillbirths in comparison with noncomplicated pregnancies

Por Günyeli, İlker, Erdemoğlu, Evrim, Ceylaner, Serdar, Zergeroğlu, Sema, Mungan, Tamer
Publicado em 2011

Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign

Por Çamtosun, Emine, Şıklar, Zeynep, Ceylaner, Serdar, Kocaay, Pınar, Berberoğlu, Merih
Publicado no J Clin Res Pediatr Endocrinol (2017)

A novel frameshift mutation of malonyl‐CoA decarboxylase deficiency: clinical signs and therapy response of a late‐diagnosed case

Por Ersoy, Melike, Akyol, Mehmet Bedir, Ceylaner, Serdar, Çakır Biçer, Nihan
Publicado no Clin Case Rep (2017)

Association of vitamin D receptor gene polymorphisms with osteosarcoma risk and prognosis

Por Nilgun Kurucu, Gurses Şahin, Neriman Sarı, Serdar Ceylaner, İnci Ergurhan İlhan
Publicado em 2019-02-01

Siblings with Ethylmalonic Encephalopathy: Case Report

Por Çiğdem Seher Kasapkara, Ayşe Aksoy, Emine Polat, Mustafa Kılıç, Serdar Ceylaner
Publicado em 2018-03-01

Prenatally diagnosed partial trisomy 3q case with an omphalocele and less severe phenotype

Por Arıkan, Deniz Cemgil, Coşkun, Ayhan, Arıkan, İlker, Kıran, Gürkan, Ceylaner, Gülay
Publicado em 2010

A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data.

Por Sayli, B S, Akarsu, A N, Sayli, U, Akhan, O, Ceylaner, S, Sarfarazi, M
Publicado em 1995

Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene

Por Evliyaoğlu, Olcay, Dokurel, İpek, Bucak, Feride, Özcabı, Bahar, Ercan, Oya, Ceylaner, Serdar
Publicado em 2013

Coexistence of Kabuki Syndrome and Autoimmune Thyroiditis

Por Gürbüz, Fatih, Özalp Yüreğir, Özge, Ceylaner, Serdar, Topaloğlu, Ali Kemal, Yüksel, Bilgin
Publicado no J Clin Res Pediatr Endocrinol (2016)

p.R220L Is a Likely Pathogenic Novel GLA Gene Mutation Responsible for Fabry Disease

Por Hasan Ali Barman, Adem Atıcı, Serhan Özyıldırım, Serdar Ceylaner, Memduh Dursun, Sait Mesut Doğan
Publicado em 2022-05-01

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...

Por Meliha Demiral, Hüseyin Demirbilek, Edip Unal, Ceren Damla Durmaz, Serdar Ceylaner, Mehmet Nuri Özbek
Publicado em 2020-09-01

Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene

Por Aycan, Zehra, Ağladıoğlu, Sebahat Yılmaz, Ceylaner, Serdar, Çetinkaya, Semra, Baş, Veysel Nijat, Peltek Kendirici, Havva Nur
Publicado em 2010

A Rare Cause of Elevated Chitotriosidase Activity: Glycogen Storage Disease Type IV

Por Hizarcioglu-Gulsen, Hayriye, Yuce, Aysel, Akcoren, Zuhal, Berberoglu-Ates, Burcu, Aydemir, Yusuf, Sag, Erdal, Ceylaner, Serdar
Publicado no JIMD Rep (2014)

Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene

Por Özcabı, Bahar, Tahmiscioğlu Bucak, Feride, Ceylaner, Serdar, Özcan, Rahşan, Büyükünal, Cenk, Ercan, Oya, Tüysüz, Beyhan, Evliyaoğlu, Olcay
Publicado no J Clin Res Pediatr Endocrinol (2015)