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Serdar Ceylaner

Showing results (21-30 of 244) with videos related to

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Cornea|March 18, 2021
A Novel mRNA Modification Mutation in a Patient With Ligneous Conjunctivitis Coexisting With Heterozygous Familial Mediterranean Fever MutationNeslihan D Koseoglu, Serdar Ceylaner, Nilgun Yildirim
Epilepsy & Behavior Case Reports|February 11, 2015
Stimulus-induced myoclonus treated effectively with clonazepam in genetically confirmed Coffin-Lowry syndromeElif Acar Arslan, Serdar Ceylaner, Güzide Turanlı
The Turkish Journal of Pediatrics|February 28, 2020
Ataxia, tremor, intellectual disability: a case of STXBP1 encephalopathy with a new mutationAydan Değerliyurt, Gamze Gezgen Kesen, Serdar Ceylaner
The Turkish Journal of Pediatrics|April 30, 2021
Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disordersBerna Şeker Yılmaz, Serdar Ceylaner, Neslihan Önenli Mungan
Journal of Clinical Research in Pediatric Endocrinology|May 20, 2021
Central Precocious Puberty in an Infant with Sotos Syndrome and Response to TreatmentTuğba Kontbay, Zeynep Şıklar, Serdar Ceylaner, et al.
Clinical Dysmorphology|May 22, 2012
Hydranencephaly, pituitary hypoplasia, and anophthalmia in a male infantMurat Köstü, Oğuz Tuncer, Serdar Ceylaner, et al.
Hormone Research in Paediatrics|November 1, 2016
Two Frameshift Mutations in MKRN3 in Turkish Patients with Familial Central Precocious PubertyEnver Simsek, Meliha Demiral, Serdar Ceylaner, et al.
Sudanese Journal of Paediatrics|August 7, 2019
Importance of pedigree in patients with familial epilepsy and intellectual disabilityHüseyin Çaksen, Fesih Aktar, Gökçen Yıldırım, et al.
Pediatric Neurology|April 22, 2009
Hypomelanosis of Ito and Sturge-Weber syndrome without facial nevus: an association or a new syndrome?Aydan Değerliyurt, Asli Kantar, Serdar Ceylaner, et al.
Prenatal Diagnosis|September 13, 2013
Are low maternal estriol levels a predictor for pro-opiomelanocortin (POMC) deficiency caused by POMC mutation during pregnancy?Ozgur Aldemir, Samim Ozen, Cigdem Sanlialp, et al.
Pageof 25

Showing results (21-30 of 244) with videos related to

Sort By:
Pageof 25
Cornea|March 18, 2021
A Novel mRNA Modification Mutation in a Patient With Ligneous Conjunctivitis Coexisting With Heterozygous Familial Mediterranean Fever MutationNeslihan D Koseoglu, Serdar Ceylaner, Nilgun Yildirim
Epilepsy & Behavior Case Reports|February 11, 2015
Stimulus-induced myoclonus treated effectively with clonazepam in genetically confirmed Coffin-Lowry syndromeElif Acar Arslan, Serdar Ceylaner, Güzide Turanlı
The Turkish Journal of Pediatrics|February 28, 2020
Ataxia, tremor, intellectual disability: a case of STXBP1 encephalopathy with a new mutationAydan Değerliyurt, Gamze Gezgen Kesen, Serdar Ceylaner
The Turkish Journal of Pediatrics|April 30, 2021
Brown Vialetto Van Laere syndrome: presenting with left ventricular non-compaction and mimicking mitochondrial disordersBerna Şeker Yılmaz, Serdar Ceylaner, Neslihan Önenli Mungan
Journal of Clinical Research in Pediatric Endocrinology|May 20, 2021
Central Precocious Puberty in an Infant with Sotos Syndrome and Response to TreatmentTuğba Kontbay, Zeynep Şıklar, Serdar Ceylaner, et al.
Clinical Dysmorphology|May 22, 2012
Hydranencephaly, pituitary hypoplasia, and anophthalmia in a male infantMurat Köstü, Oğuz Tuncer, Serdar Ceylaner, et al.
Hormone Research in Paediatrics|November 1, 2016
Two Frameshift Mutations in MKRN3 in Turkish Patients with Familial Central Precocious PubertyEnver Simsek, Meliha Demiral, Serdar Ceylaner, et al.
Sudanese Journal of Paediatrics|August 7, 2019
Importance of pedigree in patients with familial epilepsy and intellectual disabilityHüseyin Çaksen, Fesih Aktar, Gökçen Yıldırım, et al.
Pediatric Neurology|April 22, 2009
Hypomelanosis of Ito and Sturge-Weber syndrome without facial nevus: an association or a new syndrome?Aydan Değerliyurt, Asli Kantar, Serdar Ceylaner, et al.
Prenatal Diagnosis|September 13, 2013
Are low maternal estriol levels a predictor for pro-opiomelanocortin (POMC) deficiency caused by POMC mutation during pregnancy?Ozgur Aldemir, Samim Ozen, Cigdem Sanlialp, et al.
Pageof 25