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Serdar Ceylaner

Showing results (111-120 of 244) with videos related to

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Journal of Obstetrics and Gynaecology of India|August 9, 2019
Prenatal Diagnosis of Osteogenesis Imperfecta Type IIIMehmet Tunc Canda, Serdar Ceylaner, Latife Doganay Caglayan, et al.
Neuromuscular Disorders : NMD|August 3, 2022
Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up studyGulshan Yunisova, Serdar Ceylaner, Piraye Oflazer, et al.
Prenatal Diagnosis|August 21, 2007
Chromosomal heteromorphisms may help for the diagnosis of uniparental disomy (UPD): a case reportGülay Ceylaner, Serdar Ceylaner, Nuri Danişman, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 1, 2017
A Mutation in INSR in a Child Presenting with Severe Acanthosis NigricansHale Tuhan, Serdar Ceylaner, Özlem Nalbantoğlu, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|December 31, 2019
A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in <i>CYP17A1</i> geneEdip Unal, Ruken Yıldırım, Funda Feryal Taş, et al.
Clinical Dysmorphology|February 20, 2020
A novel mutation which causes a frameshift in the PHOX2B gene causes Haddad syndromeNilufer Guzoglu, Mustafa K Aslan, Yasemin D Gunay, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 1, 2017
The variable clinical phenotype of three patients with hepatic glycogen synthase deficiencyÇiğdem Seher Kasapkara, Zehra Aycan, Esma Açoğlu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2021
Molecular and clinical findings of Turkish patients with hereditary fructose intoleranceMehmet Gunduz, Özlem Ünal-Uzun, Nevra Koç, et al.
Klinische Padiatrie|July 20, 2021
Horizontal Gaze Palsy with Progressive Scoliosis in an Infant Diagnosed Before Developing Scoliosis: MRI and DTI FindingsBerna Ucan, Seda Kaynak Sahap, Derya Bako, et al.
Anatolian Journal of Cardiology|May 13, 2022
p.R220L Is a Likely Pathogenic Novel GLA Gene Mutation Responsible for Fabry DiseaseHasan Ali Barman, Adem Atıcı, Serhan Özyıldırım, et al.
Pageof 25

Showing results (111-120 of 244) with videos related to

Sort By:
Pageof 25
Journal of Obstetrics and Gynaecology of India|August 9, 2019
Prenatal Diagnosis of Osteogenesis Imperfecta Type IIIMehmet Tunc Canda, Serdar Ceylaner, Latife Doganay Caglayan, et al.
Neuromuscular Disorders : NMD|August 3, 2022
Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up studyGulshan Yunisova, Serdar Ceylaner, Piraye Oflazer, et al.
Prenatal Diagnosis|August 21, 2007
Chromosomal heteromorphisms may help for the diagnosis of uniparental disomy (UPD): a case reportGülay Ceylaner, Serdar Ceylaner, Nuri Danişman, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 1, 2017
A Mutation in INSR in a Child Presenting with Severe Acanthosis NigricansHale Tuhan, Serdar Ceylaner, Özlem Nalbantoğlu, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|December 31, 2019
A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in <i>CYP17A1</i> geneEdip Unal, Ruken Yıldırım, Funda Feryal Taş, et al.
Clinical Dysmorphology|February 20, 2020
A novel mutation which causes a frameshift in the PHOX2B gene causes Haddad syndromeNilufer Guzoglu, Mustafa K Aslan, Yasemin D Gunay, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 1, 2017
The variable clinical phenotype of three patients with hepatic glycogen synthase deficiencyÇiğdem Seher Kasapkara, Zehra Aycan, Esma Açoğlu, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 23, 2021
Molecular and clinical findings of Turkish patients with hereditary fructose intoleranceMehmet Gunduz, Özlem Ünal-Uzun, Nevra Koç, et al.
Klinische Padiatrie|July 20, 2021
Horizontal Gaze Palsy with Progressive Scoliosis in an Infant Diagnosed Before Developing Scoliosis: MRI and DTI FindingsBerna Ucan, Seda Kaynak Sahap, Derya Bako, et al.
Anatolian Journal of Cardiology|May 13, 2022
p.R220L Is a Likely Pathogenic Novel GLA Gene Mutation Responsible for Fabry DiseaseHasan Ali Barman, Adem Atıcı, Serhan Özyıldırım, et al.
Pageof 25