Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Serdar Ceylaner

Showing results (51-60 of 244) with videos related to

Pageof 25
Sort By:
Human Fertility (Cambridge, England)|April 25, 2012
Genetic evaluation of severe male factor infertility in Turkey: a cross-sectional studySabri Cavkaytar, Sertaç Batioglu, Mufit Gunel, et al.
Hepatology Forum|July 5, 2022
A novel insight into the pathophysiology of autoimmune hepatitis: An immune activator mutation in the FLT3 receptorMuhammed Yuksel, Ayse Armutlu, Farinaz Nazmi, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 24, 2016
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 SignEmine Çamtosun, Zeynep Şıklar, Serdar Ceylaner, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 3, 2019
A novel mutation in the GP1BA gene in Bernard-Soulier syndromeZeynep C Özdemir, Yeter Düzenli Kar, Serdar Ceylaner, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 9, 2021
Niemann-Pick type C disease with a novel intronic mutation: three Turkish cases from the same familyGonca Kılıç Yıldırım, Coşkun Yarar, Berna Şeker Yılmaz, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|October 25, 2021
Successful therapeutic plasma exchange in a case with extremely severe hypertriglyceridemia secondary to diabetic ketoacidosis concomitant with type IX glycogen storage diseaseMerve Kisioglu, Osman Yesilbas, Burcu Guven, et al.
Journal of the Turkish German Gynecological Association|March 5, 2014
Histopathological analysis of the placental lesions in pregnancies complicated with IUGR and stillbirths in comparison with noncomplicated pregnanciesIlker Günyeli, Evrim Erdemoğlu, Serdar Ceylaner, et al.
Journal of Pediatric Surgery|September 11, 2004
Three new cases of disorganizationlike syndrome: one with accessory extrophia vesicalisHasan Ilkehan, Y Kenan Coban, Melih A Guven, et al.
American Journal of Medical Genetics. Part A|February 11, 2005
Craniosynostosis and ectopia lentis in a propositus whose parents are cousinsDilek Güven, Serdar Ceylaner, Defne Kalayci, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|March 5, 2020
Importance of DNA Sequencing for Abnormal Hemoglobins Detected by HPLC ScreeningDuran Canatan, Abdullah Çim, Serpil Delibaş, et al.
Pageof 25

Showing results (51-60 of 244) with videos related to

Sort By:
Pageof 25
Human Fertility (Cambridge, England)|April 25, 2012
Genetic evaluation of severe male factor infertility in Turkey: a cross-sectional studySabri Cavkaytar, Sertaç Batioglu, Mufit Gunel, et al.
Hepatology Forum|July 5, 2022
A novel insight into the pathophysiology of autoimmune hepatitis: An immune activator mutation in the FLT3 receptorMuhammed Yuksel, Ayse Armutlu, Farinaz Nazmi, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 24, 2016
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 SignEmine Çamtosun, Zeynep Şıklar, Serdar Ceylaner, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 3, 2019
A novel mutation in the GP1BA gene in Bernard-Soulier syndromeZeynep C Özdemir, Yeter Düzenli Kar, Serdar Ceylaner, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 9, 2021
Niemann-Pick type C disease with a novel intronic mutation: three Turkish cases from the same familyGonca Kılıç Yıldırım, Coşkun Yarar, Berna Şeker Yılmaz, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|October 25, 2021
Successful therapeutic plasma exchange in a case with extremely severe hypertriglyceridemia secondary to diabetic ketoacidosis concomitant with type IX glycogen storage diseaseMerve Kisioglu, Osman Yesilbas, Burcu Guven, et al.
Journal of the Turkish German Gynecological Association|March 5, 2014
Histopathological analysis of the placental lesions in pregnancies complicated with IUGR and stillbirths in comparison with noncomplicated pregnanciesIlker Günyeli, Evrim Erdemoğlu, Serdar Ceylaner, et al.
Journal of Pediatric Surgery|September 11, 2004
Three new cases of disorganizationlike syndrome: one with accessory extrophia vesicalisHasan Ilkehan, Y Kenan Coban, Melih A Guven, et al.
American Journal of Medical Genetics. Part A|February 11, 2005
Craniosynostosis and ectopia lentis in a propositus whose parents are cousinsDilek Güven, Serdar Ceylaner, Defne Kalayci, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|March 5, 2020
Importance of DNA Sequencing for Abnormal Hemoglobins Detected by HPLC ScreeningDuran Canatan, Abdullah Çim, Serpil Delibaş, et al.
Pageof 25