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Serdar Ceylaner

Showing results (141-150 of 244) with videos related to

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Minerva Pediatrica|October 11, 2018
A rare cause of fever of unknown origin: hypohidrotic ectodermal dysplasia with a splice site mutationMelahat M Oguz, Meltem Akcaboy, Asuman Gurkan, et al.
Pediatric Nephrology (Berlin, Germany)|November 1, 2019
Hypokalemia and hearing loss in a 3-year-old boy: AnswersOzlem Yuksel Aksoy, Fatma Semsa Cayci, Serdar Ceylaner, et al.
Turkish Journal of Medical Sciences|January 17, 2021
Clinical and molecular findings in 37 Turkish patients with isolated methylmalonic acidemiaBerna Şeker Yılmaz, Deniz Kor, Fatma Derya Bulut, et al.
Fertility and Sterility|July 22, 2010
An uncommon complementary isochromosome of 46,XY, i(9)(p10),i(9)(q10) in an infertile oligoasthenoteratozoospermic manEmine Seda Guvendag Guven, Serdar Dilbaz, Serdar Ceylaner, et al.
Hormone Research in Paediatrics|January 10, 2019
Clinical, Histochemical, and Molecular Study of Three Turkish Siblings Diagnosed with H Syndrome, and Literature ReviewEnver Simsek, Tulay Simsek, Makbule Eren, et al.
Journal of Pediatric Hematology/Oncology|July 5, 2024
Familial Hemophagocytic Lymphohistiocytosis Screening in Neonatal SepsisZuhre Kadi Ozan, Erol Erduran, Serdar Ceylaner, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 29, 2011
Sporadic nonautoimmune neonatal hyperthyroidism due to A623V germline mutation in the thyrotropin receptor geneZehra Aycan, Sebahat Yılmaz Ağladıoğlu, Serdar Ceylaner, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 20, 2021
Is Bioavailable Vitamin D Better Than Total Vitamin D to Evaluate Vitamin D Status in Obese Children?Gülin Karacan Küçükali, Özlem Gülbahar, Şervan Özalkak, et al.
Pediatric Nephrology (Berlin, Germany)|November 1, 2019
Hypokalemia and hearing loss in a 3-year-old boy: QuestionsOzlem Yuksel Aksoy, Fatma Semsa Cayci, Serdar Ceylaner, et al.
JIMD Reports|August 27, 2014
A Rare Cause of Elevated Chitotriosidase Activity: Glycogen Storage Disease Type IVHayriye Hizarcioglu-Gulsen, Aysel Yuce, Zuhal Akcoren, et al.
Pageof 25

Showing results (141-150 of 244) with videos related to

Sort By:
Pageof 25
Minerva Pediatrica|October 11, 2018
A rare cause of fever of unknown origin: hypohidrotic ectodermal dysplasia with a splice site mutationMelahat M Oguz, Meltem Akcaboy, Asuman Gurkan, et al.
Pediatric Nephrology (Berlin, Germany)|November 1, 2019
Hypokalemia and hearing loss in a 3-year-old boy: AnswersOzlem Yuksel Aksoy, Fatma Semsa Cayci, Serdar Ceylaner, et al.
Turkish Journal of Medical Sciences|January 17, 2021
Clinical and molecular findings in 37 Turkish patients with isolated methylmalonic acidemiaBerna Şeker Yılmaz, Deniz Kor, Fatma Derya Bulut, et al.
Fertility and Sterility|July 22, 2010
An uncommon complementary isochromosome of 46,XY, i(9)(p10),i(9)(q10) in an infertile oligoasthenoteratozoospermic manEmine Seda Guvendag Guven, Serdar Dilbaz, Serdar Ceylaner, et al.
Hormone Research in Paediatrics|January 10, 2019
Clinical, Histochemical, and Molecular Study of Three Turkish Siblings Diagnosed with H Syndrome, and Literature ReviewEnver Simsek, Tulay Simsek, Makbule Eren, et al.
Journal of Pediatric Hematology/Oncology|July 5, 2024
Familial Hemophagocytic Lymphohistiocytosis Screening in Neonatal SepsisZuhre Kadi Ozan, Erol Erduran, Serdar Ceylaner, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 29, 2011
Sporadic nonautoimmune neonatal hyperthyroidism due to A623V germline mutation in the thyrotropin receptor geneZehra Aycan, Sebahat Yılmaz Ağladıoğlu, Serdar Ceylaner, et al.
Journal of Clinical Research in Pediatric Endocrinology|May 20, 2021
Is Bioavailable Vitamin D Better Than Total Vitamin D to Evaluate Vitamin D Status in Obese Children?Gülin Karacan Küçükali, Özlem Gülbahar, Şervan Özalkak, et al.
Pediatric Nephrology (Berlin, Germany)|November 1, 2019
Hypokalemia and hearing loss in a 3-year-old boy: QuestionsOzlem Yuksel Aksoy, Fatma Semsa Cayci, Serdar Ceylaner, et al.
JIMD Reports|August 27, 2014
A Rare Cause of Elevated Chitotriosidase Activity: Glycogen Storage Disease Type IVHayriye Hizarcioglu-Gulsen, Aysel Yuce, Zuhal Akcoren, et al.
Pageof 25