Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Melikşah KESKİN"'
Autor:
Elif Özsu, Semra Çetinkaya, Semih Bolu, Nihal Hatipoğlu, Şenay Savaş Erdeve, Olcay Evliyaoğlu, Firdevs Baş, Atilla Çayır, İsmail Dündar, Emine Demet Akbaş, Seyid Ahmet Uçaktürk, Merih Berberoğlu, Zeynep Şıklar, Şervan Özalkak, Nursel Muratoğlu Şahin, Melikşah Keskin, Ülkü Gül Şiraz, Hande Turan, Ayşe Pınar Öztürk, Eda Mengen, Elif Sağsak, Fatma Dursun, Nesibe Akyürek, Sevinç Odabaşı Güneş, Zehra Aycan
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 297-305 (2024)
INTRODUCTION: Maturity onset diabetes of the young (MODY) occurs due to mutations in genes involved in pancreatic beta cell function and insulin secretion, has heterogeneous clinical and laboratory features, and account for 1-5% of all diabetes cases
Externí odkaz:
https://doaj.org/article/eb7e190aaeb24a0bb6a30c654ca0303b
Autor:
Zülfikar Akelma, Melikşah Keskin, Şenay Savaş Erdeve, Nurbanu Bursa, Osman Çelik, Ersan İmrat, Mustafa Mahir Ülgü, Murat Çağlayan, Naim Ata, Şuayip Birinci
Publikováno v:
Gülhane Tıp Dergisi, Vol 64, Iss 3, Pp 268-273 (2022)
Aims:Vitamin D deficiency results from malabsorption in Celiac disease (CD), and it may also be involved in the pathogenesis of CD. There is no clarity regarding vitamin D deficiency in CD. We investigated the frequency of vitamin D deficiency in chi
Externí odkaz:
https://doaj.org/article/ae3dd5bfe0e04df1820af68fe2d4bcfc
Publikováno v:
JCRPE, Vol 13, Iss 3, Pp 300-307 (2021)
Objective:Familial hypomagnesemia with secondary hypocalcemia (HSH) is an autosomal recessive disease caused by a mutation in the transient receptor potential melastatin 6 (TRPM6) gene and is characterized by selective magnesium malabsorption. Affect
Externí odkaz:
https://doaj.org/article/a3afbbe7354b4ce7a0ba3d3fc0204635
Autor:
Nursel Muratoğlu Şahin, Elvan Bayramoğlu, Hatice Nursun Özcan, Erdal Kurnaz, Melikşah Keskin, Şenay Savaş-Erdeve, Semra Çetinkaya, Zehra Aycan
Publikováno v:
JCRPE, Vol 11, Iss 3, Pp 287-292 (2019)
Objective:Antimüllerian hormone (AMH) concentrations in mini puberty are higher than those reported for the prepubertal period. In this study we investigated AMH concentrations in infants with premature thelarche (PT). A healthy control group was us
Externí odkaz:
https://doaj.org/article/b718f12a043c46d6a598ec00a75877c9
Publikováno v:
JCRPE, Vol 13, Iss 3, Pp 300-307 (2021)
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology
Objective: Familial hypomagnesemia with secondary hypocalcemia (HSH) is an autosomal recessive disease caused by a mutation in the transient receptor potential melastatin 6 (TRPM6) gene and is characterized by selective magnesium malabsorption. Affec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4947715c89f0937239232387f284142e
https://doi.org/10.4274/jcrpe.galenos.2021.2020.0192
https://doi.org/10.4274/jcrpe.galenos.2021.2020.0192
Publikováno v:
Turkish Journal of Obstetrics and Gynecology
In recent years, interest in the evaluation of vitamin D levels and the possible outcomes of their deficiency during pregnancy has increased. However, there is no consensus on when to start vitamin D supplementation, its duration, dosage, and the opt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4371e7975e6b02aa45fc42f42e4d9682
https://doi.org/10.4274/tjod.galenos.2021.90023
https://doi.org/10.4274/tjod.galenos.2021.90023
Publikováno v:
Journal of Academic Research in Medicine. 11:81-85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af75b6da25666871cb2014c40fa3685e
https://doi.org/10.4274/jarem.galenos.2021.22932
https://doi.org/10.4274/jarem.galenos.2021.22932
Autor:
Burçe, Orman, Senem, Esen, Melikşah, Keskin, Nursel, Muratoğlu Şahin, Şenay, Savaş Erdeve, Semra, Çetinkaya
Publikováno v:
Turkish archives of pediatrics. 57(3)
The onset of puberty in children is occurring at an increasingly earlier ages. During the coronavirus 2019 pandemic, children experienced epidemic-related changes such as stress, sedentary lifestyle, and weight gain.Auxological, clinical, endocrinolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::23a5835d6e3f1bb0af4690e4edbfbbf9
https://pubmed.ncbi.nlm.nih.gov/35781240
https://pubmed.ncbi.nlm.nih.gov/35781240
Autor:
Zehra Aycan, Melikşah Keskin, Naz Güleray Lafcı, Şenay Savaş-Erdeve, Firdevs Baş, Şükran Poyrazoğlu, Pınar Öztürk, Mesut Parlak, Oya Ercan, Tülay Güran, Nihal Hatipoğlu, Seyit Ahmet Uçaktürk, Gönül Çatlı, Nesibe Akyürek, Aşan Önder, Suna Kılınç, Semra Çetinkaya
Testicular adrenal rest tumor (TART) is one of the important complications that can cause infertility in male patients with congenital adrenal hyperplasia (CAH) and should therefore be diagnosed and treated at an early age. The factors that result in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c7df7f69c984e6eb8e31cccc545cd28
https://hdl.handle.net/20.500.12713/3423
https://hdl.handle.net/20.500.12713/3423
Autor:
Elvan Bayramoğlu, Erdal Kurnaz, Hatice Nursun Özcan, Zehra Aycan, Semra Çetinkaya, Melikşah Keskin, Nursel Muratoglu Sahin, Şenay Savaş-Erdeve
Publikováno v:
JCRPE, Vol 11, Iss 3, Pp 287-292 (2019)
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology
Objective Antimullerian hormone (AMH) concentrations in mini puberty are higher than those reported for the prepubertal period. In this study we investigated AMH concentrations in infants with premature thelarche (PT). A healthy control group was use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52bc64bea61d85f49cc77a7f27d64027
https://doi.org/10.4274/jcrpe.galenos.2019.2018.0293
https://doi.org/10.4274/jcrpe.galenos.2019.2018.0293