Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Pinar Vatansever"'
Autor:
Gulin Sunter, Ece Oge Enver, Azad Akbarzade, Serap Turan, Pinar Vatansever, Dilek Ince Gunal, Goncagul Haklar, Abdullah Bereket, Kadriye Agan, Tulay Guran
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Congenital sphingosine-1-phosphate (S1P) lyase deficiency due to biallelic mutations in SGPL1 gene has recently been described in association with primary adrenal insufficiency and steroid-resistant nephrotic syndrome. S1P lyase,
Externí odkaz:
https://doaj.org/article/bd219541ea214e42ad4d4ea3ea85a112
Autor:
Yasemin Gokdemir, Pinar Vatansever, Bulent Karadag, Tuncay Seyrekel, Ozgur Baykan, Nilay Bas Ikızoglu, Refika Ersu, Fazilet Karakoc, Goncagul Haklar
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
Background: The objective of the study was to assess the diagnostic efficacy of the coulometric endpoint method and compare it with classic Gibson&Cooke and chloridometer methods.Methods: This study is a prospective clinical study comparing two conve
Externí odkaz:
https://doaj.org/article/9f9d1e2b2c9942d6bb5210cdba7f56bc
Autor:
Ece Oge Enver, Goncagül Haklar, Pinar Vatansever, Abdullah Bereket, Tulay Guran, Leyla Bilgin, Perran Boran, Omer Guran, Serap Turan
Publikováno v:
Pediatric research. 92(1)
BACKGROUND Interpretation of the results of steroid hormone measurements is challenging at early infancy. The liquid chromatography-tandem mass spectrometry (LC-MS/MS) method provides a powerful tool for diagnosing steroidogenesis disorders. We aimed
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 33(11)
Background Sclerostin and osteoprotegerin (OPG) are new markers of chronic kidney disease (CKD) mediated mineral bone disease (CKD-MBD) which were extensively evaluated in adult population. We aimed to evaluate the associations between serum levels o
Publikováno v:
International Journal of Hypertension, Vol 2020 (2020)
International Journal of Hypertension
International Journal of Hypertension
Aim: to compare the plasma N-terminal pro-C-type natriuretic peptide concentrations of normotensive pregnant women, patients with mild preeclampsia, and patients with severe preeclampsia. Methods: we collected venous blood samples from 25 normotensiv
Autor:
Tulay Guran, Ece Oge Enver, Abdullah Bereket, Serap Turan, Dilek Ince Gunal, Goncagül Haklar, Kadriye Agan, Gulin Sunter, Pinar Vatansever, Azad Akbarzade
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
BMC Neurology
BMC Neurology
Background Congenital sphingosine-1-phosphate (S1P) lyase deficiency due to biallelic mutations in SGPL1 gene has recently been described in association with primary adrenal insufficiency and steroid-resistant nephrotic syndrome. S1P lyase, on the ot
Publikováno v:
International Journal of Hypertension, Vol 2020 (2020)
Aim. To compare the plasma N-terminal pro-C-type natriuretic peptide concentrations of normotensive pregnant women, patients with mild preeclampsia, and patients with severe preeclampsia. Methods. We collected venous blood samples from 25 normotensiv
Externí odkaz:
https://doaj.org/article/a2aba4cbdcba4909bb05d4ad4370c0e5