Zobrazeno 1 - 10
of 18
pro vyhledávání: '"İlhan Asya Tanju"'
Autor:
Rabia Gonul Sezer, Gokhan Aydemir, Abdulkadir Bozaykut, Serdar Hira, Ilhan Asya Tanju, Ömer Özcan
Publikováno v:
Annals of Thoracic Medicine, Vol 8, Iss 4, Pp 209-213 (2013)
Aims: Matrix metalloproteinases (MMP) have been associated with neonatal lung morbidity and MMP dysregulation contributes to the pathology of chronic and acute lung disorders. Most of the previous studies were performed in the 1 st weeks of life of t
Externí odkaz:
https://doaj.org/article/96783b5fe8dd4573a0dd24ca7d35dc21
Publikováno v:
Haseki Tıp Bülteni, Vol 48, Iss 9, Pp 99-102 (2010)
Aim: We aimed to determine the frequency of cases with developmental hip dysplasia during the neonatal period and the associated risk factors. Methods: Hip ultrasound images of 258 full-term newborns aged one month were evaluated prospectively in
Externí odkaz:
https://doaj.org/article/890a33de66ff4944a20f98c1d0571a19
Publikováno v:
Medical Hypotheses. 82:341-345
The mean platelet volume (MPV), the accurate measure of platelet size, is considered a marker and determinant of platelet function. MPV can be a potentially useful prognostic biomarker in patients with cardiovascular disease. After reviewing literatu
WOS: 000358667900009
Objective: The purpose of this study was to investigate the association of prenatal, natal and postnatal factors with maternal attachment in mothers having infants aged 1-4 months and defining no mental health problems. Meth
Objective: The purpose of this study was to investigate the association of prenatal, natal and postnatal factors with maternal attachment in mothers having infants aged 1-4 months and defining no mental health problems. Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21355cebc4e9abe69231619dac24d305
https://hdl.handle.net/20.500.12415/1728
https://hdl.handle.net/20.500.12415/1728
Publikováno v:
Psychiatry research. 235
WOS: 000369472600023
PubMed ID: 26699881
It is suggested that salivary alpha-amylase (sAA) may be a marker of sympathoadrenal medullary system activity. Thus, it can be a possible relationship sAA and anxiety disorders. The aim of this stud
PubMed ID: 26699881
It is suggested that salivary alpha-amylase (sAA) may be a marker of sympathoadrenal medullary system activity. Thus, it can be a possible relationship sAA and anxiety disorders. The aim of this stud
Publikováno v:
Hepatitis Monthly
Background: Hepatitis B virus (HBV), hepatitis C Virus (HCV), and human immunodeficiency virus (HIV) infections are significant causes of morbidity and mortality all over the world, especially in underdeveloped countries like Afghanistan. Limited dat
Autor:
Ferhat Cekmez, Ilhan Asya Tanju, İsmail Göçmen, Cihan Meral, Teoman Dogru, Ferhan Karademir, Emre Tascilar, Osman Metin Ipcioglu, Cemal Nuri Ercin
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 23(5)
Background Apelin is a novel adipocytokine produced by white adipose tissue that binds the APJ receptor with high affinity. Insulin may have a role in regulation of apelin synthesis and secretion from the adipose tissue. Objective To investigate bloo
Autor:
Ferhat Cekmez, Ferhan Karademir, Ozgur Pirgon, Osman Metin Ipcioglu, Ilhan Asya Tanju, İsmail Göçmen, Cihan Meral
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 24(1)
The aim of this study was to assess the adiponectin and visfatin concentrations in small-for-gestational age (SGA), appropriate-for-gestational age (AGA), and large-for-gestational age (LGA) newborns and their mothers. Sixty parturients giving birth
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
PubMed: 21274310
Alström syndrome is a rare autosomal recessive disorder characterized by retinal degeneration, sensorineural hearing loss, early-onset obesity, and non-insulin-dependent diabetes mellitus. Affected individuals have normal birth
Alström syndrome is a rare autosomal recessive disorder characterized by retinal degeneration, sensorineural hearing loss, early-onset obesity, and non-insulin-dependent diabetes mellitus. Affected individuals have normal birth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d91cb0a591a5ba0f14d28f58fcad3f5a
https://hdl.handle.net/20.500.12395/24161
https://hdl.handle.net/20.500.12395/24161
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 21