Search Results - "Akşit, M. Arif"
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Blood lead levels of maternal-cord pairs, children and adults who live in a central urban area in Turkey
Published in Turkish journal of pediatrics (01-04-2005)“…Lead levels were measured in blood samples of 99 adults, 180 children and 143 pregnant women living in Eskişehir, an urban area in Turkey. One hundred and…”
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Low-mannose-binding lectin levels in susceptibility to neonatal sepsis in preterm neonates with fetal inflammatory response syndrome
Published in The journal of maternal-fetal & neonatal medicine (01-09-2010)“…Aim. In this study, we aimed to evaluate cord blood mannose binding levels (MBL), to evaluate possible relationship between cord blood MBL levels with neonatal…”
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Serum Amyloid A, Procalcitonin, Tumor Necrosis Factor-α, and Interleukin-1β Levels in Neonatal Late-Onset Sepsis
Published in Mediators of Inflammation (01-01-2008)“…Background. Sepsis is an important cause of mortality in newborns. However, a single reliable marker is not available for the diagnosis of neonatal late-onset…”
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Macrocephaly−Cutis marmorata telangiectatica congenita with atrial septal aneurysm and magnetic resonance imaging (MRI) findings
Published in Pediatrics international (01-06-2004)Get full text
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Role of nitric oxide in hypoxia-induced changes in newborn rats
Published in Biology of the neonate (01-10-2000)“…In order to investigate the role of nitric oxide (NO) in hypoxic tissue damage in newborns, we studied the effects of systemic administration of an inhibitor…”
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Clinical and laboratory findings of two newborns with Wiedemann-Rautenstrauch syndrome: additional features, evaluation of bone turnover and review of the literature
Published in Journal of pediatric endocrinology & metabolism : JPEM (01-06-2008)“…Wiedemann-Rautenstrauch syndrome (WRS) is a rare autosomal recessive condition which represents a complex of symptoms and laboratory findings with unknown…”
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Severe fatal course of axial mesodermal dysplasia spectrum associated with complex cardiac defect in an infant of a mother with insulin dependent diabetes
Published in American journal of medical genetics. Part A (15-09-2007)“…Axial mesodermal dysplasia spectrum (AMDS) includes the features of other malformation complexes or sequences, such as oculo‐auriculo‐vertebral spectrum (OAVS)…”
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Cord blood IGF-1 and IGFBP-3 levels in asphyxiated term newborns
Published in Neuro-endocrinology letters (01-12-2006)“…Determination and pathogenesis of perinatal asphyxia is still an important problem. During the asphyxial insult and recovery phase, alteration of the growth…”
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SECONDARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS ASSOCIATED WITH MENINGOCOCCEMIA
Published in Pediatric hematology and oncology (01-12-2006)Get full text
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Serum amyloid A, procalcitonin, tumor necrosis factor-alpha, and interleukin-1beta levels in neonatal late-onset sepsis
Published in Mediators of inflammation (2008)“…Sepsis is an important cause of mortality in newborns. However, a single reliable marker is not available for the diagnosis of neonatal late-onset sepsis…”
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Thrombocytopenia-Absent Radius Syndrome with Hemolytic Anemia and Cow’s Milk Intolerance in a Neonate
Published in Türkiye çocuk hastalıkları dergisi (01-04-2016)Get full text
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The role of Nitric Oxide (NO) in Hypoxia-Induced Changes in Newborn Rats† 1041
Published in Pediatric research (01-04-1998)Get full text
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Bölgemizde 2-24 ay arasındaki sağlıklı çocukların sol el-elbileği grafilerinde kemiklerin olgunlaşma derecelerinin Greutich-pyle iskelet gelişme atlasına göre uyumluluğunun karşılaştırılması
Published in T.C. Uludağ Üniversitesi Tıp Fakültesi dergisi (2004)“…Bu çalışma, kronolojik yaşları belli olan 2-24 ay arasındaki 700 çocuk içinden, sağlıklı olan 242'sinin sol el-elbilek grafilerinde kemik matürasyonlarının…”
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Camptodactyly, myopia, and fibrosis of the medial rectus of the eye in two sibs born to consanguineous parents: Autosomal recessive entity?
Published in American journal of medical genetics (28-04-1998)“…Unaffected but consanguineous parents suggest autosomal recessive inheritance of a previously apparently undescribed syndrome of camptodactyly, fibrosis of the…”
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