Search Results - "Akşit, M. Arif"

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  1. 1

    Blood lead levels of maternal-cord pairs, children and adults who live in a central urban area in Turkey by Kirel, Birgül, Akşit, M Arif, Bulut, Hakan

    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 by Ozdemir, Ozgur, Dinleyici, Ener Cagri, Tekin, Neslihan, Colak, Omer, Aksit, M. Arif

    “…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 by Ucar, Birsen, Yildiz, Bilal, Aksit, M. Arif, Yarar, Coskun, Colak, Omer, Akbay, Yildiz, Colak, Ertugrul

    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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    Role of nitric oxide in hypoxia-induced changes in newborn rats by Kiliç, I, Kiliç, B A, Güven, C, Demirpençe, E, Akşit, M A

    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 by Dinleyici, Ener Cagri, Tekin, Neslihan, Dinleyici, Meltem, Aksit, M Arif

    “…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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  8. 8

    Severe fatal course of axial mesodermal dysplasia spectrum associated with complex cardiac defect in an infant of a mother with insulin dependent diabetes by Dinleyici, Ener Cagri, Tekin, Neslihan, Dinleyici, Meltem, Kilic, Zubeyir, Adapinar, Baki, Aksit, M. Arif

    “…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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  9. 9

    Cord blood IGF-1 and IGFBP-3 levels in asphyxiated term newborns by Dinleyici, Ener Cagri, Tekin, Neslihan, Colak, Omer, Aksit, M Arif

    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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    Serum amyloid A, procalcitonin, tumor necrosis factor-alpha, and interleukin-1beta levels in neonatal late-onset sepsis by Ucar, Birsen, Yildiz, Bilal, Aksit, M Arif, Yarar, Coskun, Colak, Omer, Akbay, Yildiz, Colak, Ertugrul

    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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    Bölgemizde 2-24 ay arasındaki sağlıklı çocukların sol el-elbileği grafilerinde kemiklerin olgunlaşma derecelerinin Greutich-pyle iskelet gelişme atlasına göre uyumluluğunun karşılaştırılması by ZİYLAN, S. Zeki, YÜZÜGÜLLÜ, Sıdıka, AKŞİT, M. Arif

    “…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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  17. 17

    Camptodactyly, myopia, and fibrosis of the medial rectus of the eye in two sibs born to consanguineous parents: Autosomal recessive entity? by Kilic, İlknur, Kilic, B. Alper, Ergin, Hacer, Aygün, Meral Günay, Aksit, M. Arif

    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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