Arşiv logosu
  • Türkçe
  • English
  • Giriş
    Yeni kullanıcı mısınız? Kayıt için tıklayın. Şifrenizi mi unuttunuz?
Arşiv logosu
  • Koleksiyonlar
  • Sistem İçeriği
  • Analiz
  • Talep/Soru
  • Türkçe
  • English
  • Giriş
    Yeni kullanıcı mısınız? Kayıt için tıklayın. Şifrenizi mi unuttunuz?
  1. Ana Sayfa
  2. Yazara Göre Listele

Yazar "Dogan, D. G." seçeneğine göre listele

Listeleniyor 1 - 12 / 12
Sayfa Başına Sonuç
Sıralama seçenekleri
  • Küçük Resim Yok
    Öğe
    BILATERAL SPLIT FEET: A NEW FINDING IN CORNELIA DE LANGE SYNDROME
    (Medecine Et Hygiene, 2010) Dogan, D. G.; Dogan, M.; Aslan, M.; Karabiber, H.
    Bilateral split feet: a new finding in Cornelia de Lange Syndrome: We report on a male infant with Cornelia de Lange syndrome and bilateral split feet. Bilateral split feet do not appear to have ever been a reported feature in any of the published cases of Cornelia de Lange syndrome.
  • Küçük Resim Yok
    Öğe
    A COLLODION BABY WITH HYPOTHYROIDISM
    (Medecine Et Hygiene, 2010) Dogan, D. G.; Aslan, M.; Karabiber, H.
    A Collodion baby with hypothyroidism: Collodion baby is a rare keratinizing congenital disorder. Although it is milder in degree than harlequin fetus, the infant is at risk for increased water loss, thermal instability, percutaneous toxicity, and infection as a result of an impaired skin barrier function. Here we report on an 11 days-old collodion baby with hypernatremic dehydratation, septicemia and congenital hypothyroidism. To our knowledge congenital hypothyroidism associated with collodion baby is reported in only one case up to date.
  • Küçük Resim Yok
    Öğe
    Congenital brucellosis: case report
    (Maney Publishing, 2010) Dogan, D. G.; Aslan, M.; Menekse, E.; Yakinci, C.
    A 6-hour-old infant was admitted with severe respiratory distress and hepatosplenomegaly. Her mother had arthralgia for 4 weeks in the 7/8th month of pregnancy and the infant was born at 31 weeks. Brucella spp was detected in blood culture and serology in mother and infant, supporting the diagnosis of brucellosis with presumed transplacental transmission.
  • Küçük Resim Yok
    Öğe
    Diffuse edema and bilateral massive pleural effusion as the presentation of systemic lupus erythematosus
    (Sage Publications Ltd, 2011) Aslan, M.; Bicak, U.; Dogan, D. G.; Dogan, M.; Yakinci, C.
    A rare case of systemic lupus erythematosus (SLE), with massive bilateral pleural effusions and generalized edema as the first manifestations, is reported. The patient was a previously healthy 13-year-old boy. He presented with a history of fever, lack of appetite, gradually increasing fatigue, cough, diffuse edema, and moderate dyspnea. He responded well to corticosteroids with resolution of the pleural effusions, and edema. SLE should always be kept in mind in cases of massive pleural effusions and/or diffuse edema, even in the absence of other clinical manifestations of the disease. Lupus (2011) 20, 308-310.
  • Küçük Resim Yok
    Öğe
    HALLERMANN-STREIFF SYNDROME WITH HEMIHYPERTROPHY
    (Medecine Et Hygiene, 2010) Dogan, D. G.; Karabiber, H.; Erhan, M. D.; Garipardic, M.; Davutoglu, M.; Guler, E.
    Hallerrnann-Streiff syndrome with hemihypertrophy: We report on a five year old girl with Hallermann-Streiff syndrome and hemihypertrophy. Hemihypertrophy does not appear to have ever been associated with Hallermann-Streiff syndrome.
  • Küçük Resim Yok
    Öğe
    HANHART SYNDROME
    (Medecine Et Hygiene, 2010) Dogan, D. G.; Dogan, M.; Aslan, M.; Menekse, E.; Yakinci, C.
    Hanhart syndrome: We report on a male infant with Hanhart Syndrome. It is classified in oromandibular limb hypogenesis syndromes which are a group of rare conditions involving congenital malformations of tongue, mandible, and limbs.
  • Küçük Resim Yok
    Öğe
    Hospitalisation: A Good Opportunity to Detect Developmental Difficulty in Children
    (Medcom Ltd, 2018) Kum, Y. E.; Dogan, D. G.; Canaloglu, S. K.; Kivilcim, M.
    This study aimed to determine children at risk of developmental difficulty by using a developmental monitoring tool during their hospital stay. The development of 113 hospitalised children aged 2-42 months was evaluated by using expressive and receptive language, fine and gross motor, social-emotional and relational functions, play, and self-help skills areas of the Guide for Monitoring Child Development (GMCD). There were 49 (42.4%) children with developmental difficulties. Developmental difficulty was found in 72.9% of the children of mothers who expressed a concern (p<0.001). Developmental difficulties were significantly more common in children of mothers without regular prenatal follow-up (p<0.001), with low educational level (p<0.001), and who had previously suffered stillbirth (p<0.013); and in children with a birth weight below 2500 g (p<0.002), and with consanguineous parents (p<0.007). The hospitalisation period is a good opportunity to identify children at risk of developmental problems and refer them for further assessment and early intervention.
  • Küçük Resim Yok
    Öğe
    Hospitalisation: a good opportunity to detect developmental difficulty in children
    (Medcom ltd, room 504-5, cheung tat centre, 18 cheung lee st, chaı wan, hong kong 00000, peoples r chına, 2018) Kum, Y. E.; Dogan, D. G.; Canaloglu, S. K.; Kivilcim, M.
    This study aimed to determine children at risk of developmental difficulty by using a developmental monitoring tool during their hospital stay. The development of 113 hospitalised children aged 2-42 months was evaluated by using expressive and receptive language, fine and gross motor, social-emotional and relational functions, play, and self-help skills areas of the Guide for Monitoring Child Development (GMCD). There were 49 (42.4%) children with developmental difficulties. Developmental difficulty was found in 72.9% of the children of mothers who expressed a concern (p<0.001). Developmental difficulties were significantly more common in children of mothers without regular prenatal follow-up (p<0.001), with low educational level (p<0.001), and who had previously suffered stillbirth (p<0.013); and in children with a birth weight below 2500 g (p<0.002), and with consanguineous parents (p<0.007). The hospitalisation period is a good opportunity to identify children at risk of developmental problems and refer them for further assessment and early intervention.
  • Küçük Resim Yok
    Öğe
    Human milk banking and milk kinship: perspectives of religious officers in a Muslim country
    (Springernature, 2015) Ozdemir, R.; Ak, M.; Karatas, M.; Ozer, A.; Dogan, D. G.; Karadag, A.
    OBJECTIVE: The present study aims to determine the knowledge, attitudes and views of the Muslim religious officers regarding infant feeding, breast milk, wet nursing, milk kinship and human milk banks (HMBs). STUDY DESIGN: A total of 401 religious officers were included in the study. Participants included 355 community service religious officers and 46 faculty religious officers. RESULTS: Two hundred fifty-four (63.3%) participants were in favor of administering donor human milk when breast milk is not available from the mothers. To the question 'What kind of human milk bank would you approve as far as the religious sensitivity is concerned?' a majority of the religious officers (71.3%) responded that they would only approve if the milk pool contained a restricted HMB where a limited number of recipients were allowed to use the mixtures in these milk pools. Only 7 (1.7%) participants advocated initiating Western-style HMBs in Turkey. CONCLUSION: Turkish religious officers have revealed that they would only approve the establishment of an alternative HMB by a maximum three donors where up to three recipients whose identities are known by one another are allowed to use donor milk from each milk pool.
  • Küçük Resim Yok
    Öğe
    Maternal serum and cord blood preptin levels in gestational diabetes mellitus
    (Nature Publishing Group, 2011) Aslan, M.; Celik, O.; Karsavuran, N.; Celik, N.; Dogan, D. G.; Botan, E.; Kafkasli, A.
    Objective: To assess preptin concentrations in pregnant women with and without gestational diabetes mellitus (GDM) and in the cord blood of their fetuses. Study Design: In all, 31 pregnant women with GDM and 31 gestational age-matched healthy pregnant subjects participated. Maternal serum and cord blood preptin levels were measured with ELISA. The relationships between maternal serum and cord blood preptin levels, anthropometric and metabolic parameters were also assessed. Result: Maternal serum and cord blood preptin levels were found higher in patients with GDM compared with control pregnant women. Preptin concentration in maternal serum was positively correlated with maternal age, fasting insulin levels, 1-h blood glucose after glucose load and cord preptin concentrations at birth. However, relationships between maternal and/or cord serum preptin and fetal growth parameters at birth were not detected. Conclusion: Our results indicate that preptin concentrations increase in maternal serum of women with GDM. Preptin levels may provide a novel approach to identify women with GDM. Journal of Perinatology (2011) 31, 350-355; doi:10.1038/jp.2010.125; published online 16 December 2010
  • Küçük Resim Yok
    Öğe
    Multiple dural arteriovenous fistulas involving the cavernous sinus, transverse sinus, sigmoid sinus and spinal drainage: CT angiography findings in 14-year-old boy
    (Verduci Publisher, 2012) Dogan, M.; Kahraman, A. S.; Firat, C.; Ak, M.; Yildirim, O.; Dogan, D. G.
    Dural arteriovenous fistulas (DAVF) are rare and constitute 10% to 15% of all intracranial arteriovenous malformations. Only few cases of DAVFs are reported in children. Here is the first case report describing CT angiographic findings in a 14 year old child having multiple DAVFs involving spinal canal, both cavernous and cerebral sinuses.
  • Küçük Resim Yok
    Öğe
    Spectral changes in electrical activity of pylorus due to L-NAME induced hypertrophic pyloric stenosis
    (Comenius Univ, 2011) Aslan, M.; Celik, O.; Dogan, D. G.; Tagluk, M. E.; Ulas, M.; Aydin, E.
    Objectives: To investigate the relation between hypertrophic pyloric stenosis (HPS) and the changes in the myoelectrical activity of the pyloric and gastric areas. Methods: Three pregnant females, at 14 days of gestation two of which were named as D14n (NOS inhibitor group) and one was named as D14c (control). From the beginning of the study until the end of gestation, rats in D14n group received nitric oxide synthase inhibitor L-NAME for administrating their pups, and the rat in D14c group was drinking water for 21 days. The pups of each group underwent laparotomy at 42 days of their life and myoelectrical signals of their pyloric and gastric regions were recorded via bipolar electrodes and then evaluated through signal processing. Results: Signal analysis showed that HPS induced pyloric segment reveals a suppressed spectral component that was detected in normal pyloric segment. The HPS induced pyloric segment also revealed higher power/min and +/- SD compared to that of normal and gastric areas. In the pyloric segment, while the number of interstitial cells of Cajal (ICC) was lesser, the number of smooth muscle cells was higher than in the pyloric segment of controls. Conclusions: The spectral differentials depend on the type, population and condition of locally specialized muscular mechanism which can be affected from HPS. The HPS also has a relation to specific cells, such as ICC that generates NO, provoke the spontaneous pacemakers and biological slow waves (Tab. 1, Fig. 1, Ref. 19). Full Text in free PDF www.bmj.sk.

| İnönü Üniversitesi | Kütüphane | Rehber | OAI-PMH |

Bu site Creative Commons Alıntı-Gayri Ticari-Türetilemez 4.0 Uluslararası Lisansı ile korunmaktadır.


İnönü Üniversitesi, Battalgazi, Malatya, TÜRKİYE
İçerikte herhangi bir hata görürseniz lütfen bize bildirin

DSpace 7.6.1, Powered by İdeal DSpace

DSpace yazılımı telif hakkı © 2002-2025 LYRASIS

  • Çerez Ayarları
  • Gizlilik Politikası
  • Son Kullanıcı Sözleşmesi
  • Geri Bildirim