Search Results - "Kiper, Nural"

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  1. 1

    European protocols for the diagnosis and initial treatment of interstitial lung disease in children by Bush, Andrew, Cunningham, Steve, de Blic, Jacques, Barbato, Angelo, Clement, Annick, Epaud, Ralph, Hengst, Meike, Kiper, Nural, Nicholson, Andrew G, Wetzke, Martin, Snijders, Deborah, Schwerk, Nicolaus, Griese, Matthias

    Published in Thorax (01-11-2015)
    “…Interstitial lung disease in children (chILD) is rare, and most centres will only see a few cases/year. There are numerous possible underlying diagnoses, with…”
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    Journal Article
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    Does cystic fibrosis make susceptible to celiac disease? by Emiralioglu, Nagehan, Ademhan Tural, Dilber, Hizarcioglu Gulsen, Hayriye, Ergen, Yasin Maruf, Ozsezen, Beste, Sunman, Birce, Saltık Temizel, İncinur, Yalcin, Ebru, Dogru, Deniz, Ozcelik, Uğur, Kiper, Nural

    Published in European journal of pediatrics (01-09-2021)
    “…Patients with cystic fibrosis (CF) have a higher incidence of celiac disease (CD) than the healthy population; however, the actual incidence of coexisting CF…”
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    The role of flexible bronchoscopy in the diagnostic pathway of children with unexplained peripheral eosinophilia by Hızal, Mina, Eryilmaz Polat, Sanem, Emiralioğlu, Nagehan, Cinel, Guzin, Yalcin, Ebru, Dogru, Deniz, Ozcelik, Ugur, Kiper, Nural

    Published in Pediatrics international (01-01-2023)
    “…Background Many possible underlying causes can be seen in children with unexplained peripheral eosinophilia (UPE) with suspected pulmonary involvement. Here,…”
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    Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis by Hildebrandt, Jenna, Yalcin, Ebru, Bresser, Hans-Georg, Cinel, Guzin, Gappa, Monika, Haghighi, Alireza, Kiper, Nural, Khalilzadeh, Soheila, Reiter, Karl, Sayer, John, Schwerk, Nicolaus, Sibbersen, Anke, Van Daele, Sabine, Nübling, Georg, Lohse, Peter, Griese, Matthias

    Published in Orphanet journal of rare diseases (26-11-2014)
    “…Juvenile pulmonary alveolar proteinosis (PAP) due to CSF2RA mutations is a rare disorder with only a few cases described worldwide. We identified nine children…”
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  8. 8

    Increased Plasma YKL-40 Level and Chitotriosidase Activity in Cystic Fibrosis Patients by Topcu, Dilara Bal, Tugcu, Gokcen, Er, Berrin, Polat, Sanem Eryilmaz, Hizal, Mina, Yalcin, Ebru Elmas, Ersoz, Deniz Dogru, Coplu, Lutfi, Ozcelik, Ugur, Kiper, Nural, Lay, Incilay, Oztas, Yesim

    Published in Inflammation (01-04-2022)
    “…We investigated plasma YKL-40 levels and chitotriosidase (CHIT1) activity in patients with cystic fibrosis (CF) lung disease and evaluated clinically relevant…”
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  9. 9

    Human bocavirus and human metapneumovirus in children with lower respiratory tract infections: Effects on clinical, microbiological features and disease severity by Ademhan Tural, Dilber, Yalcin, Ebru, Emiralioglu, Nagehan, Ozsezen, Beste, Alp, Alpaslan, Sunman, Birce, Gozmen, Onur, Dogru, Deniz, Ozcelik, Ugur, Kiper, Nural

    Published in Pediatrics international (01-01-2022)
    “…Background We aimed to compare the clinical findings of human bocavirus (HBoV) and human metapneumovirus (HMPV) infections, and to analyze the effects of…”
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    The frequency and related factors of non‐tuberculosis mycobacteria infections among patients with cystic fibrosis by Ademhan Tural, Dilber, Emiralioglu, Nagehan, Ozsezen, Beste, Saribas, Zeynep, Ozcan, Nursun, Alp, Alpaslan, Sunman, Birce, Hizal, Mina, Eryilmaz Polat, Sanem, Yalcin, Ebru, Dogru, Deniz, Ozcelik, Ugur, Kiper, Nural

    Published in Pediatrics international (01-11-2021)
    “…Background Non‐tuberculous mycobacteria (NTM) can cause chronic lung infection particularly in patients who have structural lung disease such as cystic…”
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  12. 12

    Interactions between physicians and drug industry by Begul Yagci Kupeli, Nural Kiper

    “…Ethical issues involving drug industry physician relationship have resulted in an ongoing debate about its appropriateness for many years in medical World. The…”
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  13. 13

    Different features of lung involvement in Niemann-Pick disease and Gaucher disease by Gülhan, Bora, Özçelik, Uğur, Gürakan, Figen, Güçer, Şafak, Orhan, Diclehan, Cinel, Güzin, Yalçn, Ebru, Ersöz, Deniz Doğru, Kiper, Nural, Yüce, Aysel, Kale, Gülsev

    Published in Respiratory medicine (01-09-2012)
    “…Summary Background Niemann-Pick disease (NPD) and Gaucher disease (GD) are well-known lysosomal storage diseases. Respiratory system involvement is an…”
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  14. 14

    Congenital Tuberculosis after in-vitro Fertilisation in a Woman Previously Undiagnosed with Tuberculosis Salpingitis by Emiralioglu, Nagehan, MD, Dogru, Deniz, Dr, Oguz, Berna, Dr, Yalcin, Ebru, Dr, Ozcelik, Ugur, Dr, Konuskan, Bahadir, Dr, Cengiz, Ali Bulent, Dr, Kiper, Nural, Dr

    Published in Pediatrics and neonatology (01-12-2016)
    “…Abstract The diagnosis of congenital tuberculosis (TB) is often difficult as clinical signs are nonspecific and maternal history of TB remains an important…”
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    Long‐term results of disodium etidronate treatment in pulmonary alveolar microlithiasis by Ozcelik, Ugur, Yalcin, Ebru, Arıyurek, Macit, Ersoz, Deniz Dogru, Cinel, Guzin, Gulhan, Bora, Kiper, Nural

    Published in Pediatric pulmonology (01-05-2010)
    “…Pulmonary alveolar microlithiasis (PAM) is a rare disease with alveolar microliths mainly composed of calcium phosphate. The gene responsible for the disease…”
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    Diagnosis and treatment of pulmonary alveolar microlithiasis by Emiralioglu, Nagehan, Beken, Burcin, Ozcan, Hatice Nursun, Yalcin, Ebru, Dogru, Deniz, Ozcelik, Ugur, Haliloglu, Mithat, Kiper, Nural

    Published in Pediatrics international (01-08-2016)
    “…Pulmonary alveolar microlithiasis (PAM) is a rare genetic disease caused by mutations in sodium–phosphate co‐transporter (SLC34A2), which encodes a type 2b…”
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    Pneumomediastinum, pneumorrhachis and subcutaneous emphysema associated with viral infections: Report of three cases by Emiralioğlu, Nagehan, Ozcan, H Nursun, Oğuz, Berna, Yalçın, Ebru, Doğru, Deniz, Özçelik, Uğur, Kiper, Nural

    Published in Pediatrics international (01-10-2015)
    “…Spontaneous pneumomediastinum is usually secondary to alveolar rupture in the pulmonary interstitium, associated with subcutaneous emphysema and occasionally…”
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    Does Helicobacter pylori play a role in the pathogenesis of non-cystic fibrosis bronchiectasis? by Aydın Teke, Turkan, Akyön, Yakut, Yalcin, Ebru, Ozen, Hasan, Doğru, Deniz, Kiper, Nural, Ozcelik, Ugur

    Published in Pediatrics international (01-09-2016)
    “…Background The aim of this study was to investigate whether Helicobacter pylori plays a role in the pathogenesis and severity of non‐cystic fibrosis…”
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    Do we neglect nutrition in childhood interstitial lung disease? by Emiralioglu, Nagehan, Kiper, Nural

    Published in European journal of clinical nutrition (06-08-2024)
    “…Growth failure and inadequate weight gain are common problems in childhood interstitial lung diseases (chILD) and these children usually need high calories. It…”
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    Medical treatment of pulmonary hydatid disease: for which child? by Doğru, Deniz, Kiper, Nural, Özçelik, Uğur, Yalçın, Ebru, Göçmen, Ayhan

    Published in Parasitology international (01-06-2005)
    “…There have been many encouraging studies on medical treatment of pulmonary hydatid disease due to Echinococcus granulosus infection. Our aims were to…”
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