Search Results - "Kiper, Nural"
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European protocols for the diagnosis and initial treatment of interstitial lung disease in children
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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International management platform for children's interstitial lung disease (chILD-EU)
Published in Thorax (01-03-2018)“…Children's interstitial lung diseases (chILD) cover many rare entities, frequently not diagnosed or studied in detail. There is a great need for specialised…”
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3
Does cystic fibrosis make susceptible to celiac disease?
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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4
Obstructive sleep apnea in children with Down syndrome: is it possible to predict severe apnea?
Published in European journal of pediatrics (01-02-2022)“…The objectives are to explore the demographic and polysomnographic features of children with Down syndrome and to determine the predictive factors associated…”
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The role of flexible bronchoscopy in the diagnostic pathway of children with unexplained peripheral eosinophilia
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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The effect of Pseudomonas aeruginosa eradication regimens on chronic colonization and clinical outcomes in pediatric patients with cystic fibrosis
Published in Pediatrics international (01-01-2022)“…Background Chronic Pseudomonas aeruginosa colonization (Pa‐CC) affects cystic fibrosis (CF) progression, including pulmonary exacerbations and pulmonary…”
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Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis
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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Increased Plasma YKL-40 Level and Chitotriosidase Activity in Cystic Fibrosis Patients
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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Human bocavirus and human metapneumovirus in children with lower respiratory tract infections: Effects on clinical, microbiological features and disease severity
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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Prospective evaluation of hydroxychloroquine in pediatric interstitial lung diseases: Study protocol for an investigator-initiated, randomized controlled, parallel-group clinical trial
Published in Current controlled trials in cardiovascular medicine (03-04-2020)“…Interstitial lung diseases in children (chILD) are rare and consist of many different entities that affect the parenchyma of the lungs, leading to a chronic…”
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The frequency and related factors of non‐tuberculosis mycobacteria infections among patients with cystic fibrosis
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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Interactions between physicians and drug industry
Published in Çukurova Üniversitesi tip fakültesi dergisi (01-12-2016)“…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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Different features of lung involvement in Niemann-Pick disease and Gaucher disease
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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Congenital Tuberculosis after in-vitro Fertilisation in a Woman Previously Undiagnosed with Tuberculosis Salpingitis
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
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
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
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?
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?
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?
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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