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Profil bibliographique

Nihat Sapan

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

357Publications signalées
807Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Allergic Rhinitis and SensitizationAsthma and respiratory diseasesFood Allergy and Anaphylaxis ResearchCystic Fibrosis Research AdvancesCultural and Sociopolitical Studies

Les publications récentes

Accès ouvert 2026 article OpenAlex

Clinical features associated with Pseudomonas aeruginosa colonization in children under 2 years of age: a retrospective study of Cystic Fibrosis Registry

Ece Ocak, Güzin Cinel, Gökçen Dilşa Tuğcu, Sanem Eryılmaz Polat et autres

BACKGROUND: Respiratory colonization with Pseudomonas aeruginosa is associated with increased morbidity and mortality in cystic fibrosis (CF) patients. This study aims to assess the clinical characteristics and associated factors of CF infants under two years of age with P. aeruginosa colonization in …

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0 citations The Turkish Journal of Pediatrics
Accès ouvert 2026 article OpenAlex

Evaluation of Asthma Control in Patients with Asthma and Factors Affecting Asthma Control in Childhood Asthma

Nihat Sapan, Sabahattin Karakaya, Şükrü Çekiç, Yakup Canıtez et autres

Objective: Asthma is the most common chronic disease of childhood. The goal of asthma treatment is to achieve complete control of the damage. This study aimed to investigate the control status of children diagnosed with asthma aged 4-18 years, using asthma control …

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0 citations Çocuk Dergisi / Journal of Child
Accès ouvert 2025 article OpenAlex

Phenotypes of Food Allergies in Patients with Atopic Dermatitis Aged Under 24 Months: A Multicenter Study

Müjde Tuba Çöğürlü, Metin Aydoğan, Özlem Cavkaytar, Pınar Uysal et autres

Background: Atopic dermatitis (AD) and food allergy (FA) are common allergic diseases in early childhood. AD may be concomitant with FA, particularly in young children. Although studies report the prevalence of FA in children with AD, there is insufficient data regarding different …

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1 citation Diagnostics
Accès ouvert 2025 article OpenAlex

Potentially Overlooked Risk for Neuropsychiatric Symptoms in Children: Montelukast Treatment

Seda Tunca, Özge Yılmaz, Merve Öcalan, Mustafa Arga et autres

BACKGROUND: Montelukast is a leukotriene receptor antagonist commonly used in allergic diseases. In this study, we investigated the frequency, severity and risk factors for neuropsychiatric side effects and sleep disorders associated with montelukast in children. METHOD: Children aged 6 months to 17 …

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7 citations Journal of Paediatrics and Child Health
2025 article OpenAlex

The Efficacy of Different Dosing Regimens of Omalizumab in Children and Adolescents with Chronic Spontaneous Urticaria Based on Real-Life Data

Yakup Canıtez, Deniz Özçeker, Pınar Uysal, Öner Özdemır et autres

INTRODUCTION: Limited data are available regarding the effectiveness of different omalizumab-dosing strategies in childhood chronic spontaneous urticaria (CSU). This study aimed to investigate the efficacy of omalizumab initiated at different doses in children and adolescents with CSU based on real-life data. METHODS: …

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2 citations International Archives of Allergy and Immunology
2024 article OpenAlex

Factors associated with pulmonary function decline of patients in the cystic fibrosis registry of Turkey: A retrospective cohort study

Nagehan Emiralioğlu, Banu Cakir, Ahmet Sertçelik, Ebru Elmas Yalcin et autres

BACKGROUND: The decline in pulmonary function is a predictor of disease progression in patients with cystic fibrosis (CF). This study aimed to determine the decline rate of percent predicted forced expiratory volume in 1 s (ppFEV1) based on the data of the …

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3 citations Pediatric Pulmonology
2023 article OpenAlex

Patients with cystic fibrosis who could not receive the CFTR modulator treatment: What did they lose in 1 year?

Salih Uytun, Güzin Cinel, Sanem Eryılmaz Polat, Satı Özkan Tabakçı et autres

BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disorder caused by CF transmembrane conductance regulator (CFTR) genetic variants. CFTR modulators improve pulmonary function and reduce respiratory infections in CF. This study investigated the clinical and laboratory follow-up parameters over 1 year in …

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9 citations Pediatric Pulmonology

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