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Author

Fatih Kurt

Observed names: Fatih KURT, Kurt, Fatih
Observed institution: Düzce Üniversitesi
ORCID: 0000-0003-1975-6492
Observed ORCID: 0000-0003-1975-6492
OpenAlex ID: A5048957007
Investigation of plasma vitamin D, vitamin B12, and folate levels in newborns with pathological jaundice without risk factors
2025 · Fatih Kurt, Fatih Davran, et al. · Egyptian Pediatric Association Gazette · 25
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The rising threat of antibiotic and multidrug resistance in neonatal urinary tract infections
2025 · Mukaddes Kılıç Sağlam, Emine Yanaşoğlu, et al. · BMC Pediatrics · 6
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Refugee and asylum‐seeker children and health problems in the city of Duzce, Türkiye
2024 · Hatice Mine Cakmak, Kenan Kocabay, et al. · Child Care Health and Development · 4
Evaluation of mass mercury poisoning cases occurring in a center in Türkiye: symptomatology, treatment methods, and follow-up processes
2025 · Fatih Kurt, Abdullah Akcil, et al. · European Journal of Pediatrics · 3
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Investigation of Microvascular Involvement Through Nailfold Capillaroscopic Examination in Children with Familial Mediterranean Fever
2025 · Fatih Kurt, Belkız Uyar, et al. · Medicina · 2
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Evaluation of clinical and laboratory findings in cases of infantile hypertrophic pyloric stenosis
2025 · Fatih Kurt, Murat Kaya · Journal of Health Sciences and Medicine · 1
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Adenoid hypertrophy detection inventory in children for primary care physicians and pediatricians
2025 · Fatih Kurt, Abdullah Belada, et al. · European Archives of Oto-Rhino-Laryngology · 1
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Kışlar Hep Çetin Geçer: Çocuklarda Alt Solunum Yolu Enfeksiyonu Etkenleri ve Prognozu Etkileyen Faktörler
2025 · Fatih Kurt, Ramazan Cahit Temizkan, et al. · Sağlık Bilimlerinde Değer · 1
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Attention! One of the Causes of Second-Degree Mobitz Type 1 AV Block: Pheniramine Maleate
2024 · Fatih Kurt, Selmin Karademir · Konuralp Tıp Dergisi · 1
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Apoptosis-associated speck-like protein containing a CARD (ASC), TNF Like Factor 1a(TL-1a) and B Cell Chemoattractant Chemokine Ligand 13(CXCL-13) expression profiles in familial Mediterranean fever (FMF) patients
2023 · Fatih KURT, Recep ERÖZ, et al. · Konuralp Tıp Dergisi · 1
The diagnosis to be kept in mind in resistant epilepsy; tuberous sclerosis
2022 · Fatih Kurt, Recep Eröz, et al. · Northwestern Medical Journal · 1
Causes of baby abandonment and associated factors: a descriptive study
2026 · Fatih Kurt, Abdullah Akcil, et al. · Humanities and Social Sciences Communications
May Long-Term Follow-Up in Alport Syndrome Assess Potential Cardiovascular Risks?
2026 · İbrahim Halil Damar, Fatih Kurt, et al. · Sağlık Bilimlerinde Değer
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Examination of Symptoms, Findings, and Molecular Analysis Results in Pediatric Cases Diagnosed with Familial Renal Glucosuria
2026 · Fatih Kurt · Haydarpaşa Numune medical journal (Online)
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Examination of Cases Who Had Molecular Testing with the Presumptive Diagnosis of Cystic Fibrosis: Experience of a Single Center
2025 · Fatih Kurt, Recep Eröz · Online Türk Sağlık Bilimleri Dergisi
Kistik Fibrozis Öntanısıyla Moleküler Test Yapılan Olguların İncelenmesi: Tek Merkez Deneyimi
2025 · Kurt, Fatih, Eröz, Recep · Online Türk Sağlık Bilimleri Dergisi
Artificial Intelligence in Pediatrics: A Comparative Analysis of Gpt-3.5 and Gpt-4 Models
2025 · Nadide Melike Sav, Ahmet Berk Gökmen, et al. · SSRN Electronic Journal
Clinical Characteristics of Cases Developing Neonatal Pneumothorax: 10 Years of Experience
2024 · Fatih Kurt, Abdulkadir Kaya, et al. · Medical Records
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What is the ideal thyroid-stimulating hormone (TSH) threshold value in congenital hypothyroidism screening? Twin study
2024 · Fatih Kurt, Busra Olcay Oz, et al. · Medicine
Kronik Öksürükte Vasküler Ring Anomalilerine Dikkat
2024 · Fatih KURT · Sağlık Bilimlerinde Değer
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A new neurological complication of COVID-19 infection; ulnar sensory neuropathy
2022 · Fatih Kurt · Northwestern Medical Journal
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İletişimsizliğin Çocuk Sağlığına Etkilerinden Biri: Nutrisyonel Rikets
2022 · Fatih KURT, Nilgün YALÇIN, et al. · Sağlık Bilimlerinde Değer
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Charcott-Marie-Tooth Disease Type 4c Caused from a Pathogenic Homozygous c.1897delG (p.Ala633Profs * 12) Variation in The SH3TC2 Gene
2021 · Fatih Kurt, Mustafa Dogan, et al. · Hong Kong Journal of Paediatrics Research
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A Novel Variant of Tuberosclerosis: c.2458A>T p.(Lys820*) in the TSC1 Gene 19th Exon
2021 · Fatih Kurt, Mustafa Dogan, et al. · Hong Kong Journal of Paediatrics Research
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Works count: 24
Citation count: 46
H-index: 3
I10-index: 1
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