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Emek Uyur Yalçın

Observed names: E Uyur Yalcin, Emek Uyur Yalçın, Emek UYUR YALÇIN, Emek Uyur, Emek Uyur Yalcin, Emek Uyur Yalçin, Emek Uyur-Yalçın, UYUR YALÇIN, EMEK
ORCID: 0000-0001-6071-6375
Observed ORCID: 0000-0001-6071-6375
OpenAlex ID: A5020160968
The efficacy of nebulized salbutamol, hypertonic saline and salbutamol/hypertonic saline combination in moderate bronchiolitis
2011 · Ilke Ozahı Ipek, Emek Uyur Yalcin, et al. · Pulmonary Pharmacology & Therapeutics · 56
Clinical outcomes in children with herpes simplex encephalitis receiving steroid therapy
2016 · Hülya Maraş Genç, Emek Uyur Yalçın, et al. · Journal of Clinical Virology · 31
An overview of smell and taste problems in paediatric COVID‐19 patients
2020 · Ozlem Erdede, Erdal Sarı, et al. · Acta Paediatrica · 20
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Long-term clinical and radiologic follow-up of Schilder's disease
2017 · Hülya Maraş Genç, Bülent Kara, et al. · Multiple Sclerosis and Related Disorders · 18
TSEN54 gene-related pontocerebellar hypoplasia type 2 presenting with exaggerated startle response: report of two cases in a family
2015 · Hülya Maraş-Genç, Emek Uyur-Yalçın, et al. · The Turkish Journal of Pediatrics · 16
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Pyruvate dehydrogenase-E1α deficiency presenting as recurrent acute proximal muscle weakness of upper and lower extremities in an 8-year-old boy
2016 · Bülent Kara, Hülya Maraş Genç, et al. · Neuromuscular Disorders · 14
Neurodevelopmental Outcome in Patients with Typical Imaging Features of Injury as a Result of Neonatal Hypoglycemia
2021 · Emek Uyur Yalçın, Hülya Maraş Genç, et al. · Nöro Psikiyatri Arşivi · 10
Genetic and clinical evaluation of congenital myasthenic syndromes with long-term follow-up: experience of a tertiary center in Turkey
2022 · Edibe Pembegul Yildiz, Mehmet Akif Kilic, et al. · Acta Neurologica Belgica · 6
BEND4 as a Candidate Gene for an Infection-Induced Acute Encephalopathy Characterized by a Cyst and Calcification of the Pons and Cerebellar Atrophy
2021 · Bülent Kara, Oya Uyguner, et al. · Molecular Syndromology · 6
Clinical and neuroradiologic variability of Aicardi-Goutiéres syndrome: Two siblings with RNASEH2C mutation and a boy with TREX1 mutation
2015 · Emek Uyur Yalçın, Hülya Maraş Genç, et al. · The Turkish Journal of Pediatrics · 6
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Relationship Between Lactate Levels and Length of Hospital Stay in Infants with Lower Respiratory Tract Infection
2021 · Emek Uyur Yalçin, Furkan Erdogan, et al. · Pediatric Allergy Immunology and Pulmonology · 5
Comprehensive Evaluation of Inflammatory Biomarkers and Osmolarity to Distinguish Simple and Complex Febrile Seizures in Children
2023 · Özlem Erdede, Erdal Sarı, et al. · Children · 4
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New-Onset Dizziness Associated With COVID-19
2020 · Erdal Sarı, Nihan Uygur Külcü, et al. · Pediatric Neurology · 4
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Intracranial Calcification after Probable Disseminated Bacillus Calmette–Guérin Infection in a Child with Severe Combined Immunodeficiency
2018 · Isil Eser, Zeynep Seda Uyan, et al. · Journal of Pediatric Infectious Diseases · 4
A Case of Sotos Syndrome Caused by a Novel Variant in the NSD1 Gene: A Proposed Rationale to Treat Accompanying Precocious Puberty
2020 · B Ozcabi, G Akay, et al. · Acta Endocrinologica (Bucharest) · 3
Acute ophthalmoparesis and persistent mydriasis: expanding the clinical spectrum of anti-GQ1b positive cranial neuropathy in a 5.5-year-old girl
2019 · Ayfer Sakarya Güneş, Hülya Maraş Genç, et al. · The Turkish Journal of Pediatrics · 3
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A comparative randomized-controlled trial of serial casting and exercises on ankle range of motion, toe walking severity, walking balance, and functional health-related quality of life in children with idiopathic toe walking
2025 · Esra Giray, Pinar Akpinar, et al. · Journal of Pediatric Orthopaedics B · 2
Effectiveness and Safety of Epilepsy Surgery for Pediatric Patients with Intractable Epilepsy: A Clinical Retrospective Study from a Single-Center Experience
2023 · Müge Dolgun, Duygu Dölen, et al. · Pediatric Neurosurgery · 2
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study
2023 · Çağatay Günay, Duygu Aykol, et al. · Neuropediatrics · 2
Proteomic Analysis of m.8296A>G Variation in the Mitochondrial tRNALys Gene
2022 · Hülya Maraş Genç, Gürler Akpınar, et al. · Molecular Syndromology · 2
Clinical features and EEG findings in pediatric migraine: A retrospective analysis of 148 patients
2025 · Emek Uyur, Nilüfer Eldeş Hacıfazlıoğlu · Cephalalgia Reports · 1
Spine ultrasound evaluation in occult spinal dysraphism: A 5-year retrospective observation
2023 · Özlem Erdede, Kutlay Gür, et al. · The Annals of Clinical and Analytical Medicine · 1
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Are Interictal Discharges Associated with Neuronal Cell Loss in Electrical Status Epilepticus in Sleep?
2022 · Hüseyin Kılıç, Kübra Yılmaz, et al. · Turkish Archives of Pediatrics · 1
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Global aphasia without hemiparesis may be caused by blunt head trauma: An adolescent boy with transient aphasia
2017 · Sevim Şahin, Dilşad Türkdoğan, et al. · Journal of Clinical Neuroscience · 1
Prevalence and risk factors of acquired undescended testis in boys with cerebral palsy: A cross-sectional study
2026 · Dora Selda Seçim, Sabri Cansaran, et al. · Journal of Pediatric Urology
Works count: 38
Citation count: 217
H-index: 7
I10-index: 7
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