İlknur Sürücü Kara

Ankara University — Turkey

Medicine · Health Sciences

6h-index104citations43works1.32yr avg
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Research Topics

Lysosomal Storage Disorders Research(6), Metabolism and Genetic Disorders(6), Folate and B Vitamins Research(4), Biotin and Related Studies(4), Click Chemistry and Applications(3)

Publications43 total

Long-term clinical evaluation of patients with alpha-mannosidosis - a multicenter study
Molecular Genetics and Metabolism·2026Open Access
Untargeted Metabolomic and Lipidomic Profiling Reveals Distinct Biochemical Patterns in Treated Biotinidase Deficiency
International Journal of Molecular Sciences·2026Open Access
The Nutritional Parameters in Children with Delays in Speech
Cerrahpasa Medical Journal·2025Open Access
NOD-m: a novel clinical score for predicting hearing loss in inherited metabolic disorders
European Archives of Oto-Rhino-Laryngology·2025Open Access
Clinical and biochemical spectrum of APOB-related hypobetalipoproteinemia: Insights from a retrospective cohort study
Journal of clinical lipidology·2025· 2 cited
Challenges Faced by Newborns with Inherited Metabolic Disorders and Their Mothers During Antepartum, Intrapartum, and Postpartum Periods
Fetal and Pediatric Pathology·2025
Anemia, inflammation, circadian rhythm and season effects in febrile convulsions
Northern Clinics of Istanbul·2025Open Access
Siblings with a Homozygous Variant in the NHP2 Gene: A Case Report and Review of Literature
Molecular Syndromology·2024Open Access
Quality of Life and Related Factors in Patients Diagnosed with Mucopolysaccharidosis and Their Caregivers
Klinische Pädiatrie·2024· 1 cited
Evaluating the gonads of left-handed children using ultrasonography and comparing the findings with those of right-handed ones
European Journal of Pediatrics·2024
Hemogram Parameters of Children with Bell’s Palsy at the Time of Admission and Their Findings in the Follow-up
Turkish Journal of Pediatric Disease·2024Open Access
Newborn Screening for Biotinidase Deficiency
2024· 6 cited
Screening Tests Performed in the Newborn Period in Our Country for Congenital Endocrine and Metabolic Diseases: Definition and Their Importance
2024
Long-term clinical evaluation of patients with alpha-mannosidosis – A multicenter study
European Journal of Medical Genetics·2024· 4 citedOpen Access
Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in <i>GRN</i> gene: case report and review of literature
Journal of Pediatric Endocrinology and Metabolism·2024· 6 cited
Risk Factors for Lower Respiratory Tract Infection and Recurrent Lower Respiratory Tract Infection in Children
Van Medical Journal·2024· 1 citedOpen Access
Concurrent medulloblastoma and Chiari Type-I deformity in a pediatric case
Çukurova medical journal (Online)/Çukurova medical journal·2023Open Access
A different approach to the evaluation of the genotype-phenotype relationship in biotinidase deficiency: repeated measurement of biotinidase enzyme activity
Journal of Pediatric Endocrinology and Metabolism·2023· 7 cited
Vitamin B12 Level in Children
Güncel Pediatri·2023· 5 citedOpen Access
A Different Approach to the Evaluation of the Genotype-Phenotype Relationship in Biotinidase Deficiency: Repeated Measurement of Biotinidase Enzyme Activity
Research Square (Research Square)·2023Open Access
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Frequent Co-authors

Engi̇n Köse(11), Fatma Tuba Eminoğlu(11), Necla Aydın Peker(9), Yusuf Kemal Arslan(7), Merve Koç Yekedüz(6), Cuma Mertoğlu(6), Zerrin Orbak(5), Gamze Gök(3), Özcan Erel(3), İsmail Topal(3), Neslihan Doğulu(2), Ümmühan Öncül(2), Şeyma Karatekin(2), İsmail Topal(2), Gülsah Siranli(2), İlke Dolğun(2), Ahmet Cevdet Ceylan(2), Aslı İnci(2), Leyla Tümer(2), ENGİN KÖSE(2)