Ceyda Tuna-Kırsaclıoglu
Ankara, Turkey
Last Updated: 09/26/2026
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Found 26 publications
Challenge of diagnosing celiac disease in pediatric type 1 diabetes mellitus: lessons from long-term serological surveillance.
Journal: Postgraduate medicine
Published: June 13, 2026
Use of a specialized peptide-based enteral formula containing medium-chain triglycerides for enteral tube feeding in children with cerebral palsy and previous tube feeding intolerance on standard enteral formula: a prospective observational TolerUP study.
Journal: Frontiers in pediatrics
Published: June 13, 2024
A Rare Case of "Periportal Cuffing" as an Incidental Finding on 18F-FDG PET/CT.
Journal: Molecular imaging and radionuclide therapy
Published: October 23, 2023
Evaluation of Gastrointestinal System Complaints and Comorbidities in Pediatric Familial Mediterranean Fever Patients.
Journal: Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases
Published: September 19, 2023
The frequency of Duchenne muscular dystrophy/Becker muscular dystrophy and Pompe disease in children with isolated transaminase elevation: results from the observational VICTORIA study.
Journal: Frontiers in pediatrics
Published: August 03, 2023
Management of gastrointestinal and nutritional problems in children on home invasive mechanical ventilation.
Journal: Pediatric pulmonology
Published: August 01, 2023
Very-early-onset Inflammatory Bowel Disease in an Infant with a Partial RIPK1 Deletion.
Journal: Journal of clinical immunology
Published: June 23, 2023
Growth, tolerance and safety outcomes with use of an extensively hydrolyzed casein-based formula in infants with cow's milk protein allergy.
Journal: Frontiers in pediatrics
Published: May 29, 2023
Neonatal ichthyosis-sclerosing cholangitis syndrome: report of a novel mutation and a review of the literature.
Journal: Clinical dysmorphology
Published: February 13, 2023
Not all enteropathies are coeliac disease! Report of an infant with microvillus inclusion disease.
Journal: Gastroenterology and hepatology from bed to bench
Published: January 16, 2023
Coexistence of spinocerebellar ataxia autosomal recessive type 21 and Ehlers-Danlos syndrome spondylodysplastic type 3 in a patient.
Journal: Clinical dysmorphology
Published: December 12, 2022
A Rare Contiguous Gene Deletion Leading to Trichothiodystrophy Type 4 and Glutaric Aciduria Type 3.
Journal: Molecular syndromology
Published: February 18, 2022
Last Updated: 09/26/2026