Arzu M. Demir
Ankara, Turkey
Last Updated: 09/26/2026
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Found 24 publications
Ultra-short celiac disease in children: histological and autoimmune features.
Journal: European journal of pediatrics
Published: September 21, 2025
Thoracic Duct Embolization in a Case of Congenital Chylothorax.
Journal: Pediatric pulmonology
Published: June 27, 2025
Early Pulmonary Complications After Paediatric Liver Transplantation: A Single Center Experience.
Journal: Pediatric pulmonology
Published: June 18, 2025
Wolcott-Rallison syndrome: late-onset diabetes, multiple epiphyseal dysplasia, and acute liver failure - a case report.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: March 02, 2025
Congenital enteropathy caused by ezrin deficiency.
Journal: Human genetics
Published: November 11, 2024
Altered chaperone-nonmuscle myosin II interactions drive pathogenicity of the UNC45A c.710T>C variant in osteo-oto-hepato-enteric syndrome.
Journal: JCI insight
Published: July 31, 2024
A rare and challenging pediatric case of drug toxicity and immune reconstitution inflammatory syndrome during the treatment of intracranial tuberculoma: A case report.
Journal: Experimental and therapeutic medicine
Published: July 25, 2024
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
Celiac crisis with thrombocytopenia and coagulopathy in a child.
Journal: The Turkish journal of pediatrics
Published: December 30, 2022
Pediatric dysphagia overview: best practice recommendation study by multidisciplinary experts.
Journal: World journal of pediatrics : WJP
Published: April 12, 2022
Cancer and constitutional Mismatch Repair Deficiency syndrome due to homozygous MSH 6 mutation in children with Café au Lait Spots and review of literature.
Journal: The Turkish journal of pediatrics
Published: November 05, 2021
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
Journal: The Journal of clinical investigation
Published: September 15, 2021
Last Updated: 09/26/2026