Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism Reports|September 14, 2020
Ethylmalonic encephalopathy: Clinical course and therapy response in an uncommon mild case with a severe ETHE1 mutationMelike Ersoy, Valeria Tiranti, Massimo Zeviani
Clinical Case Reports|August 8, 2017
A novel frameshift mutation of malonyl-CoA decarboxylase deficiency: clinical signs and therapy response of a late-diagnosed caseMelike Ersoy, Mehmet Bedir Akyol, Serdar Ceylaner, et al.
Journal of Clinical Research in Pediatric Endocrinology|August 8, 2024
Endocrine Disorders in Children with Primary Mitochondrial Diseases: Single Center ExperienceEsra Deniz Papatya Çakır, Melike Ersoy, Nihan Çakır Biçer, et al.
Wilderness & Environmental Medicine|August 21, 2023
Occupational Silica Exposure as a Potential Risk for Microscopic PolyangiitisAlper Alp, Melike Ersoy, İbrahim Meteoğlu, et al.
Pediatric Nephrology (Berlin, Germany)|March 21, 2018
Hemolytic uremic syndrome with dual caution in an infant: cobalamin C defect and complement dysregulation successfully treated with eculizumabUlkem Kocoglu Barlas, Hasan Serdar Kıhtır, Nilufer Goknar, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 17, 2025
Dual molecular genetic diagnosis with combined malonic and methylmalonic aciduria (CMAMMA): implications of coexisting genetic disorders on clinical presentationMelike Ersoy, Zehra Yavas Abali, Esra Deniz Papatya Cakir, et al.
Psychiatry and Clinical Psychopharmacology|December 4, 2024
Very Early-Onset Schizophrenia with Accompanying Obsessive-Compulsive Symptoms: A Case Report of a Female with 16p13.11 DuplicationKerim Kızıltan, Ebru Özbezen Kızıltan, Elif Yerlikaya Oral, et al.
Pageof 3