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Nutrients|October 16, 2024
Evaluation of Body Composition and Biochemical Parameters in Adult PhenylketonuriaMehmet Cihan Balci, Meryem Karaca, Dilek Gunes, et al.
Pediatric Research|September 23, 2025
Choline supplementation in classic homocystinuria: impact on homocysteine and hepatic steatosisSevde Kahraman, Asuman Gedikbasi, Meryem Karaca, et al.
JIMD Reports|March 9, 2016
Rapid Desensitization for Immediate Hypersensitivity to Galsulfase Therapy in Patients with MPS VIZeynep Tamay, Gulden Gokcay, Fatih Dilek, et al.
Healthcare (Basel, Switzerland)|October 25, 2024
Challenging Childhood Obesity: The Influence of Education and Close Monitoring on Obesity-Related BehaviorsEda Sunnetci Silistre, Alihan Yesil, Tugba Kozanoglu, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|November 4, 2022
Cardiologic evaluation of Turkish mitochondrial fatty acid oxidation disordersMehmet Cihan Balci, Meryem Karaca, Yakup Ergul, et al.
International Journal of Molecular Sciences|October 16, 2025
Evaluation of Serum FGF21 Levels in Patients with Mitochondrial Aminoacyl-tRNA Synthetase DeficiencySebnem Tekin Neijmann, Dilek Gunes, Meryem Karaca, et al.
Molecular Genetics and Metabolism Reports|December 13, 2023
A different perspective into clinical symptoms in CPT I deficiencyMehmet Cihan Balci, Meryem Karaca, Arzu Selamioglu, et al.
Scientific Reports|November 20, 2024
Oxidative damage and mitochondrial dysfunction in cystathionine beta-synthase deficiencyMehmet Cihan Balci, Asuman Gedikbasi, Sukru Anil Dogan, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 5, 2023
Evaluation of the risk factors for noncommunicable diseases in patients with inborn errors of amino acid metabolism receiving nutrition therapyMehmet Cihan Balci, Meryem Karaca, Alihan Yesil, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 28, 2023
Reanalysis of exome sequencing data reveals a treatable neurometabolic origin in two previously undiagnosed siblings with neurodevelopmental disorderSeda Susgun, Yesim Kesim, Dovlat Khalilov, et al.
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