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Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia.
Hacıhamdioğlu B, Özgürhan G, Çaran B, Meydan-Aksanlı E, Keskin E. Hacıhamdioğlu B, et al. Among authors: keskin e. Turk J Pediatr. 2018;60(5):581-583. doi: 10.24953/turkjped.2018.05.018. Turk J Pediatr. 2018. PMID: 30968641 Free article.
Hacihamdioglu B, Ozgurhan G, Caran B, Meydan-Aksanli E, Keskin E. Glycogen storage disease type 0 due to a novel frameshift mutation in glycogen synthase 2 (GYS2) gene in a child presenting with fasting hypoglycemia and postprandial hyperglycemia. ...
Hacihamdioglu B, Ozgurhan G, Caran B, Meydan-Aksanli E, Keskin E. Glycogen storage disease type 0 due to a novel frames …
Is there a comparable Mp-MRI for incidental prostate uptake on 18 F-FDG PET/CT?
Şam Özdemir M, Kaya N, Savun M, Keskin ET, Yüzkan S, Arslan FZ, Budak B, Omak Ö, Yardımcı AH, Özdemir H. Şam Özdemir M, et al. Among authors: keskin et. World J Surg Oncol. 2024 Dec 20;22(1):339. doi: 10.1186/s12957-024-03578-0. World J Surg Oncol. 2024. PMID: 39707383 Free PMC article.
233 results