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Page 1
[Hennekam syndrome].
Erkan T, Kutlu T, Cullu F, Celik M, Demir T, Tüysüz B, Tümay GT. Erkan T, et al. Among authors: demir t. Arch Pediatr. 1998 Dec;5(12):1344-6. doi: 10.1016/s0929-693x(99)80054-2. Arch Pediatr. 1998. PMID: 9885742 French.
Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey.
Akinci B, Onay H, Demir T, Ozen S, Kayserili H, Akinci G, Nur B, Tuysuz B, Nuri Ozbek M, Gungor A, Yildirim Simsir I, Altay C, Demir L, Simsek E, Atmaca M, Topaloglu H, Bilen H, Atmaca H, Atik T, Cavdar U, Altunoglu U, Aslanger A, Mihci E, Secil M, Saygili F, Comlekci A, Garg A. Akinci B, et al. Among authors: demir t, demir l. J Clin Endocrinol Metab. 2016 Jul;101(7):2759-67. doi: 10.1210/jc.2016-1005. Epub 2016 May 4. J Clin Endocrinol Metab. 2016. PMID: 27144933 Free PMC article.
Partial lipodystrophy of the limbs in a diabetes clinic setting.
Demir T, Akinci B, Demir L, Altay C, Atik T, Cavdar U, Secil M, Comlekci A. Demir T, et al. Among authors: demir l. Prim Care Diabetes. 2016 Aug;10(4):293-9. doi: 10.1016/j.pcd.2015.12.006. Epub 2016 Jan 8. Prim Care Diabetes. 2016. PMID: 26776282
Clinical presentations, metabolic abnormalities and end-organ complications in patients with familial partial lipodystrophy.
Akinci B, Onay H, Demir T, Savas-Erdeve Ş, Gen R, Simsir IY, Keskin FE, Erturk MS, Uzum AK, Yaylali GF, Ozdemir NK, Atik T, Ozen S, Yurekli BS, Apaydin T, Altay C, Akinci G, Demir L, Comlekci A, Secil M, Oral EA. Akinci B, et al. Among authors: demir t, demir l. Metabolism. 2017 Jul;72:109-119. doi: 10.1016/j.metabol.2017.04.010. Epub 2017 Apr 27. Metabolism. 2017. PMID: 28641778
Renal complications of lipodystrophy: A closer look at the natural history of kidney disease.
Akinci B, Unlu SM, Celik A, Simsir IY, Sen S, Nur B, Keskin FE, Ozgen Saydam B, Kutbay Ozdemir N, Sarer Yurekli B, Ergur BU, Sonmez M, Atik T, Arslan A, Demir T, Altay C, Tunc UA, Arkan T, Gen R, Eren E, Akinci G, Yilmaz AA, Bilen H, Ozen S, Celtik A, Savas Erdeve S, Cetinkaya S, Onay H, Sarioglu S, Oral EA. Akinci B, et al. Among authors: demir t. Clin Endocrinol (Oxf). 2018 Jul;89(1):65-75. doi: 10.1111/cen.13732. Epub 2018 May 17. Clin Endocrinol (Oxf). 2018. PMID: 29722904 Free PMC article.
Magnetic resonance spectroscopy to assess hepatic steatosis in patients with lipodystrophy.
Altay C, Seçil M, Adıyaman SC, Özgen Saydam B, Demir T, Akıncı G, Simsir IY, Eren E, Temeloğlu Keskin E, Demir L, Onay H, Topaloğlu H, Sarer Yürekli B, Özdemir Kutbay N, Gen R, Akıncı B. Altay C, et al. Among authors: demir t, demir l. Turk J Gastroenterol. 2020 Aug;31(8):588-595. doi: 10.5152/tjg.2020.19114. Turk J Gastroenterol. 2020. PMID: 32915147 Free PMC article.
Familial partial lipodystrophy linked to a novel peroxisome proliferator activator receptor -γ (PPARG) mutation, H449L: a comparison of people with this mutation and those with classic codon 482 Lamin A/C (LMNA) mutations.
Demir T, Onay H, Savage DB, Temeloglu E, Uzum AK, Kadioglu P, Altay C, Ozen S, Demir L, Cavdar U, Akinci B. Demir T, et al. Among authors: demir l. Diabet Med. 2016 Oct;33(10):1445-50. doi: 10.1111/dme.13061. Epub 2016 Feb 5. Diabet Med. 2016. PMID: 26756202
470 results