Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Tamer Tetiker"'
Autor:
Fahri Bayram, Alper Sonmez, Cem Haymana, Tevfik Sabuncu, Oguzhan Sitki Dizdar, Eren Gurkan, Ayse Kargili Carlioglu, Kemal Agbaht, Didem Ozdemir, Ibrahim Demirci, Cem Barcin, Serpil Salman, Tamer Tetiker, Mustafa Kemal Balci, Nur Kebapci, Canan Ersoy, Volkan Yumuk, Peter P. Toth, Ilhan Satman, TEMD Study Group
Publikováno v:
Lipids in Health and Disease, Vol 19, Iss 1, Pp 1-11 (2020)
Abstract Background Attaining acceptable levels of LDL Cholesterol (LDL-C) significantly improves cardiovascular (CV) outcomes in patients with type 2 diabetes mellitus (T2DM). The LDL-C target attainment and the characteristics of patients attaining
Externí odkaz:
https://doaj.org/article/3bd78abe0da7469881d7892af599876c
Autor:
Gamze Akkuş, Isa Burak Güney, Fesih Ok, Mehtap Evran, Volkan Izol, Şeyda Erdoğan, Yıldırım Bayazıt, Murat Sert, Tamer Tetiker
Publikováno v:
Endocrine Connections, Vol 8, Iss 7, Pp 838-845 (2019)
Background: The management of adrenal incidentaloma is still a challenge with respect to determining its functionality (hormone secretion) and malignancy. In this light, we performed 18F-FDG PET/CT scan to assess the SUVmax values in different adrena
Externí odkaz:
https://doaj.org/article/48793e4efc974ca2a6d068c7969fb3f7
Autor:
Rıfat Emral, Tamer Tetiker, Ibrahim Sahin, Ramazan Sari, Ahmet Kaya, İlhan Yetkin, Sefika Uslu Cil, Neslihan Başcıl Tütüncü, on behalf of the IO HAT investigator group
Publikováno v:
BMC Endocrine Disorders, Vol 18, Iss 1, Pp 1-11 (2018)
Abstract Background Limited real-world data are currently available on hypoglycemia in diabetes patients. The International Operations Hypoglycemia Assessment Tool (IO HAT) study was designed to estimate hypoglycemia in insulin-treated type I (T1DM)
Externí odkaz:
https://doaj.org/article/a629e9cd9ded42deb1f450130452b54a
Publikováno v:
Cukurova Medical Journal, Vol 43, Iss 1, Pp 260-262 (2018)
Externí odkaz:
https://doaj.org/article/1285a163ba1646b18886d735521dbf51
Publikováno v:
Cukurova Medical Journal, Vol 41, Iss 2, Pp 363-369 (2016)
Adrenal incidentalomas are masses that are discovered by imaging tests performed for other reasons. Today, in line with the increased use of imaging methods as computerized tomography and magnetic resonance imaging, the prevalence of diagnosis of adr
Externí odkaz:
https://doaj.org/article/326de0c09d2e47aab3b1d075acf66dc9
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 40, Iss 4, Pp 836-840 (2015)
Bilateral Striopallidodentat Calcinosis also called Fahrs disease (FH); basal ganglia, thalamus, and cerebellar dentate nucleus is a disease characterized by symmetric calcifications in the cerebral white matter. Calcifications are often drawn attent
Externí odkaz:
https://doaj.org/article/ac86c578a158468786e9b20b463b038f
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 4, Pp 836-840 (2015)
Bilateral Striopallidodentat Kalsinozis olarak da isimlendirilen Fahr Hastalığı (FH); bazal ganglion, talamus, serebellar dentat nükleus ve serebral beyaz cevherde simetrik kalsifikasyonlar ile karakterize bir hastalıktır. Kalsifikasyonlar gene
Externí odkaz:
https://doaj.org/article/b73b4d6d8bc84d4b91d9b7650e659d6b
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 40, Iss 3, Pp 593-596 (2015)
Pheochromocytoma is a rare tumor in which seen an incidence of 1 per 100.000 in the general population. Pheochromocytoma is a catecholamine producing neuroendocrine tumor arising from adrenal medulla. A 46-year-old man experienced headache, sweating
Externí odkaz:
https://doaj.org/article/2dab0123aa4c45bb859ba001b8f17355
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 3, Pp 593-596 (2015)
Feokromasitoma 100.000 kişide bir görülebilen nadir tümörlerden birisidir. Genel olarak adrenal medulladan katekolamin salınımı ile karakterizedir. Kırk altı yaşında erkek hasta baş ağrısı, terleme, çarpıntı şikayeti ile kliniğim
Externí odkaz:
https://doaj.org/article/b4327f0723cf417b9137fd8b4cc9dce3
Publikováno v:
Case Reports in Medicine, Vol 2009 (2009)
We report the clinical course of two siblings with Werner's syndrome (WS) who were diagnosed and followed at our clinics for 12 years. Initial diagnosis of the first sibling (sister) was at age 20, the second (brother) at 16. At the initial diagnosis
Externí odkaz:
https://doaj.org/article/470f71d14cbd472aaf7fde27e8eb12ed