Search Results - "Nilüfer Özdemir Kutbay"

Determining residual adipose tissue characteristics with MRI in patients with various subtypes of lipodystrophy by Altay, Canan, Seçil, Mustafa, Demir, Tevfik, Atik, Tahir, Akıncı, Gülçin, Özdemir Kutbay, Nilüfer, Keskin Temeloğlu, Ela, Yıldırım Şimşir, Ilgın, Özışık, Seçil, Demir, Leyla, Eren, Erdal, Tuna, Emine Burçin, Aytaç, Hasibe, Onay, Hüseyin, Akıncı, Barış

“…We aimed to investigate residual adipose tissue with whole-body magnetic resonance imaging to differentiate between subtypes of lipodystrophy. A total of 32…”
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Magnetic resonance spectroscopy to assess hepatic steatosis in patients with lipodystrophy by Altay, Canan, Secil, Mustafa, Adiyaman, Suleyman Cem, Saydam, Basak Ozgen, Demir, Tevfik, Akinci, Gulcin, Simsir, Ilgin Yildirim, Eren, Erdal, Keskin, Ela Temeloglu, Demir, Leyla, Onay, Huseyin, Topaloglu, Haluk, Yurekli, Banu Sarer, Kutbay, Nilufer Ozdemir, Gen, Ramazan, Akinci, Baris

“…Background/Aims: Lipodystrophy is a rare metabolic disorder characterized by a near-total or partial lack of subcutaneous adipose tissue and is associated with…”
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A Case of Thyroid Hemiagenesis: An Exceptional Case by Banu Pinar ŞARER YÜREKLİ, KUTBAY, Nilüfer ÖZDEMİR, ERDOĞAN, Mehmet, Özer MAKAY, İÇÖZ, Recep Gökhan, ÖZGEN, Gökhan

“…Thyroid hemiagenesis is a rare congenital anomaly in which one thyroid lobe fails to develop. We recently observed a case of thyroid hemiagenesis accompanied…”
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Two Siblings with Triple-A Syndrome: Endocrinologic and Neurologic Features by ÖZDEMİR KUTBAY, Nilüfer, KEKLİK, Fatma, SARER YÜREKLİ, Banu, KAVASOĞLU, Gökçe, ORUÇ, Nevin, ERDOĞAN, Mehmet, ÇETİNKALP, Şevki, ÖZGEN, Gökhan, SAYGILI, Füsun

“…Triple-A syndrome is a rare, multi-systemic disease and is characterized by adrenal insufficiency, achalasia, or alacrima. The symptoms may also involve…”
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Could Retroperitoneal Ganglioneuroma be a Dopamine Secreting Ganglioneuroma? by ÖZIŞIK, Hatice, YÜREKLİ, Banu Sarer, ÖZDEMİR KUTLAY, Nilüfer, EKER, Barış, ERTAN, Yeşim, SAYGILI, Füsun

“…Ganglioneuromas are rarely occurring benign tumors characterized by hyperplasia of mature ganglia and satellite cells. They are well-differentiated, slow…”
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Preoperative and Postoperative (1st and 3rd Month) Metabolic Data of Patients Who Underwent Bariatric Surgery by Kutbay, Nilüfer Özdemir, Yürekli, Banu Sarer, Özisik, Hatice, Altun, Ilker, Suner, Asli, Simsir, Ilgin Yildirim, Firat, Özgür, Erdogan, Mehmet, Çetinkalp, Sevki, Özgen, Gökhan, Saygili, Füsun

“…Purpose: The growing prevalence of obesity has become a major concern. The efficacy of medical treatment, diet and behavior therapy in morbidly obese patients…”
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Effects of metformin and pioglitazone combination on apoptosis and AMPK/mTOR signaling pathway in human anaplastic thyroid cancer cells by Ozdemir Kutbay, Nilufer, Biray Avci, Cigir, Sarer Yurekli, Banu, Caliskan Kurt, Cansu, Shademan, Behrouz, Gunduz, Cumhur, Erdogan, Mehmet

“…Anaplastic cancer constitutes 1% of thyroid cancers, and it is one of the most aggressive cancers. Treatment options are external radiation therapy and/or…”
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Cardiac phenotype in familial partial lipodystrophy by Eldin, Abdelwahab Jalal, Akinci, Baris, Rocha, Andre Monteiro, Meral, Rasimcan, Simsir, Ilgin Yildirim, Adiyaman, Suleyman Cem, Ozpelit, Ebru, Bhave, Nicole, Gen, Ramazan, Yurekli, Banu, Ozdemir Kutbay, Nilufer, Siklar, Zeynep, Neidert, Adam H., Hench, Rita, Tayeh, Marwan K., Innis, Jeffrey W., Jalife, Jose, Oral, Hakan, Oral, Elif A.

“…Objectives LMNA variants have been previously associated with cardiac abnormalities independent of lipodystrophy. We aimed to assess cardiac impact of familial…”
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Renal complications of lipodystrophy: A closer look at the natural history of kidney disease by Akinci, Baris, Unlu, Sadiye Mehtat, Celik, Ali, Simsir, Ilgin Yildirim, Sen, Sait, Nur, Banu, Keskin, Fatma Ela, Ozgen Saydam, Basak, Kutbay Ozdemir, Nilufer, Sarer Yurekli, Banu, Ergur, Bekir Ugur, Sonmez, Melda, Atik, Tahir, Arslan, Atakan, Demir, Tevfik, Altay, Canan, Tunc, Ulku Aybuke, Arkan, Tugba, Gen, Ramazan, Eren, Erdal, Akinci, Gulcin, Yilmaz, Aslihan Arasli, Bilen, Habib, Ozen, Samim, Celtik, Aygul, Savas Erdeve, Senay, Cetinkaya, Semra, Onay, Huseyin, Sarioglu, Sulen, Oral, Elif Arioglu

“…Summary Objectives Lipodystrophy syndromes are a group of heterogeneous disorders characterized by adipose tissue loss. Proteinuria is a remarkable finding in…”
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Osteogenesis Imperfecta: Case Report by Nilüfer Özdemir Kutbay, Yürekli, Banu Şarer, Özışık, Hatice, Diri, Halit

“…Osteogenesis imperfecta is a genetic disorder characterized by osteoporosis, recurrent bone fractures and, consequently, deformities. In many cases, it is…”
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Dopamine Agonist-Induced Impulse Control Disorders in Patients With Prolactinoma: A Cross-Sectional Multicenter Study by Dogansen, Sema Ciftci, Cikrikcili, Ugur, Oruk, Gonca, Kutbay, Nilufer Ozdemir, Tanrikulu, Seher, Hekimsoy, Zeliha, Hadzalic, Aysa, Gorar, Suheyla, Omma, Tulay, Mert, Meral, Akbaba, Gulhan, Yalin, Gulsah Yenidunya, Bayram, Fahri, Ozkan, Mine, Yarman, Sema

“…Abstract Context Dopamine agonist (DA)-induced impulse control disorder (ICD) in patients with prolactinomas is not sufficiently known. Objective To evaluate…”
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Characteristics and Treatment Results of 5 Patients with Fibrous Dysplasia and Review of the Literature by Sahin, Serap Baydur, Kartal Baykan, Emine, Sarer Yurekli, Banu, Ozdemir Kutbay, Nilufer, Saygili, Fusun

“…Aim. Fibrous dysplasia is a rare bone disease caused by missense mutation leading to abnormal fibroblast and osteoblast proliferation and increased bone…”
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A Case of MEN 2A: D631Y Mutation by Yürekli, Banu Şarer, Özışık, Hatice, Nilüfer Özdemir Kutbay, Onay, Hüseyin, Özgen, Gökhan

“…Multiple endocrine neoplasia 2A (MEN 2A) is a hereditary disease comprising medullary thyroid carcinoma (MTC) (95%), pheochromocytoma (50%), parathyroid…”
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Two Cases of Klinefelter Syndrome by Özışık, Hatice, Yürekli, Banu Şarer, Nilüfer Özdemir Kutbay, Onay, Hüseyin, Erdoğan, Mehmet, Çetinkalp, Şevki, Özgen, Gökhan, Saygılı, Füsun

“…Klinefelter syndrome is the most commonly seen sex chromosomal disorder in males. The typical clinical features of this syndrome are symptoms of hypogonadism…”
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A Distinct Clinical Phenotype in Two Siblings with X-linked Adrenoleukodystrophy by Ozdemir Kutbay, Nilufer, Ozbek, Mehmet Nuri, Sarer Yurekli, Banu, Demirbilek, Huseyin

“…X-linked adrenoleukodystrophy(X-ALD) is a rare X-linked recessive metabolic disorder. The mutations in the ATP Binding Cassette Subfamily D Member 1 (ABCD1)…”
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A Case of Polyglandular Autoimmune Syndrome Type One with Hypercalcemia and Hypotension by Kutbay, Nilüfer Özdemir, Yürekli, Banu Sarer, Yaman, Miray, Erdogan, Mehmet, Çetinkalp, Sevki, Saygili, L Füsun, Darcan, Sükran, Özgen, A Gökhan

“…Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is also known as autoimmune polyendocrine syndrome type 1 (APS-1). We present a case of…”
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A Young Diabetic Case with Bloom Syndrome by Kutbay, Nilüfer Özdemir, Yürekli, Banu Sarer, Erdogan, Mehmet, Çetinkalp, Sevki, Çogulu, Özgür, Özgen, A Gökhan, Saygili, L Füsun

“…Bloom syndrome (BS) is a rare autosomal recessive disorder characterized by short stature, telangiectasias, and a rash on the face triggered by the sun. Other…”
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Identifying Clinical Characteristics of Hypoparathyroidism in Turkey: HIPOPARATURK-NET Study by Konca Degertekin, Ceyla, Gogas Yavuz, Dilek, Pekkolay, Zafer, Saygili, Emre, Ugur, Kader, Or Koca, Arzu, Unubol, Mustafa, Topaloglu, Omercan, Aydogan, Berna Imge, Ozdemir Kutbay, Nilufer, Hekimsoy, Zeliha, Yilmaz, Nusret, Balci, Mustafa Kemal, Tanrikulu, Seher, Aydogan Unsal, Yasemin, Ersoy, Canan, Omma, Tulay, Keskin, Muge, Yalcin, Mehmet Muhittin, Yetkin, Ilhan, Soylu, Hikmet, Karakose, Melia, Yilmaz, Merve, Karakilic, Ersen, Piskinpasa, Hamide, Batman, Adnan, Akbaba, Gulhan, Elbuken, Gulsah, Tura Bahadir, Cigdem, Kilinc, Faruk, Bilginer, Muhammet Cuneyt, Turhan Iyidir, Ozlem, Canturk, Zeynep, Aktas Yilmaz, Banu, Sayiner, Zeynel Abidin, Eroglu, Mustafa

“…Hypoparathyroidism is an orphan disease with ill-defined epidemiology that is subject to geographic variability. We conducted this study to assess the…”
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Features of Nine Adult Cases of Osteogenesis Imperfecta by Kutbay, Nilüfer Özdemir, Yürekli, Banu Sarer, Keklik, Fatma, Altun, Ilker, Erdogan, Mehmet, Çetinkalp, Sevki, Özgen, A Gökhan, Göksen, Damla, Saygili, L Füsun

“…Introduction: Osteogenesis imperfecta (OI) is a congenital bone disorder characterized by common osteoporosis, recurrent fractures and deformities. Most cases…”
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Olfactory Sulcus Hypoplasia Images in a Case of Kallmann Syndrome by Yürekli, Banu Sarer, Kutbay, Nilüfer Özdemir, Karaca, Emin, Erdogan, Mehmet, Çetinkalp, Sevki, Kitis, Ömer, Özgen, A Gökhan, Özkinay, Ferda, Saygili, L Füsun

“…Introduction: Kallmann syndrome is a form of hypogonadotropic hypogonadism accompanied by anosmia or hyposmia. It is transmitted genetically in autosomal…”
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