Search Results - "Karakilic, E."

PP-032 A RARE CAUSE OF HEMATURIA IN AN IMMUNOSUPPRESSED PATIENT: BK VIRUS NEPHROPATHY by Karakilic, E, Karaman, S, Uysalol, E, Aydogdu, S, Karakas, Z, Unuvar, A, Devecioglu, O, Anak, S

Get full text

The importance of some angiogenic markers in spontaneous abortion by Ozturk, N, Gozukara, I, Kamalak, Z, Gul, M A, Bayraktutan, Z, Baygutalp, N K, Kiziltunc, A, Bakan, E, Karakilic E U

“…In this study, the authors aimed to determine the serum levels of vascular endothelial growth factor (VEGF), angiopoietin-l (ang-1) and angiopoietin-2 (ang-2)…”
Get full text

Assessment of traumatic deaths in a level one trauma center in Ankara, Turkey by Arslan, E. D., Kaya, E., Sonmez, M., Kavalci, C., Solakoglu, A., Yilmaz, F., Durdu, T., Karakilic, E.

“…Trauma management shows significant progress in last decades. Determining the time and place of deaths indicate where to focus to improve our knowledge about…”
Get full text

Effect of heparin on neuroprotection against spinal cord ischemia and reperfusion in rats by Korkmaz, K, Gedik, H S, Budak, A B, Erdem, H, Lafci, G, Karakilic, E, Nacar, O A, Yildirim, L, Ankarali, H

“…Paraplegia due to ischemia/reperfusion (I/R) injury of the spinal cord is a devastating and undesired complication of thoraco-abdominal aortic surgery…”
Get more information

Rethinking intellectual property rights in the cognitive and digital age of capitalism: An autonomist Marxist reading by Karakilic, Emrah

“…The transition from industrial capitalism to cognitive capitalism and the rise of the digital revolution have brought the subject of intellectual property…”
Get full text

Novel variants ensued genomic imprinting in familial central precocious puberty by Karaman, V., Karakilic-Ozturan, E., Poyrazoglu, S., Gelmez, M. Y., Bas, F., Darendeliler, F., Uyguner, Z. O.

“…Introduction Central precocious puberty (CPP) is characterized by the early onset of puberty and is associated with the critical processes involved in the…”
Get full text

Diagnostic Value of Ischemia-Modified Albumin as a Biomarker in Patients with Peripheral Vertigo at Emergency Department of State Hospital in Ankara: A Cross-Sectional Study by Karakılıç, E, Çelikel, E, Uysal, P I, Topçuoğlu, C, Turhan, T, Özakın, E

“…In previous studies, it was shown that ischemia-modified albumin (IMA) is an early marker of ischemia and different pathologies. However, IMA level change is…”
Get full text

Is computed tomography necessary to determine liver injury in pediatric trauma patients with negative ultrasonography? by Kaya, U., Çavuş, U. Y., Karakılıç, M. E., Erdem, A. B., Aydın, K., Işık, B., Abacıoğlu, S., Büyükcam, F.

“…Purpose Abdominal trauma is the third most common cause of all trauma-related deaths in children. Liver injury is the second most common, but the most fatal…”
Get full text

Breast cancer with diabetes insipidus by Dogan, M, Karakilic, E, Oz, I I, Zorlu, F, Akbulut, H

“…Diabetes insipidus (DI) is a rare clinical condition, which is usually caused by neurohypophyseal or pituitary stalk infiltration in cancer patients. we…”
Get more information

SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS by Karakilic-Ozturan, E, Ozturk, A P, Oney, C, Kardelen Al, A D, Yildirim, Z Y, Balci, H I, Poyrazoglu, S, Bas, F, Darendeliler, F

“…Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a rare autosomal recessive disorder, which is characterized by renal phosphate wasting,…”
Get full text

Heart and Aorta Anomalies in Turner Syndrome and Relation with Karyotype by Kardelen Al, A D, Gencay, G, Bayramoglu, Z, Aliyev, B, Karakilic-Ozturan, E, Poyrazoglu, S, Nişli, K, Bas, F, Darendeliler, F

“…Turner Syndrome (TS) is associated with a high risk of cardiac anomalies and cardiovascular disease. We aimed to evaluate patients with TS (n=33) for cardiac…”
Get full text

Characterization of V804M-mutated RET proto-oncogene associated with familial medullary thyroid cancer, report of the largest Turkish family by Basaran, M. N., Tuna, M. M., Karakılıç, E., Doğan, B. A., İmga, N. N., Berker, D., Güler, S.

“…Purpose Analysis of the RET proto-oncogen is very important for diagnosis and prognosis of medullary thyroid cancer (MTC). Genotype–phenotype correlation is…”
Get full text

Same effect of sublingual and oral captopril in hypertensive crisis by Karakiliç, E, Büyükcam, F, Kocalar, G, Gedik, S, Atalar, E

“…Hypertensive crisis is a condition characterized by rapid and inappropriate symptomatic elevation of blood pressure (BP) that is commonly seen in Emergency…”
Get more information

Could Vital Signs Predict Carbon Monoxide Intoxication? by Aksu, NM, Akkaş, M, Çoşkun, F, Karakiliç, E, Günalp, M, Akküçük, H, Ataman, DK, Özcan, H, Özmen, MM

“…OBJECTIVE: This retrospective study examined the correlation between carboxyhaemoglobin (COHb) levels and vital signs in patients with carbon monoxide (CO)…”
Get full text

Underdiagnosis of anaphylaxis in the emergency department: misdiagnosed or miscoded? by Hocagil, H, Karakilic, E, Hocagil, C, Senlikci, H, Buyukcam, F

“…To distinguish allergic reactions and anaphylaxis, and to highlight the importance of anaphylaxis. Case series. Adult emergency department of the medical…”
Get full text

SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS by Karakilic-Ozturan, E., Ozturk, A.P., Oney, C., Kardelen Al, A.D., Yildirim, Z.Y., Balci, H.I., Poyrazoglu, S., Bas, F., Darendeliler, F.

Get full text

Occupational injury patterns of Turkey by Celik, Kaan, Yilmaz, Fevzi, Kavalci, Cemil, Ozlem, Miray, Demir, Ali, Durdu, Tamer, Sonmez, Bedriye Müge, Yilmaz, Muhittin Serkan, Karakilic, Muhammed Evvah, Arslan, Engin Deniz, Yel, Cihat

“…Each year, a significant number of people die or become handicapped due to preventable occupational accidents or occupational diseases. The aim of this study…”
Get full text

5-azacytidine treatment results in myelodysplastic syndrome by Bakanay, S. M., Karakiliç, E., Civriz-Bozdag, S., Arat, M., Ozcan, M., Gurman, G., Ilhan, O., Beksac, M., Konuk, N., Arslan, O.

“…Abstract only e18003 Background: Myelodysplastic syndrome (MDS) is a clonal disease of hematopoiesis characterized by dysplasia in one or more series…”
Get full text

SLC34A3 GENE MUTATION AS A RARE CAUSE OF HYPOPHOSPHATEMIA IN TWO SIBLINGS by Karakilic-Ozturan, E, Ozturk, A P, Oney, C, Kardelen Al, A D, Yildirim, Z Y, Balci, H I, Poyrazoglu, S, Bas, F, Darendeliler, F

“…ContextHereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a rare autosomal recessive disorder, which is characterized by renal phosphate…”
Get full text

Heart and Aorta Anomalies in Turner Syndrome and Relation with Karyotype by Kardelen Al, A D, Gencay, G, Bayramoglu, Z, Aliyev, B, Karakilic-Ozturan, E, Poyrazoglu, S, Nişli, K, Bas, F, Darendeliler, F

“…OBJECTIVESTurner Syndrome (TS) is associated with a high risk of cardiac anomalies and cardiovascular disease. We aimed to evaluate patients with TS (n=33) for…”
Get full text