Zobrazeno 1 - 10
of 375
pro vyhledávání: '"Saatçi U"'
Autor:
Agras, P.I., Baskin, E., Saatci, U., Colak, T., Cengiz, N., Kinik, S.T., Isiklar, I., Haberal, A., Mert, I., Haberal, M.
Publikováno v:
In Transplantation Proceedings 2005 37(7):3106-3108
Publikováno v:
In Transplantation Proceedings 2005 37(7):2915-2917
Publikováno v:
In Transplantation Proceedings 2002 34(6):2041-2043
Publikováno v:
Acta Paediatrica. 94:1055-1059
Aim: To evaluate left ventricular (LV) diastolic function in children with end-stage renal disease (ESRD) using conventional pulsed-Doppler echocardiography and Doppler tissue imaging (DTI), and to compare the findings with these two modalities. Meth
Publikováno v:
Acta Paediatrica. 94:1732-1737
Aim: To examine the relationship between inflammation criteria and body mass index in otherwise-healthy obese school-children and to evaluate the effect of obesity on renal functions. Methods: Sixty-five otherwise-healthy obese children (median age 1
Autor:
Mehmet Haberal, Saatçi U, Turan Colak, Pinar Isik Agras, Ayşegül Haberal, Nurcan Cengiz, Namik Ozbek, Hamdi Karakayali, Esra Baskin
Publikováno v:
Transplant Immunology. 15:241-245
Objectives Leptin, the Ob gene product, centrally regulates weight control. Transplant recipients are exposed to many factors affecting body mass. Leptin has been reported to activate the peripheral immune system. In this study, we evaluated serum le
Publikováno v:
Renal Failure. 26:393-397
Restless Legs Syndrome (RLS), a common problem increasing morbidity and mortality in hemodialysis (HD) patients, affects 20-30% of uremic patients. Our aim was to find the efficacy of gabapentin in the treatment of RLS in HD patients by comparing a l
Autor:
Akgün Hiçsönmez, A. Ebru Sakallioglu, Füsun Alehan, Saatçi U, Sibel Bayil Oguzkan, Pinar Isik Agras, Murat Derbent, Esra Baskin, Sukriye Ayter, I.Serdar Arda
Publikováno v:
Journal of Child Neurology. 18:68-72
Neurofibromatosis 1 is an autosomal dominant disorder. Noonan's syndrome is known to be associated with neurofibromatoses. Patients with neurofibromatosis are predisposed to developing malignant tumors. The relationship between the genetic changes in
Publikováno v:
Pediatric Nephrology. 16:623-626
Jeune syndrome is a rare autosomal recessive disease characterized by narrow thoracic cage and short-limbed dwarfism. Seventy percent of affected individuals die in early childhood from pulmonary hypoplasia and respiratory distress due to the small s
Publikováno v:
Transplantation Proceedings. 37:2915-2917
Cardiovascular disease is one of the most important causes of morbidity and mortality in children with end-stage renal failure. Chronic inflammation and malnutrition have been suggested to be risk factors for cardiovascular disease. However, to date,