Konu "Sağlık Bilimleri" için Avesis listeleme
Toplam kayıt 505, listelenen: 1-20
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A case of Horner's syndrome after the surgical treatment of pulmonary hydatid cyst.
We report a case of right-sided iatrogenic Horner’s syndrome developed after surgical treatment for pulmonary hydatid cyst. This occurred in a 10 year old girl who had been diagnosed as having a ruptured lung hydatid cyst ... -
A genome screen for linkage disequilibrium in Turkish multiple sclerosis
(2003)A genome screen for linkage disequilibrium in Turkish multiple sclerosisM. Eraksoya,*,1, A. Hensiekb,1, M. Kurtuncua,b, G. Akman-Demira, M. Kılıncc,M. Gedizlioglud, B. Petek-Balcıe, O¨ . Anlarf, C. Kutlug, G. Saruhan-Dir ... -
A New Marker For Endothelial Function in Peritoneal Dialysis Patients: Apelin
(2013)Aim: The most important cause of death in end-stage renal disease is cardiovascular diseases (CVDs). Endothelial dysfunction (ED) is one of the most important steps in the pathogenesis of CVD. Apelin is a peptide recently ... -
A rare case of peritonitis: Streptococcus salivarius
(2015)Streptococcus salivarius is a Gram-positive bacteria that may cause infections like endocarditis and meningitis. However, it has not been reported as a causative agent of peritonitis in peritoneal dialysis patients. In ... -
A Rare Cause of Massive Gastrointestinal Bleeding: Henoch-Schönlein Purpura
Introduction: Henoch-Schonlein Purpura (HSP) is a vasculitis mediated by IgA immune complex. It is usually seen in children and young adults, but rarely in advanced age. Cases of gastrointestinal bleeding have been reported ... -
A rare urea cycle disorder in a neonate: N-acetylglutamate synthetase deficiency
(2020)Urea cycle disorders (UCD), are genetically inherited diseases that may have a poor outcome due to to profound hyperammonemia. We report the case of a baby girl diagnosed as N-acetylglutamate synthase (NAGS) deficiency. ... -
A whole genome screen for linkage in Turkish multiple sclerosis
(2003)A whole genome screen for linkage in Turkish multiple sclerosisM. Eraksoya,*,1, M. Kurtuncua,b,1, G. Akman-Demira, M. Kılıncc, M. Gedizlioglud, M. Mirzae,O¨. Anlarf, C. Kutlug, M. Demirkıranh, H.A. I˙drisoglua, A. Compstonb, ... -
Abruptio placentae after amnioreduction in twin to twin transfusion syndrome.
(2017)özeti ektedir