Ara
Toplam kayıt 35, listelenen: 31-35
Characterization of the apelin-1860T>C polymorphism in Turkish coronary artery disease patients and healthy individuals
(E-Century Publishing Corporation, 2015)
To evaluate the association between the apelin -1860T>C polymorphism and plasma apelin levels in Turkish patients with coronary artery disease (CAD). A total of 276 individuals were enrolled in the present study, including ...
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
(Nature Publishing Group, 2016)
Purpose:Noonan syndrome (NS) is an autosomal-dominant disorder characterized by craniofacial dysmorphism, growth retardation, cardiac abnormalities, and learning difficulties. It belongs to the RASopathies, which are caused ...
Abdominal aorta and its branches: Morphometry - Variations in autopsy cases
(TIP ARASTIRMALARI DERNEGI, 2010)
Aim: Knowing the morphology of abdominal aorta (AA) and its branches are important as regards to diagnosis and surgical treatment. The aims of this study were to a) make morphometric measurements of AA and its branches, ...
Complex variation of median nerve: A case report
(2013)
During routine dissections we saw complex variation of median nerve in the right arm of an adult male cadaver. Lateral cord continued as lateral root of median nerve without giving off musculocutaneous nerve and it formed ...
Sialolipoma of the parotid gland: Case report
(Turkiye Klinikleri, 2017)
Sialolipoma which is composed of adipocyte cells and glandular tissue is a rare salivary gland tumor. Sialolipomas can be found in the major and minor salivary glands but most commonly in the parotid gland. Sixty year old ...