Ara
Toplam kayıt 239, listelenen: 51-60
The use of sealants in modern thoracic surgery: A survey
(2009)
[No abstract available]
Treatment of type 3 arthrofibrosis following arthroscopic reconstruction of ACL and posterolateral corner injury with tibia plateau fracture in a professional dancer: A case report
(SAGE Publications Ltd, 2014)
Objectives: Arthrofibrosis is a serious complication following the reconstruction of anterior cruciate ligament (ACL) and posterolateral corner (PLC) injury. Loss of motion caused by arthrofibrosis can be disabling in young ...
No scientific support for linking dietary saturated fat to CHD
(2012)
[No abstract available]
Merkel cell carcinoma: Literature review
(Via Medica, 2017)
Merkel cell carcinoma (MCC) was given a such name after the German histopathologist Friedrich Merkel, who first in 1875, described the Merkel cells, as small round or oval basophilic cells located at the end of nerve axons ...
Hepatosplenomegaly and pernicious anaemia
(Journal of Clinical and Diagnostic Research, 2014)
[No abstract available]
Autoimmune Diseases Associated with Epilepsy
(KARE PUBL, 2016)
Involvement of the central nervous system (CNS) during the course of systemic autoimmune diseases is not rare. Connective tissue disorders such as systemic lupus erythematosus (SLE), rheumatoid arthritis, Behcet's disease; ...
The Role of Neuroprotection in Subarachnoid Haemorrhage
(AVES, 2018)
…
Evaluation of Plateletcrit and Platelet Distribution Width in Patients with Non-Alcoholic Fatty Liver Disease: A Retrospective Chart Review Study
(Int Scientific Information, Inc, 2019)
Background: Platelets are considered to be essential in proinflammatory environments, including atherosclerosis. the de- gree of platelet activation has been demonstrated to be correlated with plateletcrit and platelet ...
2020 Issue 3 at a Glance
(Turkish Ophthalmological Soc, 2020)
[No abstract available]
Urinary Findings and Biomarkers in Autosomal Dominant Polycystic Kidney Disease
(Aves, 2020)
Autosomal dominant polycystic kidney disease (ADPKD), characterized by the development of multiple cysts in the kidneys and other organs, is the most common hereditary renal disorder and the fourth leading cause of end-stage ...