Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Swapneel Mathurkar"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 04, Pp 01-03 (2024)
Marfan syndrome is an autosomal dominant hereditary connective tissue disease caused by mutations in the Fibrillin-1 gene located on chromosome 15q15-21. Fibrillin is a specific type of glycoprotein widely distributed throughout the body, contributin
Externí odkaz:
https://doaj.org/article/06845e5527e146b3ae5e1c50d4243ae2
Publikováno v:
Asian Journal of Medical Sciences, Vol 12, Iss 7, Pp 149-153 (2021)
Corona Virus Disease 2019 (COVID 19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), first identified in Wuhan city of China in December 2019. Since then, the disease has spread very rapidly which has led to the current pan
Externí odkaz:
https://doaj.org/article/0676b520384f4914ab832e35b20e10b4
Publikováno v:
Medical Science. 27:1-6
Publikováno v:
Cureus.
Aim This study aims to compare the ganglion cell complex changes in diabetic macular edema (DME) and central retinal vein occlusion (CRVO) macular edema using optical coherence tomography (OCT). Methods This was a hospital-based cross-sectional study
Autor:
Pallavi Yelne, Ruchita Kabra, Swapneel Mathurkar, Shilpa A Gaidhane, Sourya Acharya, Sunil Kumar
Publikováno v:
Cureus.
Publikováno v:
Journal of Evolution of Medical and Dental Sciences. 10:1382-1386
BACKGROUND Meibomian gland dysfunction (MGD) is one of the causes of evaporative dry eye disease. It is the terminal duct obstruction of the Meibomian gland and is associated with glandular secretion changes. These changes lead to decreased amount of
Publikováno v:
Journal of Datta Meghe Institute of Medical Sciences University. 15:696