Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Saleha Noorain"'
Autor:
Saleha Noorain, A.C. Nagamani, K.S. Subramani, Santosh Jadhav, Ravinandan Gowda, Ashita Barthur, C.N. Manjunath
Publikováno v:
IHJ Cardiovascular Case Reports, Vol 6, Iss 2, Pp 100-103 (2022)
A 30-year-old lady with severe Rheumatic Mitral stenosis underwent PTMC. Despite a good result, echocardiogram on post-op day one showed a mobile mass attached to the mitral chordae causing diagnostic dilemma between a thrombus and damaged chordae, d
Externí odkaz:
https://doaj.org/article/b1eb9c48d98c4fa4b6186ec06bffdcf8
Autor:
Saleha Noorain
Publikováno v:
Lung India, Vol 33, Iss 1, Pp 53-57 (2016)
Background: Chronic obstructive pulmonary disease (COPD) is a major cause of mortality and morbidity. It is the fourth leading cause of death worldwide. Acute exacerbations of COPD are common and are associated with worsening lung function and mortal
Externí odkaz:
https://doaj.org/article/9e863714d35646c4b4581dc87d0c1311
Publikováno v:
The Journal of the Association of Physicians of India. 67(11)
Cerebral Hyperperfusion syndrome is a relatively rare event following carotid revascularization. It can occur after both carotid endarterectomy and carotid artery stenting. It is characterized by focal neurodeficit, seizures and headache in the absen
Autor:
Nagamani Alur Chikkabasavaiah, Varshit D. Hathi, Subramani K. Shankar Rao, Manjunath C. Nanjappa, Santosh Jadhav, Saleha Noorain, Ravinandan Gowda
Publikováno v:
International Journal of Advances in Medicine. 8:839
Familial hypercholesterolemia is a rare, monogenic, co-dominant, life-threatening disorder resulting from loss of function mutations in the genes responsible for synthesis of low-density lipoprotein receptors or apo-B genes or gain of function mutati