Zobrazeno 81 - 90
of 202
pro vyhledávání: '"Ajay Bahl"'
Autor:
Prosenjit Ganguli, Sanjay Gambhir, Balram Airan, Hemant Madan, Jacob Jose, Shinjini Bhatnagar, Paul V George, Oomen K George, Rajat Datta, Aditi Pandit, Prashant Bharadwaj, Sujata Mohanty, Naveen Garg, Balram Bhargava, Mi Trial, Pravin K. Goel, Anish Bhatacharya, Sunil Thomas Chandy, Ajay Bahl, Vikram Mathews, Ritwik Sarkar, M J Jacob, Velu Nair, Kewal K. Talwar, Alka Sharma, Neelam Marwah, Chetan Patel, Soniya Nityanand, A. Srivastava, Sunil Sofat, A S Mondal
Publikováno v:
Indian Journal of Medical Research, Vol 142, Iss 2, Pp 165-174 (2015)
The Indian Journal of Medical Research
The Indian Journal of Medical Research
Background & objectives: Acute myocardial infarction (AMI) is characterized by irreparable and irreversible loss of cardiac myocytes. Despite major advances in the management of AMI, a large number of patients are left with reduced left ventricular e
Publikováno v:
Journal of Cardiology and Therapeutics. 2:115-120
Background : Few studies have focused on the prevalence of CAD in RHD. Coronary angiography should be routinely done in patients of valvular heart disease prior to surgery, especially in patients above 40 years of age. Overlooking CAD can lead to com
Autor:
Madhu Khullar, Anupam Mittal, Santanu Rana, Rajni Sharma, Vikas Arige, Sanskriti Khanna, Nitish Mahapatra, Sagartirtha Sarkar, Uma N Saikia, Ajay Bahl
Publikováno v:
Circulation Research. 121
Myocardin (MYOCD), a cardiac specific transcriptional co-activator is up-regulated in heart failure (HF). Up-regulation of MYOCD expression has been proposed to be an important adaptive response in cardiac remodelling. However, molecular mechanisms c
Publikováno v:
Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology. 37(2)
Organ failure (OF) is the most important predictor of outcome in severe acute pancreatitis (SAP). Cardiovascular failure (CVSF) occurs in a variable proportion of patients with SAP. We aimed to study myocardial dysfunction in acute pancreatitis (AP)
Autor:
Ajay Bahl, Gurjeet Kaur, Madhu Khullar, Amit Kumar, Rishikesh Prasad, Rajni Sharma, Bindu Rani
Publikováno v:
Molecular and cellular biochemistry. 438(1-2)
The marked clinical and genetic heterogeneity seen in hypertrophic (HCM) and dilated cardiomyopathies (DCM) suggests involvement of disease modifiers and environmental factors in the pathophysiology of these diseases. In the current study, we examine
Publikováno v:
Pancreas. 46(5)
Objective Persistent organ failure is a feature of severe acute pancreatitis (SAP) and the leading cause of death. Although usually defined by hypotension, cardiovascular dysfunction (CD) in early SAP has not been well characterized. We aim to charac
Publikováno v:
Journal of cardiothoracic and vascular anesthesia. 31(5)
Speckle tracking, when combined with 3-dimensional (3D) left ventricular ejection fraction, might prove to be a more sensitive marker for postoperative ventricular dysfunction. This study investigated early outcomes in a cohort of patients with left
Autor:
Nahid Akhtar Khan, Priyadharshini Selvaraj, Periyasamy Govindaraj, Calambur Narasimhan, Deepa Selvi Rani, Kumpati Premkumar, Bindu Rani, Kumarasamy Thangaraj, Vuskamalla Jyothi, Ajay Bahl, Dharma Rakshak, Madhu Khullar
Publikováno v:
Mitochondrion. 16:65-72
Hypertrophic cardiomyopathy (HCM) is a primary disorder, characterized by unexplained hypertrophy of the left ventricle that frequently involved in the inter-ventricular septum. Mitochondrial DNA (mtDNA) mutations and haplogroups have been found to b
Autor:
Perundurai S. Dhandapany, Periyasamy Govindaraj, Kumarasamy Thangaraj, Andiappan Rathinavel, Sherly Pardo, Ajay Bahl, Elisabetta Flex, Madhu Khullar, Sreejith Kunnoth, Jonathan J. Edwards, Djamel Lebeche, Giuseppe Limongelli, Bruce D. Gelb, Jeffrey Robbins, Sonia Mulero-Navarro, Rumiko Matsuoka, Ilan Riess, Michiko Furutani, Toshio Nakanishi, Tomohiro Yokota, Roger J. Hajjar, Jipo Sheng, Abdur Razzaque, Bindhu Rani, Deepa Selvi Rani, Kirsten C. Sadler, Tsutomu Nishizawa, Uthiralingam Muthusami, Marco Tartaglia
Publikováno v:
Nature Genetics. 46:635-639
Dilated cardiomyopathy (DCM) is a highly heterogeneous trait with sarcomeric gene mutations predominating. The cause of a substantial percentage of DCMs remains unknown, and no gene-specific therapy is available. On the basis of resequencing of 513 D
Publikováno v:
Journal of Clinical and Preventive Cardiology, Vol 8, Iss 3, Pp 131-135 (2019)
Background: Despite better understanding of various aspects of Sudden Cardiac Death (SCD), mortality from the disease still remains very high. Coronary artery disease (CAD) is the most common cause of SCD in all parts of India. The American College o