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The Journal of the Association of Physicians of India
|
September 1, 1991
Efficacy and safety of 1-2, dimethyl-3-hydroxypyrid-4-one (L1) as an oral iron chelator in patients of beta thalassaemia major with iron overload
M B Agarwal, S S Gupte, D Vasandani, et al.
Iscience
|
February 21, 2025
The hypertrophic cardiomyopathy-associated A331P actin variant enhances basal contractile activity and elicits resting muscle dysfunction
Matthew H Doran, Michael J Rynkiewicz, Evan Despond, et al.
Elife
|
August 14, 2018
Prolonged cross-bridge binding triggers muscle dysfunction in a <i>Drosophila</i> model of myosin-based hypertrophic cardiomyopathy
William A Kronert, Kaylyn M Bell, Meera C Viswanathan, et al.
JAMA Ophthalmology
|
December 30, 2017
Comparison of Quality and Output of Different Optimal Perimetric Testing Approaches in Children With Glaucoma
Dipesh E Patel, Phillippa M Cumberland, Bronwen C Walters, et al.
Circulation Research
|
November 15, 2005
Oxidative mediated lipid peroxidation recapitulates proarrhythmic effects on cardiac sodium channels
Koji Fukuda, Sean S Davies, Tadashi Nakajima, et al.
Cardiovascular Research
|
March 10, 2016
Profilin modulates sarcomeric organization and mediates cardiomyocyte hypertrophy
Viola Kooij, Meera C Viswanathan, Dong I Lee, et al.
Nature
|
March 10, 2001
A sodium-channel mutation causes isolated cardiac conduction disease
H L Tan, M T Bink-Boelkens, C R Bezzina, et al.
Investigative Ophthalmology & Visual Science
|
April 20, 2013
Copy number variation at chromosome 5q21.2 is associated with intraocular pressure
Abhishek Nag, Cristina Venturini, Pirro G Hysi, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
September 29, 2000
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome
E Ficker, D Thomas, P C Viswanathan, et al.
Circulation
|
May 9, 2002
Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes
Ping Yang, Hideaki Kanki, Benoit Drolet, et al.
Page
of 15
Search research articles
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Showing results (101-110 of 142) with videos related to
Sort By:
Page
of 15
The Journal of the Association of Physicians of India
|
September 1, 1991
Efficacy and safety of 1-2, dimethyl-3-hydroxypyrid-4-one (L1) as an oral iron chelator in patients of beta thalassaemia major with iron overload
M B Agarwal, S S Gupte, D Vasandani, et al.
Iscience
|
February 21, 2025
The hypertrophic cardiomyopathy-associated A331P actin variant enhances basal contractile activity and elicits resting muscle dysfunction
Matthew H Doran, Michael J Rynkiewicz, Evan Despond, et al.
Elife
|
August 14, 2018
Prolonged cross-bridge binding triggers muscle dysfunction in a <i>Drosophila</i> model of myosin-based hypertrophic cardiomyopathy
William A Kronert, Kaylyn M Bell, Meera C Viswanathan, et al.
JAMA Ophthalmology
|
December 30, 2017
Comparison of Quality and Output of Different Optimal Perimetric Testing Approaches in Children With Glaucoma
Dipesh E Patel, Phillippa M Cumberland, Bronwen C Walters, et al.
Circulation Research
|
November 15, 2005
Oxidative mediated lipid peroxidation recapitulates proarrhythmic effects on cardiac sodium channels
Koji Fukuda, Sean S Davies, Tadashi Nakajima, et al.
Cardiovascular Research
|
March 10, 2016
Profilin modulates sarcomeric organization and mediates cardiomyocyte hypertrophy
Viola Kooij, Meera C Viswanathan, Dong I Lee, et al.
Nature
|
March 10, 2001
A sodium-channel mutation causes isolated cardiac conduction disease
H L Tan, M T Bink-Boelkens, C R Bezzina, et al.
Investigative Ophthalmology & Visual Science
|
April 20, 2013
Copy number variation at chromosome 5q21.2 is associated with intraocular pressure
Abhishek Nag, Cristina Venturini, Pirro G Hysi, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
September 29, 2000
Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome
E Ficker, D Thomas, P C Viswanathan, et al.
Circulation
|
May 9, 2002
Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes
Ping Yang, Hideaki Kanki, Benoit Drolet, et al.
Page
of 15