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IEEE Applied Imagery Pattern Recognition Workshop : [Proceedings]. IEEE Applied Imagery Pattern Recognition Workshop
|
June 2, 2018
The National Library of Medicine Pill Image Recognition Challenge: An Initial Report
Ziv Yaniv, Jessica Faruque, Sally Howe, et al.
Heart Rhythm
|
May 31, 2025
The clinical and electrocardiographic phenotype of patients with genotype-negative long QT syndrome
Vanessa Karlinski Vizentin, Raquel Neves, Sahej Bains, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
February 1, 1986
Differences between basophils and mast cells: failure to detect Charcot-Leyden crystal protein (lysophospholipase) and eosinophil granule major basic protein in human mast cells
K M Leiferman, G J Gleich, G M Kephart, et al.
JACC. Clinical Electrophysiology
|
February 7, 2025
Incidence and Clinical Management of Supraventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
Brett C Austin, Gurukripa N Kowlgi, Raquel Almeida Lopes Neves, et al.
The Journal of Allergy and Clinical Immunology
|
January 27, 2020
Charcot-Leyden crystal protein/galectin-10 interacts with cationic ribonucleases and is required for eosinophil granulogenesis
Milica M Grozdanovic, Christine B Doyle, Li Liu, et al.
European Heart Journal
|
August 10, 2005
Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy
Meghan J Perkins, Sara L Van Driest, Erik G Ellsworth, et al.
Channels (Austin, Tex.)
|
July 10, 2018
Mexiletine rescues a mixed biophysical phenotype of the cardiac sodium channel arising from the SCN5A mutation, N406K, found in LQT3 patients
Rou-Mu Hu, David J Tester, Ryan Li, et al.
Journal of the American College of Cardiology
|
November 3, 2004
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
Sara L Van Driest, Vlad C Vasile, Steve R Ommen, et al.
Circulation. Arrhythmia and Electrophysiology
|
September 3, 2013
Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome
Bettina F Cuneo, Susan P Etheridge, Hitoshi Horigome, et al.
Cancer
|
December 15, 1996
Primary combined malignant melanoma and ductal carcinoma of the breast. A report of two cases
R F Padmore, J F Lara, D J Ackerman, et al.
Page
of 114
Search research articles
Search
Showing results (711-720 of 1,140) with videos related to
Sort By:
Page
of 114
IEEE Applied Imagery Pattern Recognition Workshop : [Proceedings]. IEEE Applied Imagery Pattern Recognition Workshop
|
June 2, 2018
The National Library of Medicine Pill Image Recognition Challenge: An Initial Report
Ziv Yaniv, Jessica Faruque, Sally Howe, et al.
Heart Rhythm
|
May 31, 2025
The clinical and electrocardiographic phenotype of patients with genotype-negative long QT syndrome
Vanessa Karlinski Vizentin, Raquel Neves, Sahej Bains, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
February 1, 1986
Differences between basophils and mast cells: failure to detect Charcot-Leyden crystal protein (lysophospholipase) and eosinophil granule major basic protein in human mast cells
K M Leiferman, G J Gleich, G M Kephart, et al.
JACC. Clinical Electrophysiology
|
February 7, 2025
Incidence and Clinical Management of Supraventricular Arrhythmias in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
Brett C Austin, Gurukripa N Kowlgi, Raquel Almeida Lopes Neves, et al.
The Journal of Allergy and Clinical Immunology
|
January 27, 2020
Charcot-Leyden crystal protein/galectin-10 interacts with cationic ribonucleases and is required for eosinophil granulogenesis
Milica M Grozdanovic, Christine B Doyle, Li Liu, et al.
European Heart Journal
|
August 10, 2005
Gene-specific modifying effects of pro-LVH polymorphisms involving the renin-angiotensin-aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy
Meghan J Perkins, Sara L Van Driest, Erik G Ellsworth, et al.
Channels (Austin, Tex.)
|
July 10, 2018
Mexiletine rescues a mixed biophysical phenotype of the cardiac sodium channel arising from the SCN5A mutation, N406K, found in LQT3 patients
Rou-Mu Hu, David J Tester, Ryan Li, et al.
Journal of the American College of Cardiology
|
November 3, 2004
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy
Sara L Van Driest, Vlad C Vasile, Steve R Ommen, et al.
Circulation. Arrhythmia and Electrophysiology
|
September 3, 2013
Arrhythmia phenotype during fetal life suggests long-QT syndrome genotype: risk stratification of perinatal long-QT syndrome
Bettina F Cuneo, Susan P Etheridge, Hitoshi Horigome, et al.
Cancer
|
December 15, 1996
Primary combined malignant melanoma and ductal carcinoma of the breast. A report of two cases
R F Padmore, J F Lara, D J Ackerman, et al.
Page
of 114