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Cardiovascular Digital Health Journal
|
January 2, 2023
Tandem deep learning and logistic regression models to optimize hypertrophic cardiomyopathy detection in routine clinical practice
Maren Maanja, Peter A Noseworthy, Jeffrey B Geske, et al.
Protein Science : a Publication of the Protein Society
|
May 10, 2001
Identification of intrinsic order and disorder in the DNA repair protein XPA
L M Iakoucheva, A L Kimzey, C D Masselon, et al.
Circulation
|
January 28, 2021
Suppression-Replacement <i>KCNQ1</i> Gene Therapy for Type 1 Long QT Syndrome
Steven M Dotzler, C S John Kim, William A C Gendron, et al.
Transfusion
|
July 21, 1999
Clinical consequences of alterations in platelet transfusion dose: a prospective, randomized, double-blind trial
T R Klumpp, J H Herman, J P Gaughan, et al.
European Heart Journal
|
May 8, 2007
Surgical septal myectomy decreases the risk for appropriate implantable cardioverter defibrillator discharge in obstructive hypertrophic cardiomyopathy
Christopher J McLeod, Steve R Ommen, Michael J Ackerman, et al.
The Journal of Pediatrics
|
August 10, 2016
Clinical Presentation of Pediatric Patients at Risk for Sudden Cardiac Arrest
Aarti Dalal, Richard J Czosek, Joshua Kovach, et al.
Journal of Cardiovascular Electrophysiology
|
May 10, 2024
Utilizing median and maximum QTc values improves prediction of breakthrough cardiac events in pediatric long QT syndrome
Ram K Rohatgi, Andrew S Tseng, Alan M Sugrue, et al.
Circulation. Genomic and Precision Medicine
|
July 21, 2022
Acacetin, a Potent Transient Outward Current Blocker, May Be a Novel Therapeutic for <i>KCND3</i>-Encoded Kv4.3 Gain-of-Function-Associated J-Wave Syndromes
Dan Ye, Wei Zhou, Samantha K Hamrick, et al.
Neurogastroenterology and Motility
|
October 3, 2002
SCN5A is expressed in human jejunal circular smooth muscle cells
Y Ou, S J Gibbons, S M Miller, et al.
Circulation. Genomic and Precision Medicine
|
March 14, 2020
Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population
Daniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
Page
of 114
Search research articles
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Showing results (811-820 of 1,140) with videos related to
Sort By:
Page
of 114
Cardiovascular Digital Health Journal
|
January 2, 2023
Tandem deep learning and logistic regression models to optimize hypertrophic cardiomyopathy detection in routine clinical practice
Maren Maanja, Peter A Noseworthy, Jeffrey B Geske, et al.
Protein Science : a Publication of the Protein Society
|
May 10, 2001
Identification of intrinsic order and disorder in the DNA repair protein XPA
L M Iakoucheva, A L Kimzey, C D Masselon, et al.
Circulation
|
January 28, 2021
Suppression-Replacement <i>KCNQ1</i> Gene Therapy for Type 1 Long QT Syndrome
Steven M Dotzler, C S John Kim, William A C Gendron, et al.
Transfusion
|
July 21, 1999
Clinical consequences of alterations in platelet transfusion dose: a prospective, randomized, double-blind trial
T R Klumpp, J H Herman, J P Gaughan, et al.
European Heart Journal
|
May 8, 2007
Surgical septal myectomy decreases the risk for appropriate implantable cardioverter defibrillator discharge in obstructive hypertrophic cardiomyopathy
Christopher J McLeod, Steve R Ommen, Michael J Ackerman, et al.
The Journal of Pediatrics
|
August 10, 2016
Clinical Presentation of Pediatric Patients at Risk for Sudden Cardiac Arrest
Aarti Dalal, Richard J Czosek, Joshua Kovach, et al.
Journal of Cardiovascular Electrophysiology
|
May 10, 2024
Utilizing median and maximum QTc values improves prediction of breakthrough cardiac events in pediatric long QT syndrome
Ram K Rohatgi, Andrew S Tseng, Alan M Sugrue, et al.
Circulation. Genomic and Precision Medicine
|
July 21, 2022
Acacetin, a Potent Transient Outward Current Blocker, May Be a Novel Therapeutic for <i>KCND3</i>-Encoded Kv4.3 Gain-of-Function-Associated J-Wave Syndromes
Dan Ye, Wei Zhou, Samantha K Hamrick, et al.
Neurogastroenterology and Motility
|
October 3, 2002
SCN5A is expressed in human jejunal circular smooth muscle cells
Y Ou, S J Gibbons, S M Miller, et al.
Circulation. Genomic and Precision Medicine
|
March 14, 2020
Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population
Daniel J Clemens, Belinda Gray, Richard D Bagnall, et al.
Page
of 114