Search research articles
Contact Us
Filters
Showing results (41-50 of 54) with videos related to
Page
of 6
Sort By:
Pacing and Clinical Electrophysiology : PACE
|
January 31, 2002
Minimally invasive cardioverter defibrillator implantation for children: an animal model and pediatric case report
C I Berul, J K Triedman, J Forbess, et al.
The Journal of Clinical Investigation
|
February 18, 1999
DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model
C I Berul, C T Maguire, M J Aronovitz, et al.
Pacing and Clinical Electrophysiology : PACE
|
April 29, 1998
Transcoronary ethanol ablation of the atrioventricular node in a young patient with tricuspid atresia
X F Costeas, C I Berul, C B Foote, et al.
Journal of Cardiovascular Electrophysiology
|
January 22, 1998
Electrocardiographic markers of late sudden death risk in postoperative tetralogy of Fallot children
C I Berul, S L Hill, R L Geggel, et al.
Journal of Cardiovascular Electrophysiology
|
November 9, 2001
Supraventricular arrhythmias in children and young adults with implantable cardioverter defibrillators
B A Love, K S Barrett, M E Alexander, et al.
Journal of Cardiovascular Electrophysiology
|
October 12, 1999
Localization of the sites of conduction abnormalities in a mouse model of myotonic dystrophy
S Saba, B A Vanderbrink, B Luciano, et al.
Circulation
|
November 28, 2001
Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant Myosin-binding protein C gene
C I Berul, B K McConnell, H Wakimoto, et al.
The American Journal of Cardiology
|
March 12, 1999
Comparison of frequency of complications of implantable cardioverter-defibrillators in children versus adults
M S Link, S L Hill, D L Cliff, et al.
British Journal of Haematology
|
June 14, 2001
A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome
S Gritli, S Omar, E Tartaglini, et al.
The Journal of Clinical Investigation
|
July 18, 2001
Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein
H Kasahara, H Wakimoto, M Liu, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Pacing and Clinical Electrophysiology : PACE
|
January 31, 2002
Minimally invasive cardioverter defibrillator implantation for children: an animal model and pediatric case report
C I Berul, J K Triedman, J Forbess, et al.
The Journal of Clinical Investigation
|
February 18, 1999
DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model
C I Berul, C T Maguire, M J Aronovitz, et al.
Pacing and Clinical Electrophysiology : PACE
|
April 29, 1998
Transcoronary ethanol ablation of the atrioventricular node in a young patient with tricuspid atresia
X F Costeas, C I Berul, C B Foote, et al.
Journal of Cardiovascular Electrophysiology
|
January 22, 1998
Electrocardiographic markers of late sudden death risk in postoperative tetralogy of Fallot children
C I Berul, S L Hill, R L Geggel, et al.
Journal of Cardiovascular Electrophysiology
|
November 9, 2001
Supraventricular arrhythmias in children and young adults with implantable cardioverter defibrillators
B A Love, K S Barrett, M E Alexander, et al.
Journal of Cardiovascular Electrophysiology
|
October 12, 1999
Localization of the sites of conduction abnormalities in a mouse model of myotonic dystrophy
S Saba, B A Vanderbrink, B Luciano, et al.
Circulation
|
November 28, 2001
Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant Myosin-binding protein C gene
C I Berul, B K McConnell, H Wakimoto, et al.
The American Journal of Cardiology
|
March 12, 1999
Comparison of frequency of complications of implantable cardioverter-defibrillators in children versus adults
M S Link, S L Hill, D L Cliff, et al.
British Journal of Haematology
|
June 14, 2001
A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome
S Gritli, S Omar, E Tartaglini, et al.
The Journal of Clinical Investigation
|
July 18, 2001
Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein
H Kasahara, H Wakimoto, M Liu, et al.
Page
of 6