Search research articles
Contact Us
Filters
Showing results (81-90 of 167) with videos related to
Page
of 17
Sort By:
Circulation
|
February 9, 2000
Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts
R Brugada, J Brugada, C Antzelevitch, et al.
Human Genetics
|
January 27, 2000
Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy
K R Bowles, C Zintz, S E Abraham, et al.
American Journal of Medical Genetics
|
March 29, 1996
Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene
E A Putnam, M Cho, A B Zinn, et al.
The British Journal of Dermatology
|
September 16, 2015
Ventricular dysfunction and aortic dilation in patients with recessive dystrophic epidermolysis bullosa
T D Ryan, A W Lucky, E C King, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
March 16, 2001
Improved myocardial structure following LVAD support: effect of unloading on dystrophin expression
S J. Stetson, A Perez-Verdia, M Vatta, et al.
Biochemical and Molecular Medicine
|
December 1, 1995
Genetic heterogeneity in familial dilated cardiomyopathy
K R Schultz, R J Gajarski, R Pignatelli, et al.
Circulation
|
May 21, 1998
Improvement of repolarization abnormalities by a K+ channel opener in the LQT1 form of congenital long-QT syndrome
W Shimizu, T Kurita, K Matsuo, et al.
Biochemical Medicine and Metabolic Biology
|
October 1, 1989
Demonstration and characterization of human cardiac porin: a voltage-dependent channel involved in adenine nucleotide movement across the outer mitochondrial membrane
J A Towbin, M Minter, D Brdiczka, et al.
Human Genetics
|
September 1, 1989
Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus
J A Towbin, D R Wu, J Chamberlain, et al.
Genomics
|
July 1, 1990
DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis
J A Towbin, J S Chamberlain, D R Wu, et al.
Page
of 17
Search research articles
Search
Showing results (81-90 of 167) with videos related to
Sort By:
Page
of 17
Circulation
|
February 9, 2000
Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts
R Brugada, J Brugada, C Antzelevitch, et al.
Human Genetics
|
January 27, 2000
Genomic characterization of the human peptidyl-prolyl-cis-trans-isomerase, mitochondrial precursor gene: assessment of its role in familial dilated cardiomyopathy
K R Bowles, C Zintz, S E Abraham, et al.
American Journal of Medical Genetics
|
March 29, 1996
Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene
E A Putnam, M Cho, A B Zinn, et al.
The British Journal of Dermatology
|
September 16, 2015
Ventricular dysfunction and aortic dilation in patients with recessive dystrophic epidermolysis bullosa
T D Ryan, A W Lucky, E C King, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
March 16, 2001
Improved myocardial structure following LVAD support: effect of unloading on dystrophin expression
S J. Stetson, A Perez-Verdia, M Vatta, et al.
Biochemical and Molecular Medicine
|
December 1, 1995
Genetic heterogeneity in familial dilated cardiomyopathy
K R Schultz, R J Gajarski, R Pignatelli, et al.
Circulation
|
May 21, 1998
Improvement of repolarization abnormalities by a K+ channel opener in the LQT1 form of congenital long-QT syndrome
W Shimizu, T Kurita, K Matsuo, et al.
Biochemical Medicine and Metabolic Biology
|
October 1, 1989
Demonstration and characterization of human cardiac porin: a voltage-dependent channel involved in adenine nucleotide movement across the outer mitochondrial membrane
J A Towbin, M Minter, D Brdiczka, et al.
Human Genetics
|
September 1, 1989
Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus
J A Towbin, D R Wu, J Chamberlain, et al.
Genomics
|
July 1, 1990
DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis
J A Towbin, J S Chamberlain, D R Wu, et al.
Page
of 17