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Nederlands Tijdschrift Voor Geneeskunde
|
November 1, 2018
[General Data Protection Regulation and medical research: friend or foe?]
W Antoinette Groenewegen, Elise M van de Putte
Advances in Cardiology
|
May 2, 2006
Cx40 polymorphism in human atrial fibrillation
Richard N W Hauer, W Antoinette Groenewegen, Mehran Firouzi, et al.
Heart Rhythm
|
September 29, 2005
Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms
Naomasa Makita, Koji Sasaki, W Antoinette Groenewegen, et al.
Biochimica Et Biophysica Acta
|
October 20, 2006
The human Cx40 promoter polymorphism -44G-->A differentially affects transcriptional regulation by Sp1 and GATA4
Mehran Firouzi, Marti F A Bierhuizen, Bart Kok, et al.
Circulation Research
|
August 7, 2004
Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation
Mehran Firouzi, Hemanth Ramanna, Bart Kok, et al.
Neuroscience Letters
|
June 30, 2009
Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions
Linda Volkers, Martin B Rook, Joost H G Das, et al.
Cardiovascular Research
|
March 26, 2003
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics
W Antoinette Groenewegen, Connie R Bezzina, J Peter van Tintelen, et al.
Journal of Hypertension
|
March 2, 2006
Polymorphisms in human connexin40 gene promoter are associated with increased risk of hypertension in men
Mehran Firouzi, Bart Kok, Wilko Spiering, et al.
Circulation Research
|
February 8, 2003
Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system
Connie R Bezzina, Martin B Rook, W Antoinette Groenewegen, et al.
Circulation Research
|
January 11, 2003
A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill
W Antoinette Groenewegen, Mehran Firouzi, Connie R Bezzina, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Nederlands Tijdschrift Voor Geneeskunde
|
November 1, 2018
[General Data Protection Regulation and medical research: friend or foe?]
W Antoinette Groenewegen, Elise M van de Putte
Advances in Cardiology
|
May 2, 2006
Cx40 polymorphism in human atrial fibrillation
Richard N W Hauer, W Antoinette Groenewegen, Mehran Firouzi, et al.
Heart Rhythm
|
September 29, 2005
Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms
Naomasa Makita, Koji Sasaki, W Antoinette Groenewegen, et al.
Biochimica Et Biophysica Acta
|
October 20, 2006
The human Cx40 promoter polymorphism -44G-->A differentially affects transcriptional regulation by Sp1 and GATA4
Mehran Firouzi, Marti F A Bierhuizen, Bart Kok, et al.
Circulation Research
|
August 7, 2004
Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation
Mehran Firouzi, Hemanth Ramanna, Bart Kok, et al.
Neuroscience Letters
|
June 30, 2009
Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions
Linda Volkers, Martin B Rook, Joost H G Das, et al.
Cardiovascular Research
|
March 26, 2003
A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics
W Antoinette Groenewegen, Connie R Bezzina, J Peter van Tintelen, et al.
Journal of Hypertension
|
March 2, 2006
Polymorphisms in human connexin40 gene promoter are associated with increased risk of hypertension in men
Mehran Firouzi, Bart Kok, Wilko Spiering, et al.
Circulation Research
|
February 8, 2003
Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system
Connie R Bezzina, Martin B Rook, W Antoinette Groenewegen, et al.
Circulation Research
|
January 11, 2003
A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill
W Antoinette Groenewegen, Mehran Firouzi, Connie R Bezzina, et al.
Page
of 2