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Journal of Biomedical Engineering
|
January 1, 1988
New high-frequency catheter technique for His bundle ablation in dogs
A E Aubert, M Gewillig, E Witters, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 20, 2015
Immediate and intermediate results of stent therapy for aortic coarctation
A M Honing-Hemmers, W K van Putten, M Gewillig, et al.
Clinical Genetics
|
April 1, 1997
Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion
K Devriendt, R Van Hoestenberghe, C Van Hole, et al.
Prenatal Diagnosis
|
March 4, 1998
Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndrome
K Devriendt, D Van Schoubroeck, B Eyskens, et al.
Heart (British Cardiac Society)
|
February 18, 2004
Long term outcome up to 30 years after the Mustard or Senning operation: a nationwide multicentre study in Belgium
P Moons, M Gewillig, T Sluysmans, et al.
European Journal of Preventive Cardiology
|
November 6, 2012
Recommendations for physical activity, recreation sport, and exercise training in paediatric patients with congenital heart disease: a report from the Exercise, Basic & Translational Research Section of the European Association of Cardiovascular Prevention and Rehabilitation, the European Congenital Heart and Lung Exercise Group, and the Association for European Paediatric Cardiology
T Takken, A Giardini, T Reybrouck, et al.
Human Genetics
|
August 15, 2000
Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay
Z Urbán, V V Michels, S N Thibodeau, et al.
American Journal of Medical Genetics
|
September 20, 2001
Recurrent involvement of chromosomal region 6q21 in heterotaxy
H Peeters, P Debeer, P Groenen, et al.
Human Genetics
|
February 28, 2003
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse
H Peeters, P Debeer, A Bairoch, et al.
American Journal of Human Genetics
|
March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1
K Devriendt, G Matthijs, R Van Dael, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 113) with videos related to
Sort By:
Page
of 12
Journal of Biomedical Engineering
|
January 1, 1988
New high-frequency catheter technique for His bundle ablation in dogs
A E Aubert, M Gewillig, E Witters, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
|
February 20, 2015
Immediate and intermediate results of stent therapy for aortic coarctation
A M Honing-Hemmers, W K van Putten, M Gewillig, et al.
Clinical Genetics
|
April 1, 1997
Submicroscopic deletion in chromosome 22q11 in trizygous triplet siblings and their father. Clinical variability of 22q11 deletion
K Devriendt, R Van Hoestenberghe, C Van Hole, et al.
Prenatal Diagnosis
|
March 4, 1998
Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndrome
K Devriendt, D Van Schoubroeck, B Eyskens, et al.
Heart (British Cardiac Society)
|
February 18, 2004
Long term outcome up to 30 years after the Mustard or Senning operation: a nationwide multicentre study in Belgium
P Moons, M Gewillig, T Sluysmans, et al.
European Journal of Preventive Cardiology
|
November 6, 2012
Recommendations for physical activity, recreation sport, and exercise training in paediatric patients with congenital heart disease: a report from the Exercise, Basic & Translational Research Section of the European Association of Cardiovascular Prevention and Rehabilitation, the European Congenital Heart and Lung Exercise Group, and the Association for European Paediatric Cardiology
T Takken, A Giardini, T Reybrouck, et al.
Human Genetics
|
August 15, 2000
Isolated supravalvular aortic stenosis: functional haploinsufficiency of the elastin gene as a result of nonsense-mediated decay
Z Urbán, V V Michels, S N Thibodeau, et al.
American Journal of Medical Genetics
|
September 20, 2001
Recurrent involvement of chromosomal region 6q21 in heterotaxy
H Peeters, P Debeer, P Groenen, et al.
Human Genetics
|
February 28, 2003
PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouse
H Peeters, P Debeer, A Bairoch, et al.
American Journal of Human Genetics
|
March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1
K Devriendt, G Matthijs, R Van Dael, et al.
Page
of 12