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Showing results (81-90 of 172) with videos related to

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Journal of the American College of Cardiology|November 21, 2009
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysisArgelia Medeiros-Domingo, Zahurul A Bhuiyan, David J Tester, et al.
Frontiers in Immunology|January 11, 2020
Meta-Analysis of <i>in vitro</i>-Differentiated Macrophages Identifies Transcriptomic Signatures That Classify Disease Macrophages <i>in vivo</i>Hung-Jen Chen, Andrew Y F Li Yim, Guillermo R Griffith, et al.
European Journal of Epidemiology|August 27, 2005
CONCOR, an initiative towards a national registry and DNA-bank of patients with congenital heart disease in the Netherlands: rationale, design, and first resultsE T van der Velde, Velde E T Vander, J W J Vriend, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|November 13, 2018
Oxytocin receptor gene methylation in male and female PTSD patients and trauma-exposed controlsL Nawijn, I M Krzyzewska, M van Zuiden, et al.
European Journal of Human Genetics : EJHG|April 11, 2024
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment optionsNiels Vos, Lotte Kleinendorst, Liselot van der Laan, et al.
European Heart Journal|November 9, 2006
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?Nynke Hofman, Arthur A M Wilde, Stefan Kääb, et al.
Plos One|March 31, 2018
Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonatesPeter Henneman, Arjan Bouman, Adri Mul, et al.
Journal of Medical Genetics|November 8, 2005
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patientsA V Postma, I Denjoy, J Kamblock, et al.
Blood Cells, Molecules & Diseases|November 9, 2010
A monozygotic twin pair with highly discordant Gaucher phenotypesM Biegstraaten, I N van Schaik, J M F G Aerts, et al.
European Journal of Human Genetics : EJHG|June 1, 2006
New mutations in the NHS gene in Nance-Horan Syndrome families from the NetherlandsRalph J Florijn, Willem Loves, Liesbeth J J M Maillette de Buy Wenniger-Prick, et al.
Pageof 18

Showing results (81-90 of 172) with videos related to

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Pageof 18
Journal of the American College of Cardiology|November 21, 2009
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysisArgelia Medeiros-Domingo, Zahurul A Bhuiyan, David J Tester, et al.
Frontiers in Immunology|January 11, 2020
Meta-Analysis of <i>in vitro</i>-Differentiated Macrophages Identifies Transcriptomic Signatures That Classify Disease Macrophages <i>in vivo</i>Hung-Jen Chen, Andrew Y F Li Yim, Guillermo R Griffith, et al.
European Journal of Epidemiology|August 27, 2005
CONCOR, an initiative towards a national registry and DNA-bank of patients with congenital heart disease in the Netherlands: rationale, design, and first resultsE T van der Velde, Velde E T Vander, J W J Vriend, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|November 13, 2018
Oxytocin receptor gene methylation in male and female PTSD patients and trauma-exposed controlsL Nawijn, I M Krzyzewska, M van Zuiden, et al.
European Journal of Human Genetics : EJHG|April 11, 2024
Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment optionsNiels Vos, Lotte Kleinendorst, Liselot van der Laan, et al.
European Heart Journal|November 9, 2006
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?Nynke Hofman, Arthur A M Wilde, Stefan Kääb, et al.
Plos One|March 31, 2018
Widespread domain-like perturbations of DNA methylation in whole blood of Down syndrome neonatesPeter Henneman, Arjan Bouman, Adri Mul, et al.
Journal of Medical Genetics|November 8, 2005
Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patientsA V Postma, I Denjoy, J Kamblock, et al.
Blood Cells, Molecules & Diseases|November 9, 2010
A monozygotic twin pair with highly discordant Gaucher phenotypesM Biegstraaten, I N van Schaik, J M F G Aerts, et al.
European Journal of Human Genetics : EJHG|June 1, 2006
New mutations in the NHS gene in Nance-Horan Syndrome families from the NetherlandsRalph J Florijn, Willem Loves, Liesbeth J J M Maillette de Buy Wenniger-Prick, et al.
Pageof 18