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Cuno Kuiperi

Showing results (1-10 of 8) with videos related to

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Acta Cardiologica|December 31, 2015
Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropoutTomas Robyns, Cuno Kuiperi, Rik Willems, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|May 1, 2018
Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriersTomas Robyns, Dieter Nuyens, Bert Vandenberk, et al.
European Journal of Medical Genetics|September 13, 2019
Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathyTomas Robyns, Jeroen Breckpot, Dieter Nuyens, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathyTomas Robyns, Cuno Kuiperi, Jeroen Breckpot, et al.
Heart Rhythm|February 19, 2017
Individualized corrected QT interval is superior to QT interval corrected using the Bazett formula in predicting mutation carriage in families with long QT syndromeTomas Robyns, Rik Willems, Bert Vandenberk, et al.
Brain : a Journal of Neurology|April 9, 2005
Acute treatment with the PPARgamma agonist pioglitazone and ibuprofen reduces glial inflammation and Abeta1-42 levels in APPV717I transgenic miceMichael T Heneka, Magdalena Sastre, Lucia Dumitrescu-Ozimek, et al.
European Journal of Medical Genetics|October 13, 2017
Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutationAleksandra Nijak, Maaike Alaerts, Cuno Kuiperi, et al.
European Journal of Human Genetics : EJHG|April 9, 2023
Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRIJohanna Jacobs, Lucas Van Aelst, Jeroen Breckpot, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Acta Cardiologica|December 31, 2015
Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropoutTomas Robyns, Cuno Kuiperi, Rik Willems, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|May 1, 2018
Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriersTomas Robyns, Dieter Nuyens, Bert Vandenberk, et al.
European Journal of Medical Genetics|September 13, 2019
Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathyTomas Robyns, Jeroen Breckpot, Dieter Nuyens, et al.
European Journal of Human Genetics : EJHG|December 20, 2017
Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathyTomas Robyns, Cuno Kuiperi, Jeroen Breckpot, et al.
Heart Rhythm|February 19, 2017
Individualized corrected QT interval is superior to QT interval corrected using the Bazett formula in predicting mutation carriage in families with long QT syndromeTomas Robyns, Rik Willems, Bert Vandenberk, et al.
Brain : a Journal of Neurology|April 9, 2005
Acute treatment with the PPARgamma agonist pioglitazone and ibuprofen reduces glial inflammation and Abeta1-42 levels in APPV717I transgenic miceMichael T Heneka, Magdalena Sastre, Lucia Dumitrescu-Ozimek, et al.
European Journal of Medical Genetics|October 13, 2017
Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutationAleksandra Nijak, Maaike Alaerts, Cuno Kuiperi, et al.
European Journal of Human Genetics : EJHG|April 9, 2023
Tools to differentiate between Filamin C and Titin truncating variant carriers: value of MRIJohanna Jacobs, Lucas Van Aelst, Jeroen Breckpot, et al.
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