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Heart Rhythm
|
February 21, 2024
Tropomyosin-troponin complex in inherited cardiomyopathies
Christian Krijger Juárez, Vasco Sequeira, Malou van den Boogaard, et al.
European Journal of Clinical Nutrition
|
August 17, 2017
Reproducibility and relative validity of a food frequency questionnaire to estimate intake of dietary phylloquinone and menaquinones
S R Zwakenberg, A I P Engelen, G W Dalmeijer, et al.
Journal of Thrombosis and Haemostasis : JTH
|
March 26, 2011
Circulating matrix γ-carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndrome
E C M Cranenburg, K Y VAN Spaendonck-Zwarts, L Bonafe, et al.
International Journal of Molecular Sciences
|
November 27, 2021
Therapeutic Prospects of Exon Skipping for Epidermolysis Bullosa
Franciscus C Vermeer, Jeroen Bremer, Robert J Sietsma, et al.
Experimental Dermatology
|
March 24, 2022
Functional investigation of two simultaneous or separately segregating DSP variants within a single family supports the theory of a dose-dependent disease severity
Mathilde C S C Vermeer, Daniela Andrei, Duco Kramer, et al.
The British Journal of Dermatology
|
August 17, 2022
A translation re-initiation variant in KLHL24 also causes epidermolysis bullosa simplex and dilated cardiomyopathy via intermediate filament degradation
Mathilde C S C Vermeer, Mohammad Al-Shinnag, Herman H W Silljé, et al.
Journal of the American College of Cardiology
|
May 14, 2016
Dilation of the Aorta Ascendens Forms Part of the Clinical Spectrum of HCN4 Mutations
Alexa M C Vermeer, Elisabeth M Lodder, Dierk Thomas, et al.
Journal of the American College of Cardiology
|
August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy
Annalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Cardiovascular Research
|
May 20, 2014
Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutations
E Rosalie Witjas-Paalberends, Ahmet Güçlü, Tjeerd Germans, et al.
JACC. Heart Failure
|
August 11, 2023
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
Mark Jansen, Remco de Brouwer, Fahima Hassanzada, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 201) with videos related to
Sort By:
Page
of 21
Heart Rhythm
|
February 21, 2024
Tropomyosin-troponin complex in inherited cardiomyopathies
Christian Krijger Juárez, Vasco Sequeira, Malou van den Boogaard, et al.
European Journal of Clinical Nutrition
|
August 17, 2017
Reproducibility and relative validity of a food frequency questionnaire to estimate intake of dietary phylloquinone and menaquinones
S R Zwakenberg, A I P Engelen, G W Dalmeijer, et al.
Journal of Thrombosis and Haemostasis : JTH
|
March 26, 2011
Circulating matrix γ-carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndrome
E C M Cranenburg, K Y VAN Spaendonck-Zwarts, L Bonafe, et al.
International Journal of Molecular Sciences
|
November 27, 2021
Therapeutic Prospects of Exon Skipping for Epidermolysis Bullosa
Franciscus C Vermeer, Jeroen Bremer, Robert J Sietsma, et al.
Experimental Dermatology
|
March 24, 2022
Functional investigation of two simultaneous or separately segregating DSP variants within a single family supports the theory of a dose-dependent disease severity
Mathilde C S C Vermeer, Daniela Andrei, Duco Kramer, et al.
The British Journal of Dermatology
|
August 17, 2022
A translation re-initiation variant in KLHL24 also causes epidermolysis bullosa simplex and dilated cardiomyopathy via intermediate filament degradation
Mathilde C S C Vermeer, Mohammad Al-Shinnag, Herman H W Silljé, et al.
Journal of the American College of Cardiology
|
May 14, 2016
Dilation of the Aorta Ascendens Forms Part of the Clinical Spectrum of HCN4 Mutations
Alexa M C Vermeer, Elisabeth M Lodder, Dierk Thomas, et al.
Journal of the American College of Cardiology
|
August 23, 2014
HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy
Annalisa Milano, Alexa M C Vermeer, Elisabeth M Lodder, et al.
Cardiovascular Research
|
May 20, 2014
Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutations
E Rosalie Witjas-Paalberends, Ahmet Güçlü, Tjeerd Germans, et al.
JACC. Heart Failure
|
August 11, 2023
Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study
Mark Jansen, Remco de Brouwer, Fahima Hassanzada, et al.
Page
of 21