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Michael Hofbeck

Showing results (121-130 of 126) with videos related to

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Human Molecular Genetics|December 27, 2011
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsRachel Soemedi, Ana Topf, Ian J Wilson, et al.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, et al.
American Journal of Human Genetics|December 5, 2017
Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 DeletionsTiong Yang Tan, Claudia Gonzaga-Jauregui, Elizabeth J Bhoj, et al.
JACC. Basic to Translational Science|March 25, 2025
Impact of MEK Inhibition on Childhood RASopathy-Associated Hypertrophic CardiomyopathyCordula M Wolf, Martin Zenker, Olga Boleti, et al.
Cardiovascular Diagnosis and Therapy|January 24, 2022
Medical treatment of pulmonary hypertension in adults with congenital heart disease: updated and extended results from the International COMPERA-CHD RegistryAnn-Sophie Kaemmerer, Matthias Gorenflo, Dörte Huscher, et al.
Journal of Clinical Medicine|May 17, 2020
Pulmonary Hypertension in Adults with Congenital Heart Disease: Real-World Data from the International COMPERA-CHD RegistryHarald Kaemmerer, Matthias Gorenflo, Dörte Huscher, et al.
Pageof 13

Showing results (121-130 of 126) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 126 results.
Human Molecular Genetics|December 27, 2011
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsRachel Soemedi, Ana Topf, Ian J Wilson, et al.
European Heart Journal|July 2, 2025
Long QT syndrome in children and adolescents: risk factors and outcomes in a large German cohortLea Lippert, Tobias Burkard, Franziska Markel, et al.
American Journal of Human Genetics|December 5, 2017
Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 DeletionsTiong Yang Tan, Claudia Gonzaga-Jauregui, Elizabeth J Bhoj, et al.
JACC. Basic to Translational Science|March 25, 2025
Impact of MEK Inhibition on Childhood RASopathy-Associated Hypertrophic CardiomyopathyCordula M Wolf, Martin Zenker, Olga Boleti, et al.
Cardiovascular Diagnosis and Therapy|January 24, 2022
Medical treatment of pulmonary hypertension in adults with congenital heart disease: updated and extended results from the International COMPERA-CHD RegistryAnn-Sophie Kaemmerer, Matthias Gorenflo, Dörte Huscher, et al.
Journal of Clinical Medicine|May 17, 2020
Pulmonary Hypertension in Adults with Congenital Heart Disease: Real-World Data from the International COMPERA-CHD RegistryHarald Kaemmerer, Matthias Gorenflo, Dörte Huscher, et al.
Pageof 13