J.Peter van Tintelen
@jpvantintelen
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clinical geneticist, department Genetics. professor of clinical genetics; klinisch geneticus, hoogleraar klinische genetica @umcugenetica
UMC Utrecht, the Netherlands
Joined March 2011
Exercise intensity and cardiac disease development in carriers of titin truncating variants https://t.co/pQWWOI1qlk
#DCM #Athlete #exercise #Sportscardiology
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💙 Last week, https://t.co/BiJmoGzmYk & the DCM Foundation hosted a webinar on transforming cardiomyopathy care. 🧬 Genetics saves lives. 🤝 Support networks matter. Read the recap & watch the replay: https://t.co/kWGImBkhRh
#Cardiomyopathy #LMNA #GeneticTesting #HeartHealth
lmnacardiac.org
Hosted by the DCM Foundation and LMNAcardiac.org Earlier this week, the DCM Foundation and LMNAcardiac.org co-hosted a powerful webinar titled “Transforming Cardiomyopathy Care” — bringing together...
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🔴 Titin-related familial dilated cardiomyopathy: factors associated with disease onset @ESC_Journals #Cardiology #CardioEd #FOAMed
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💙 Most people have never heard of Arrhythmogenic Cardiomyopathy (ACM), also known as Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)—help us change that. Visit https://t.co/NhZ2bA53in to learn more.
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Clinical care of family members of patients with dilated cardiomyopathy: a clinical consensus statement just published in #EHJ 👉 https://t.co/X67pJrtLau
@RoccoMontone @ehj_ed #cardiomyopathies #DCM
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Prognostic Role of Myocarditis-Like Episodes and Their Treatment in Patients With Pathogenic Desmoplakin Variants | Circulation
ahajournals.org
BACKGROUND: Inflammatory, myocarditis-like episodes precede and are associated with higher risk of sustained ventricular arrhythmias and heart failure in patients with pathogenic or likely pathogenic...
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Nieuwe studie in npj Digital Medicine! Angst triggert klikken, liefde bouwt community—echte verhalen zorgen voor betrokkenheid. Trots op Myrthe Kuipers & team @UvA_Amsterdam @amsterdamumc . Lees meer: https://t.co/pvOMSzXzZk
#boezemfibrilleren #onderzoek #stichtingafip
afiponline.org
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CRY has developed a series of booklets that contain personal stories from bereaved mums, dads, siblings, partners and friends. The series focuses on the grief specific to the relationship an individual has with the deceased. Read online here: https://t.co/jySKRsmKYd
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#GeneticWorkforce limitations call for paradigm shifts. “Genetics First,” program empowers non-geneticist physicians to play an active role in the process of genetic consultation and testing. https://t.co/KTeMcD1QbV
#GeneticEducation #TestingAccessibility
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Nieuwe blog van Cora Aalfs @UMCUgenetica in Medisch contact: https://t.co/ApMdS3CLoK... Sofie (33) heeft Noonan syndroom. De medische feiten kende ze al vroeg, maar pas jaren later ontdekte ze hoe belangrijk het is om óók over emoties en vermoeidheid te praten.
medischcontact.nl
Blogs en columns van artsen met verschillende achtergronden en specialismen.
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Personalized Sudden Cardiac Death Risk Prediction in Genetic Heart Diseases: Beyond One-Size-Fits-All #OpenAccess
https://t.co/7ijJm0BVhp
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Major arrhythmias in non-dilated left ventricular cardiomyopathy: a novel prediction score https://t.co/eCZz2IeFX2
academic.oup.com
AbstractBackground and Aims. The prediction of the first major arrhythmic event (MAE) is still an unmet need in the recently defined scenario of non-dilate
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We are calling for papers for a special issue of EJHG exploring the role of DNA in public health screening. We welcome: -Original research -Reviews -Commentaries Deadline: December 31st, 2025 Submit via: https://t.co/rQj05HX5vU
@eshgsociety
nature.com
The rapid technological progress makes it possible to use DNA testing in settings outside of clinical genetics services. This implies that public health ...
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🔴 The Relevance of the Type of Ventricular Arrhythmia in Titin-Related Dilated Cardiomyopathy: A Multicenter Study @JACCJournals #Cardiology #CardioEd #Epeeps
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An evidence-based Plakophilin-2 specific longitudinal screening algorithm for arrhythmogenic right ventricular cardiomyopathy may improve patient care and efficiency of clinical resource allocation @ProfPim @SCYap77 @jpvantintelen
https://t.co/2UCpD9vTFF
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Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy - ScienceDirect
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Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy: The American Journal of Human Genetics
cell.com
Bi-allelic variants in POPDC2 cause a recessive syndrome characterized by sinus node dysfunction, AV block, and hypertrophic cardiomyopathy. Modeling and electrophysiological studies suggest effects...
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EHRA Level 3 (DAS CAM) is ready for the Next edition! Applications are possible until May 5th. Your next chance to be part of the DAS CAM community- one of the strongest networks in EP💪. @martaderiva @EHRAPresident @MBergonti @AGEP_DGK @YoungDgk @kvernooy @JordiHeijman
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What a fabulous first day for our 9th edition of the Hereditary Cardiovascular Diseases Course! Thank you to all the fantastic speakers, and see you all today at noon (CET time)! @arbelo_e @IacopoOlivotto @ProtonotariosA @bogdan_popescu1 @rbarvil @dr_pavia @KristinaHaugaa
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Save the date for our upcoming webinar featuring Rachel Lampert, M.D., who will discuss risk assessment and treatment strategies to help determine safe levels of exercise and sports participation for kids with cardiomyopathy. Register: https://t.co/7GZICAPLT3
#KeepKidsInGame
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