[Familial degeneration of the conduction system (author's transl)]

Evidence of Nuclear Geometry-Driven Anisotropic Flow in O+O and Ne+Ne Collisions at sqrt[s_{NN}]=5.36 TeV.

Physical review letters·2026

Evidence for J/ψ Suppression in Incoherent Photonuclear Production.

Physical review letters·2026

Long-Range Transverse-Momentum Correlations and Radial Flow in Pb-Pb Collisions at the LHC.

Physical review letters·2026

Search for Quasiparticle Scattering in the Quark-Gluon Plasma with Jet Splittings in pp and Pb-Pb Collisions at sqrt[s_{NN}]=5.02 TeV.

Physical review letters·2025

First Measurement of A=4 Hypernuclei and Antihypernuclei at the LHC.

Physical review letters·2025

Probing Strangeness Hadronization with Event-by-Event Production of Multistrange Hadrons.

Physical review letters·2025

Cardiac tamponade: an unusual, fatal complication of infective endocarditis.

Giornale italiano di cardiologia·2000

Incessant ventricular tachycardia early after acute myocardial infarction: efficacy of radiofrequency catheter ablation but not of optimal coronary revascularization.

Giornale italiano di cardiologia·2000

Treatment of a native right coronary artery with the PercuSurge Guardwire protection system during PTCA and stenting.

Giornale italiano di cardiologia·2000

Relief of an early pulmonary pathway obstruction with stenting after modified Fontan operation in an adult.

Giornale italiano di cardiologia·2000

[Clinical characteristics, familial distribution and preliminary genetic data in 9 different families with "Brugada's syndrome"].

Giornale italiano di cardiologia·2000

[Clinical course of pre- and post-natal isolated congenital atrioventricular block diagnosed in utero].

Giornale italiano di cardiologia·2000

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Pediatric blood & cancer·2026

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Frontiers in pediatrics·2026

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

European journal of human genetics : EJHG·2026

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Annals of medicine·2026

Familial short stature: genetic architecture, risk stratification, and precision management.

Frontiers in endocrinology·2026

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026

Related Experiment Videos

[Familial degeneration of the conduction system (author's transl)]

Related Concept Videos

Evidence of Nuclear Geometry-Driven Anisotropic Flow in O+O and Ne+Ne Collisions at sqrt[s_{NN}]=5.36 TeV.

Evidence for J/ψ Suppression in Incoherent Photonuclear Production.

Long-Range Transverse-Momentum Correlations and Radial Flow in Pb-Pb Collisions at the LHC.

Search for Quasiparticle Scattering in the Quark-Gluon Plasma with Jet Splittings in pp and Pb-Pb Collisions at sqrt[s_{NN}]=5.02 TeV.

First Measurement of A=4 Hypernuclei and Antihypernuclei at the LHC.

Probing Strangeness Hadronization with Event-by-Event Production of Multistrange Hadrons.

Cardiac tamponade: an unusual, fatal complication of infective endocarditis.

Incessant ventricular tachycardia early after acute myocardial infarction: efficacy of radiofrequency catheter ablation but not of optimal coronary revascularization.

Treatment of a native right coronary artery with the PercuSurge Guardwire protection system during PTCA and stenting.

Relief of an early pulmonary pathway obstruction with stenting after modified Fontan operation in an adult.

[Clinical characteristics, familial distribution and preliminary genetic data in 9 different families with "Brugada's syndrome"].

[Clinical course of pre- and post-natal isolated congenital atrioventricular block diagnosed in utero].

A Situational Assessment of the Diagnostic Landscape and Organizational Readiness to Implement Next-Generation Sequencing at Two Childhood Cancer Treatment Centers in Ghana.

Case Report: Clinical and molecular genetic analysis of a patient with coexisting complete androgen insensitivity syndrome and neurofibromatosis type 1 and 15pstk + polymorphism.

Three-dimensional facial gestalt analysis for three neurodevelopmental disorders: Koolen-de Vries, Jansen-de Vries and KBG syndrome.

Identification of rare maternal copy number variants by genome-wide analysis of noninvasive prenatal screening data in 113,017 pregnant women.

Familial short stature: genetic architecture, risk stratification, and precision management.

Shared genetic architecture between DTI-ALPS traits and neurodegenerative diseases.

Related Experiment Videos

[Familial degeneration of the conduction system (author's transl)]

Related Concept Videos

Related Articles