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Thomas Pickardt

national registry for congenital heart defects
H指数:21
被引数:2,012

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DNA methylation analysis of NOTCH1 variants reveals the first episignature for non-syndromic congenital heart defects

NOTCH1基因变异的DNA甲基化分析揭示了非综合征性先天性心脏病的第一种表观遗传标志物

2026-01-070
OAAI
Novel Deep Learning Aligned Strain Techniques in Repaired Tetralogy of Fallot

新型与深度学习对齐的应变技术在修复后的法洛四联症中的应用

2024-11-120
PRE
Prognostic Value of Speckle Tracking Echocardiography-Derived Strain in Unmasking Risk for Arrhythmias in Children with Myocarditis
2024-10-162
OAAI
Clinical course and follow-up of pediatric patients with COVID-19 vaccine-associated myocarditis compared to non-vaccine-associated myocarditis within the prospective multicenter registry-MYKKE
2024-01-013
OAAI
Clinical characteristics and outcome of biopsy-proven myocarditis in children - Results of the German prospective multicentre registry MYKKE
2022-06-0111
OAAI
Le Cœur en Sabot: shape associations with adverse events in repaired tetralogy of Fallot

Le c œ ur en Sabot: 法洛四联症修复后的形状与不良事件的关联

2022-01-016
OAAI
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease (vol 17, e1009679, 2021)

基因组变异的综合分析揭示了候选单倍体不足基因与先天性心脏病的新关联 (第17卷,e1009679,2021)

2021-09-210
OAAI
Arterial tissue transcriptional profiles associate with tissue remodeling and cardiovascular phenotype in children with end-stage kidney disease
2019-07-1610
OAAI
Toward evidence-based diagnosis of myocarditis in children and adolescents: Rationale, design, and first baseline data of MYKKE, a multicenter registry and study platform
2017-05-0131
PREAI
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
2016-08-01332
OAAI