Found: 12
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Tachycardia-induced cardiomyopathy in infants with multifocal atrial tachycardia.
- Published in:
- Cardiology in the Young, 2022, v. 32, p. S164
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- Publication type:
- Article
Tachycardia-induced cardiomyopathy in infants with multifocal atrial tachycardia.
- Published in:
- Cardiology in the Young, 2022, v. 32, n. S2, p. S164, doi. 10.1017/S1047951122001950
- By:
- Publication type:
- Article
Right ventricular endomyocardial biopsy in children and adolescents with drug-refractory arrhythmia.
- Published in:
- 2017
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- Publication type:
- journal article
Modified technique for coarctation of aorta with hypoplastic distal aortic arch.
- Published in:
- 2021
- By:
- Publication type:
- journal article
COVID-19 Heart Lesions in Children: Clinical, Diagnostic and Immunological Changes.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 2, p. 1147, doi. 10.3390/ijms24021147
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- Publication type:
- Article
RBM20 -Associated Ventricular Arrhythmias in a Patient with Structurally Normal Heart.
- Published in:
- Genes, 2021, v. 12, n. 1, p. 94, doi. 10.3390/genes12010094
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- Publication type:
- Article
Two New Cases of Hypertrophic Cardiomyopathy and Skeletal Muscle Features Associated with ALPK3 Homozygous and Compound Heterozygous Variants.
- Published in:
- Genes, 2020, v. 11, n. 10, p. 1201, doi. 10.3390/genes11101201
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- Publication type:
- Article
Functional Analysis of SCN5A Genetic Variants Associated with Brugada Syndrome.
- Published in:
- Cardiology, 2022, v. 147, n. 1, p. 35, doi. 10.1159/000519857
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- Publication type:
- Article
Genetic Spectrum of Left Ventricular Non-Compaction in Paediatric Patients.
- Published in:
- Cardiology, 2020, v. 145, n. 11, p. 746, doi. 10.1159/000510439
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- Publication type:
- Article
A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.
- Published in:
- BMC Medical Genomics, 2020, v. 13, n. 1, p. N.PAG, doi. 10.1186/s12920-020-00821-x
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- Publication type:
- Article
A cryptic splice-altering KCNQ1 variant in trans with R259L leading to Jervell and Lange-Nielsen syndrome.
- Published in:
- NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00183-y
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- Publication type:
- Article
Severe Course of COVID-19 and Long-COVID-19 in Children: Difficulties in Diagnosis.
- Published in:
- Life (2075-1729), 2023, v. 13, n. 3, p. 781, doi. 10.3390/life13030781
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- Publication type:
- Article