Anita Hiippala
Helsinki, Finland
Last Updated: 09/26/2026
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Found 13 publications
Multicenter cohort study on duration of antiarrhythmic medication for supraventricular tachycardia in infants.
Journal: European journal of pediatrics
Published: September 01, 2022
Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International Study.
Journal: Circulation. Genomic and precision medicine
Published: May 13, 2022
Genetic Basis of Severe Childhood-Onset Cardiomyopathies.
Journal: Journal of the American College of Cardiology
Published: February 13, 2018
Cardiovascular magnetic resonance findings in patients with PRKAG2 gene mutations.
Journal: Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
Published: August 17, 2015
The rare Costello variant HRAS c.173C>T (p.T58I) with severe neonatal hypertrophic cardiomyopathy.
Journal: American journal of medical genetics. Part A
Published: May 09, 2015
Follow-up of 316 molecularly defined pediatric long-QT syndrome patients: clinical course, treatments, and side effects.
Journal: Circulation. Arrhythmia and electrophysiology
Published: December 16, 2014
Expanding the phenotype of Timothy syndrome type 2: an adolescent with ventricular fibrillation but normal development.
Journal: American journal of medical genetics. Part A
Published: June 19, 2014
Population-based single-center outcome for pediatric catheter ablation of common supraventricular tachycardias.
Journal: Pacing and clinical electrophysiology : PACE
Published: January 14, 2014
Cryoablation in the treatment of cardiac arrhythmias
Journal: Duodecim; laaketieteellinen aikakauskirja
Published: July 04, 2013
Permanent cardiac pacing in children: choosing the optimal pacing site: a multicenter study.
Journal: Circulation
Published: January 01, 2013
Long-term performance of beat-to-beat automatic ventricular threshold adjustment in infants with congenital atrioventricular block.
Journal: Pacing and clinical electrophysiology : PACE
Published: September 04, 2012
New mutation of mitochondrial DNAJC19 causing dilated and noncompaction cardiomyopathy, anemia, ataxia, and male genital anomalies.
Journal: Pediatric research
Published: July 17, 2012
Last Updated: 09/26/2026