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Kidney International|February 18, 2011
Chronic potassium depletion increases adrenal progesterone production that is necessary for efficient renal retention of potassiumBoutaïna Elabida, Aurélie Edwards, Amel Salhi, et al.International Journal of Cardiology|October 7, 2006
Beta1-adrenergic receptor polymorphisms, QTc interval and occurrence of symptoms in type 1 of long QT syndromeKristian J Paavonen, Heikki Swan, Kirsi Piippo, et al.Annals of Medicine|June 7, 2006
Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patientsHeidi Fodstad, Saïd Bendahhou, Jean-Sébastien Rougier, et al.Frontiers in Genetics|July 5, 2021
Case Report: A Rare Truncating Variant of the CFHR5 Gene in IgA NephropathyGabriella Guzzo, Salima Sadallah, Heidi Fodstad, et al.Journal of the American College of Cardiology|January 3, 2006
Ratio of late to early T-wave peak amplitude in 24-h electrocardiographic recordings as indicator of symptom history in patients with long-QT Syndrome types 1 and 2Matti Viitasalo, Lasse Oikarinen, Heikki Swan, et al.Journal of the American College of Cardiology|July 27, 2002
Association between HERG K897T polymorphism and QT interval in middle-aged Finnish womenEeva Pietilä, Heidi Fodstad, Elmo Niskasaari, et al.Journal of Medical Genetics|January 30, 2024
Mosaic RASopathies concept: different skin lesions, same systemic manifestations?Marie-Anne Morren, Heidi Fodstad, Hilde Brems, et al.Cardiovascular Research|September 23, 2003
Functional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH2 (HERG)Kristian J Paavonen, Hugh Chapman, Päivi J Laitinen, et al.BMC Neurology|January 15, 2020
Childhood neurodegeneration associated with a specific UBTF variant: a new case report and review of the literatureFilipa Bastos, Mathieu Quinodoz, Marie-Claude Addor, et al.American Journal of Medical Genetics. Part A|July 23, 2021
Homozygous GLI3 variants observed in three unrelated patients presenting with syndromic polydactylyAhmed El Mouatani, Géraldine Van Winckel, Khaoula Zaafrane-Khachnaoui, et al.Pageof 3