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European Archives of Paediatric Dentistry : Official Journal of the European Academy of Paediatric Dentistry|September 15, 2016
Oral health among children with congenital heart defects in Western NorwayT B Sivertsen, J Aßmus, G Greve, et al.
International Journal of Experimental Pathology|September 19, 1998
Regional activation of the immediate-early response gene c-fos in infarcted rat heartsT H Larsen, R Skar, E K Frotjold, et al.
BMC Medical Genomics|June 27, 2021
Repeat to gene expression ratios in leukemic blast cells can stratify risk prediction in acute myeloid leukemiaM Onishi-Seebacher, G Erikson, Z Sawitzki, et al.
Experimental Physiology|September 26, 2001
Right ventricular distension alters monophasic action potential duration during pulmonary arterial occlusion in anaesthetised lambs: evidence for arrhythmogenic right ventricular mechanoelectrical feedbackG Greve, M J Lab, R Chen, et al.
The Journal of Clinical Investigation|January 1, 1994
Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathyR Anan, G Greve, L Thierfelder, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|June 30, 2017
Mid-childhood outcomes after pre-viable preterm premature rupture of membranesM H Bentsen, E Satrell, H Reigstad, et al.
Neurourology and Urodynamics|September 27, 2007
Development and validation of the pelvic floor inventories Leiden (PelFIs)Petra J Voorham-van der Zalm, Anne M Stiggelbout, Ilona Aardoom, et al.
Human Genetics|January 5, 2001
Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?M J Baptista, U L Fairbrother, C M Howard, et al.
Annals of Surgery|October 20, 2004
Pylorus preserving pancreaticoduodenectomy versus standard Whipple procedure: a prospective, randomized, multicenter analysis of 170 patients with pancreatic and periampullary tumorsKhe T C Tran, Hans G Smeenk, Casper H J van Eijck, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|August 30, 2008
Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriersK E Berge, K H Haugaa, A Früh, et al.
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