Ulla‐Maija Koivisto

Author

Ulla‐Maija Koivisto

Also Known As

U M Koivisto, U.-M. Koivisto, U.‐M. KOIVISTO, U.‐M. Koivisto, ULLA-MAIJA KOIVISTO, Ulla-Maija Koivisto, Ulla‐Maija Koivisto

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University of Helsinki North Karelia Central Hospital University of Oulu Hospital for Sick Children University of Turku

About

Ulla‐Maija Koivisto is an author at University of Helsinki specializing in medicine, metabolic syndrome, and atherosclerosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	340
2	Public Health	3	3	196
3	Biochemistry	2	2	207
4	Health Sciences	1	1	101
5	Cell Biology	1	1	101

Ulla‐Maija Koivisto

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Differential regulation of the GLUT-1 and GLUT-4 glucose transport systems by glucose and insulin in L6 muscle cells in culture Ulla‐Maija Koivisto, Héctor Martínez-Valdez, Philip J. Bilan, Journal of Biological Chemistry	1991	160
EuroEco (European Health Economic Trial on Home Monitoring in ICD Patients): a provider perspective in five European countries on costs and net financial impact of follow-up with or without remote monitoring Hein Heidbüchel, G Hindricks, Paul Broadhurst, European Heart Journal	2014	114
Laminin and its neurite outgrowth‐promoting domain in the brain in Alzheimer's disease and Down's syndrome patients Sanna Murtomäki, Juha Risteli, Leila Risteli, Journal of Neuroscience Research	1992	108
The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finland. Ulla‐Maija Koivisto, Hannu Turtola, Katriina Aalto‐Setälä, Journal of Clinical Investigation GeneticsGenetic EpidemiologyPathologyHyperlipidemiaMetabolic Syndrome	1992	106
A single-base substitution in the proximal Sp1 site of the human low density lipoprotein receptor promoter as a cause of heterozygous familial hypercholesterolemia. Ulla‐Maija Koivisto, Jorma J. Palvimo, Olli A. Jänne, Proceedings of the National Academy of Sciences	1994	104
Glucose transport activity in L6 muscle cells is regulated by the coordinate control of subcellular glucose transporter distribution, biosynthesis, and mRNA transcription. Patricia S. Walker, Toolsie Ramlal, Vivian Sarabia, Journal of Biological Chemistry Cellular PhysiologyInsulin SignalingMetabolic SyndromeGlucose DeprivationChronic Glucose Deprivation	1990	101
Diagnosis of heterozygous familial hypercholesterolemia. DNA analysis complements clinical examination and analysis of serum lipid levels. Pekka Koivisto, Ulla‐Maija Koivisto, T.A. Miettinen, Arteriosclerosis and Thrombosis A Journal of Vascular Biology Genetic TestingGeneticsGenetic EpidemiologyDna AnalysisHuman Polymorphism	1992	69
Molecular characterization of minor gene rearrangements in Finnish patients with heterozygous familial hypercholesterolemia: identification of two common missense mutations (Gly823-->Asp and Leu380-->His) and eight rare mutations of the LDL receptor gene. Ulla‐Maija Koivisto, Jorma Viikari, Kimmo Kontula PubMed	1995	57
Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences Alpo Vuorio, Katriina Aalto‐Setälä, Ulla‐Maija Koivisto, Annals of Medicine	2001	55
Safety of pacemaker and implantable cardioverter–defibrillator implantation during uninterrupted warfarin treatment — The FinPAC study Juhani Airaksinen, Petri Korkeila, Juha Lund, International Journal of Cardiology Implantable Cardioverter–defibrillator ImplantationThrombosisCardiovascular DiseasePatient SafetyUninterrupted Warfarin Treatment	2013	43

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