Preview
Sign-in for full Details 
Sign-in free and Explore the Exciting World of BiomedExperts:
- Over 1.500.000 Profiles
- More than 1.800 Organizations worldwide
- State of the Art Network Visualizations
- Manage your own Profile
- Locate Experts in your Country/Region
- Locate Experts in your 1. and 2. Level Network
- Connect to Experts Worldwide
NetworkView
Seppo Helisalmi
This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers
together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles
free of charge to researchers worldwide.
Research Profile (preview)
Disorders
Chemicals & Drugs
Geographic Areas
Physiology
Genes & Molecular Sequences
Concepts & Ideas
Procedures
Sign-in to see full Profile
Network (preview)
61
Soininen, Hilkka
50
Hiltunen, Mikko
40
Mannermaa, Arto
32
Lehtovirta, Maarit
24
Heinonen, Seppo
20
Riekkinen, PJ
18
Ryynänen, Markku
17
Koivisto, Anne Maria
16
Alafuzoff, Irina
14
Punnonen, Kari
13
Vepsäläinen, Saila
11
Iivonen, Susan
10
Romppanen, Eeva-Liisa
8
Laakso, Markku
7
Pirskanen, Mia
Sign-in to see all Coauthors
Publications
Sign-in to see all Publications
Sign in free and see...
Visualized networks:
See your personal network in
sophisticated graphical views
GeoTargeted Searches:
Locate experts around the world
and connect with global collaborators
Research Profiles:
See the visualized research activity
of experts around the globe
Sign-in to see more
Geonetwork of Seppo Helisalmi (preview)
Cities where this author has publications
Cities where co-authors of this author have publications
Sign-in to see more
All Publications
-
2009: Vepsäläinen S; Helisalmi S; Mannermaa A; Pirttilä T; Soininen H; Hiltunen M
Combined risk effects of IDE and NEP gene variants on Alzheimer disease.
Journal of neurology, neurosurgery, and psychiatry 2009;80(11):1268-70.
-
2009: Viswanathan Jayashree; Mäkinen Petra; Helisalmi Seppo; Haapasalo Annakaisa; Soininen Hilkka; Hiltunen Mikko
An association study between granulin gene polymorphisms and Alzheimer's disease in Finnish population.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(5):747-50.
-
2009: Alafuzoff I; Aho L; Helisalmi S; Mannermaa A; Soininen H
Beta-amyloid deposition in brains of subjects with diabetes.
Neuropathology and applied neurobiology 2009;35(1):60-8.
-
2009: Helisalmi Seppo; Väkevä Antti; Hiltunen Mikko; Soininen Hilkka
Flanking markers of cystatin c (CST3) gene do not show association with Alzheimer's disease.
Dementia and geriatric cognitive disorders 2009;27(4):318-21.
-
2008: Jaaskelainen E; Keski-Nisula L; Toivonen S; Paattiniemi E-L; Helisalmi S; Punnonen K; Heinonen S
Polymorphism of the interleukin 1 receptor antagonist (IL1Ra) gene and placental abruption.
Journal of reproductive immunology 2008;79(1):58-62.
-
2008: Helisalmi Seppo; Tarvainen Timo; Vepsäläinen Saila; Koivisto Anne Mari; Hiltunen Mikko; Soininen Hilkka
Lack of genetic association between PPARG gene polymorphisms and Finnish late-onset Alzheimer's disease.
Neuroscience letters 2008;441(2):233-6.
-
2008: Vepsäläinen Saila; Hiltunen Mikko; Helisalmi Seppo; Wang Jun; van Groen Thomas; Tanila Heikki; Soininen Hilkka
Increased expression of Abeta degrading enzyme IDE in the cortex of transgenic mice with Alzheimer's disease-like neuropathology.
Neuroscience letters 2008;438(2):216-20.
-
2008: Lämsä R; Helisalmi S; Herukka S-K; Tapiola T; Pirttilä T; Vepsäläinen S; Hiltunen M; Soininen H
Genetic study evaluating LDLR polymorphisms and Alzheimer's disease.
Neurobiology of aging 2008;29(6):848-55.
-
2008: Helisalmi S; Vepsäläinen S; Hiltunen M; Koivisto A M; Salminen A; Laakso M; Soininen H
Genetic study between SIRT1, PPARD, PGC-1alpha genes and Alzheimer's disease.
Journal of neurology 2008;255(5):668-73.
-
2008: Blom Elin S; Viswanathan Jayashree; Kilander Lena; Helisalmi Seppo; Soininen Hilkka; Lannfelt Lars; Ingelsson Martin; Glaser Anna; Hiltunen Mikko
Low prevalence of APP duplications in Swedish and Finnish patients with early-onset Alzheimer's disease.
European journal of human genetics : EJHG 2008;16(2):171-5.
-
2008: Jääskeläinen Ester; Toivonen Sari; Keski-Nisula Leea; Paattiniemi Eeva-Liisa; Helisalmi Seppo; Punnonen Kari; Heinonen Seppo
CTLA-4 polymorphism 49A-G is associated with placental abruption and preeclampsia in Finnish women.
Clinical chemistry and laboratory medicine : CCLM / FESCC 2008;46(2):169-73.
-
2008: Laasanen Jaana; Helisalmi Seppo; Iivonen Susan; Eloranta M-L; Hiltunen Mikko; Heinonen Seppo
Gamma 2 actin gene (enteric type) polymorphism is not associated with obstetric cholestasis or preeclampsia.
Fetal diagnosis and therapy 2008;23(1):36-40.
-
2007: Vepsäläinen Saila; Helisalmi Seppo; Koivisto Anne M; Tapaninen Toni; Hiltunen Mikko; Soininen Hilkka
Somatostatin genetic variants modify the risk for Alzheimer's disease among Finnish patients.
Journal of neurology 2007;254(11):1504-8.
-
2007: Lämsä R; Helisalmi S; Hiltunen M; Herukka S-K; Tapiola T; Pirttilä T; Vepsäläinen S; Soininen H
The association study between DHCR24 polymorphisms and Alzheimer's disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(7):906-10.
-
2007: Vepsäläinen Saila; Parkinson Michele; Helisalmi Seppo; Mannermaa Arto; Soininen Hilkka; Tanzi Rudolph E; Bertram Lars; Hiltunen Mikko
Insulin-degrading enzyme is genetically associated with Alzheimer's disease in the Finnish population.
Journal of medical genetics 2007;44(9):606-8.
-
2007: Herukka Sanna-Kaisa; Helisalmi Seppo; Hallikainen Merja; Tervo Susanna; Soininen Hilkka; Pirttilä Tuula
CSF Abeta42, Tau and phosphorylated Tau, APOE epsilon4 allele and MCI type in progressive MCI.
Neurobiology of aging 2007;28(4):507-14.
-
2007: Lamsa R; Helisalmi S; Herukka S-K; Tapiola T; Pirttila T; Vepsalainen S; Hiltunen M; Soininen H
Study on the association between SOAT1 polymorphisms, Alzheimer's disease risk and the level of CSF biomarkers.
Dementia and geriatric cognitive disorders 2007;24(2):146-50.
-
2006: Tuhkanen Hanna; Anttila Maarit; Kosma Veli-Matti; Heinonen Seppo; Juhola Matti; Helisalmi Seppo; Kataja Vesa; Mannermaa Arto
Frequent gene dosage alterations in stromal cells of epithelial ovarian carcinomas.
International journal of cancer. Journal international du cancer 2006;119(6):1345-53.
-
2006: Saarela Tanja; Hiltunen Mikko; Helisalmi Seppo; Heinonen Seppo; Laakso Markku
Polymorphisms of interleukin-6, hepatic lipase and calpain-10 genes, and preeclampsia.
European journal of obstetrics, gynecology, and reproductive biology 2006;128(1-2):175-9.
-
2006: Helisalmi S; Vepsäläinen S; Koivisto A M; Mannermaa A; Iivonen S; Hiltunen M; Kiviniemi V; Soininen H
Association of CYP46 intron 2 polymorphism in Finnish Alzheimer's disease samples and a global scale summary.
Journal of neurology, neurosurgery, and psychiatry 2006;77(3):421-2.
-
2006: Koivisto Anne M; Helisalmi Seppo; Pihlajamaki Jussi; Hiltunen Mikko; Koivisto Keijo; Moilanen Leena; Kuusisto Johanna; Helkala Eeva-Liisa; Hanninen Tuomo; Kervinen Kari; Kesaniemi Y Antero; Laakso Markku; Soininen Hilkka
Association analysis of peroxisome proliferator-activated receptor gamma polymorphisms and late onset Alzheimer's disease in the Finnish population.
Dementia and geriatric cognitive disorders 2006;22(5-6):449-53.
-
2006: Jääskeläinen Ester; Keski-Nisula Leea; Toivonen Sari; Romppanen Eeva-Liisa; Helisalmi Seppo; Punnonen Kari; Heinonen Seppo
MTHFR C677T polymorphism is not associated with placental abruption or preeclampsia in Finnish women.
Hypertension in pregnancy : official journal of the International Society for the Study of Hypertension in Pregnancy 2006;25(2):73-80.
-
2006: Saarela Tanja; Hiltunen Mikko; Helisalmi Seppo; Heinonen Seppo; Laakso Markku
Adiponectin gene haplotype is associated with preeclampsia.
Genetic testing 2006;10(1):35-9.
-
2006: Iivonen S; Heikkinen T; Puoliväli J; Helisalmi S; Hiltunen M; Soininen H; Tanila H
Effects of estradiol on spatial learning, hippocampal cytochrome P450 19, and estrogen alpha and beta mRNA levels in ovariectomized female mice.
Neuroscience 2006;137(4):1143-52.
-
2006: Saarela Tanja; Hiltunen Mikko; Helisalmi Seppo; Heinonen Seppo; Laakso Markku
Plasma cell membrane glycoprotein-1 K121Q polymorphism in preeclampsia.
Gynecologic and obstetric investigation 2006;61(3):124-7.
-
2005: Toivonen Sari; Keski-Nisula Leea; Romppanen Eeva-Liisa; Helisalmi Seppo; Punnonen Kari; Heinonen Seppo
Endothelial nitric oxide synthase polymorphism is not associated with placental abruption in Finnish women.
Fetal diagnosis and therapy 2005;20(6):508-11.
-
2005: Heinonen Seppo; Korhonen Seija; Helisalmi Seppo; Koivunen Riitta; Tapanainen Juha; Hippeläinen Maritta; Laakso Markku
Associations between two single nucleotide polymorphisms in the adiponectin gene and polycystic ovary syndrome.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2005;21(3):165-9.
-
2005: Pirskanen Mia; Hiltunen Mikko; Mannermaa Arto; Helisalmi Seppo; Lehtovirta Maarit; Hänninen Tuomo; Soininen Hilkka
Estrogen receptor beta gene variants are associated with increased risk of Alzheimer's disease in women.
European journal of human genetics : EJHG 2005;13(9):1000-6.
-
2005: Koivisto Anne M; Helisalmi Seppo; Pihlajamäki Jussi; Moilanen Leena; Kuusisto Johanna; Laakso Markku; Hiltunen Mikko; Keijo Koivisto; Hänninen Tuomo; Helkala Eeva-Liisa; Kervinen Kari; Kesäniemi Y Antero; Soininen Hilkka
Interleukin-6 promoter polymorphism and late-onset Alzheimer's disease in the Finnish population.
Journal of neurogenetics 2005;19(3-4):155-61.
-
2005: Saarela Tanja; Hiltunen Mikko; Helisalmi Seppo; Heinonen Seppo; Laakso Markku
Tumour necrosis factor-alpha gene haplotype is associated with pre-eclampsia.
Molecular human reproduction 2005;11(6):437-40.
-
2005: Vepsäläinen Saila; Castren Eero; Helisalmi Seppo; Iivonen Susan; Mannermaa Arto; Lehtovirta Maarit; Hänninen Tuomo; Soininen Hilkka; Hiltunen Mikko
Genetic analysis of BDNF and TrkB gene polymorphisms in Alzheimer's disease.
Journal of neurology 2005;252(4):423-8.
-
2004: Toivonen Sari; Romppanen Eeva-Liisa; Hiltunen Mikko; Helisalmi Seppo; Keski-Nisula Leea; Punnonen Kari; Heinonen Seppo
Low-activity haplotype of the microsomal epoxide hydrolase gene is protective against placental abruption.
Journal of the Society for Gynecologic Investigation 2004;11(8):540-4.
-
2004: Helisalmi S; Hiltunen M; Vepsäläinen S; Iivonen S; Mannermaa A; Lehtovirta M; Koivisto A M; Alafuzoff I; Soininen H
Polymorphisms in neprilysin gene affect the risk of Alzheimer's disease in Finnish patients.
Journal of neurology, neurosurgery, and psychiatry 2004;75(12):1746-8.
-
2004: Jääskeläinen E; Toivonen S; Romppanen E-L; Helisalmi S; Keski-Nisula L; Punnonen K; Heinonen S
M385T polymorphism in the factor V gene, but not Leiden mutation, is associated with placental abruption in Finnish women.
Placenta 2004;25(8-9):730-4.
-
2004: Heinonen Seppo; Korhonen Seija; Helisalmi Seppo; Koivunen Riitta; Tapanainen Juha S; Laakso Markku
The 121Q allele of the plasma cell membrane glycoprotein 1 gene predisposes to polycystic ovary syndrome.
Fertility and sterility 2004;82(3):743-5.
-
2004: Helisalmi Seppo; Hiltunen Mikko; Vepsäläinen Saila; Iivonen Susan; Corder Elizabeth H; Lehtovirta Maarit; Mannermaa Arto; Koivisto Anne Maria; Soininen Hilkka
Genetic variation in apolipoprotein D and Alzheimer's disease.
Journal of neurology 2004;251(8):951-7.
-
2004: Helisalmi S; Dermaut B; Hiltunen M; Mannermaa A; Van den Broeck M; Lehtovirta M; Koivisto A M; Iivonen S; Cruts M; Soininen H; Van Broeckhoven C
Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population.
Neurology 2004;63(1):173-5.
-
2004: Iivonen S; Corder E; Lehtovirta M; Helisalmi S; Mannermaa A; Vepsäläinen S; Hänninen T; Soininen H; Hiltunen M
Polymorphisms in the CYP19 gene confer increased risk for Alzheimer disease.
Neurology 2004;62(7):1170-6.
-
2004: Faisel Fareeza; Romppanen Eeva-Liisa; Hiltunen Mikko; Helisalmi Seppo; Laasanen Jaana; Punnonen Kari; Salonen Jukka T; Heinonen Seppo
Susceptibility to pre-eclampsia in Finnish women is associated with R485K polymorphism in the factor V gene, not with Leiden mutation.
European journal of human genetics : EJHG 2004;12(3):187-91.
-
2004: Hiltunen Mikko; Helisalmi Seppo; Kivipelto Miia; Soininen Hilkka
[Genetics of Alzheimer's disease]
Duodecim; lääketieteellinen aikakauskirja 2004;120(20):2425-31.
-
2003: Iivonen Susan; Helisalmi Seppo; Mannermaa Arto; Alafuzoff Irina; Lehtovirta Maarit; Soininen Hilkka; Hiltunen Mikko
Heparan sulfate proteoglycan 2 polymorphism in Alzheimer's disease and correlation with neuropathology.
Neuroscience letters 2003;352(2):146-50.
-
2003: Faisel Fareeza; Romppanen Eeva-Liisa; Hiltunen Mikko; Helisalmi Seppo; Punnonen Kari; Salonen Jukka; Heinonen Seppo
Polymorphism in the interleukin 1 receptor antagonist gene in women with preeclampsia.
Journal of reproductive immunology 2003;60(1):61-70.
-
2003: Eloranta M L; Häkli T; Hiltunen M; Helisalmi S; Punnonen K; Heinonen S
Association of single nucleotide polymorphisms of the bile salt export pump gene with intrahepatic cholestasis of pregnancy.
Scandinavian journal of gastroenterology 2003;38(6):648-52.
-
2003: Korhonen Seija; Romppanen Eeva Liisa; Hiltunen Mikko; Helisalmi Seppo; Punnonen Kari; Hippeläinen Maritta; Heinonen Seppo
Two exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are associated with polycystic ovary syndrome.
Fertility and sterility 2003;79(6):1353-7.
-
2003: Häkli Tanja; Romppanen Eeva-Liisa; Hiltunen Mikko; Helisalmi Seppo; Punnonen Kari; Heinonen Seppo
Endothelial nitric oxide synthase polymorphism in preeclampsia.
Journal of the Society for Gynecologic Investigation 2003;10(3):154-7.
-
2003: Korhonen S; Heinonen S; Hiltunen M; Helisalmi S; Hippeläinen M; Koivunen R; Tapanainen J S; Laakso M
Polymorphism in the peroxisome proliferator-activated receptor-gamma gene in women with polycystic ovary syndrome.
Human reproduction (Oxford, England) 2003;18(3):540-3.
-
2003: Häkli Tanja; Romppanen Eeva-Liisa; Hiltunen Mikko; Helisalmi Seppo; Punnonen Kari; Heinonen Seppo
Plasminogen activator inhibitor-1 polymorphism in women with pre-eclampsia.
Genetic testing 2003;7(3):265-8.
-
2002: Laasanen Jaana; Romppanen Eeva-Liisa; Hiltunen Mikko; Helisalmi Seppo; Mannermaa Arto; Punnonen Kari; Heinonen Seppo
Two exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are jointly associated with preeclampsia.
European journal of human genetics : EJHG 2002;10(9):569-73.
-
2002: Pirskanen Mia; Hiltunen Mikko; Mannermaa Arto; Iivonen Susan; Helisalmi Seppo; Lehtovirta Maarit; Koivisto Anne Maria; Laakso Markku; Soininen Hilkka; Alafuzoff Irina
Interleukin 1 alpha gene polymorphism as a susceptibility factor in Alzheimer's disease and its influence on the extent of histopathological hallmark lesions of Alzheimer's disease.
Dementia and geriatric cognitive disorders 2002;14(3):123-7.
-
2002: Iivonen S; Hiltunen M; Alafuzoff I; Mannermaa A; Kerokoski P; Puoliväli J; Salminen A; Helisalmi S; Soininen H
Seladin-1 transcription is linked to neuronal degeneration in Alzheimer's disease.
Neuroscience 2002;113(2):301-10.
-
2001: Hiltunen M; Mannermaa A; Thompson D; Easton D; Pirskanen M; Helisalmi S; Koivisto A M; Lehtovirta M; Ryynänen M; Soininen H
Genome-wide linkage disequilibrium mapping of late-onset Alzheimer's disease in Finland.
Neurology 2001;57(9):1663-8.
-
2001: Pirskanen M; Alafuzoff I; Hiltunen M; Mannermaa A; Helisalmi S; Lehtovirta M; Koivisto A M; Laakso M; Soininen H
An association between a subset of Finnish late-onset Alzheimer's disease and alpha2-macroglobulin.
Neurogenetics 2001;3(3):171-2.
-
2001: Heinonen S; Eloranta M L; Heiskanen J; Punnonen K; Helisalmi S; Mannermaa A; Hiltunen M
Maternal susceptibility locus for obstetric cholestasis maps to chromosome region 2p13 in Finnish patients.
Scandinavian journal of gastroenterology 2001;36(7):766-70.
-
2001: Kraszpulski M; Soininen H; Helisalmi S; Alafuzoff I
The load and distribution of beta-amyloid in brain tissue of patients with Alzheimer's disease.
Acta neurologica Scandinavica 2001;103(2):88-92.
-
2000: Overmyer M; Kraszpulski M; Helisalmi S; Soininen H; Alafuzoff I
DNA fragmentation, gliosis and histological hallmarks of Alzheimer's disease.
Acta neuropathologica 2000;100(6):681-7.
-
2000: Reynolds W F; Hiltunen M; Pirskanen M; Mannermaa A; Helisalmi S; Lehtovirta M; Alafuzoff I; Soininen H
MPO and APOEepsilon4 polymorphisms interact to increase risk for AD in Finnish males.
Neurology 2000;55(9):1284-90.
-
2000: Eloranta M L; Heiskanen J; Hiltunen M; Helisalmi S; Mannermaa A; Heinonen S
Apolipoprotein E alleles in women with intrahepatic cholestasis of pregnancy.
Scandinavian journal of gastroenterology 2000;35(9):966-8.
-
2000: Helisalmi S; Valve R; Karvonen M K; Hiltunen M; Pirskanen M; Mannermaa A; Koulu M; Pesonen U; Uusitupa M; Soininen H
The leucine (7)-to-proline (7) polymorphism in the signal peptide of neuropeptide Y is not associated with Alzheimer's disease or the link apolipoprotein E.
Neuroscience letters 2000;287(1):25-8.
-
2000: Hiltunen M; Helisalmi S; Mannermaa A; Alafuzoff I; Koivisto A M; Lehtovirta M; Pirskanen M; Sulkava R; Verkkoniemi A; Soininen H
Identification of a novel 4.6-kb genomic deletion in presenilin-1 gene which results in exclusion of exon 9 in a Finnish early onset Alzheimer's disease family: an Alu core sequence-stimulated recombination?
European journal of human genetics : EJHG 2000;8(4):259-66.
-
2000: Alafuzoff I; Helisalmi S; Mannermaa A; Soininen H
Severity of cardiovascular disease, apolipoprotein E genotype, and brain pathology in aging and dementia.
Annals of the New York Academy of Sciences 2000;903():244-51.
-
2000: Alafuzoff I; Helisalmi S; Heinonen E H; Reinikainen K; Hallikainen M; Soininen H; Koivisto K
Selegiline treatment and the extent of degenerative changes in brain tissue of patients with Alzheimer's disease.
European journal of clinical pharmacology 2000;55(11-12):815-9.
-
2000: Helisalmi S; Hiltunen M; Mannermaa A; Koivisto A M; Lehtovirta M; Alafuzoff I; Ryynänen M; Soininen H
Is the presenilin-1 E318G missense mutation a risk factor for Alzheimer's disease?
Neuroscience letters 2000;278(1-2):65-8.
-
2000: Lehtovirta M; Partanen J; Könönen M; Hiltunen J; Helisalmi S; Hartikainen P; Riekkinen P; Soininen H
A longitudinal quantitative EEG study of Alzheimer's disease: relation to apolipoprotein E polymorphism.
Dementia and geriatric cognitive disorders 2000;11(1):29-35.
-
1999: Helisalmi S; Hiltunen M; Valonen P; Mannermaa A; Koivisto A M; Lehtovirta M; Ryynänen M; Soininen H
Promoter polymorphism (-491A/T) in the APOE gene of Finnish Alzheimer's disease patients and control individuals.
Journal of neurology 1999;246(9):821-4.
-
1999: Hiltunen M; Mannermaa A; Koivisto A M; Lehtovirta M; Helisalmi S; Ryynänen M; Riekkinen P; Soininen H
Linkage disequilibrium in the 13q12 region in Finnish late onset Alzheimer's disease patients.
European journal of human genetics : EJHG 1999;7(6):652-8.
-
1999: Overmyer M; Helisalmi S; Soininen H; Laakso M; Riekkinen P; Alafuzoff I
Astrogliosis and the ApoE genotype. an immunohistochemical study of postmortem human brain tissue.
Dementia and geriatric cognitive disorders 1999;10(4):252-7.
-
1999: Overmyer M; Helisalmi S; Soininen H; Laakso M; Riekkinen P; Alafuzoff I
Reactive microglia in aging and dementia: an immunohistochemical study of postmortem human brain tissue.
Acta neuropathologica 1999;97(4):383-92.
-
1998: Juottonen K; Lehtovirta M; Helisalmi S; Riekkinen P J; Soininen H
Major decrease in the volume of the entorhinal cortex in patients with Alzheimer's disease carrying the apolipoprotein E epsilon4 allele.
Journal of neurology, neurosurgery, and psychiatry 1998;65(3):322-7.
-
1998: Hiltunen M; Mannermaa A; Helisalmi S; Koivisto A; Lehtovirta M; Ryynänen M; Riekkinen P; Soininen H
Butyrylcholinesterase K variant and apolipoprotein E4 genes do not act in synergy in Finnish late-onset Alzheimer's disease patients.
Neuroscience letters 1998;250(1):69-71.
-
1998: Lehtovirta M; Kuikka J; Helisalmi S; Hartikainen P; Mannermaa A; Ryynänen M; Riekkinen PSr; Soininen H
Longitudinal SPECT study in Alzheimer's disease: relation to apolipoprotein E polymorphism.
Journal of neurology, neurosurgery, and psychiatry 1998;64(6):742-6.
-
1998: Tapiola T; Lehtovirta M; Ramberg J; Helisalmi S; Linnaranta K; Riekkinen P; Soininen H
CSF tau is related to apolipoprotein E genotype in early Alzheimer's disease.
Neurology 1998;50(1):169-74.
-
1997: Tapiola T; Overmyer M; Lehtovirta M; Helisalmi S; Ramberg J; Alafuzoff I; Riekkinen P; Soininen H
The level of cerebrospinal fluid tau correlates with neurofibrillary tangles in Alzheimer's disease.
Neuroreport 1997;8(18):3961-3.
-
1997: Helisalmi S; Mannermaa A; Lehtovirta M; Ryynänen M; Riekkinen P; Soininen H
No association between alpha1-antichymotrypsin polymorphism, apolipoprotein E and patients with late-onset Alzheimer's disease.
Neuroscience letters 1997;231(1):56-8.
-
1996: Lehtovirta M; Partanen J; Könönen M; Soininen H; Helisalmi S; Mannermaa A; Ryynänen M; Hartikainen P; Riekkinen P
Spectral analysis of EEG in Alzheimer's disease: relation to apolipoprotein E polymorphism.
Neurobiology of aging 1996;17(4):523-6.
-
1996: Lehtovirta M; Soininen H; Laakso M P; Partanen K; Helisalmi S; Mannermaa A; Ryynänen M; Kuikka J; Hartikainen P; Riekkinen P J
SPECT and MRI analysis in Alzheimer's disease: relation to apolipoprotein E epsilon 4 allele.
Journal of neurology, neurosurgery, and psychiatry 1996;60(6):644-9.
-
1996: Helisalmi S; Mannermaa A; Lehtovirta M; Ryynänen M; Riekkinen P; Soininen H
Screening for amyloid beta precursor protein codon 665, 670/671 and 717 mutations in Finnish patients with Alzheimer's disease.
Neuroscience letters 1996;205(1):68-70.
-
1996: Helisalmi S; Linnaranta K; Lehtovirta M; Mannermaa A; Heinonen O; Ryynänen M; Riekkinen P; Soininen H
Apolipoprotein E polymorphism in patients with different neurodegenerative disorders.
Neuroscience letters 1996;205(1):61-4.
-
1996: Lehtovirta M; Soininen H; Helisalmi S; Mannermaa A; Helkala E L; Hartikainen P; Hänninen T; Ryynänen M; Riekkinen P J
Clinical and neuropsychological characteristics in familial and sporadic Alzheimer's disease: relation to apolipoprotein E polymorphism.
Neurology 1996;46(2):413-9.
-
1995: Soininen H; Lehtovirta M; Helisalmi S; Linnaranta K; Heinonen O; Riekkinen P
Increased acetylcholinesterase activity in the CSF of Alzheimer patients carrying apolipoprotein epsilon4 allele.
Neuroreport 1995;6(18):2518-20.
-
1995: Heinonen O; Lehtovirta M; Soininen H; Helisalmi S; Mannermaa A; Sorvari H; Kosunen O; Paljärvi L; Ryynänen M; Riekkinen P J
Alzheimer pathology of patients carrying apolipoprotein E epsilon 4 allele.
Neurobiology of aging 1995;16(4):505-13.
-
1995: Lehtovirta M; Laakso M P; Soininen H; Helisalmi S; Mannermaa A; Helkala E L; Partanen K; Ryynänen M; Vainio P; Hartikainen P
Volumes of hippocampus, amygdala and frontal lobe in Alzheimer patients with different apolipoprotein E genotypes.
Neuroscience 1995;67(1):65-72.
-
1995: Kosunen O; Talasniemi S; Lehtovirta M; Heinonen O; Helisalmi S; Mannermaa A; Paljärvi L; Ryynänen M; Riekkinen P J; Soininen H
Relation of coronary atherosclerosis and apolipoprotein E genotypes in Alzheimer patients.
Stroke; a journal of cerebral circulation 1995;26(5):743-8.
-
1995: Soininen H; Kosunen O; Helisalmi S; Mannermaa A; Paljärvi L; Talasniemi S; Ryynänen M; Riekkinen P
A severe loss of choline acetyltransferase in the frontal cortex of Alzheimer patients carrying apolipoprotein epsilon 4 allele.
Neuroscience letters 1995;187(2):79-82.
-
1995: Soininen H; Partanen K; Pitkänen A; Hallikainen M; Hänninen T; Helisalmi S; Mannermaa A; Ryynänen M; Koivisto K; Riekkinen P
Decreased hippocampal volume asymmetry on MRIs in nondemented elderly subjects carrying the apolipoprotein E epsilon 4 allele.
Neurology 1995;45(2):391-2.
-
1995: Lehtovirta M; Helisalmi S; Mannermaa A; Soininen H; Koivisto K; Ryynänen M; Riekkinen P
Apolipoprotein E polymorphism and Alzheimer's disease in eastern Finland.
Neuroscience letters 1995;185(1):13-5.
Sign-in to see more