Hiltunen M - Search Results

1

GRN variant rs5848 reduces plasma and brain levels of granulin in Alzheimer's disease patients.

Kämäläinen A, Viswanathan J, Natunen T, Helisalmi S, Kauppinen T, Pikkarainen M, Pursiheimo JP, Alafuzoff I, Kivipelto M, Haapasalo A, Soininen H, Herukka SK, Hiltunen M. Kämäläinen A, et al. Among authors: hiltunen m. J Alzheimers Dis. 2013;33(1):23-7. doi: 10.3233/JAD-2012-120946. J Alzheimers Dis. 2013. PMID: 22890097

2

Butyrylcholinesterase K variant and apolipoprotein E4 genes do not act in synergy in Finnish late-onset Alzheimer's disease patients.

Hiltunen M, Mannermaa A, Helisalmi S, Koivisto A, Lehtovirta M, Ryynänen M, Riekkinen P Sr, Soininen H. Hiltunen M, et al. Neurosci Lett. 1998 Jun 26;250(1):69-71. doi: 10.1016/s0304-3940(98)00453-4. Neurosci Lett. 1998. PMID: 9696068

3

Linkage disequilibrium in the 13q12 region in Finnish late onset Alzheimer's disease patients.

Hiltunen M, Mannermaa A, Koivisto AM, Lehtovirta M, Helisalmi S, Ryynänen M, Riekkinen P Sr, Soininen H. Hiltunen M, et al. Eur J Hum Genet. 1999 Sep;7(6):652-8. doi: 10.1038/sj.ejhg.5200342. Eur J Hum Genet. 1999. PMID: 10482953

4

Promoter polymorphism (-491A/T) in the APOE gene of Finnish Alzheimer's disease patients and control individuals.

Helisalmi S, Hiltunen M, Valonen P, Mannermaa A, Koivisto AM, Lehtovirta M, Ryynänen M, Soininen H. Helisalmi S, et al. Among authors: hiltunen m. J Neurol. 1999 Sep;246(9):821-4. doi: 10.1007/s004150050461. J Neurol. 1999. PMID: 10525981 Clinical Trial.

5

Is the presenilin-1 E318G missense mutation a risk factor for Alzheimer's disease?

Helisalmi S, Hiltunen M, Mannermaa A, Koivisto AM, Lehtovirta M, Alafuzoff I, Ryynänen M, Soininen H. Helisalmi S, et al. Among authors: hiltunen m. Neurosci Lett. 2000 Jan 7;278(1-2):65-8. doi: 10.1016/s0304-3940(99)00891-5. Neurosci Lett. 2000. PMID: 10643802

6

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.

Helisalmi S, Valve R, Karvonen MK, Hiltunen M, Pirskanen M, Mannermaa A, Koulu M, Pesonen U, Uusitupa M, Soininen H. Helisalmi S, et al. Among authors: hiltunen m. Neurosci Lett. 2000 Jun 16;287(1):25-8. doi: 10.1016/s0304-3940(00)01126-5. Neurosci Lett. 2000. PMID: 10841982

7

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?

Hiltunen M, Helisalmi S, Mannermaa A, Alafuzoff I, Koivisto AM, Lehtovirta M, Pirskanen M, Sulkava R, Verkkoniemi A, Soininen H. Hiltunen M, et al. Eur J Hum Genet. 2000 Apr;8(4):259-66. doi: 10.1038/sj.ejhg.5200423. Eur J Hum Genet. 2000. PMID: 10854108

8

Apolipoprotein E alleles in women with intrahepatic cholestasis of pregnancy.

Eloranta ML, Heiskanen J, Hiltunen M, Helisalmi S, Mannermaa A, Heinonen S. Eloranta ML, et al. Among authors: hiltunen m. Scand J Gastroenterol. 2000 Sep;35(9):966-8. doi: 10.1080/003655200750023048. Scand J Gastroenterol. 2000. PMID: 11063158

9

MPO and APOEepsilon4 polymorphisms interact to increase risk for AD in Finnish males.

Reynolds WF, Hiltunen M, Pirskanen M, Mannermaa A, Helisalmi S, Lehtovirta M, Alafuzoff I, Soininen H. Reynolds WF, et al. Among authors: hiltunen m. Neurology. 2000 Nov 14;55(9):1284-90. doi: 10.1212/wnl.55.9.1284. Neurology. 2000. PMID: 11087769

10

Maternal susceptibility locus for obstetric cholestasis maps to chromosome region 2p13 in Finnish patients.

Heinonen S, Eloranta ML, Heiskanen J, Punnonen K, Helisalmi S, Mannermaa A, Hiltunen M. Heinonen S, et al. Among authors: hiltunen m. Scand J Gastroenterol. 2001 Jul;36(7):766-70. doi: 10.1080/003655201300192049. Scand J Gastroenterol. 2001. PMID: 11444477

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