Ryynänen M - Search Results

1

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. Among authors: ryynanen m. Neurosci Lett. 1998 Jun 26;250(1):69-71. doi: 10.1016/s0304-3940(98)00453-4. Neurosci Lett. 1998. PMID: 9696068

2

Apolipoprotein E polymorphism in patients with different neurodegenerative disorders.

Helisalmi S, Linnaranta K, Lehtovirta M, Mannermaa A, Heinonen O, Ryynänen M, Riekkinen P Sr, Soininen H. Helisalmi S, et al. Among authors: ryynanen m. Neurosci Lett. 1996 Feb 16;205(1):61-4. doi: 10.1016/0304-3940(96)12373-9. Neurosci Lett. 1996. PMID: 8867021

3

Screening for amyloid beta precursor protein codon 665, 670/671 and 717 mutations in Finnish patients with Alzheimer's disease.

Helisalmi S, Mannermaa A, Lehtovirta M, Ryynänen M, Riekkinen P Sr, Soininen H. Helisalmi S, et al. Among authors: ryynanen m. Neurosci Lett. 1996 Feb 16;205(1):68-70. doi: 10.1016/0304-3940(96)12364-8. Neurosci Lett. 1996. PMID: 8867023

4

No association between alpha1-antichymotrypsin polymorphism, apolipoprotein E and patients with late-onset Alzheimer's disease.

Helisalmi S, Mannermaa A, Lehtovirta M, Ryynänen M, Riekkinen P Sr, Soininen H. Helisalmi S, et al. Among authors: ryynanen m. Neurosci Lett. 1997 Aug 1;231(1):56-8. doi: 10.1016/s0304-3940(97)00525-9. Neurosci Lett. 1997. PMID: 9280167

5

Longitudinal SPECT study in Alzheimer's disease: relation to apolipoprotein E polymorphism.

Lehtovirta M, Kuikka J, Helisalmi S, Hartikainen P, Mannermaa A, Ryynänen M, Riekkinen PSr, Soininen H. Lehtovirta M, et al. Among authors: ryynanen m. J Neurol Neurosurg Psychiatry. 1998 Jun;64(6):742-6. doi: 10.1136/jnnp.64.6.742. J Neurol Neurosurg Psychiatry. 1998. PMID: 9647302 Free PMC article.

6

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. Among authors: ryynanen m. Eur J Hum Genet. 1999 Sep;7(6):652-8. doi: 10.1038/sj.ejhg.5200342. Eur J Hum Genet. 1999. PMID: 10482953

7

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: ryynanen m. J Neurol. 1999 Sep;246(9):821-4. doi: 10.1007/s004150050461. J Neurol. 1999. PMID: 10525981 Clinical Trial.

8

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: ryynanen m. Neurosci Lett. 2000 Jan 7;278(1-2):65-8. doi: 10.1016/s0304-3940(99)00891-5. Neurosci Lett. 2000. PMID: 10643802

9

Genome-wide linkage disequilibrium mapping of late-onset Alzheimer's disease in Finland.

Hiltunen M, Mannermaa A, Thompson D, Easton D, Pirskanen M, Helisalmi S, Koivisto AM, Lehtovirta M, Ryynänen M, Soininen H. Hiltunen M, et al. Among authors: ryynanen m. Neurology. 2001 Nov 13;57(9):1663-8. doi: 10.1212/wnl.57.9.1663. Neurology. 2001. PMID: 11706108

10

Volumes of hippocampus, amygdala and frontal lobe in Alzheimer patients with different apolipoprotein E genotypes.

Lehtovirta M, Laakso MP, Soininen H, Helisalmi S, Mannermaa A, Helkala EL, Partanen K, Ryynänen M, Vainio P, Hartikainen P, et al. Lehtovirta M, et al. Among authors: ryynanen m. Neuroscience. 1995 Jul;67(1):65-72. doi: 10.1016/0306-4522(95)00014-a. Neuroscience. 1995. PMID: 7477910 Clinical Trial.

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