Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

334 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Leber's hereditary optic neuroretinopathy, a mitochondrial disease?
Nikoskelainen E, Hassinen IE, Paljärvi L, Lang H, Kalimo H. Nikoskelainen E, et al. Among authors: kalimo h. Lancet. 1984 Dec 22;2(8417-8418):1474. doi: 10.1016/s0140-6736(84)91669-6. Lancet. 1984. PMID: 6151084 No abstract available.
Dipeptidyl carboxypeptidase 1 (DCP1) and butyrylcholinesterase (BCHE) gene interactions with the apolipoprotein E epsilon4 allele as risk factors in Alzheimer's disease and in Parkinson's disease with coexisting Alzheimer pathology.
Mattila KM, Rinne JO, Röyttä M, Laippala P, Pietilä T, Kalimo H, Koivula T, Frey H, Lehtimäki T. Mattila KM, et al. Among authors: kalimo h. J Med Genet. 2000 Oct;37(10):766-70. doi: 10.1136/jmg.37.10.766. J Med Genet. 2000. PMID: 11015454 Free PMC article.
[Facioscapulohumeral muscular dystrophy].
Halonen P, Alanen A, Falck B, Kalimo H, Kiuru A, Lang H, Savontaus ML, Sonninen V. Halonen P, et al. Among authors: kalimo h. Duodecim. 1990;106(17):1210-8. Duodecim. 1990. PMID: 1670542 Review. Finnish. No abstract available.
Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL.
Annunen-Rasila J, Finnilä S, Mykkänen K, Moilanen JS, Veijola J, Pöyhönen M, Viitanen M, Kalimo H, Majamaa K. Annunen-Rasila J, et al. Among authors: kalimo h. Neurogenetics. 2006 Jul;7(3):185-94. doi: 10.1007/s10048-006-0049-x. Epub 2006 Jun 29. Neurogenetics. 2006. PMID: 16807713
Detection of the founder effect in Finnish CADASIL families.
Mykkänen K, Savontaus ML, Juvonen V, Sistonen P, Tuisku S, Tuominen S, Penttinen M, Lundkvist J, Viitanen M, Kalimo H, Pöyhönen M. Mykkänen K, et al. Among authors: kalimo h. Eur J Hum Genet. 2004 Oct;12(10):813-9. doi: 10.1038/sj.ejhg.5201221. Eur J Hum Genet. 2004. PMID: 15378071
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene.
Kousi M, Anttila V, Schulz A, Calafato S, Jakkula E, Riesch E, Myllykangas L, Kalimo H, Topçu M, Gökben S, Alehan F, Lemke JR, Alber M, Palotie A, Kopra O, Lehesjoki AE. Kousi M, et al. Among authors: kalimo h. J Med Genet. 2012 Jun;49(6):391-9. doi: 10.1136/jmedgenet-2012-100859. J Med Genet. 2012. PMID: 22693283 Free PMC article.
334 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page