Nokelainen P - Search Results

1

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.

Nokelainen P, Alanen-Kurki L, Winqvist R, Falck B, Somer H, Leisti J, Johnson K, Savontaus ML, Peltonen L. Nokelainen P, et al. Hum Genet. 1990 Oct;85(5):541-5. doi: 10.1007/BF00194234. Hum Genet. 1990. PMID: 1977684

2

Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy.

Nokelainen PT, Alanen-Kurki L, Somer HV, Pihko SH, Peltonen L. Nokelainen PT, et al. Muscle Nerve. 1991 May;14(5):451-6. doi: 10.1002/mus.880140511. Muscle Nerve. 1991. PMID: 1678492

3

The DM mutation; diagnostic applications in the Finnish population.

Nokelainen P, Shelbourne P, Shaw D, Brook JD, Harley HG, Johnson K, Somer H, Savontaus ML, Peltonen L. Nokelainen P, et al. Clin Genet. 1993 Apr;43(4):190-5. doi: 10.1111/j.1399-0004.1993.tb04446.x. Clin Genet. 1993. PMID: 8101149

4

Linkage analyses in tibial muscular dystrophy.

Nokelainen P, Udd B, Somer H, Peltonen L. Nokelainen P, et al. Hum Hered. 1996 Mar-Apr;46(2):98-107. doi: 10.1159/000154334. Hum Hered. 1996. PMID: 8666419

5

A microsatellite polymorphism in the von Willebrand factor gene: comparison of allele frequencies in different population samples and evaluation for forensic medicine.

Sajantila A, Pacek P, Lukka M, Syvänen AC, Nokelainen P, Sistonen P, Peltonen L, Budowle B. Sajantila A, et al. Among authors: nokelainen p. Forensic Sci Int. 1994 Sep 16;68(2):91-102. doi: 10.1016/0379-0738(94)90307-7. Forensic Sci Int. 1994. PMID: 7988968

6

Meiotic drive at the myotonic dystrophy locus?

Carey N, Johnson K, Nokelainen P, Peltonen L, Savontaus ML, Juvonen V, Anvret M, Grandell U, Chotai K, Robertson E, et al. Carey N, et al. Among authors: nokelainen p. Nat Genet. 1994 Feb;6(2):117-8. doi: 10.1038/ng0294-117. Nat Genet. 1994. PMID: 8162064 No abstract available.

7

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.

Davies J, Yamagata H, Shelbourne P, Buxton J, Ogihara T, Nokelainen P, Nakagawa M, Williamson R, Johnson K, Miki T. Davies J, et al. Among authors: nokelainen p. J Med Genet. 1992 Nov;29(11):766-9. doi: 10.1136/jmg.29.11.766. J Med Genet. 1992. PMID: 1453423 Free PMC article.

8

Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy.

Udd B, Rapola J, Nokelainen P, Arikawa E, Somer H. Udd B, et al. Among authors: nokelainen p. J Neurol Sci. 1992 Dec;113(2):214-21. doi: 10.1016/0022-510x(92)90249-k. J Neurol Sci. 1992. PMID: 1487757

9

A patient with 2 different repeat expansion mutations.

Nokelainen P, Heiskala H, Lehesjoki AE, Kaski M. Nokelainen P, et al. Arch Neurol. 2000 Aug;57(8):1199-203. doi: 10.1001/archneur.57.8.1199. Arch Neurol. 2000. PMID: 10927802

10

Two brothers with macrocephaly, progressive cerebral atrophy and abnormal white matter, severe mental retardation, and Lennox-Gastaut spectrum type epilepsy: an inherited encephalopathy of childhood?

Nokelainen P, Heiskala H, Raininko R, Autti T, Wirtavuori K, Häkkinen AM, Flint J. Nokelainen P, et al. Am J Med Genet. 2001 Oct 15;103(3):198-206. doi: 10.1002/ajmg.1536.abs. Am J Med Genet. 2001. PMID: 11745991

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