Silander K - Search Results

1

Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies.

Silander K, Meretoja P, Juvonen V, Ignatius J, Pihko H, Saarinen A, Wallden T, Herrgård E, Aula P, Savontaus ML. Silander K, et al. Hum Mutat. 1998;12(1):59-68. doi: 10.1002/(SICI)1098-1004(1998)12:1<59::AID-HUMU9>3.0.CO;2-A. Hum Mutat. 1998. PMID: 9633821

2

A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patients.

Silander K, Meretoja P, Nelis E, Timmerman V, Van Broeckhoven C, Aula P, Savontaus ML. Silander K, et al. Hum Mutat. 1996;8(4):304-10. doi: 10.1002/(SICI)1098-1004(1996)8:4<304::AID-HUMU2>3.0.CO;2-7. Hum Mutat. 1996. PMID: 8956034

3

Screening for connexin 32 mutations in Charcot-Marie-Tooth disease families with possible X-linked inheritance.

Silander K, Meretoja P, Pihko H, Juvonen V, Issakainen J, Aula P, Savontaus ML. Silander K, et al. Hum Genet. 1997 Sep;100(3-4):391-7. doi: 10.1007/s004390050522. Hum Genet. 1997. PMID: 9272161

4

DNA analysis in Finnish patients with hereditary neuropathy with liability to pressure palsies (HNPP).

Silander K, Halonen P, Sara R, Kalimo H, Falck B, Savontaus ML. Silander K, et al. J Neurol Neurosurg Psychiatry. 1994 Oct;57(10):1260-2. doi: 10.1136/jnnp.57.10.1260. J Neurol Neurosurg Psychiatry. 1994. PMID: 7931393 Free PMC article.

5

Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study.

Nelis E, Van Broeckhoven C, De Jonghe P, Löfgren A, Vandenberghe A, Latour P, Le Guern E, Brice A, Mostacciuolo ML, Schiavon F, Palau F, Bort S, Upadhyaya M, Rocchi M, Archidiacono N, Mandich P, Bellone E, Silander K, Savontaus ML, Navon R, Goldberg-Stern H, Estivill X, Volpini V, Friedl W, Gal A, et al. Nelis E, et al. Among authors: silander k. Eur J Hum Genet. 1996;4(1):25-33. doi: 10.1159/000472166. Eur J Hum Genet. 1996. PMID: 8800924 Free article.

6

Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western Finland.

Meretoja P, Silander K, Kalimo H, Aula P, Meretoja A, Savontaus ML. Meretoja P, et al. Among authors: silander k. Neuromuscul Disord. 1997 Dec;7(8):529-32. doi: 10.1016/s0960-8966(97)00100-4. Neuromuscul Disord. 1997. PMID: 9447611

7

[Hereditary neuropathy with liability to pressure palsies--a more common neuropathy than generally thought].

Meretoja P, Silander K, Savontaus ML, Kalimo H. Meretoja P, et al. Among authors: silander k. Duodecim. 1998;114(24):2569-74. Duodecim. 1998. PMID: 11757129 Review. Finnish. No abstract available.

8

Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP.

Lopes J, Tardieu S, Silander K, Blair I, Vandenberghe A, Palau F, Ruberg M, Brice A, LeGuern E. Lopes J, et al. Among authors: silander k. Hum Mol Genet. 1999 Nov;8(12):2285-92. doi: 10.1093/hmg/8.12.2285. Hum Mol Genet. 1999. PMID: 10545609

9

Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts.

Alanne M, Kristiansson K, Auro K, Silander K, Kuulasmaa K, Peltonen L, Salomaa V, Perola M. Alanne M, et al. Among authors: silander k. Hum Genet. 2007 Nov;122(3-4):355-65. doi: 10.1007/s00439-007-0402-7. Epub 2007 Jul 20. Hum Genet. 2007. PMID: 17641917

10

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.

Ghosh S, Watanabe RM, Valle TT, Hauser ER, Magnuson VL, Langefeld CD, Ally DS, Mohlke KL, Silander K, Kohtamäki K, Chines P, Balow J Jr, Birznieks G, Chang J, Eldridge W, Erdos MR, Karanjawala ZE, Knapp JI, Kudelko K, Martin C, Morales-Mena A, Musick A, Musick T, Pfahl C, Porter R, Rayman JB. Ghosh S, et al. Among authors: silander k. Am J Hum Genet. 2000 Nov;67(5):1174-85. Epub 2000 Oct 13. Am J Hum Genet. 2000. PMID: 11032783 Free PMC article.

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