Wahlström J - Search Results

1

Mutations and sequence variation in the human myosin heavy chain IIa gene (MYH2).

Tajsharghi H, Darin N, Rekabdar E, Kyllerman M, Wahlström J, Martinsson T, Oldfors A. Tajsharghi H, et al. Among authors: wahlstrom j. Eur J Hum Genet. 2005 May;13(5):617-22. doi: 10.1038/sj.ejhg.5201375. Eur J Hum Genet. 2005. PMID: 15741996

2

Dominant hereditary inclusion-body myopathy gene (IBM3) maps to chromosome region 17p13.1.

Martinsson T, Darin N, Kyllerman M, Oldfors A, Hallberg B, Wahlström J. Martinsson T, et al. Among authors: wahlstrom j. Am J Hum Genet. 1999 May;64(5):1420-6. doi: 10.1086/302375. Am J Hum Genet. 1999. PMID: 10205275 Free PMC article.

3

Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene.

Martinsson T, Oldfors A, Darin N, Berg K, Tajsharghi H, Kyllerman M, Wahlstrom J. Martinsson T, et al. Among authors: wahlstrom j. Proc Natl Acad Sci U S A. 2000 Dec 19;97(26):14614-9. doi: 10.1073/pnas.250289597. Proc Natl Acad Sci U S A. 2000. PMID: 11114175 Free PMC article.

4

Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age.

Tajsharghi H, Thornell LE, Darin N, Martinsson T, Kyllerman M, Wahlström J, Oldfors A. Tajsharghi H, et al. Among authors: wahlstrom j. Neurology. 2002 Mar 12;58(5):780-6. doi: 10.1212/wnl.58.5.780. Neurology. 2002. PMID: 11889243

5

Dilated cardiomyopathy and the dystrophin gene: an illustrated review.

Oldfors A, Eriksson BO, Kyllerman M, Martinsson T, Wahlström J. Oldfors A, et al. Among authors: wahlstrom j. Br Heart J. 1994 Oct;72(4):344-8. doi: 10.1136/hrt.72.4.344. Br Heart J. 1994. PMID: 7833192 Free PMC article. Review.

6

Duchenne muscular dystrophy and spinal muscular atrophy type I segregating in the same family.

Oldfors A, Martinsson T, Tessin I, Wahlström J, Wang S. Oldfors A, et al. Among authors: wahlstrom j. Clin Genet. 1994 Feb;45(2):97-103. doi: 10.1111/j.1399-0004.1994.tb04002.x. Clin Genet. 1994. PMID: 8004806

7

Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles.

Darin N, Kyllerman M, Wahlström J, Martinsson T, Oldfors A. Darin N, et al. Among authors: wahlstrom j. Ann Neurol. 1998 Aug;44(2):242-8. doi: 10.1002/ana.410440215. Ann Neurol. 1998. PMID: 9708547

8

Cytogenetic analysis of 477 psoriatics revealed an increased frequency of aberrations involving chromosome region 11q.

Enerbäck C, Holmqvist D, Inerot A, Enlund F, Samuelsson L, Torinsson A, Wahlström J, Swanbeck G, Martinsson T. Enerbäck C, et al. Among authors: wahlstrom j. Eur J Hum Genet. 1999 Apr;7(3):339-44. doi: 10.1038/sj.ejhg.5200311. Eur J Hum Genet. 1999. PMID: 10234510

9

Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy.

Jansson M, Darin N, Kyllerman M, Martinsson T, Wahlström J, Oldfors A. Jansson M, et al. Among authors: wahlstrom j. Acta Neuropathol. 2000 Jul;100(1):23-8. doi: 10.1007/s004010051188. Acta Neuropathol. 2000. PMID: 10912916

10

Scandinavian CDG-Ia patients: genotype/phenotype correlation and geographic origin of founder mutations.

Erlandson A, Bjursell C, Stibler H, Kristiansson B, Wahlström J, Martinsson T. Erlandson A, et al. Among authors: wahlstrom j. Hum Genet. 2001 May;108(5):359-67. doi: 10.1007/s004390100489. Hum Genet. 2001. PMID: 11409861

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