Wahlström J - Search Results

1

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.

2

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

3

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

4

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

5

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.

6

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

7

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

8

X-linked myotubular myopathy: clinical and pathological findings in a family.

Oldfors A, Kyllerman M, Wahlström J, Darnfors C, Henriksson KG. Oldfors A, et al. Among authors: wahlstrom j. Clin Genet. 1989 Jul;36(1):5-14. doi: 10.1111/j.1399-0004.1989.tb03360.x. Clin Genet. 1989. PMID: 2670345 Review.

9

Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406.

Martinsson T, Bjursell C, Stibler H, Kristiansson B, Skovby F, Jaeken J, Blennow G, Strömme P, Hanefeld F, Wahlström J. Martinsson T, et al. Among authors: wahlstrom j. Hum Mol Genet. 1994 Nov;3(11):2037-42. Hum Mol Genet. 1994. PMID: 7874123

10

A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family.

Nordling M, Karlsson P, Wahlström J, Engwall Y, Wallgren A, Martinsson T. Nordling M, et al. Among authors: wahlstrom j. Cancer Res. 1998 Apr 1;58(7):1372-5. Cancer Res. 1998. PMID: 9537232

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