Edström L - Search Results

1

A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.

Xiang F, Almqvist EW, Huq M, Lundin A, Hayden MR, Edström L, Anvret M, Zhang Z. Xiang F, et al. Among authors: edstrom l. Am J Hum Genet. 1998 Nov;63(5):1431-8. doi: 10.1086/302093. Am J Hum Genet. 1998. PMID: 9792871 Free PMC article.

2

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.

Xiang F, Zhang Z, Clarke A, Joseluiz P, Sakkubai N, Sarojini B, Delozier-Blanchet CD, Hansmann I, Edström L, Anvret M. Xiang F, et al. Among authors: edstrom l. J Med Genet. 1998 Apr;35(4):297-300. doi: 10.1136/jmg.35.4.297. J Med Genet. 1998. PMID: 9598723 Free PMC article.

3

Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q.

Nicolao P, Xiang F, Gunnarsson LG, Giometto B, Edström L, Anvret M, Zhang Z. Nicolao P, et al. Among authors: edstrom l. Am J Hum Genet. 1999 Mar;64(3):788-92. doi: 10.1086/302281. Am J Hum Genet. 1999. PMID: 10053013 Free PMC article.

4

A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21.

Xiang F, Nicolao P, Chapon F, Edström L, Anvret M, Zhang Z. Xiang F, et al. Among authors: edstrom l. Neuromuscul Disord. 1999 Jul;9(5):308-12. doi: 10.1016/s0960-8966(99)00030-9. Neuromuscul Disord. 1999. PMID: 10407851

5

Huntington disease phenocopy is a familial prion disease.

Moore RC, Xiang F, Monaghan J, Han D, Zhang Z, Edström L, Anvret M, Prusiner SB. Moore RC, et al. Among authors: edstrom l. Am J Hum Genet. 2001 Dec;69(6):1385-8. doi: 10.1086/324414. Epub 2001 Oct 9. Am J Hum Genet. 2001. PMID: 11593450 Free PMC article.

6

Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy.

Anvret M, Ahlberg G, Grandell U, Hedberg B, Johnson K, Edström L. Anvret M, et al. Among authors: edstrom l. Hum Mol Genet. 1993 Sep;2(9):1397-400. doi: 10.1093/hmg/2.9.1397. Hum Mol Genet. 1993. PMID: 8242063

7

Welander distal myopathy is not linked to other defined distal myopathy gene loci.

Ahlberg G, Borg K, Edström L, Anvret M. Ahlberg G, et al. Among authors: edstrom l. Neuromuscul Disord. 1997 Jun;7(4):256-60. doi: 10.1016/s0960-8966(97)00451-3. Neuromuscul Disord. 1997. PMID: 9196908

8

Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies.

Ahlberg G, Borg K, Edström L, Anvret M. Ahlberg G, et al. Among authors: edstrom l. Neuromuscul Disord. 1998 Apr;8(2):111-4. doi: 10.1016/s0960-8966(98)00007-8. Neuromuscul Disord. 1998. PMID: 9608564

9

Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levels.

Eriksson M, Ansved T, Edström L, Anvret M, Carey N. Eriksson M, et al. Among authors: edstrom l. Hum Mol Genet. 1999 Jun;8(6):1053-60. doi: 10.1093/hmg/8.6.1053. Hum Mol Genet. 1999. PMID: 10332037

10

Genetic linkage of Welander distal myopathy to chromosome 2p13.

Ahlberg G, von Tell D, Borg K, Edström L, Anvret M. Ahlberg G, et al. Among authors: edstrom l. Ann Neurol. 1999 Sep;46(3):399-404. doi: 10.1002/1531-8249(199909)46:3<399::aid-ana16>3.0.co;2-q. Ann Neurol. 1999. PMID: 10482271

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