Tyson J - Search Results

1

Jervell and Lange-Nielsen syndrome: a Norwegian perspective.

Tranebjaerg L, Bathen J, Tyson J, Bitner-Glindzicz M. Tranebjaerg L, et al. Among authors: tyson j. Am J Med Genet. 1999 Sep 24;89(3):137-46. Am J Med Genet. 1999. PMID: 10704188 Review.

2

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.

Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sørland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M. Tyson J, et al. Hum Mol Genet. 1997 Nov;6(12):2179-85. doi: 10.1093/hmg/6.12.2179. Hum Mol Genet. 1997. PMID: 9328483

3

Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen.

Tyson J, Tranebjaerg L, McEntagart M, Larsen LA, Christiansen M, Whiteford ML, Bathen J, Aslaksen B, Sørland SJ, Lund O, Pembrey ME, Malcolm S, Bitner-Glindzicz M. Tyson J, et al. Hum Genet. 2000 Nov;107(5):499-503. doi: 10.1007/s004390000402. Hum Genet. 2000. PMID: 11140949

4

Mapping of DFN2 to Xq22.

Tyson J, Bellman S, Newton V, Simpson P, Malcolm S, Pembrey ME, Bitner-Glindzicz M. Tyson J, et al. Hum Mol Genet. 1996 Dec;5(12):2055-60. doi: 10.1093/hmg/5.12.2055. Hum Mol Genet. 1996. PMID: 8968763

5

Molecular basis of the long-QT syndrome.

Bitner-Glindzicz M, Tyson J, Jamieson R. Bitner-Glindzicz M, et al. Among authors: tyson j. N Engl J Med. 1997 Oct 2;337(14):1011-3. doi: 10.1056/NEJM199710023371416. N Engl J Med. 1997. PMID: 9312674 No abstract available.

6

A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome.

de Vries BB, Bitner-Glindzicz M, Knight SJ, Tyson J, MacDermont KD, Flint J, Malcolm S, Winter RM. de Vries BB, et al. Among authors: tyson j. Clin Genet. 2000 Dec;58(6):483-7. doi: 10.1034/j.1399-0004.2000.580610.x. Clin Genet. 2000. PMID: 11149619

7

Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome.

Kelberman D, Tyson J, Chandler DC, McInerney AM, Slee J, Albert D, Aymat A, Botma M, Calvert M, Goldblatt J, Haan EA, Laing NG, Lim J, Malcolm S, Singer SL, Winter RM, Bitner-Glindzicz M. Kelberman D, et al. Among authors: tyson j. Hum Genet. 2001 Dec;109(6):638-45. doi: 10.1007/s00439-001-0626-x. Epub 2001 Oct 26. Hum Genet. 2001. PMID: 11810276

8

Splice mutations in KVLQT1?

Tyson J, Malcolm S, Bitner-Glindzicz M. Tyson J, et al. Circulation. 1999 May 11;99(18):2476-7. Circulation. 1999. PMID: 10318740 No abstract available.

9

DFN2.

Bitner-Glindzicz M, Tyson J. Bitner-Glindzicz M, et al. Among authors: tyson j. Adv Otorhinolaryngol. 2000;56:181-3. doi: 10.1159/000059099. Adv Otorhinolaryngol. 2000. PMID: 10868233 Review. No abstract available.

10

Blepharospasm and limb dystonia caused by Mohr-Tranebjaerg syndrome with a novel splice-site mutation in the deafness/dystonia peptide gene.

Kim HT, Edwards MJ, Tyson J, Quinn NP, Bitner-Glindzicz M, Bhatia KP. Kim HT, et al. Among authors: tyson j. Mov Disord. 2007 Jul 15;22(9):1328-31. doi: 10.1002/mds.21351. Mov Disord. 2007. PMID: 17534980

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