Khajavi M - Search Results

1

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T. Matsuura T, et al. Among authors: khajavi m. Nat Genet. 2000 Oct;26(2):191-4. doi: 10.1038/79911. Nat Genet. 2000. PMID: 11017075

2

Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10.

Matsuura T, Fang P, Lin X, Khajavi M, Tsuji K, Rasmussen A, Grewal RP, Achari M, Alonso ME, Pulst SM, Zoghbi HY, Nelson DL, Roa BB, Ashizawa T. Matsuura T, et al. Among authors: khajavi m. Am J Hum Genet. 2004 Jun;74(6):1216-24. doi: 10.1086/421526. Epub 2004 May 4. Am J Hum Genet. 2004. PMID: 15127363 Free PMC article.

3

Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy.

Matsuura T, Achari M, Khajavi M, Bachinski LL, Zoghbi HY, Ashizawa T. Matsuura T, et al. Among authors: khajavi m. Ann Neurol. 1999 Mar;45(3):407-11. doi: 10.1002/1531-8249(199903)45:3<407::aid-ana21>3.0.co;2-d. Ann Neurol. 1999. PMID: 10072060

4

Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?

Tan EK, Matsuura T, Nagamitsu S, Khajavi M, Jankovic J, Ashizawa T. Tan EK, et al. Among authors: khajavi m. Neurology. 2000 Mar 14;54(5):1195-8. doi: 10.1212/wnl.54.5.1195. Neurology. 2000. PMID: 10720300

5

Alcohol dehydrogenase polymorphism and Parkinson's disease.

Tan EK, Nagamitsu S, Matsuura T, Khajavi M, Jankovic J, Ondo W, Ashizawa T. Tan EK, et al. Among authors: khajavi m. Neurosci Lett. 2001 Jun 1;305(1):70-2. doi: 10.1016/s0304-3940(01)01770-0. Neurosci Lett. 2001. PMID: 11356310

6

"Mitotic drive" of expanded CTG repeats in myotonic dystrophy type 1 (DM1).

Khajavi M, Tari AM, Patel NB, Tsuji K, Siwak DR, Meistrich ML, Terry NH, Ashizawa T. Khajavi M, et al. Hum Mol Genet. 2001 Apr 1;10(8):855-63. doi: 10.1093/hmg/10.8.855. Hum Mol Genet. 2001. PMID: 11285251

7

A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene.

Nagamitsu S, Matsuura T, Khajavi M, Armstrong R, Gooch C, Harati Y, Ashizawa T. Nagamitsu S, et al. Among authors: khajavi m. Neurology. 2000 Dec 12;55(11):1697-703. doi: 10.1212/wnl.55.11.1697. Neurology. 2000. PMID: 11113225

8

Variability and validity of polymorphism association studies in Parkinson's disease.

Tan EK, Khajavi M, Thornby JI, Nagamitsu S, Jankovic J, Ashizawa T. Tan EK, et al. Among authors: khajavi m. Neurology. 2000 Aug 22;55(4):533-8. doi: 10.1212/wnl.55.4.533. Neurology. 2000. PMID: 10953187

9

The G209A mutation in the alpha-synuclein gene is not detected in familial cases of Parkinson disease in non-Greek and/or Italian populations.

Wang WW, Khajavi M, Patel BJ, Beach J, Jankovic J, Ashizawa T. Wang WW, et al. Among authors: khajavi m. Arch Neurol. 1998 Dec;55(12):1521-3. doi: 10.1001/archneur.55.12.1521. Arch Neurol. 1998. PMID: 9865795

10

Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients.

Hashem VI, Pytlos MJ, Klysik EA, Tsuji K, Khajavi M, Ashizawa T, Sinden RR. Hashem VI, et al. Among authors: khajavi m. Nucleic Acids Res. 2004 Dec 1;32(21):6334-46. doi: 10.1093/nar/gkh976. Print 2004. Nucleic Acids Res. 2004. PMID: 15576360 Free PMC article.

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