Seltzer WK - Search Results

1

Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes.

Street VA, Meekins G, Lipe HP, Seltzer WK, Carter GT, Kraft GH, Bird TD. Street VA, et al. Among authors: seltzer wk. Neuromuscul Disord. 2002 Oct;12(7-8):643-50. doi: 10.1016/s0960-8966(02)00021-4. Neuromuscul Disord. 2002. PMID: 12207932

2

Late-onset hereditary axonal neuropathies.

Bennett CL, Lawson VH, Brickell KL, Isaacs K, Seltzer W, Lipe HP, Weiss MD, Carter GT, Flanigan KM, Chance PF, Bird TD. Bennett CL, et al. Neurology. 2008 Jul 1;71(1):14-20. doi: 10.1212/01.wnl.0000304048.94023.73. Epub 2008 May 21. Neurology. 2008. PMID: 18495953

3

Demyelinating neuropathy in a patient with multiple sclerosis and genotypical HMSN-1.

Almsaddi M, Bertorini TE, Seltzer WK. Almsaddi M, et al. Among authors: seltzer wk. Neuromuscul Disord. 1998 Apr;8(2):87-9. doi: 10.1016/s0960-8966(98)00016-9. Neuromuscul Disord. 1998. PMID: 9608561

4

SCA2 may present as levodopa-responsive parkinsonism.

Payami H, Nutt J, Gancher S, Bird T, McNeal MG, Seltzer WK, Hussey J, Lockhart P, Gwinn-Hardy K, Singleton AA, Singleton AB, Hardy J, Farrer M. Payami H, et al. Among authors: seltzer wk. Mov Disord. 2003 Apr;18(4):425-9. doi: 10.1002/mds.10375. Mov Disord. 2003. PMID: 12671950

5

Spinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxia.

Ikeda Y, Dalton JC, Moseley ML, Gardner KL, Bird TD, Ashizawa T, Seltzer WK, Pandolfo M, Milunsky A, Potter NT, Shoji M, Vincent JB, Day JW, Ranum LP. Ikeda Y, et al. Among authors: seltzer wk. Am J Hum Genet. 2004 Jul;75(1):3-16. doi: 10.1086/422014. Epub 2004 May 19. Am J Hum Genet. 2004. PMID: 15152344 Free PMC article.

6

Huntington's Disease-like 2 (HDL2) in North America and Japan.

Margolis RL, Holmes SE, Rosenblatt A, Gourley L, O'Hearn E, Ross CA, Seltzer WK, Walker RH, Ashizawa T, Rasmussen A, Hayden M, Almqvist EW, Harris J, Fahn S, MacDonald ME, Mysore J, Shimohata T, Tsuji S, Potter N, Nakaso K, Adachi Y, Nakashima K, Bird T, Krause A, Greenstein P. Margolis RL, et al. Among authors: seltzer wk. Ann Neurol. 2004 Nov;56(5):670-4. doi: 10.1002/ana.20248. Ann Neurol. 2004. PMID: 15468075

7

Severe X-linked Charcot-Marie-Tooth neuropathy due to new mutations [G59R(G-->C), W44X(G-->A)] in the connexin 32 gene.

Felice KJ, Seltzer WK. Felice KJ, et al. Among authors: seltzer wk. Eur Neurol. 2000;44(1):61-3. doi: 10.1159/000008196. Eur Neurol. 2000. PMID: 10894999 No abstract available.

8

Clinical and genetic analysis of CMT1B in a Nigerian family.

Kakar R, Ma W, Dutra A, Seltzer WK, Grewal RP. Kakar R, et al. Among authors: seltzer wk. Muscle Nerve. 2003 May;27(5):628-30. doi: 10.1002/mus.10344. Muscle Nerve. 2003. PMID: 12707985

9

Fatal infantile X-linked neuropathy.

Sekul E, Carroll JE, Yaghmai F, Armstrong DL, Seltzer WK. Sekul E, et al. Among authors: seltzer wk. J Child Neurol. 2000 Dec;15(12):829-30. doi: 10.1177/088307380001501217. J Child Neurol. 2000. PMID: 11198505

10

Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.

Gwinn-Hardy K, Chen JY, Liu HC, Liu TY, Boss M, Seltzer W, Adam A, Singleton A, Koroshetz W, Waters C, Hardy J, Farrer M. Gwinn-Hardy K, et al. Neurology. 2000 Sep 26;55(6):800-5. doi: 10.1212/wnl.55.6.800. Neurology. 2000. PMID: 10993999

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