Lipe H - Search Results

1

CMT2C with vocal cord paresis associated with short stature and mutations in the TRPV4 gene.

Chen DH, Sul Y, Weiss M, Hillel A, Lipe H, Wolff J, Matsushita M, Raskind W, Bird T. Chen DH, et al. Among authors: lipe h. Neurology. 2010 Nov 30;75(22):1968-75. doi: 10.1212/WNL.0b013e3181ffe4bb. Neurology. 2010. PMID: 21115951 Free PMC article.

2

Impotence associated with the Charcot-Marie-Tooth syndrome.

Bird TD, Lipe HP, Crabtree LD. Bird TD, et al. Among authors: lipe hp. Eur Neurol. 1994;34(3):155-7. doi: 10.1159/000117029. Eur Neurol. 1994. PMID: 8033941

3

Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.

Bird TD, Kraft GH, Lipe HP, Kenney KL, Sumi SM. Bird TD, et al. Among authors: lipe hp. Ann Neurol. 1997 Apr;41(4):463-9. doi: 10.1002/ana.410410409. Ann Neurol. 1997. PMID: 9124803

4

The clinical and genetic spectrum of spinocerebellar ataxia 14.

Chen DH, Cimino PJ, Ranum LP, Zoghbi HY, Yabe I, Schut L, Margolis RL, Lipe HP, Feleke A, Matsushita M, Wolff J, Morgan C, Lau D, Fernandez M, Sasaki H, Raskind WH, Bird TD. Chen DH, et al. Among authors: lipe hp. Neurology. 2005 Apr 12;64(7):1258-60. doi: 10.1212/01.WNL.0000156801.64549.6B. Neurology. 2005. PMID: 15824357

5

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. Among authors: lipe hp. Neurology. 2008 Jul 1;71(1):14-20. doi: 10.1212/01.wnl.0000304048.94023.73. Epub 2008 May 21. Neurology. 2008. PMID: 18495953

6

Familial dyskinesia and facial myokymia (FDFM): a novel movement disorder.

Fernandez M, Raskind W, Wolff J, Matsushita M, Yuen E, Graf W, Lipe H, Bird T. Fernandez M, et al. Among authors: lipe h. Ann Neurol. 2001 Apr;49(4):486-92. Ann Neurol. 2001. PMID: 11310626

7

Hereditary benign chorea: clinical and genetic features of a distinct disease.

Fernandez M, Raskind W, Matsushita M, Wolff J, Lipe H, Bird T. Fernandez M, et al. Among authors: lipe h. Neurology. 2001 Jul 10;57(1):106-10. doi: 10.1212/wnl.57.1.106. Neurology. 2001. PMID: 11445636

8

A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.

Brkanac Z, Bylenok L, Fernandez M, Matsushita M, Lipe H, Wolff J, Nochlin D, Raskind WH, Bird TD. Brkanac Z, et al. Among authors: lipe h. Arch Neurol. 2002 Aug;59(8):1291-5. doi: 10.1001/archneur.59.8.1291. Arch Neurol. 2002. PMID: 12164726

9

Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.

Chen DH, Matsushita M, Rainier S, Meaney B, Tisch L, Feleke A, Wolff J, Lipe H, Fink J, Bird TD, Raskind WH. Chen DH, et al. Among authors: lipe h. Arch Neurol. 2005 Apr;62(4):597-600. doi: 10.1001/archneur.62.4.597. Arch Neurol. 2005. PMID: 15824259

10

A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: phenotypic spectrum and structural study of FHL1 mutations.

Chen DH, Raskind WH, Parson WW, Sonnen JA, Vu T, Zheng Y, Matsushita M, Wolff J, Lipe H, Bird TD. Chen DH, et al. Among authors: lipe h. J Neurol Sci. 2010 Sep 15;296(1-2):22-9. doi: 10.1016/j.jns.2010.06.017. Epub 2010 Jul 14. J Neurol Sci. 2010. PMID: 20633900 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

53 results

Search Page