Ueno S - Search Results

1

Global and region-specific analyses of apparent diffusion coefficient in dentatorubral-pallidoluysian atrophy.

Kin T, Hirano M, Taoka T, Furiya Y, Kataoka H, Kichikawa K, Ueno S. Kin T, et al. Among authors: ueno s. AJNR Am J Neuroradiol. 2006 Aug;27(7):1463-6. AJNR Am J Neuroradiol. 2006. PMID: 16908559 Free PMC article.

2

Mutant GTP cyclohydrolase I in autosomal dominant dystonia and recessive hyperphenylalaninemia.

Hirano M, Ueno S. Hirano M, et al. Among authors: ueno s. Neurology. 1999 Jan 1;52(1):182-4. doi: 10.1212/wnl.52.1.182. Neurology. 1999. PMID: 9921872

3

Missense mutants inactivate guanosine triphosphate cyclohydrolase I in hereditary progressive dystonia.

Ueno S, Hirano M. Ueno S, et al. Brain Dev. 2000 Sep;22 Suppl 1:S111-4. doi: 10.1016/s0387-7604(00)00135-2. Brain Dev. 2000. PMID: 10984670

4

Coexistence of Ramsay Hunt syndrome and varicella-zoster virus encephalitis.

Kin T, Hirano M, Tonomura Y, Ueno S. Kin T, et al. Among authors: ueno s. Infection. 2006 Dec;34(6):352-4. doi: 10.1007/s15010-006-5669-4. Infection. 2006. PMID: 17180593 Review.

5

A novel missense mutant inactivates GTP cyclohydrolase I in dopa-responsive dystonia.

Hirano M, Komure O, Ueno S. Hirano M, et al. Among authors: ueno s. Neurosci Lett. 1999 Feb 5;260(3):181-4. doi: 10.1016/s0304-3940(98)00984-7. Neurosci Lett. 1999. PMID: 10076897

6

Differential splicing of the GTP cyclohydrolase I RNA in dopa-responsive dystonia.

Hirano M, Imaiso Y, Ueno S. Hirano M, et al. Among authors: ueno s. Biochem Biophys Res Commun. 1997 May 19;234(2):316-9. doi: 10.1006/bbrc.1997.6632. Biochem Biophys Res Commun. 1997. PMID: 9177267

7

Dominant negative effect of GTP cyclohydrolase I mutations in dopa-responsive hereditary progressive dystonia.

Hirano M, Yanagihara T, Ueno S. Hirano M, et al. Among authors: ueno s. Ann Neurol. 1998 Sep;44(3):365-71. doi: 10.1002/ana.410440312. Ann Neurol. 1998. PMID: 9749603

8

Teaching NeuroImages: Hemiatrophy as a clinical presentation in facioscapulohumeral muscular dystrophy.

Sugie K, Hayashi YK, Kin T, Goto K, Nishino I, Ueno S. Sugie K, et al. Among authors: ueno s. Neurology. 2009 Aug 4;73(5):e24. doi: 10.1212/WNL.0b013e3181b04af9. Neurology. 2009. PMID: 19652136 No abstract available.

9

A carrier of human T-lymphotropic virus type I with periodic limb movements progressing to myelopathy.

Okahashi Y, Kataoka H, Kawahara M, Tamaru T, Ueno S. Okahashi Y, et al. Among authors: ueno s. Neurology. 2005 Sep 27;65(6):965-6. doi: 10.1212/01.wnl.0000175985.33134.70. Neurology. 2005. PMID: 16186552 No abstract available.

10

Mosaicism and phenotype in ring chromosome 20 syndrome.

Nishiwaki T, Hirano M, Kumazawa M, Ueno S. Nishiwaki T, et al. Among authors: ueno s. Acta Neurol Scand. 2005 Mar;111(3):205-8. doi: 10.1111/j.1600-0404.2005.00298.x. Acta Neurol Scand. 2005. PMID: 15691292

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