Uyama E - Search Results

1

Genetic localization of the familial adult myoclonic epilepsy (FAME) gene to chromosome 8q24.

Plaster NM, Uyama E, Uchino M, Ikeda T, Flanigan KM, Kondo I, Ptácek LJ. Plaster NM, et al. Among authors: uyama e. Neurology. 1999 Oct 12;53(6):1180-3. doi: 10.1212/wnl.53.6.1180. Neurology. 1999. PMID: 10522869

2

Familial adult myoclonic epilepsy (FAME).

Uyama E, Fu YH, Ptácek LJ. Uyama E, et al. Adv Neurol. 2005;95:281-8. Adv Neurol. 2005. PMID: 15508931 Review. No abstract available.

3

Benign adult familial myoclonus epilepsy (BAFME): an autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) gene.

Kuwano A, Takakubo F, Morimoto Y, Uyama E, Uchino M, Ando M, Yasuda T, Terao A, Hayama T, Kobayashi R, Kondo I. Kuwano A, et al. Among authors: uyama e. J Med Genet. 1996 Jan;33(1):80-1. doi: 10.1136/jmg.33.1.80. J Med Genet. 1996. PMID: 8825056 Free PMC article.

4

Comments on "type 3 GM1 gangliosidosis: clinical and neuroradiological findings in an 11-year-old girl".

Uyama E, Uchino M, Ando M. Uyama E, et al. J Neurol. 1996 Mar;243(3):295-7. doi: 10.1007/BF00868530. J Neurol. 1996. PMID: 8936363 No abstract available.

5

Balint's syndrome.

Uyama E, Uchino M, Ando M. Uyama E, et al. Neurology. 1995 Nov;45(11):2118-9. doi: 10.1212/wnl.45.11.2118. Neurology. 1995. PMID: 7501184 No abstract available.

6

Oculopharyngeal muscular dystrophy in two unrelated Japanese families.

Uyama E, Nohira O, Chateau D, Tokunaga M, Uchino M, Okabe T, Ando M, Tome FM. Uyama E, et al. Neurology. 1996 Mar;46(3):773-8. doi: 10.1212/wnl.46.3.773. Neurology. 1996. PMID: 8618681

7

Autosomal recessive oculopharyngodistal myopathy in light of distal myopathy with rimmed vacuoles and oculopharyngeal muscular dystrophy.

Uyama E, Uchino M, Chateau D, Tomé FM. Uyama E, et al. Neuromuscul Disord. 1998 Apr;8(2):119-25. doi: 10.1016/s0960-8966(98)00002-9. Neuromuscul Disord. 1998. PMID: 9608566

8

[Identification of Notch 3 mutation in the first Japanese CADASIL family].

Uyama E, Uchino M, Tabira T. Uyama E, et al. Rinsho Shinkeigaku. 1999 Jan;39(1):53. Rinsho Shinkeigaku. 1999. PMID: 10377801 Japanese. No abstract available.

9

Dentatorubral-pallidoluysian atrophy (DRPLA): clinical, genetic, and neuroradiologic studies in a family.

Uyama E, Kondo I, Uchino M, Fukushima T, Murayama N, Kuwano A, Inokuchi N, Ohtani Y, Ando M. Uyama E, et al. J Neurol Sci. 1995 Jun;130(2):146-53. doi: 10.1016/0022-510x(95)00019-x. J Neurol Sci. 1995. PMID: 8586978

10

A Japanese family with FEOM1-linked congenital fibrosis of the extraocular muscles type 1 associated with spinal canal stenosis and refinement of the FEOM1 critical region.

Uyama E, Yamada K, Kawano H, Chan WM, Andrews C, Yoshioka M, Uchino M, Engle EC. Uyama E, et al. Neuromuscul Disord. 2003 Aug;13(6):472-8. doi: 10.1016/s0960-8966(03)00065-8. Neuromuscul Disord. 2003. PMID: 12899874

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