Kondo R - Search Results

1

Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findings.

Koide R, Onodera O, Ikeuchi T, Kondo R, Tanaka H, Tokiguchi S, Tomoda A, Miike T, Isa F, Beppu H, Shimizu N, Watanabe Y, Horikawa Y, Shimohata T, Hirota K, Ishikawa A, Tsuji S. Koide R, et al. Among authors: kondo r. Neurology. 1997 Dec;49(6):1605-12. doi: 10.1212/wnl.49.6.1605. Neurology. 1997. PMID: 9409354

2

Dentatorubral-pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat.

Ikeuchi T, Koide R, Tanaka H, Onodera O, Igarashi S, Takahashi H, Kondo R, Ishikawa A, Tomoda A, Miike T, et al. Ikeuchi T, et al. Among authors: kondo r. Ann Neurol. 1995 Jun;37(6):769-75. doi: 10.1002/ana.410370610. Ann Neurol. 1995. PMID: 7778850

3

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).

Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T, et al. Koide R, et al. Among authors: kondo r. Nat Genet. 1994 Jan;6(1):9-13. doi: 10.1038/ng0194-9. Nat Genet. 1994. PMID: 8136840

4

[A case of cerebrotendinous xanthomatosis with spastic paraparesis, epilepsy, and bradykinesia].

Kondo R, Wakamatsu N, Ishikawa A, Yuasa T, Miyatake T. Kondo R, et al. Rinsho Shinkeigaku. 1991 Jun;31(6):677-9. Rinsho Shinkeigaku. 1991. PMID: 1934787 Japanese.

5

Uniform tissue distribution of tRNA(Lys) mutation in mitochondrial DNA in MERRF patients.

Tanno Y, Yoneda M, Tanaka K, Kondo R, Hozumi I, Wakabayashi K, Yamada M, Fukuhara N, Ikuta F, Tsuji S. Tanno Y, et al. Among authors: kondo r. Neurology. 1993 Jun;43(6):1198-200. doi: 10.1212/wnl.43.6.1198. Neurology. 1993. PMID: 8170566

6

Identification of a mutation in the arylsulfatase A gene of a patient with adult-type metachromatic leukodystrophy.

Kondo R, Wakamatsu N, Yoshino H, Fukuhara N, Miyatake T, Tsuji S. Kondo R, et al. Am J Hum Genet. 1991 May;48(5):971-8. Am J Hum Genet. 1991. PMID: 1673291 Free PMC article.

7

Mutations producing premature termination of translation and an amino acid substitution in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis associated with parkinsonism.

Wakamatsu N, Hayashi M, Kawai H, Kondo H, Gotoda Y, Nishida Y, Kondo R, Tsuji S, Matsumoto T. Wakamatsu N, et al. Among authors: kondo r, kondo h. J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):195-8. doi: 10.1136/jnnp.67.2.195. J Neurol Neurosurg Psychiatry. 1999. PMID: 10406988 Free PMC article.

8

An adult-type metachromatic leukodystrophy caused by substitution of serine for glycine-122 in arylsulfatase A.

Honke K, Kobayashi T, Fujii T, Gasa S, Xu M, Takamaru Y, Kondo R, Tsuji S, Makita A. Honke K, et al. Among authors: kondo r. Hum Genet. 1993 Nov;92(5):451-6. doi: 10.1007/BF00216449. Hum Genet. 1993. PMID: 7902317

9

Chronotoxicity of glufosinate ammonium in mice.

Yoshiyama Y, Kobayashi T, Kondo R, Tomonaga F, Ohwada T. Yoshiyama Y, et al. Among authors: kondo r. Vet Hum Toxicol. 1995 Feb;37(1):22-3. Vet Hum Toxicol. 1995. PMID: 7709584

10

Pharmacokinetic study of mannitol in subjects with increased ICP.

Kobayashi T, Ichikawa T, Kondo R, Yoshiyama Y, Tomonaga F, Ohwada T. Kobayashi T, et al. Among authors: kondo r. Acta Neurochir Suppl (Wien). 1994;60:538-40. doi: 10.1007/978-3-7091-9334-1_148. Acta Neurochir Suppl (Wien). 1994. PMID: 7976642

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