Kaido M - Search Results

1

New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1.

Himoro M, Yoshikawa H, Matsui T, Mitsui Y, Takahashi M, Kaido M, Nishimura T, Sawaishi Y, Takada G, Hayasaka K. Himoro M, et al. Among authors: kaido m. Biochem Mol Biol Int. 1993 Sep;31(1):169-73. Biochem Mol Biol Int. 1993. PMID: 7505151

2

Cation binding at the node of Ranvier in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies.

Yoshikawa H, Nishimura T, Kaido M, Toyooka K, Fujimura H, Sakoda S, Yanagihara T. Yoshikawa H, et al. Among authors: kaido m. Acta Neuropathol. 1996;91(6):587-94. doi: 10.1007/s004010050471. Acta Neuropathol. 1996. PMID: 8781657

3

Familial amyloid polyneuropathy associated with transthyretin Gly42 mutation: a quantitative light and electron microscopic study of the peripheral nervous system.

Toyooka K, Fujimura H, Ueno S, Yoshikawa H, Kaido M, Nishimura T, Yorifuji S, Yanagihara T. Toyooka K, et al. Among authors: kaido m. Acta Neuropathol. 1995;90(5):516-25. doi: 10.1007/BF00294814. Acta Neuropathol. 1995. PMID: 8560986

4

Alzheimer-type pathology in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).

Kaido M, Fujimura H, Soga F, Toyooka K, Yoshikawa H, Nishimura T, Higashi T, Inui K, Imanishi H, Yorifuji S, Yanagihara T. Kaido M, et al. Acta Neuropathol. 1996 Sep;92(3):312-8. doi: 10.1007/s004010050524. Acta Neuropathol. 1996. PMID: 8870835

5

A clinicopathological study of a patient with familial amyotrophic lateral sclerosis associated with a two base pair deletion in the copper/zinc superoxide dismutase (SOD1) gene.

Kadekawa J, Fujimura H, Ogawa Y, Hattori N, Kaido M, Nishimura T, Yoshikawa H, Shirahata N, Sakoda S, Yanagihara T. Kadekawa J, et al. Among authors: kaido m. Acta Neuropathol. 1997 Dec;94(6):617-22. doi: 10.1007/s004010050758. Acta Neuropathol. 1997. PMID: 9444365

6

Mitochondrial abnormalities in a murine model of primary carnitine deficiency. Systemic pathology and trial of replacement therapy.

Kaido M, Fujimura H, Ono A, Toyooka K, Yoshikawa H, Nishimura T, Ozaki K, Narama I, Kuwajima M. Kaido M, et al. Eur Neurol. 1997;38(4):302-9. doi: 10.1159/000113399. Eur Neurol. 1997. PMID: 9434090

7

Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy.

Hattori N, Kaido M, Nishigaki T, Inui K, Fujimura H, Nishimura T, Naka T, Hazama T. Hattori N, et al. Among authors: kaido m. Neuromuscul Disord. 1999 Jun;9(4):220-6. doi: 10.1016/s0960-8966(99)00005-x. Neuromuscul Disord. 1999. PMID: 10399748

8

Focal cytochrome c oxidase deficiency in the brain and dorsal root ganglia in a case with mitochondrial encephalomyopathy (tRNA(Ile) 4269 mutation): histochemical, immunohistochemical, and ultrastructural study.

Kaido M, Fujimura H, Taniike M, Yoshikawa H, Toyooka K, Yorifuji S, Inui K, Okada S, Sparaco M, Yanagihara T. Kaido M, et al. J Neurol Sci. 1995 Aug;131(2):170-6. doi: 10.1016/0022-510x(95)00111-e. J Neurol Sci. 1995. PMID: 7595643 Free article.

9

[A case of spinal muscular atrophy with marked calf hypertrophy and adolescent onset].

Hattori N, Nishigaki T, Inui K, Kaido M, Nishimura T, Hazama T, Nakata T. Hattori N, et al. Among authors: kaido m. Rinsho Shinkeigaku. 2000 Feb;40(2):170-3. Rinsho Shinkeigaku. 2000. PMID: 10835940 Japanese.

10

Clinical utility of somatosensory evoked potentials in diabetes mellitus.

Nakamura Y, Takahashi M, Kitaguchi M, Kaido M, Imaoka H, Kono N, Tarui S. Nakamura Y, et al. Among authors: kaido m. Diabetes Res Clin Pract. 1989 Jun 20;7(1):17-23. doi: 10.1016/0168-8227(89)90039-9. Diabetes Res Clin Pract. 1989. PMID: 2752886

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