Kuroiwa Y - Search Results

1

[Family with hereditary polyneuropthy assoicated with pyramidal signs].

Doi H, Shibasaki H, Goto I, Kuroiwa Y, Ohta M. Doi H, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1976 Sep;16(9):642-8. Rinsho Shinkeigaku. 1976. PMID: 1034548 Japanese. No abstract available.

2

[A case of peroneal muscular atrophy with cerebellar ataxia, pyramidal signs and loss of deep sensations].

Shinoda H, Kitaguchi T, Kobayashi T, Goto I, Kuroiwa Y. Shinoda H, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1987 Mar;27(3):356-9. Rinsho Shinkeigaku. 1987. PMID: 3608327 Japanese. No abstract available.

3

[Case of mitochondrial myopathy].

Shibasaki H, Mita T, Kuroiwa Y. Shibasaki H, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1973 Jan;13(1):45-51. Rinsho Shinkeigaku. 1973. PMID: 4736065 Japanese. No abstract available.

4

Rigid spine syndrome: clinical and histological problems.

Goto I, Muraoka S, Fujii N, Ohta M, Kuroiwa Y. Goto I, et al. Among authors: kuroiwa y. J Neurol. 1981;226(2):143-8. doi: 10.1007/BF00313443. J Neurol. 1981. PMID: 6186785

5

[A simple form of adult onset familial sudanophilic leukodystrophy manifesting pyramidal tract involvement and presenile dementia].

Suzuki S, Tabira T, Goto I, Kuroiwa Y, Anraku S. Suzuki S, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1983 Jan;23(1):32-7. Rinsho Shinkeigaku. 1983. PMID: 6851351 Japanese. No abstract available.

6

[Oculocraniosomatic neuromuscular disease with "ragged-red" fibers (Olson)--a case study].

Hosokawa S, Santa T, Shibasaki H, Kato M, Kuroiwa Y. Hosokawa S, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1975 May;15(5):303-10. Rinsho Shinkeigaku. 1975. PMID: 1238221 Japanese. No abstract available.

7

[Familial juvenile neuronal storage disease. Cherry red spots and dyssynergia cerebellaris myoclonica without dementia type (author's transl)].

Itoyama Y, Shibasaki H, Goto I, Kuroiwa Y, Kawabuchi M. Itoyama Y, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1976 Aug 1;16(8):558-65. Rinsho Shinkeigaku. 1976. PMID: 184996 Japanese. No abstract available.

8

[Cerebrotendinous xanthomatosis with hyperthyroidism (author's transl)].

Murakami S, Yamashita Y, Goto I, Kuroiwa Y, Ohnishi A. Murakami S, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1978 Jun;18(6):312-20. Rinsho Shinkeigaku. 1978. PMID: 699435 Japanese. No abstract available.

9

[A case of demyelinating disease with acute transverse myelitis and polyradiculoneuropathy (author's transl)].

Nogaki H, Tabira T, Shibasaki H, Ohnishi A, Kuroiwa Y. Nogaki H, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1978 Nov;18(11):685-90. Rinsho Shinkeigaku. 1978. PMID: 750134 Japanese. No abstract available.

10

[McArdle's disease. Clinical, electromyographic and histological studies of the 1st case reported in Japan].

Itoyama Y, Santa T, Shibasaki H, Goto I, Kuroiwa Y. Itoyama Y, et al. Among authors: kuroiwa y. Rinsho Shinkeigaku. 1975 Jul;15(7):450-7. Rinsho Shinkeigaku. 1975. PMID: 1059511 Japanese. No abstract available.

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