Okubo R - Search Results

1

Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.

Arisato T, Okubo R, Arata H, Abe K, Fukada K, Sakoda S, Shimizu A, Qin XH, Izumo S, Osame M, Nakagawa M. Arisato T, et al. Among authors: okubo r. Acta Neuropathol. 2003 Dec;106(6):561-8. doi: 10.1007/s00401-003-0763-5. Epub 2003 Sep 27. Acta Neuropathol. 2003. PMID: 14517684

2

[Clinical and histochemical findings in spinal muscular atrophy].

Fukunaga H, Moritoyo T, Okubo R, Higuchi I, Osame M. Fukunaga H, et al. Among authors: okubo r. No To Shinkei. 1992 Jun;44(6):547-52. No To Shinkei. 1992. PMID: 1389561 Japanese.

3

Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

Higuchi I, Yamada H, Fukunaga H, Iwaki H, Okubo R, Nakagawa M, Osame M, Roberds SL, Shimizu T, Campbell KP, et al. Higuchi I, et al. Among authors: okubo r. J Clin Invest. 1994 Aug;94(2):601-6. doi: 10.1172/JCI117375. J Clin Invest. 1994. PMID: 8040315 Free PMC article.

4

Long-term follow-up of patients with Duchenne muscular dystrophy receiving ventilatory support.

Fukunaga H, Okubo R, Moritoyo T, Kawashima N, Osame M. Fukunaga H, et al. Among authors: okubo r. Muscle Nerve. 1993 May;16(5):554-8. doi: 10.1002/mus.880160519. Muscle Nerve. 1993. PMID: 8515763

5

Abnormal expression of heparin sulfate proteoglycan on basal lamina of muscle fibers in two Japanese patients with adhalin deficiency.

Higuchi I, Fukunaga H, Matsumura K, Inose M, Izumi K, Okubo R, Nakagawa M, Shimizu T, Osame M. Higuchi I, et al. Among authors: okubo r. Neuromuscul Disord. 1995 Nov;5(6):467-74. doi: 10.1016/0960-8966(95)00010-k. Neuromuscul Disord. 1995. PMID: 8580728

6

Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.

Hirano R, Takashima H, Okubo R, Tajima K, Okamoto Y, Ishida S, Tsuruta K, Arisato T, Arata H, Nakagawa M, Osame M, Arimura K. Hirano R, et al. Among authors: okubo r. Neurogenetics. 2004 Dec;5(4):215-21. doi: 10.1007/s10048-004-0194-z. Epub 2004 Sep 29. Neurogenetics. 2004. PMID: 15455264

7

Relapsing cervical cord lesions on MRI in patients with HTLV-I-associated myelopathy.

Umehara F, Tokunaga N, Hokezu Y, Hokonohara E, Yoshishige K, Shiraishi T, Okubo R, Osame M. Umehara F, et al. Among authors: okubo r. Neurology. 2006 Jan 24;66(2):289. doi: 10.1212/01.wnl.0000194219.89668.66. Neurology. 2006. PMID: 16434682 No abstract available.

8

[n-Hexane polyneuropathy presenting with CIDP-like features].

Takata Y, Shiraishi T, Matsuura E, Arisato T, Okubo R, Higuchi I, Umehara F, Osame M, Arimura K, Hashiguchi K. Takata Y, et al. Among authors: okubo r. Nihon Naika Gakkai Zasshi. 2006 May 10;95(5):933-5. doi: 10.2169/naika.95.933. Nihon Naika Gakkai Zasshi. 2006. PMID: 16774070 Japanese. No abstract available.

9

MRI studies of spinal visceral larva migrans syndrome.

Umehara F, Ookatsu H, Hayashi D, Uchida A, Douchi Y, Kawabata H, Goto R, Hashiguchi A, Matsuura E, Okubo R, Higuchi I, Arimura K, Nawa Y, Osame M. Umehara F, et al. Among authors: okubo r. J Neurol Sci. 2006 Nov 1;249(1):7-12. doi: 10.1016/j.jns.2006.05.057. Epub 2006 Jul 3. J Neurol Sci. 2006. PMID: 16815465

10

[New era of laboratory testing. Topics: II. Particulars; 10. Novel development of biomarker in nervous disease].

Arata H, Okubo R, Watanabe O, Takashima H, Hashiguchi T. Arata H, et al. Among authors: okubo r. Nihon Naika Gakkai Zasshi. 2013 Dec 10;102(12):3174-82. doi: 10.2169/naika.102.3174. Nihon Naika Gakkai Zasshi. 2013. PMID: 24605567 Review. Japanese. No abstract available.

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