Nakagawa M - Search Results

1

Glial fibrillary acidic protein mutations in adult-onset Alexander disease: clinical features observed in 12 Japanese patients.

Yoshida T, Sasayama H, Mizuta I, Okamoto Y, Yoshida M, Riku Y, Hayashi Y, Yonezu T, Takata Y, Ohnari K, Okuda S, Aiba I, Nakagawa M. Yoshida T, et al. Among authors: nakagawa m. Acta Neurol Scand. 2011 Aug;124(2):104-8. doi: 10.1111/j.1600-0404.2010.01427.x. Epub 2010 Sep 16. Acta Neurol Scand. 2011. PMID: 20849398

2

An adult form of Alexander disease: a novel mutation in glial fibrillary acidic protein.

Ohnari K, Yamano M, Uozumi T, Hashimoto T, Tsuji S, Nakagawa M. Ohnari K, et al. Among authors: nakagawa m. J Neurol. 2007 Oct;254(10):1390-4. doi: 10.1007/s00415-007-0557-0. Epub 2007 Oct 15. J Neurol. 2007. PMID: 17934883

3

Complex visual hallucination and mirror sign in posterior cortical atrophy.

Yoshida T, Yuki N, Nakagawa M. Yoshida T, et al. Among authors: nakagawa m. Acta Psychiatr Scand. 2006 Jul;114(1):62-5. doi: 10.1111/j.1600-0447.2006.00778.x. Acta Psychiatr Scand. 2006. PMID: 16774663

4

Juvenile form of Alexander disease with GFAP mutation and mitochondrial abnormality.

Nobuhara Y, Nakahara K, Higuchi I, Yoshida T, Fushiki S, Osame M, Arimura K, Nakagawa M. Nobuhara Y, et al. Among authors: nakagawa m. Neurology. 2004 Oct 12;63(7):1302-4. doi: 10.1212/01.wnl.0000140695.90497.e2. Neurology. 2004. PMID: 15477559

5

A case of cerebral aquaporinopathy.

Tanaka A, Yoshida T, Yamada T, Isayama R, Fujiwara Y, Shiga K, Yamada K, Tanaka K, Nakagawa M. Tanaka A, et al. Among authors: nakagawa m. Mult Scler. 2010 Oct;16(10):1252-4. doi: 10.1177/1352458510377906. Epub 2010 Jul 29. Mult Scler. 2010. PMID: 20670980

6

Gastrointestinal: Esophageal stricture with esophageal intramural pseudodiverticulosis.

Kinugasa H, Okamoto Y, Nakagawa M. Kinugasa H, et al. Among authors: nakagawa m. J Gastroenterol Hepatol. 2019 Jul;34(7):1130. doi: 10.1111/jgh.14597. Epub 2019 Jan 28. J Gastroenterol Hepatol. 2019. PMID: 30693566 No abstract available.

7

Heterogeneity of glucose metabolism in corticobasal degeneration.

Taniwaki T, Yamada T, Yoshida T, Sasaki M, Kuwabara Y, Nakagawa M, Mihara F, Motomura S, Shigetou H, Kira J. Taniwaki T, et al. Among authors: nakagawa m. J Neurol Sci. 1998 Nov 26;161(1):70-6. doi: 10.1016/s0022-510x(98)00269-x. J Neurol Sci. 1998. PMID: 9879684

8

Gap junction protein beta 1 (GJB1) mutations and central nervous system symptoms in X-linked Charcot-Marie-Tooth disease.

Takashima H, Nakagawa M, Umehara F, Hirata K, Suehara M, Mayumi H, Yoshishige K, Matsuyama W, Saito M, Jonosono M, Arimura K, Osame M. Takashima H, et al. Among authors: nakagawa m. Acta Neurol Scand. 2003 Jan;107(1):31-7. doi: 10.1034/j.1600-0404.2003.01317.x. Acta Neurol Scand. 2003. PMID: 12542510

9

SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucoma.

Hirano R, Takashima H, Umehara F, Arimura H, Michizono K, Okamoto Y, Nakagawa M, Boerkoel CF, Lupski JR, Osame M, Arimura K. Hirano R, et al. Among authors: nakagawa m. Neurology. 2004 Aug 10;63(3):577-80. doi: 10.1212/01.wnl.0000133211.40288.9a. Neurology. 2004. PMID: 15304601

10

Highly stable solid-state x-ray detector array.

Takahashi T, Nakagawa M, Yoshida M, Takeuchi H. Takahashi T, et al. Among authors: nakagawa m. Med Phys. 1992 Sep-Oct;19(5):1161-6. doi: 10.1118/1.596919. Med Phys. 1992. PMID: 1435593

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