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Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.
Shibasaki Y, Tanaka H, Iwabuchi K, Kawasaki S, Kondo H, Uekawa K, Ueda M, Kamiya T, Katayama Y, Nakamura A, Takashima H, Nakagawa M, Masuda M, Utsumi H, Nakamuro T, Tada K, Kurohara K, Inoue K, Koike F, Sakai T, Tsuji S, Kobayashi H. Shibasaki Y, et al. Among authors: nakagawa m. Ann Neurol. 2000 Jul;48(1):108-12. Ann Neurol. 2000. PMID: 10894224
GFAP mutations, age at onset, and clinical subtypes in Alexander disease.
Prust M, Wang J, Morizono H, Messing A, Brenner M, Gordon E, Hartka T, Sokohl A, Schiffmann R, Gordish-Dressman H, Albin R, Amartino H, Brockman K, Dinopoulos A, Dotti MT, Fain D, Fernandez R, Ferreira J, Fleming J, Gill D, Griebel M, Heilstedt H, Kaplan P, Lewis D, Nakagawa M, Pedersen R, Reddy A, Sawaishi Y, Schneider M, Sherr E, Takiyama Y, Wakabayashi K, Gorospe JR, Vanderver A. Prust M, et al. Among authors: nakagawa m. Neurology. 2011 Sep 27;77(13):1287-94. doi: 10.1212/WNL.0b013e3182309f72. Epub 2011 Sep 14. Neurology. 2011. PMID: 21917775 Free PMC article.
Rapid disease progression correlates with instability of mutant SOD1 in familial ALS.
Sato T, Nakanishi T, Yamamoto Y, Andersen PM, Ogawa Y, Fukada K, Zhou Z, Aoike F, Sugai F, Nagano S, Hirata S, Ogawa M, Nakano R, Ohi T, Kato T, Nakagawa M, Hamasaki T, Shimizu A, Sakoda S. Sato T, et al. Among authors: nakagawa m. Neurology. 2005 Dec 27;65(12):1954-7. doi: 10.1212/01.wnl.0000188760.53922.05. Epub 2005 Nov 16. Neurology. 2005. PMID: 16291929
Brain lesions in the course of generalised tetanus.
Ijichi T, Yamada T, Yoneda S, Kajita Y, Nakajima K, Nakagawa M. Ijichi T, et al. Among authors: nakagawa m. J Neurol Neurosurg Psychiatry. 2003 Oct;74(10):1432-4. doi: 10.1136/jnnp.74.10.1432. J Neurol Neurosurg Psychiatry. 2003. PMID: 14570841 Free PMC article.
3,980 results