Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

2,466 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Age associated axonal features in HNPP with 17p11.2 deletion in Japan.
Koike H, Hirayama M, Yamamoto M, Ito H, Hattori N, Umehara F, Arimura K, Ikeda S, Ando Y, Nakazato M, Kaji R, Hayasaka K, Nakagawa M, Sakoda S, Matsumura K, Onodera O, Baba M, Yasuda H, Saito T, Kira J, Nakashima K, Oka N, Sobue G. Koike H, et al. Among authors: ando y. J Neurol Neurosurg Psychiatry. 2005 Aug;76(8):1109-14. doi: 10.1136/jnnp.2004.048140. J Neurol Neurosurg Psychiatry. 2005. PMID: 16024889 Free PMC article.
Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy.
Ohmori H, Ando Y, Makita Y, Onouchi Y, Nakajima T, Saraiva MJ, Terazaki H, Suhr O, Sobue G, Nakamura M, Yamaizumi M, Munar-Ques M, Inoue I, Uchino M, Hata A. Ohmori H, et al. Among authors: ando y. J Med Genet. 2004 Apr;41(4):e51. doi: 10.1136/jmg.2003.014803. J Med Genet. 2004. PMID: 15060127 Free PMC article. No abstract available.
2,466 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page