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

376 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Use of a modified alpha-N-acetylgalactosaminidase in the development of enzyme replacement therapy for Fabry disease.
Tajima Y, Kawashima I, Tsukimura T, Sugawara K, Kuroda M, Suzuki T, Togawa T, Chiba Y, Jigami Y, Ohno K, Fukushige T, Kanekura T, Itoh K, Ohashi T, Sakuraba H. Tajima Y, et al. Among authors: togawa t. Am J Hum Genet. 2009 Nov;85(5):569-80. doi: 10.1016/j.ajhg.2009.09.016. Epub 2009 Oct 22. Am J Hum Genet. 2009. PMID: 19853240 Free PMC article.
A case of Fabry nephropathy with histological features of oligonephropathy.
Nishida M, Kosaka K, Hasegawa K, Nishikawa K, Itoi T, Tsukimura T, Togawa T, Sakuraba H, Hamaoka K. Nishida M, et al. Among authors: togawa t. Eur J Pediatr. 2014 Aug;173(8):1111-4. doi: 10.1007/s00431-013-2118-0. Epub 2013 Aug 3. Eur J Pediatr. 2014. PMID: 23913314
376 results