Ogawa M - Search Results

1

Characterization of Danon disease in a male patient and his affected mother.

Sugie K, Koori T, Yamamoto A, Ogawa M, Hirano M, Inoue K, Nonaka I, Nishino I. Sugie K, et al. Among authors: ogawa m. Neuromuscul Disord. 2003 Nov;13(9):708-11. doi: 10.1016/s0960-8966(03)00105-6. Neuromuscul Disord. 2003. PMID: 14561493

2

Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients.

Tagawa K, Ogawa M, Kawabe K, Yamanaka G, Matsumura T, Goto K, Nonaka I, Nishino I, Hayashi YK. Tagawa K, et al. Among authors: ogawa m. J Neurol Sci. 2003 Jul 15;211(1-2):23-8. doi: 10.1016/s0022-510x(03)00041-8. J Neurol Sci. 2003. PMID: 12767493

3

Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles.

Noguchi S, Keira Y, Murayama K, Ogawa M, Fujita M, Kawahara G, Oya Y, Imazawa M, Goto Y, Hayashi YK, Nonaka I, Nishino I. Noguchi S, et al. Among authors: ogawa m. J Biol Chem. 2004 Mar 19;279(12):11402-7. doi: 10.1074/jbc.M313171200. Epub 2004 Jan 5. J Biol Chem. 2004. PMID: 14707127 Free article.

4

Subcellular localization of fukutin and fukutin-related protein in muscle cells.

Matsumoto H, Noguchi S, Sugie K, Ogawa M, Murayama K, Hayashi YK, Nishino I. Matsumoto H, et al. Among authors: ogawa m. J Biochem. 2004 Jun;135(6):709-12. doi: 10.1093/jb/mvh086. J Biochem. 2004. PMID: 15213246 Free article.

5

Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.

Matsumoto H, Hayashi YK, Kim DS, Ogawa M, Murakami T, Noguchi S, Nonaka I, Nakazawa T, Matsuo T, Futagami S, Campbell KP, Nishino I. Matsumoto H, et al. Among authors: ogawa m. Neuromuscul Disord. 2005 May;15(5):342-8. doi: 10.1016/j.nmd.2005.01.009. Neuromuscul Disord. 2005. PMID: 15833426

6

Dysferlin interacts with affixin (beta-parvin) at the sarcolemma.

Matsuda C, Kameyama K, Tagawa K, Ogawa M, Suzuki A, Yamaji S, Okamoto H, Nishino I, Hayashi YK. Matsuda C, et al. Among authors: ogawa m. J Neuropathol Exp Neurol. 2005 Apr;64(4):334-40. doi: 10.1093/jnen/64.4.334. J Neuropathol Exp Neurol. 2005. PMID: 15835269

7

Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles.

Ozawa R, Hayashi YK, Ogawa M, Kurokawa R, Matsumoto H, Noguchi S, Nonaka I, Nishino I. Ozawa R, et al. Among authors: ogawa m. Am J Pathol. 2006 Mar;168(3):907-17. doi: 10.2353/ajpath.2006.050564. Am J Pathol. 2006. PMID: 16507906 Free PMC article.

8

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness.

Murakami T, Hayashi YK, Noguchi S, Ogawa M, Nonaka I, Tanabe Y, Ogino M, Takada F, Eriguchi M, Kotooka N, Campbell KP, Osawa M, Nishino I. Murakami T, et al. Among authors: ogawa m. Ann Neurol. 2006 Nov;60(5):597-602. doi: 10.1002/ana.20973. Ann Neurol. 2006. PMID: 17036286

9

Diminished binding of mutated collagen VI to the extracellular matrix surrounding myocytes.

Kawahara G, Ogawa M, Okada M, Malicdan MC, Goto Y, Hayashi YK, Noguchi S, Nishino I. Kawahara G, et al. Among authors: ogawa m. Muscle Nerve. 2008 Sep;38(3):1192-5. doi: 10.1002/mus.21030. Muscle Nerve. 2008. PMID: 18642359

10

A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI.

Murakami T, Hayashi YK, Ogawa M, Noguchi S, Campbell KP, Togawa M, Inoue T, Oka A, Ohno K, Nonaka I, Nishino I. Murakami T, et al. Among authors: ogawa m. Brain Dev. 2009 Jun;31(6):465-8. doi: 10.1016/j.braindev.2008.08.005. Epub 2008 Sep 19. Brain Dev. 2009. PMID: 18804929 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,792 results

Search Page

Filters