Yoshida K - Search Results

1

Mandibuloacral dysplasia and a novel LMNA mutation in a woman with severe progressive skeletal changes.

Kosho T, Takahashi J, Momose T, Nakamura A, Sakurai A, Wada T, Yoshida K, Wakui K, Suzuki T, Kasuga K, Nishimura G, Kato H, Fukushima Y. Kosho T, et al. Among authors: yoshida k. Am J Med Genet A. 2007 Nov 1;143A(21):2598-603. doi: 10.1002/ajmg.a.31983. Am J Med Genet A. 2007. PMID: 17935239

2

Progression of dystrophic features and activation of mitogen-activated protein kinases and calcineurin by physical exercise, in hearts of mdx mice.

Nakamura A, Yoshida K, Takeda S, Dohi N, Ikeda S. Nakamura A, et al. Among authors: yoshida k. FEBS Lett. 2002 Jun 5;520(1-3):18-24. doi: 10.1016/s0014-5793(02)02739-4. FEBS Lett. 2002. PMID: 12044863 Free article.

3

[Analysis of 14 individuals who requested predictive genetic testing for hereditary neuromuscular diseases].

Yoshida K, Tamai M, Kubota T, Kawame H, Amano N, Ikeda S, Fukushima Y. Yoshida K, et al. Rinsho Shinkeigaku. 2002 Feb;42(2):113-7. Rinsho Shinkeigaku. 2002. PMID: 12424959 Japanese.

4

Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.

Nakamura A, Yoshida K, Ikeda S. Nakamura A, et al. Among authors: yoshida k. Clin Neurol Neurosurg. 2004 Mar;106(2):122-8. doi: 10.1016/j.clineuro.2003.10.010. Clin Neurol Neurosurg. 2004. PMID: 15003303

5

Regional features of autosomal-dominant cerebellar ataxia in Nagano: clinical and molecular genetic analysis of 86 families.

Shimizu Y, Yoshida K, Okano T, Ohara S, Hashimoto T, Fukushima Y, Ikeda SI. Shimizu Y, et al. Among authors: yoshida k. J Hum Genet. 2004;49(11):610-616. doi: 10.1007/s10038-004-0196-6. Epub 2004 Oct 8. J Hum Genet. 2004. PMID: 15480876

6

Up-regulation of mitogen activated protein kinases in mdx skeletal muscle following chronic treadmill exercise.

Nakamura A, Yoshida K, Ueda H, Takeda S, Ikeda S. Nakamura A, et al. Among authors: yoshida k. Biochim Biophys Acta. 2005 Jun 10;1740(3):326-31. doi: 10.1016/j.bbadis.2004.12.003. Epub 2004 Dec 30. Biochim Biophys Acta. 2005. PMID: 15949699 Free article.

7

A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.

Ohata T, Yoshida K, Sakai H, Hamanoue H, Mizuguchi T, Shimizu Y, Okano T, Takada F, Ishikawa K, Mizusawa H, Yoshiura KI, Fukushima Y, Ikeda SI, Matsumoto N. Ohata T, et al. Among authors: yoshida k. J Hum Genet. 2006;51(5):461-466. doi: 10.1007/s10038-006-0385-6. Epub 2006 Apr 14. J Hum Genet. 2006. PMID: 16614795

8

Congenital fibrosis of the extraocular muscles (CFEOM) syndrome associated with progressive cerebellar ataxia.

Yoshida K, Okano T, Hoshi K, Yahikozawa H, Suzuki K, Banno H, Tamura T, Sobue G, Ikeda S. Yoshida K, et al. Am J Med Genet A. 2007 Jul 1;143A(13):1494-501. doi: 10.1002/ajmg.a.31795. Am J Med Genet A. 2007. PMID: 17551929

9

Activation and localization of matrix metalloproteinase-2 and -9 in the skeletal muscle of the muscular dystrophy dog (CXMDJ).

Fukushima K, Nakamura A, Ueda H, Yuasa K, Yoshida K, Takeda S, Ikeda S. Fukushima K, et al. Among authors: yoshida k. BMC Musculoskelet Disord. 2007 Jun 28;8:54. doi: 10.1186/1471-2474-8-54. BMC Musculoskelet Disord. 2007. PMID: 17598883 Free PMC article.

10

Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan.

Yoshida K, Wada T, Sakurai A, Wakui K, Ikeda SI, Fukushima Y. Yoshida K, et al. J Hum Genet. 2007;52(8):675-679. doi: 10.1007/s10038-007-0170-1. Epub 2007 Jul 5. J Hum Genet. 2007. PMID: 17611709

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

11,874 results

Search Page

Filters