Murayama K - Search Results

1

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle.

Matsuda C, Hayashi YK, Ogawa M, Aoki M, Murayama K, Nishino I, Nonaka I, Arahata K, Brown RH Jr. Matsuda C, et al. Among authors: murayama k. Hum Mol Genet. 2001 Aug 15;10(17):1761-6. doi: 10.1093/hmg/10.17.1761. Hum Mol Genet. 2001. PMID: 11532985

2

Monomelic muscle atrophy.

Takemitsu M, Murayama K, Saga T, Michihiro N, Shiihara H, Kimizuka M, Nonaka I. Takemitsu M, et al. Among authors: murayama k. Neuromuscul Disord. 1993 Jul;3(4):311-7. doi: 10.1016/0960-8966(93)90024-e. Neuromuscul Disord. 1993. PMID: 8268728

3

Tissue-specific involvement of multiple mitochondrial DNA deletions in familial mitochondrial myopathy.

Nishizuka S, Tamura G, Goto Y, Murayama K, Konno T, Hakozaki M, Nonaka I, Tohgi H, Satodate R. Nishizuka S, et al. Among authors: murayama k. Biochem Biophys Res Commun. 1998 Jun 9;247(1):24-7. doi: 10.1006/bbrc.1998.8709. Biochem Biophys Res Commun. 1998. PMID: 9636647

4

Calpain 3 gene mutations: genetic and clinico-pathologic findings in limb-girdle muscular dystrophy.

Chae J, Minami N, Jin Y, Nakagawa M, Murayama K, Igarashi F, Nonaka I. Chae J, et al. Among authors: murayama k. Neuromuscul Disord. 2001 Sep;11(6-7):547-55. doi: 10.1016/s0960-8966(01)00197-3. Neuromuscul Disord. 2001. PMID: 11525884

5

Clinicopathological features of genetically confirmed Danon disease.

Sugie K, Yamamoto A, Murayama K, Oh SJ, Takahashi M, Mora M, Riggs JE, Colomer J, Iturriaga C, Meloni A, Lamperti C, Saitoh S, Byrne E, DiMauro S, Nonaka I, Hirano M, Nishino I. Sugie K, et al. Among authors: murayama k. Neurology. 2002 Jun 25;58(12):1773-8. doi: 10.1212/wnl.58.12.1773. Neurology. 2002. PMID: 12084876 Review.

6

Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness.

Ishikawa H, Sugie K, Murayama K, Ito M, Minami N, Nishino I, Nonaka I. Ishikawa H, et al. Among authors: murayama k. Neurology. 2002 Sep 24;59(6):920-3. doi: 10.1212/wnl.59.6.920. Neurology. 2002. PMID: 12297580

7

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.

Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M, Aoki M, Nonaka I. Nishino I, et al. Among authors: murayama k. Neurology. 2002 Dec 10;59(11):1689-93. doi: 10.1212/01.wnl.0000041631.28557.c6. Neurology. 2002. PMID: 12473753

8

Ullrich disease due to deficiency of collagen VI in the sarcolemma.

Ishikawa H, Sugie K, Murayama K, Awaya A, Suzuki Y, Noguchi S, Hayashi YK, Nonaka I, Nishino I. Ishikawa H, et al. Among authors: murayama k. Neurology. 2004 Feb 24;62(4):620-3. doi: 10.1212/01.wnl.0000113023.84421.00. Neurology. 2004. PMID: 14981181

9

A new diagnostic test for VLCAD deficiency using immunohistochemistry.

Ohashi Y, Hasegawa Y, Murayama K, Ogawa M, Hasegawa T, Kawai M, Sakata N, Yoshida K, Yarita H, Imai K, Kumagai I, Murakami K, Hasegawa H, Noguchi S, Nonaka I, Yamaguchi S, Nishino I. Ohashi Y, et al. Among authors: murayama k. Neurology. 2004 Jun 22;62(12):2209-13. doi: 10.1212/01.wnl.0000130486.54839.15. Neurology. 2004. PMID: 15210884

10

Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy.

Amouri R, Driss A, Murayama K, Kefi M, Nishino I, Hentati F. Amouri R, et al. Among authors: murayama k. Neuromuscul Disord. 2005 May;15(5):361-3. doi: 10.1016/j.nmd.2005.01.012. Neuromuscul Disord. 2005. PMID: 15833430

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