Nonaka I - Search Results

1

Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin.

Matsumura K, Nonaka I, Tomé FM, Arahata K, Collin H, Leturcq F, Récan D, Kaplan JC, Fardeau M, Campbell KP. Matsumura K, et al. Among authors: nonaka i. Am J Hum Genet. 1993 Aug;53(2):409-16. Am J Hum Genet. 1993. PMID: 8328458 Free PMC article.

2

Partial deficiency of dystrophin-associated proteins in a young girl with sporadic myopathy and normal karyotype.

Matsumura K, Nonaka I, Arahata K, Campbell KP. Matsumura K, et al. Among authors: nonaka i. Neurology. 1993 Jun;43(6):1267-8. doi: 10.1212/wnl.43.6.1267. Neurology. 1993. PMID: 8170583 No abstract available.

3

The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies.

Matsumura K, Ohlendieck K, Ionasescu VV, Tomé FM, Nonaka I, Burghes AH, Mora M, Kaplan JC, Fardeau M, Campbell KP. Matsumura K, et al. Among authors: nonaka i. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):533-5. doi: 10.1016/0960-8966(93)90110-6. Neuromuscul Disord. 1993. PMID: 8186706 Review.

4

Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy.

Matsumura K, Nonaka I, Campbell KP. Matsumura K, et al. Among authors: nonaka i. Lancet. 1993 Feb 27;341(8844):521-2. doi: 10.1016/0140-6736(93)90279-p. Lancet. 1993. PMID: 8094772

5

Muscle histology in Becker muscular dystrophy.

Kaido M, Arahata K, Hoffman EP, Nonaka I, Sugita H. Kaido M, et al. Among authors: nonaka i. Muscle Nerve. 1991 Nov;14(11):1067-73. doi: 10.1002/mus.880141105. Muscle Nerve. 1991. PMID: 1745279

6

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.

Beggs AH, Neumann PE, Arahata K, Arikawa E, Nonaka I, Anderson MS, Kunkel LM. Beggs AH, et al. Among authors: nonaka i. Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):623-7. doi: 10.1073/pnas.89.2.623. Proc Natl Acad Sci U S A. 1992. PMID: 1731332 Free PMC article.

7

Limb-girdle muscular dystrophy: clinical and pathologic reevaluation.

Yamanouchi Y, Arikawa E, Arahata K, Ozawa E, Nonaka I. Yamanouchi Y, et al. Among authors: nonaka i. J Neurol Sci. 1995 Mar;129(1):15-20. doi: 10.1016/0022-510x(94)00231-c. J Neurol Sci. 1995. PMID: 7751838

8

The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin.

Hayashi YK, Mizuno Y, Yoshida M, Nonaka I, Ozawa E, Arahata K. Hayashi YK, et al. Among authors: nonaka i. Neurology. 1995 Mar;45(3 Pt 1):551-4. doi: 10.1212/wnl.45.3.551. Neurology. 1995. PMID: 7898714

9

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: nonaka i. Hum Mol Genet. 2001 Aug 15;10(17):1761-6. doi: 10.1093/hmg/10.17.1761. Hum Mol Genet. 2001. PMID: 11532985

10

Immunocytochemical analysis of dystrophin in congenital muscular dystrophy.

Arikawa E, Ishihara T, Nonaka I, Sugita H, Arahata K. Arikawa E, et al. Among authors: nonaka i. J Neurol Sci. 1991 Sep;105(1):79-87. doi: 10.1016/0022-510x(91)90122-n. J Neurol Sci. 1991. PMID: 1795174

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