Nonaka I - Search Results

1

Negative result in search for human alpha-dystrobrevin deficiency.

Ishikawa H, Nonaka I, Nishino I. Ishikawa H, et al. Among authors: nonaka i. Muscle Nerve. 2003 Sep;28(3):387-8. doi: 10.1002/mus.10441. Muscle Nerve. 2003. PMID: 12929204 No abstract available.

2

Deficiency of laminin alpha 2-chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy.

Hayashi YK, Koga R, Tsukahara T, Ishii H, Matsuishi T, Yamashita Y, Nonaka I, Arahata K. Hayashi YK, et al. Among authors: nonaka i. Muscle Nerve. 1995 Sep;18(9):1027-30. doi: 10.1002/mus.880180918. Muscle Nerve. 1995. PMID: 7643867 No abstract available.

3

Detection of DNA fragments encompassing the deletion junction of mitochondrial genome.

Goto Y, Nishino I, Horai S, Nonaka I. Goto Y, et al. Among authors: nonaka i. Biochem Biophys Res Commun. 1996 May 15;222(2):215-9. doi: 10.1006/bbrc.1996.0724. Biochem Biophys Res Commun. 1996. PMID: 8670185

4

A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathy.

Nishino I, Seki A, Maegaki Y, Takeshita K, Horai S, Nonaka I, Goto Y. Nishino I, et al. Among authors: nonaka i. Biochem Biophys Res Commun. 1996 Aug 5;225(1):180-5. doi: 10.1006/bbrc.1996.1150. Biochem Biophys Res Commun. 1996. PMID: 8769114

5

The 3260 mutation in mitochondrial DNA can cause mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).

Nishino I, Komatsu M, Kodama S, Horai S, Nonaka I, Goto Y. Nishino I, et al. Among authors: nonaka i. Muscle Nerve. 1996 Dec;19(12):1603-4. doi: 10.1002/(SICI)1097-4598(199612)19:12<1603::AID-MUS10>3.0.CO;2-S. Muscle Nerve. 1996. PMID: 8941275 No abstract available.

6

Hypoparathyroidism and insulin-dependent diabetes mellitus in a patient with Kearns-Sayre syndrome harbouring a mitochondrial DNA deletion.

Isotani H, Fukumoto Y, Kawamura H, Furukawa K, Ohsawa N, Goto Y, Nishino I, Nonaka I. Isotani H, et al. Among authors: nonaka i. Clin Endocrinol (Oxf). 1996 Nov;45(5):637-41. doi: 10.1046/j.1365-2265.1996.00856.x. Clin Endocrinol (Oxf). 1996. PMID: 8977763

7

Mitochondrial encephalomyopathy with elderly onset of stroke-like episodes.

Minamoto H, Kawabata K, Okuda B, Shibuya N, Tachibana H, Sugita M, Goto Y, Nishino I, Nonaka I. Minamoto H, et al. Among authors: nonaka i. Intern Med. 1996 Dec;35(12):991-5. doi: 10.2169/internalmedicine.35.991. Intern Med. 1996. PMID: 9031002 Free article. Review.

8

Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families.

Ozawa M, Nishino I, Horai S, Nonaka I, Goto YI. Ozawa M, et al. Among authors: nonaka i. Muscle Nerve. 1997 Mar;20(3):271-8. doi: 10.1002/(SICI)1097-4598(199703)20:3<271::AID-MUS2>3.0.CO;2-8. Muscle Nerve. 1997. PMID: 9052804

9

A new congenital muscular dystrophy with mitochondrial structural abnormalities.

Nishino I, Kobayashi O, Goto Y, Kurihara M, Kumagai K, Fujita T, Hashimoto K, Horai S, Nonaka I. Nishino I, et al. Among authors: nonaka i. Muscle Nerve. 1998 Jan;21(1):40-7. doi: 10.1002/(sici)1097-4598(199801)21:1<40::aid-mus6>3.0.co;2-g. Muscle Nerve. 1998. PMID: 9427222

10

Mitochondrial abnormalities in selenium-deficient myopathy.

Osaki Y, Nishino I, Murakami N, Matsubayashi K, Tsuda K, Yokoyama YI, Morita M, Onishi S, Goto YI, Nonaka I. Osaki Y, et al. Among authors: nonaka i. Muscle Nerve. 1998 May;21(5):637-9. doi: 10.1002/(sici)1097-4598(199805)21:5<637::aid-mus10>3.0.co;2-s. Muscle Nerve. 1998. PMID: 9572243

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