Okinaga T - Search Results

1

A girl with 1p36 deletion syndrome and congenital fiber type disproportion myopathy.

Okamoto N, Toribe Y, Nakajima T, Okinaga T, Kurosawa K, Nonaka I, Shimokawa O, Matsumoto N. Okamoto N, et al. Among authors: okinaga t. J Hum Genet. 2002;47(10):556-9. doi: 10.1007/s100380200085. J Hum Genet. 2002. PMID: 12376748

2

Long-term response to zonisamide in patients with West syndrome.

Suzuki Y, Imai K, Toribe Y, Ueda H, Yanagihara K, Shimono K, Okinaga T, Ono J, Nagai T, Matsuoka T, Tagawa T, Abe J, Morita Y, Fujikawa Y, Arai H, Mano T, Okada S. Suzuki Y, et al. Among authors: okinaga t. Neurology. 2002 May 28;58(10):1556-9. doi: 10.1212/wnl.58.10.1556. Neurology. 2002. PMID: 12034801 Clinical Trial.

3

Epilepsy in Wolf-Hirschhorn syndrome (4p-).

Kagitani-Shimono K, Imai K, Otani K, Kamio N, Okinaga T, Toribe Y, Suzuki Y, Ozono K. Kagitani-Shimono K, et al. Among authors: okinaga t. Epilepsia. 2005 Jan;46(1):150-5. doi: 10.1111/j.0013-9580.2005.02804.x. Epilepsia. 2005. PMID: 15660782 Free article.

4

Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies.

Taniguchi M, Kurahashi H, Noguchi S, Fukudome T, Okinaga T, Tsukahara T, Tajima Y, Ozono K, Nishino I, Nonaka I, Toda T. Taniguchi M, et al. Among authors: okinaga t. Hum Mol Genet. 2006 Apr 15;15(8):1279-89. doi: 10.1093/hmg/ddl045. Epub 2006 Mar 10. Hum Mol Genet. 2006. PMID: 16531417

5

[Effect of carbamazepine on epilepsy with 1p36 deletion syndrome].

Nabatame S, Okinaga T, Imai K, Kamio N, Kagitani-Shimono K, Nagai T, Kurosawa K, Ozono K. Nabatame S, et al. Among authors: okinaga t. No To Hattatsu. 2007 Jul;39(4):289-94. No To Hattatsu. 2007. PMID: 17633087 Japanese.

6

SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome.

Hashimoto N, Kagitani-Shimono K, Sakai N, Otomo T, Tominaga K, Nabatame S, Mogami Y, Takahashi Y, Imai K, Yanagihara K, Okinaga T, Nagai T, Taniike M, Ozono K. Hashimoto N, et al. Among authors: okinaga t. J Hum Genet. 2011 Dec;56(12):846-51. doi: 10.1038/jhg.2011.115. Epub 2011 Oct 20. J Hum Genet. 2011. PMID: 22011817

7

Molecular characterization of an X(p21.2;q28) chromosomal inversion in a Duchenne muscular dystrophy patient with mental retardation reveals a novel long non-coding gene on Xq28.

Tran TH, Zhang Z, Yagi M, Lee T, Awano H, Nishida A, Okinaga T, Takeshima Y, Matsuo M. Tran TH, et al. Among authors: okinaga t. J Hum Genet. 2013 Jan;58(1):33-9. doi: 10.1038/jhg.2012.131. Epub 2012 Dec 6. J Hum Genet. 2013. PMID: 23223008

8

Association between cerebrospinal fluid parameters and developmental and neurological status in glucose transporter 1 deficiency syndrome.

Nabatame S, Tanigawa J, Tominaga K, Kagitani-Shimono K, Yanagihara K, Imai K, Ando T, Tsuyusaki Y, Araya N, Matsufuji M, Natsume J, Yuge K, Bratkovic D, Arai H, Okinaga T, Matsushige T, Azuma Y, Ishihara N, Miyatake S, Kato M, Matsumoto N, Okamoto N, Takahashi S, Hattori S, Ozono K. Nabatame S, et al. Among authors: okinaga t. J Neurol Sci. 2023 Apr 15;447:120597. doi: 10.1016/j.jns.2023.120597. Epub 2023 Mar 2. J Neurol Sci. 2023. PMID: 36965413 Free article.

9

Interstitial deletion of 14q, 46, XY, del (14) (q24.3q32.1) associated with status nonepileptic myoclonia and delayed myelination.

Ono J, Kurahashi H, Okinaga T, Mano T, Imai K, Inui K, Okada S. Ono J, et al. Among authors: okinaga t. J Child Neurol. 1999 Nov;14(11):756-8. doi: 10.1177/088307389901401116. J Child Neurol. 1999. PMID: 10593558 Review.

10

Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?

Taniguchi M, Kurahashi H, Noguchi S, Sese J, Okinaga T, Tsukahara T, Guicheney P, Ozono K, Nishino I, Morishita S, Toda T. Taniguchi M, et al. Among authors: okinaga t. Biochem Biophys Res Commun. 2006 Apr 7;342(2):489-502. doi: 10.1016/j.bbrc.2005.12.224. Epub 2006 Feb 3. Biochem Biophys Res Commun. 2006. PMID: 16487936

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