Okinaga T - Search Results

1

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

2

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.

3

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

4

[Liposteroid therapy for refractory epileptic spasms].

Shimono KK, Imai K, Idoguchi R, Kamio N, Okinaga T, Ozono K. Shimono KK, et al. Among authors: okinaga t. No To Hattatsu. 2003 Nov;35(6):527-31. No To Hattatsu. 2003. PMID: 14631751 Japanese.

5

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.

6

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

7

Neuronal intranuclear hyaline inclusion disease with rapidly progressive neurological symptoms.

Mano T, Takizawa S, Mohri I, Okinaga T, Shimono K, Imai K, Taniike M, Ozono K, Fujimura H. Mano T, et al. Among authors: okinaga t. J Child Neurol. 2007 Jan;22(1):60-6. doi: 10.1177/0883073807299952. J Child Neurol. 2007. PMID: 17608307

8

[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.

9

Sleep disordered breathing in childhood-onset acid maltase deficiency.

Nabatame S, Taniike M, Sakai N, Kato-Nishimura K, Mohri I, Kagitani-Shimono K, Okinaga T, Tachibana N, Ozono K. Nabatame S, et al. Among authors: okinaga t. Brain Dev. 2009 Mar;31(3):234-9. doi: 10.1016/j.braindev.2008.03.007. Epub 2008 May 21. Brain Dev. 2009. PMID: 18495398

10

Localized donor cells in brain of a Hunter disease patient after cord blood stem cell transplantation.

Araya K, Sakai N, Mohri I, Kagitani-Shimono K, Okinaga T, Hashii Y, Ohta H, Nakamichi I, Aozasa K, Taniike M, Ozono K. Araya K, et al. Among authors: okinaga t. Mol Genet Metab. 2009 Nov;98(3):255-63. doi: 10.1016/j.ymgme.2009.05.006. Epub 2009 May 24. Mol Genet Metab. 2009. PMID: 19556155

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