Shiraishi K - Search Results

1

A case of congenital myopathy accompanied by tremor due to a MYBPC1 mutation.

Shiraishi K, Tsuburaya RS, Mukaida S, Yano N, Yoshida T. Shiraishi K, et al. Pediatr Int. 2022 Jan;64(1):e15061. doi: 10.1111/ped.15061. Pediatr Int. 2022. PMID: 35510679 No abstract available.

2

Utility of real-time three-dimensional echocardiography for Duchenne muscular dystrophy with echocardiographic limitations.

Tsuburaya RS, Uchizumi H, Ueda M, Demura Y, Mukaida S, Sudou S, Irahara K, Sakai N, Shiraishi K. Tsuburaya RS, et al. Among authors: shiraishi k. Neuromuscul Disord. 2014 May;24(5):402-8. doi: 10.1016/j.nmd.2013.12.007. Epub 2013 Dec 25. Neuromuscul Disord. 2014. PMID: 24444550

3

Anti-myelin oligodendrocyte glycoprotein (MOG) antibodies in a Japanese boy with recurrent optic neuritis.

Tsuburaya RS, Miki N, Tanaka K, Kageyama T, Irahara K, Mukaida S, Shiraishi K, Tanaka M. Tsuburaya RS, et al. Among authors: shiraishi k. Brain Dev. 2015 Jan;37(1):145-8. doi: 10.1016/j.braindev.2014.02.002. Epub 2014 Feb 28. Brain Dev. 2015. PMID: 24582475

4

Congenital fiber type disproportion: severe form with marked improvement.

Tsuji M, Higuchi Y, Shiraishi K, Mitsuyoshi I, Hattori H. Tsuji M, et al. Among authors: shiraishi k. Pediatr Neurol. 1999 Sep;21(3):658-60. doi: 10.1016/s0887-8994(99)00056-9. Pediatr Neurol. 1999. PMID: 10513694

5

Dystonia in a 13-year-old boy with secondary progressive multiple sclerosis.

Shiraishi K, Higuchi Y, Ozawa K. Shiraishi K, et al. Brain Dev. 2004 Dec;26(8):539-41. doi: 10.1016/j.braindev.2004.02.014. Brain Dev. 2004. PMID: 15533657

6

Protective effect of aminoguanidine on hypoxic-ischemic brain damage and temporal profile of brain nitric oxide in neonatal rat.

Tsuji M, Higuchi Y, Shiraishi K, Kume T, Akaike A, Hattori H. Tsuji M, et al. Among authors: shiraishi k. Pediatr Res. 2000 Jan;47(1):79-83. doi: 10.1203/00006450-200001000-00015. Pediatr Res. 2000. PMID: 10625086

7

Early phase 2 trial of TAS-205 in patients with Duchenne muscular dystrophy.

Komaki H, Maegaki Y, Matsumura T, Shiraishi K, Awano H, Nakamura A, Kinoshita S, Ogata K, Ishigaki K, Saitoh S, Funato M, Kuru S, Nakayama T, Iwata Y, Yajima H, Takeda S. Komaki H, et al. Among authors: shiraishi k. Ann Clin Transl Neurol. 2020 Feb;7(2):181-190. doi: 10.1002/acn3.50978. Epub 2020 Jan 20. Ann Clin Transl Neurol. 2020. PMID: 31957953 Free PMC article. Clinical Trial.

8

[Anti-NMDA receptor antibody encephalitis with recurrent optic neuritis and epilepsy].

Motoyama R, Shiraishi K, Tanaka K, Kinoshita M, Tanaka M. Motoyama R, et al. Among authors: shiraishi k. Rinsho Shinkeigaku. 2010 Aug;50(8):585-8. doi: 10.5692/clinicalneurol.50.585. Rinsho Shinkeigaku. 2010. PMID: 20803970 Japanese.

9

Clinical features in very early-onset demyelinating disease with anti-MOG antibody.

Nishiyama M, Nagase H, Matsumoto M, Tomioka K, Awano H, Tanaka T, Toyoshima D, Fujita K, Maruyama A, Oyazato Y, Saeki K, Shiraishi K, Takada S, Kaneko K, Takahashi T, Nakashima I, Iijima K. Nishiyama M, et al. Among authors: shiraishi k. Brain Dev. 2017 Oct;39(9):756-762. doi: 10.1016/j.braindev.2017.05.004. Epub 2017 May 24. Brain Dev. 2017. PMID: 28551039

10

[Clinical features of congenital myasthenic syndrome in Japan].

Irahara K, Komaki H, Honda R, Okumura A, Shiraishi K, Kobayashi Y, Azuma Y, Nakata T, Ohya Y, Sasaki M. Irahara K, et al. Among authors: shiraishi k. No To Hattatsu. 2012 Nov;44(6):450-4. No To Hattatsu. 2012. PMID: 23240525 Japanese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,069 results

Search Page