Kida H - Search Results

1

Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in Japan.

Tanabe H, Higuchi Y, Yuan JH, Hashiguchi A, Yoshimura A, Ishihara S, Nozuma S, Okamoto Y, Matsuura E, Ishiura H, Mitsui J, Takashima R, Kokubun N, Maeda K, Asano Y, Sunami Y, Kono Y, Ishigaki Y, Yanamoto S, Fukae J, Kida H, Morita M, Tsuji S, Takashima H. Tanabe H, et al. Among authors: kida h. J Peripher Nerv Syst. 2018 Mar;23(1):40-48. doi: 10.1111/jns.12252. Epub 2018 Feb 14. J Peripher Nerv Syst. 2018. PMID: 29381233 Free PMC article.

2

Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough.

Miura S, Shibata H, Kida H, Noda K, Tomiyasu K, Yamamoto K, Iwaki A, Ayabe M, Aizawa H, Taniwaki T, Fukumaki Y. Miura S, et al. Among authors: kida h. J Neurol Sci. 2008 Oct 15;273(1-2):88-92. doi: 10.1016/j.jns.2008.06.027. Epub 2008 Jul 26. J Neurol Sci. 2008. PMID: 18662816

3

Partial SPAST and DPY30 deletions in a Japanese spastic paraplegia type 4 family.

Miura S, Shibata H, Kida H, Noda K, Toyama T, Iwasaki N, Iwaki A, Ayabe M, Aizawa H, Taniwaki T, Fukumaki Y. Miura S, et al. Among authors: kida h. Neurogenetics. 2011 Feb;12(1):25-31. doi: 10.1007/s10048-010-0260-7. Epub 2010 Sep 22. Neurogenetics. 2011. PMID: 20857310

4

A novel missense mutation of RYR1 in familial idiopathic hyper CK-emia.

Sano K, Miura S, Fujiwara T, Fujioka R, Yorita A, Noda K, Kida H, Azuma K, Kaieda S, Yamamoto K, Taniwaki T, Fukumaki Y, Shibata H. Sano K, et al. Among authors: kida h. J Neurol Sci. 2015 Sep 15;356(1-2):142-7. doi: 10.1016/j.jns.2015.06.035. Epub 2015 Jun 19. J Neurol Sci. 2015. PMID: 26119398

5

Disrupted connectivity of motor loops in Parkinson's disease during self-initiated but not externally-triggered movements.

Taniwaki T, Yoshiura T, Ogata K, Togao O, Yamashita K, Kida H, Miura S, Kira J, Tobimatsu S. Taniwaki T, et al. Among authors: kida h. Brain Res. 2013 May 28;1512:45-59. doi: 10.1016/j.brainres.2013.03.027. Epub 2013 Mar 30. Brain Res. 2013. PMID: 23548595

6

MIBG myocardial scintigraphy in progressive supranuclear palsy.

Kamada T, Miura S, Kida H, Irie KI, Yamanishi Y, Hoshino T, Taniwaki T. Kamada T, et al. Among authors: kida h. J Neurol Sci. 2019 Jan 15;396:3-7. doi: 10.1016/j.jns.2018.10.019. Epub 2018 Oct 22. J Neurol Sci. 2019. PMID: 30391822

7

Reversible Conduction Failure in Anti-lactosylceramide-antibody-positive Combined Central and Peripheral Demyelination.

Harada M, Miura S, Kida H, Moritaka T, Irie KI, Kamada T, Uchiyama Y, Shima S, Mutoh T, Hoshino T, Taniwaki T. Harada M, et al. Among authors: kida h. Front Neurol. 2019 Jun 7;10:600. doi: 10.3389/fneur.2019.00600. eCollection 2019. Front Neurol. 2019. PMID: 31231307 Free PMC article.

8

Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome.

Kida H, Takahashi T, Nakamura Y, Kinoshita T, Hara M, Okamoto M, Okayama S, Nakamura K, Kosai KI, Taniwaki T, Yamashita Y, Matsuishi T. Kida H, et al. Sci Rep. 2017 Sep 20;7(1):12032. doi: 10.1038/s41598-017-12293-8. Sci Rep. 2017. PMID: 28931890 Free PMC article.

9

Defining the kinetic effects of infection with influenza virus A/PR8/34 (H1N1) on sphingosine-1-phosphate signaling in mice by targeted LC/MS.

Gowda D, Ohno M, B Gowda SG, Chiba H, Shingai M, Kida H, Hui SP. Gowda D, et al. Among authors: kida h. Sci Rep. 2021 Oct 11;11(1):20161. doi: 10.1038/s41598-021-99765-0. Sci Rep. 2021. PMID: 34635791 Free PMC article.

10

Critical role of oxidized LDL receptor-1 in intravascular thrombosis in a severe influenza mouse model.

Ohno M, Kakino A, Sekiya T, Nomura N, Shingai M, Sawamura T, Kida H. Ohno M, et al. Among authors: kida h. Sci Rep. 2021 Aug 3;11(1):15675. doi: 10.1038/s41598-021-95046-y. Sci Rep. 2021. PMID: 34344944 Free PMC article.

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