Miyauchi A - Search Results

1

Miglustat therapy in a case of early-infantile Niemann-Pick type C.

Usui M, Miyauchi A, Nakano Y, Nakamura S, Jimbo E, Itamura S, Adachi K, Nanba E, Narita A, Yamagata T, Osaka H. Usui M, et al. Among authors: miyauchi a. Brain Dev. 2017 Nov;39(10):886-890. doi: 10.1016/j.braindev.2017.05.006. Epub 2017 Jun 3. Brain Dev. 2017. PMID: 28587793

2

Persistent presence of the anti-myelin oligodendrocyte glycoprotein autoantibody in a pediatric case of acute disseminated encephalomyelitis followed by optic neuritis.

Miyauchi A, Monden Y, Watanabe M, Sugie H, Morita M, Kezuka T, Momoi M, Yamagata T. Miyauchi A, et al. Neuropediatrics. 2014 Jun;45(3):196-9. doi: 10.1055/s-0034-1371179. Epub 2014 Mar 7. Neuropediatrics. 2014. PMID: 24610298

3

Role of an adaptor protein Lin-7B in brain development: possible involvement in autism spectrum disorders.

Mizuno M, Matsumoto A, Hamada N, Ito H, Miyauchi A, Jimbo EF, Momoi MY, Tabata H, Yamagata T, Nagata K. Mizuno M, et al. Among authors: miyauchi a. J Neurochem. 2015 Jan;132(1):61-9. doi: 10.1111/jnc.12943. Epub 2014 Sep 26. J Neurochem. 2015. PMID: 25196215 Free article.

4

A case of anti-NMDAR encephalitis presented hypotensive shock during plasma exchange.

Miyauchi A, Monden Y, Osaka H, Takahashi Y, Yamagata T. Miyauchi A, et al. Brain Dev. 2016 Apr;38(4):427-30. doi: 10.1016/j.braindev.2015.10.009. Epub 2015 Oct 31. Brain Dev. 2016. PMID: 26524986

5

A female case of aromatic l-amino acid decarboxylase deficiency responsive to MAO-B inhibition.

Kojima K, Anzai R, Ohba C, Goto T, Miyauchi A, Thöny B, Saitsu H, Matsumoto N, Osaka H, Yamagata T. Kojima K, et al. Among authors: miyauchi a. Brain Dev. 2016 Nov;38(10):959-963. doi: 10.1016/j.braindev.2016.06.002. Epub 2016 Jun 29. Brain Dev. 2016. PMID: 27371992

6

Mesalazine allergy in a boy with ulcerative colitis: clinical usefulness of mucosal biopsy criteria.

Wada S, Kumagai H, Yokoyama K, Ito T, Miyauchi A, Sakamoto S, Imagawa T, Tulyeu J, Tanaka M, Yamagata T. Wada S, et al. Among authors: miyauchi a. Clin J Gastroenterol. 2016 Oct;9(5):302-5. doi: 10.1007/s12328-016-0675-2. Epub 2016 Aug 8. Clin J Gastroenterol. 2016. PMID: 27503129

7

A case of severe movement disorder with GNAO1 mutation responsive to topiramate.

Sakamoto S, Monden Y, Fukai R, Miyake N, Saito H, Miyauchi A, Matsumoto A, Nagashima M, Osaka H, Matsumoto N, Yamagata T. Sakamoto S, et al. Among authors: miyauchi a. Brain Dev. 2017 May;39(5):439-443. doi: 10.1016/j.braindev.2016.11.009. Epub 2017 Jan 6. Brain Dev. 2017. PMID: 27916449

8

Novel biallelic SZT2 mutations in 3 cases of early-onset epileptic encephalopathy.

Tsuchida N, Nakashima M, Miyauchi A, Yoshitomi S, Kimizu T, Ganesan V, Teik KW, Ch'ng GS, Kato M, Mizuguchi T, Takata A, Miyatake S, Miyake N, Osaka H, Yamagata T, Nakajima H, Saitsu H, Matsumoto N. Tsuchida N, et al. Among authors: miyauchi a. Clin Genet. 2018 Feb;93(2):266-274. doi: 10.1111/cge.13061. Epub 2017 Sep 18. Clin Genet. 2018. PMID: 28556953

9

A patient with early myoclonic encephalopathy (EME) with a de novo KCNQ2 mutation.

Kojima K, Shirai K, Kobayashi M, Miyauchi A, Saitsu H, Matsumoto N, Osaka H, Yamagata T. Kojima K, et al. Among authors: miyauchi a. Brain Dev. 2018 Jan;40(1):69-73. doi: 10.1016/j.braindev.2017.06.004. Epub 2017 Jul 4. Brain Dev. 2018. PMID: 28687180

10

Japanese Leigh syndrome case treated with EPI-743.

Kouga T, Takagi M, Miyauchi A, Shimbo H, Iai M, Yamashita S, Murayama K, Klein MB, Miller G, Goto T, Osaka H. Kouga T, et al. Among authors: miyauchi a. Brain Dev. 2018 Feb;40(2):145-149. doi: 10.1016/j.braindev.2017.08.005. Epub 2017 Sep 12. Brain Dev. 2018. PMID: 28916229

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