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Scientific Reports|May 7, 2020
Validation of a mitochondrial RNA therapeutic strategy using fibroblasts from a Leigh syndrome patient with a mutation in the mitochondrial ND3 geneYuma Yamada, Kana Somiya, Akihiko Miyauchi, et al.Brain & Development|November 4, 2015
A case of anti-NMDAR encephalitis presented hypotensive shock during plasma exchangeAkihiko Miyauchi, Yukifumi Monden, Hitoshi Osaka, et al.Mitochondrion|July 30, 2019
Apomorphine rescues reactive oxygen species-induced apoptosis of fibroblasts with mitochondrial diseaseAkihiko Miyauchi, Takeshi Kouga, Eriko F Jimbo, et al.Brain & Development|July 9, 2017
A patient with early myoclonic encephalopathy (EME) with a de novo KCNQ2 mutationKarin Kojima, Kentaro Shirai, Mizuki Kobayashi, et al.Neuropediatrics|March 11, 2014
Persistent presence of the anti-myelin oligodendrocyte glycoprotein autoantibody in a pediatric case of acute disseminated encephalomyelitis followed by optic neuritisAkihiko Miyauchi, Yukifumi Monden, Meri Watanabe, et al.JIMD Reports|January 14, 2022
Low donor chimerism may be sufficient to prevent demyelination in adrenoleukodystrophyTakahiro Ikeda, Yuta Kawahara, Akihiko Miyauchi, et al.Multiple Sclerosis and Related Disorders|July 5, 2020
MOG-Ab titer-guided approach for steroid tapering to prevent relapse in children with mog antibody-associated adem diseases: A case reportKoyuru Kurane, Yukifumi Monden, Daisuke Tanaka, et al.Clinical Journal of Gastroenterology|August 10, 2016
Mesalazine allergy in a boy with ulcerative colitis: clinical usefulness of mucosal biopsy criteriaShoya Wada, Hideki Kumagai, Koji Yokoyama, et al.Brain & Development|June 7, 2021
Two cases of DYNC1H1 mutations with intractable epilepsyAyumi Matsumoto, Karin Kojima, Fuyuki Miya, et al.Brain & Development|July 4, 2016
A female case of aromatic l-amino acid decarboxylase deficiency responsive to MAO-B inhibitionKarin Kojima, Rie Anzai, Chihiro Ohba, et al.Pageof 3