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Akihiko Miyauchi

TitlePostdoc Fellows and Associates
InstitutionBaylor College of Medicine
DepartmentPostDoc
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Miyauchi A, Watanabe C, Yamada N, Jimbo EF, Kobayashi M, Ohishi N, Nagayoshi A, Aoki S, Kishita Y, Ohtake A, Ohno N, Takahashi M, Yamagata T, Osaka H. Apomorphine is a potent inhibitor of ferroptosis independent of dopaminergic receptors. Sci Rep. 2024 02 27; 14(1):4820. PMID: 38413694; PMCID: PMC10899610.
      Citations:    Fields:    Translation:Humans
    2. Miyauchi A, Osaka H, Lourenco CM, Arakaki N, Honjo RS, Kim CA, Mitsuhashi S, Frith MC, Saito K, Ohori S, Sengoku T, Ogata K, Seyama R, Tsuchida N, Uchiyama Y, Koshimizu E, Hamanaka K, Misawa K, Miyatake S, Mizuguchi T, Fujita A, Matsumoto N. Biallelic structural variations within FGF12 detected by long-read sequencing in epilepsy. Life Sci Alliance. 2023 08; 6(8). PMID: 37286232; PMCID: PMC10248215.
      Citations:    Fields:    Translation:Humans
    3. Watanabe C, Osaka H, Watanabe M, Miyauchi A, Jimbo EF, Tokuyama T, Uosaki H, Kishita Y, Okazaki Y, Onuki T, Ebihara T, Aizawa K, Murayama K, Ohtake A, Yamagata T. Total and reduced/oxidized forms of coenzyme Q10 in fibroblasts of patients with mitochondrial disease. Mol Genet Metab Rep. 2023 Mar; 34:100951. PMID: 36632326; PMCID: PMC9826971.
      Citations:    
    4. Shimozawa H, Sato T, Osaka H, Takeda A, Miyauchi A, Omika N, Yada Y, Kono Y, Murayama K, Okazaki Y, Kishita Y, Yamagata T. A Case of Infantile Mitochondrial Cardiomyopathy Treated with a Combination of Low-Dose Propranolol and Cibenzoline for Left Ventricular Outflow Tract Stenosis. Int Heart J. 2022 Sep 30; 63(5):970-977. PMID: 36104228.
      Citations:    
    5. Ikeda T, Kawahara Y, Miyauchi A, Niijima H, Furukawa R, Shimozawa N, Morimoto A, Osaka H, Yamagata T. Low donor chimerism may be sufficient to prevent demyelination in adrenoleukodystrophy. JIMD Rep. 2022 Jan; 63(1):19-24. PMID: 35028267; PMCID: PMC8743339.
      Citations:    
    6. Matsumoto A, Kojima K, Miya F, Miyauchi A, Watanabe K, Iwamoto S, Kawai K, Kato M, Takahashi Y, Yamagata T. Two cases of DYNC1H1 mutations with intractable epilepsy. Brain Dev. 2021 Sep; 43(8):857-862. PMID: 34092403.
      Citations:    
    7. Kurane K, Monden Y, Tanaka D, Gunji Y, Ikeda T, Miyauchi A, Osaka H, Takahashi T, Yamagata T. MOG-Ab titer-guided approach for steroid tapering to prevent relapse in children with mog antibody-associated adem diseases: A case report. Mult Scler Relat Disord. 2020 Oct; 45:102320. PMID: 32622298.
      Citations:    
    8. Yamada Y, Somiya K, Miyauchi A, Osaka H, Harashima H. Validation of a mitochondrial RNA therapeutic strategy using fibroblasts from a Leigh syndrome patient with a mutation in the mitochondrial ND3 gene. Sci Rep. 2020 05 05; 10(1):7511. PMID: 32371897; PMCID: PMC7200808.
      Citations:    
    9. Hamanaka K, Imagawa E, Koshimizu E, Miyatake S, Tohyama J, Yamagata T, Miyauchi A, Ekhilevitch N, Nakamura F, Kawashima T, Goshima Y, Mohamed AR, Ch'ng GS, Fujita A, Azuma Y, Yasuda K, Imamura S, Nakashima M, Saitsu H, Mitsuhashi S, Mizuguchi T, Takata A, Miyake N, Matsumoto N. De Novo Truncating Variants in the Last Exon of SEMA6B Cause Progressive Myoclonic Epilepsy. Am J Hum Genet. 2020 04 02; 106(4):549-558. PMID: 32169168; PMCID: PMC7118575.
      Citations:    
    10. Miyauchi A, Kouga T, Jimbo EF, Matsuhashi T, Abe T, Yamagata T, Osaka H. Apomorphine rescues reactive oxygen species-induced apoptosis of fibroblasts with mitochondrial disease. Mitochondrion. 2019 11; 49:111-120. PMID: 31356884.
      Citations:    
    11. Kojima K, Nakajima T, Taga N, Miyauchi A, Kato M, Matsumoto A, Ikeda T, Nakamura K, Kubota T, Mizukami H, Ono S, Onuki Y, Sato T, Osaka H, Muramatsu SI, Yamagata T. Gene therapy improves motor and mental function of aromatic l-amino acid decarboxylase deficiency. Brain. 2019 02 01; 142(2):322-333. PMID: 30689738; PMCID: PMC6377184.
      Citations:    
    12. Osaka H, Miyauchi A. Reply to the Letter, "Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation". Brain Dev. 2019 Feb; 41(2):224. PMID: 30458972.
      Citations:    
    13. Nagashima M, Osaka H, Ikeda T, Matsumoto A, Miyauchi A, Kaneko K, Nakashima I, Nakano Y, Wakabayashi K, Monden Y, Yamagata T. Rituximab was effective for acute disseminated encephalomyelitis followed by recurrent optic neuritis with anti-myelin oligodendrocyte glycoprotein antibodies. Brain Dev. 2018 Aug; 40(7):607-611. PMID: 29661590.
      Citations:    
    14. Miyauchi A, Osaka H, Nagashima M, Kuwajima M, Monden Y, Kohda M, Kishita Y, Okazaki Y, Murayama K, Ohtake A, Yamagata T. Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation. Brain Dev. 2018 Jun; 40(6):498-502. PMID: 29506883.
      Citations:    
    15. Kouga T, Takagi M, Miyauchi A, Shimbo H, Iai M, Yamashita S, Murayama K, Klein MB, Miller G, Goto T, Osaka H. Japanese Leigh syndrome case treated with EPI-743. Brain Dev. 2018 Feb; 40(2):145-149. PMID: 28916229.
      Citations:    
    16. Kojima K, Shirai K, Kobayashi M, Miyauchi A, Saitsu H, Matsumoto N, Osaka H, Yamagata T. A patient with early myoclonic encephalopathy (EME) with a de novo KCNQ2 mutation. Brain Dev. 2018 Jan; 40(1):69-73. PMID: 28687180.
      Citations:    
    17. Usui M, Miyauchi A, Nakano Y, Nakamura S, Jimbo E, Itamura S, Adachi K, Nanba E, Narita A, Yamagata T, Osaka H. Miglustat therapy in a case of early-infantile Niemann-Pick type C. Brain Dev. 2017 Nov; 39(10):886-890. PMID: 28587793.
      Citations:    
    18. Sakamoto S, Monden Y, Fukai R, Miyake N, Saito H, Miyauchi A, Matsumoto A, Nagashima M, Osaka H, Matsumoto N, Yamagata T. A case of severe movement disorder with GNAO1 mutation responsive to topiramate. Brain Dev. 2017 May; 39(5):439-443. PMID: 27916449.
      Citations:    
    19. Wada S, Kumagai H, Yokoyama K, Ito T, Miyauchi A, Sakamoto S, Imagawa T, Tulyeu J, Tanaka M, Yamagata T. Mesalazine allergy in a boy with ulcerative colitis: clinical usefulness of mucosal biopsy criteria. Clin J Gastroenterol. 2016 Oct; 9(5):302-5. PMID: 27503129.
      Citations:    
    20. Kojima K, Anzai R, Ohba C, Goto T, Miyauchi A, Th?ny B, Saitsu H, Matsumoto N, Osaka H, Yamagata T. A female case of aromatic l-amino acid decarboxylase deficiency responsive to MAO-B inhibition. Brain Dev. 2016 Nov; 38(10):959-963. PMID: 27371992.
      Citations:    
    21. Miyauchi A, Monden Y, Osaka H, Takahashi Y, Yamagata T. A case of anti-NMDAR encephalitis presented hypotensive shock during plasma exchange. Brain Dev. 2016 Apr; 38(4):427-30. PMID: 26524986.
      Citations:    
    22. Mizuno M, Matsumoto A, Hamada N, Ito H, Miyauchi A, Jimbo EF, Momoi MY, Tabata H, Yamagata T, Nagata K. Role of an adaptor protein Lin-7B in brain development: possible involvement in autism spectrum disorders. J Neurochem. 2015 Jan; 132(1):61-9. PMID: 25196215.
      Citations:    
    23. Miyauchi A, Monden Y, Watanabe M, Sugie H, Morita M, Kezuka T, Momoi M, Yamagata T. Persistent presence of the anti-myelin oligodendrocyte glycoprotein autoantibody in a pediatric case of acute disseminated encephalomyelitis followed by optic neuritis. Neuropediatrics. 2014 Jun; 45(3):196-9. PMID: 24610298.
      Citations:    
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