記事一覧

• 越智雅之，大八木保政
  難渋症例から学ぶ診療のエッセンス：ビタミンB12欠乏症を合併したレビー小体型認知症．
  日本医事新報 2021; 5046:10-11.

• 大八木保政
  四国健康ナビ：ALS発症早期に確実な診断を．
  毎日新聞 2021; 4月7日

• 大八木保政
  アルツハイマー病．
  今日の治療指針 2021; 979-981.

• 越智博文
  視神経脊髄炎．
  今日の治療指針 2021; 975-977.

• Miura S, Ochi M, Ochi H, Igase M, Kawaguchi N, Miyagawa M, Uchiyama Y, Ohyagi Y.
  Bilateral parkinsonism in a patient with infarcts involving the unilateral basal ganglia.
  eNeurologicalSci 2020; 21:100291

• Goto T, Kuramoto E, Dhar A, Wang RPH, Seki H, Iwai H, Yamanaka A, Matsumoto S, Hara H, Michikawa M, Ohyagi Y, Leung WK, Chang RCC.
  Tooth loss accelerates the onset of dementia in 3xTg Alzheimer’s disease model mice.
  J Alzheimers Dis 2020; 76:1443-1459.

• Miura S, Kosaka K, Shimojo T, Matsuura E, Noda K, Fujioka R, Mori SI, Umehara F, Iwaki T, Yamamoto K, Saitsu H, Shibata H.
  Intronic variant in IQGAP3 responsible for hereditary neuropathy with proximal lower dominancy, urinary disturbance, and paroxysmal dry cough.
  J Hum Genet 2020; 65:717-725.

• Imamura T, Yanagihara YT, Ohyagi Y, Nakamura N, Iinuma KM, Yamasaki R, Asai H, Maeda M, Murakami K, Irie K, Kira JI
  Insulin deficiency promotes formation of toxic amyloid-β42 conformer co-aggregating with hyper-phophorylated tau oligomer in an Alzheimer’s disease model.
  Neurobiol Dis 2020; 137:104739

• Hamatani M, Yamashita H, Ochi H, Ashida S, Hashi Y, Okada Y, Fujii C, Kawamura K, Kitazawa R, Nakagawa M, Mizuno T, Takahashi R, Kondo T.
  Altered features of monocytes in adult onset leukoencephalopathy with axonal spheroids and pigmented glia: A clue to the pathomechanism of microglial dyshomeostasis
  Neurobiol Dis 2020; 140:104867

• Ohyagi Y, Takei SI.
  Insulin signaling as a therapeutic target in Alzheimer’s disease: Efficacy of apomorphine.
  Neurol Clin Neurosci 2020; 8:146-154.

• Senzaki K, Miura S, Ochi M, Katoh T, Okada Y, Matsumoto S, Shiraoka A, Ochi H, Igase M, Kitazawa R, Zhu B, Ikeuchi T, Ohyagi Y.
  Sporadic Japanese case of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia causes by a de novo p.Phe849del mutation in CSF1R.
  Neurol Clin Neurosci 2020; 8:96-98.

• Tabara Y, Kohara K, Okada Y, Ohyagi Y, Igase M.
  Creatinine to cystatin C ratio as a marker of bone property in older adults: The J-SHIPP study.
  J Nutr Health Aging 2020; 24:277-281.