トップ ＞ 脳神経内科医を目指す皆さんへ ＞ 大学院生・後期研修医筆頭著者の最近の発表論文

大学院生・後期研修医筆頭著者の代表的な発表論文

  1. Nakamura N, Izumi R, Hoshi Y, Takai Y, Ono R, Suzuki N, Nagai T, Ishii Y, Ishii T, Harigae H, Okada S, Aiba S, Okiyama N, Fujimoto M, Kuroda H, Tateyama M, Aoki M. FDG-PET detects extensive calcinosis cutis in anti-NXP2 antibody-positive dermatomyositis. Rheumatology (Oxford). 2019 Mar 16.
  2. Yoshida S, Hasegawa T, Suzuki M, Sugeno N, Kobayashi J, Ueyama M, Fukuda M, Ido-Fujibayashi A, Sekiguchi K, Ezura M, Kikuchi A, Baba T, Takeda A, Mochizuki H, Nagai Y, Aoki M. Parkinson's disease-linked DNAJC13 mutation aggravates alpha-synuclein-induced neurotoxicity through perturbation of endosomal trafficking. Hum Mol Genet. 2018 Mar 1;27(5):823-836
  3. Temma Soga, Naoto Sugeno, Toru Baba, Xiaoyi Jin, Tomoyuki Koike, Takafumi Hasegawa, Masashi Aoki. PEG‐J tube breakage in a patient with Parkinson's disease receiving levodopa-carbidopa intestinal gel therapy. Neurology and Clinical Neuroscience. 2018, 197-198
  4. Kaneko K, Sato DK, Nakashima I, Ogawa R, Akaishi T, Takai Y, Nishiyama S, Takahashi T, Misu T, Kuroda H, Tanaka S, Nomura K, Hashimoto Y, Callegaro D, Steinman L, Fujihara K, Aoki M. CSF cytokine profile in MOG-IgG+ neurological disease is similar to AQP4-IgG+ NMOSD but distinct from MS: a cross-sectional study and potential therapeutic implications. J Neurol Neurosurg Psychiatry. 2018 Sep;89(9):927-936.
  5. Ikenouchi H, Sugeno N, Nakamura T, Kobayashi J, Oshima R, Kuroda H, Aoki M. Paradoxical Cerebral Embolism after Gastrointestinal Endoscopy in a Patient with Crohn's Disease. J Stroke Cerebrovasc Dis. 2018 Jul;27(7):e117-e118
  6. Akaishi T, Nakashima I, Mugikura S, Aoki M, Fujihara K. Whole brain and grey matter volume of Japanese patients with multiple sclerosis. J Neuroimmunol. 2017; 306: 68-75.
  7. Nishiyama A, Niihori T, Warita H, Izumi R, Akiyama T, Kato M, Suzuki N, Aoki Y, Aoki M. Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis. Neurobiol Aging. 2017; 53: 194.e1-194.e8.
  8. Ogawa R, Nakashima I, Takahashi T, Kaneko K, Akaishi T, Takai Y, Sato DK, Nishiyama S, Misu T, Kuroda H, Aoki M, Fujihara K. MOG antibody-positive, benign, unilateral, cerebral cortical encephalitis with epilepsy. Neurol Neuroimmunol Neuroinflamm. 2017; 4(2): e322.
  9. Akaishi T, Suzuki Y, Imai T, Tsuda E, Minami N, Nagane Y, Uzawa A, Kawaguchi N, Masuda M, Konno S, Suzuki H, Murai H, Aoki M, Utsugisawa K. Response to treatment of myasthenia gravis according to clinical subtype. BMC Neurol. 2016; 16(1): 225.
  10. Akaishi T, Konno M, Nakashima I, Aoki M. Intractable Hiccup in Demyelinating Disease with Anti-Myelin Oligodendrocyte Glycoprotein (MOG) Antibody. Intern Med. 2016; 55(19): 2905-2906.
  11. Akaishi T, Nakashima I, Takeshita T, Kaneko K, Mugikura S, Sato DK, Takahashi T, Nakazawa T, Aoki M, Fujihara K. Different etiologies and prognoses of optic neuritis in demyelinating diseases. J Neuroimmunol. 2016; 299: 152-157.
  12. Nishiyama A, Warita H, Takahashi T, Suzuki N, Nishiyama S, Tano O, Akiyama T, Watanabe Y, Takahashi K, Kuroda H, Kato M, Tateyama M, Niihori T, Aoki Y, Aoki M. Prominent sensory involvement in a case of familial amyotrophic lateral sclerosis carrying the L8V SOD1 mutation. Clin Neurol Neurosurg. 2016; 150: 194-196.
  13. Shijo T, Nishiyama S, Mukai Y, Tateyama M, Kuroda H, Aoki M. A mismatch between MRI lesions and SPECT hypoperfusion in tacrolimus-related encephalopathy. J Neurol Sci. 2016; 367: 308-10.
  14. Oshima R, Hasegawa T, Tamai K, Sugeno N, Yoshida S, Kobayashi J, Kikuchi A, Baba T, Futatsugi A, Sato I, Satoh K, Takeda A, Aoki M, Tanaka N. ESCRT-0 dysfunction compromises autophagic degradation of protein aggregates and facilitates ER stress-mediated neurodegeneration via apoptotic and necroptotic pathways. Sci Rep. 2016; 6: 24997.
  15. Ando D, Kobayashi J, Kuroda H, Aoki M. Cancer-related Stroke due to Mural Thrombus in the Extracranial Carotid Artery. Intern Med. 2016; 55(11): 1497-9.
  16. Akaishi T, Nakashima I, Takeshita T, Mugikura S, Sato DK, Takahashi T, Nishiyama S, Kurosawa K, Misu T, Nakazawa T, Aoki M, Fujihara K. Lesion length of optic neuritis impacts visual prognosis in neuromyelitis optica. J Neuroimmunol. 2016; 293: 28-33.
  17. Akiyama T, Warita H, Kato M, Nishiyama A, Izumi R, Ikeda C, Kamada M, Suzuki N, Aoki M. Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan. Muscle Nerve. 2016; 54(3): 398-404.
  18. Kaneko K, Sato DK, Nakashima I, Nishiyama S, Tanaka S, Marignier R, Hyun JW, Oliveira LM, Reindl M, Seifert-Held T, Sepulveda M, Siritho S, Waters PJ, Kurosawa K, Akaishi T, Kuroda H, Misu T, Prayoonwiwat N, Berger T, Saiz A, Kim HJ, Nomura K, Callegaro D, Fujihara K, Aoki M. Myelin injury without astrocytopathy in neuroinflammatory disorders with MOG antibodies. J Neurol Neurosurg Psychiatry. 2016; 87(11): 1257-1259.
  19. Shibui A, Kobayashi J, Kuroda H, Aoki M. Dorsal root enhancement in paraneoplastic sensory ataxic neuropathy with anti-Hu antibody. Neurology and Clinical Neuroscience. 2016; 4: 22-24.
  20. Kurosawa K, Misu T, Takai Y, Sato DK, Takahashi T, Abe Y, Iwanari H, Ogawa R, Nakashima I, Fujihara K, Hamakubo T, Yasui M, Aoki M. Severely exacerbated neuromyelitis optica rat model with extensive astrocytopathy by high affinity anti-aquaporin-4 monoclonal antibody. Acta Neuropathol Commun. 2015; 3: 82.
  21. Akaishi T, Kuroda H, Tateyama M, Yoshida Y, Otsuki T, Watanabe M, Yaegashi N, Aoki M. Recurrent cerebral infarction synchronous with menorrhagia caused by endometrial stromal sarcoma. J Neurol Sci. 2015; 358(1-2): 509-11.
  22. Kobayashi J, Sugeno N, Shibui A, Aoki M. Girdle Sensation Caused by Radiculitis due to Neurosarcoidosis. Intern Med. 2015; 54(12): 1567-8.
    23. Akaishi T, Nakashima I, Misu T, Fujihara K, Aoki M. Depressive state and chronic fatigue in multiple sclerosis and neuromyelitis optica. J Neuroimmunol. 2015; 283: 70-3.
  23. Akaishi T, Sato DK, Nakashima I, Takeshita T, Takahashi T, Doi H, Kurosawa K, Kaneko K, Kuroda H, Nishiyama S, Misu T, Nakazawa T, Fujihara K, Aoki M. MRI and retinal abnormalities in isolated optic neuritis with myelin oligodendrocyte glycoprotein and aquaporin-4 antibodies: a comparative study. J Neurol Neurosurg Psychiatry. 2016; 87(4): 446-8.
  24. Ikeda K, Kiyota N, Kuroda H, Sato DK, Nishiyama S, Takahashi T, Misu T, Nakashima I, Fujihara K, Aoki M. Severe demyelination but no astrocytopathy in clinically definite neuromyelitis optica with anti-myelin-oligodendrocyte glycoprotein antibody. Mult Scler. 2015; 21(5): 656-9.
  25. Ikeda K, Kuroda H, Ono H, Miura E, Suzuki N, Misu T, Motomura M, Aoki M. Non-paraneoplastic Lambert-Eaton myasthenic syndrome presenting dropped head and respiratory failure with normoreflexia. Neurology and Clinical Neuroscience. 2015; 3: 188-189.
  26. Kobayashi J, Kuroda H, Ezura M, Sugeno N, Shibui A, Takahashi T, Misu T, Fujihara K, Mori E, Aoki M. Acute callosal disconnection syndrome as an initial manifestation of neuromyelitis optica spectrum disorders. Neurology and Clinical Neuroscience. 2015; 3: 137-139.
  27. Akaishi T, Narikawa K, Suzuki Y, Mitsuzawa S, Tsukita K, Kuroda H, Nakashima I, Fujiwara K, Aoki M. Importance of the quotient of albumin, quotient of immunoglobulin G and Reibergram in inflammatory neurological disorders with disease-specific patterns of blood-brain barrier permeability. Neurology and Clinical Neuroscience. 2015; 3: 94-100.
  28. Izumi R, Niihori T, Suzuki N, Sasahara Y, Rikiishi T, Nishiyama A, Nishiyama S, Endo K, Kato M, Warita H, Konno H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Nakayama K, Kure S, Matsubara Y, Aoki Y, Aoki M. GNE myopathy associated with congenital thrombocytopenia: a report of two siblings. Neuromuscul Disord. 2014; 24(12): 1068-72.
  29. Kato K, Jin K, Itabashi H, Iwasaki M, Kakisaka Y, Aoki M, Nakasato N. Earlier tachycardia onset in right than left mesial temporal lobe seizures. Neurology. 2014; 83(15): 1332-6.
  30. Akaishi T, Yamaguchi T, Suzuki Y, Nagane Y, Suzuki S, Murai H, Imai T, Motomura M, Fujihara K, Aoki M, Utsugisawa K. Insights into the classification of myasthenia gravis. PLoS One. 2014; 9(9): e106757.
    31. Tsuboi H, Sugeno N, Tateyama M, Nakashima I, Hasegawa T, Kuroda H, Kaneko K, Kobayashi M, Ishigaki A, Fujimori J, Aoki M. Retrospective analysis of Guillain-Barre syndrome and Fisher syndrome after the Great East Japan Earthquake. Brain Behav. 2014; 4(4): 595-7.
  31. Miura E, Hasegawa T, Konno M, Suzuki M, Sugeno N, Fujikake N, Geisler S, Tabuchi M, Oshima R, Kikuchi A, Baba T, Wada K, Nagai Y, Takeda A, Aoki M. VPS35 dysfunction impairs lysosomal degradation of α-synuclein and exacerbates neurotoxicity in a Drosophila model of Parkinson's disease. Neurobiol Dis. 2014; 71: 1-13.
  32. Kaneko K, Sato DK, Misu T, Kurosawa K, Nakashima I, Fujihara K, Aoki M. Anti-N-methyl-D-aspartate receptor encephalitis with multiphasic demyelination. Ann Neurol. 2014; 76(3): 462-4.
  33. Akaishi T, Tateyama M, Kato K, Miura E, Izumi R, Endo K, Sugeno N, Suzuki N, Baba T, Misu T, Kikuchi A, Hasegawa T, Konosu-Fukaya S, Fujishima F, Suzuki H, Nakashima I, Aoki M. An autopsy case involving a 12-year history of amyotrophic lateral sclerosis with CIDP-like polyneuropathy. Intern Med. 2014; 53(12): 1371-5.
  34. Kaneko K, Kuroda H, Izumi R, Tateyama M, Kato M, Sugimura K, Sakata Y, Ikeda Y, Hirano K, Aoki M. A novel mutation in PNPLA2 causes neutral lipid storage disease with myopathy and triglyceride deposit cardiomyovasculopathy: a case report and literature review. Neuromuscul Disord. 2014; 24(7): 634-41.
  35. Yoshida S, Kikuchi A, Tateyama M, Tano O, Nishiyama A, Akaishi T, Kato M, Aoki M. A case of steroid-responsive MADSAM with late appearance of a partial conduction block in the forearm. J Neurol. 2014; 261(4): 825-7.
  36. Nishiyama A, Sugeno N, Tateyama M, Nishiyama S, Kato M, Aoki M. Postural leg tremor in X-linked spinal and bulbar muscular atrophy. J Clin Neurosci. 2014; 21(5): 799-802.
  37. Shijo T, Sugeno N, Kuroda H, Hasegawa T, Takeda A, Aoki M. Isolated posterior column lesion in a case with mixed connective tissue disease. Neurology and Clinical Neuroscience. 2014; 2: 95.
  38. Kaneko K, Sugeno N, Tateyama M, Misu T, Suzuki N, Aoki M. Hereditary neuropathy with liability to pressure palsy emerging after hypothyroidism. Neurology and Clinical Neuroscience 2013; 1: 160-161.
  39. Yoshida S, Kikuchi A, Tateyama M, Aoki M. T2-hyperintensity of the middle cerebellar peduncles in a patient with SCA7. Intern Med. 2013; 52(12): 1433-4.
  40. 田野大人, 金子仁彦, 菊池昭夫, 長谷川隆文, 武田篤, 青木正志. ドパミン作動薬誘発性開顎ジストニアを合併した進行性核上性麻痺の1例. 臨床神経学 2013;53:308-311.
  41. 坪井博文, 菅野直人, 西山亜由美, 竪山真規, 青木正志. 撓骨神経麻痺が前景に立った神経痛性筋萎縮症の1例. 臨床神経学 2013; 53: 312-315.
  42. Kaneko K, Tano O, Kikuchi A, Hasegawa T, Tateyama M, Yoshioka M, Saito H, Watanabe O, Takeda A, Aoki M. Anti-voltage-gated potassium channel antibody is associated with chronic autonomic and sensory neuropathy. J Neurol 2013; 260: 315-317.
  43. Izumi R, Niihori T, Aoki Y, Suzuki N, Kato M, Warita H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Abe K, Nakayama K, Aoki M, Matsubara Y. Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure. J Hum Genet 2013; 58(5): 259-66.
  44. Takai Y, Misu T, Nakashima I, Takahashi T, Itoyama Y, Fujihara K, Aoki M. Two cases of lumbosacral myeloradiculitis with anti-aquaporin-4 antibody. Neurology 2012; 79: 1826-1828.
  45. Konno M, Hasegawa T, Baba T, Miura E, Sugeno N, Kikuchi A, Fiesel FC, Sasaki T, Aoki M, Itoyama Y, Takeda A. Suppression of dynamin GTPase decreases alpha-synuclein uptake by neuronal and oligodendroglial cells: a potent therapeutic target for synucleinopathy. Mol Neurodegener 2012; 7: 38.
  46. Kawaguchi N, Suzuki N, Tateyama M, Takai Y, Misu T, Nakashima I, Itoyama Y, Aoki M. Two cases of elderly-onset hereditary neuropathy with liability to pressure palsy manifesting bilateral peroneal nerve palsies. Case Rep Neurol 2012; 4: 149-155.
  47. Baba T, Kikuchi A, Hirayama K, Nishio Y, Hosokai Y, Kanno S, Hasegawa T, Sugeno N, Konno M, Suzuki K, Takahashi S, Fukuda H, Aoki M, Itoyama Y, Mori E, Takeda A. Severe olfactory dysfunction is a prodromal symptom of dementia associated with Parkinson's disease: a 3 year longitudinal study. Brain 2012; 135: 161-169.
  48. Izumi R, Suzuki N, Nagata M, Hasegawa T, Abe Y, Saito Y, Mochizuki H, Tateyama M, Aoki M. A case of late onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency manifesting as recurrent rhabdomyolysis and acute renal failure. Intern Med 2011; 50: 2663-2668.

 

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