Search Results1-8 of  8

  • St George-Hyslop Peter H. ID: 9000009292698

    Articles in CiNii:1

    • アルツハイマー病 解けてきた発症の謎 (脳と心のミステリー--心はなぜ病むのか) -- (第2部 脳と心の謎を解く) (2002)
  • St George-Hyslop Peter H. ID: 9000009932411

    Articles in CiNii:1

    • アルツハイマー病--解けてきた発症の謎 (エイジング研究の最前線--心とからだの健康学) -- (CHAPTER3 老化が引き起こす病気) (2004)
  • St.George-Hyslop Peter H. ID: 9000016538737

    Articles in CiNii:1

    • 早期発症型家族性アルツハイマ-病の原因遺伝子S182(presenilin-1) (特集 遺伝子疾患としてアルツハイマ-病を捉える) (1996)
  • St George-Hyslop Peter H. ID: 9000025015927

    Articles in CiNii:1

    • アルツハイマー病の解けてきた発症の謎 (2001)
  • GEORGE-HYSLOP Peter St ID: 9000019147836

    Centre for Research in Neurodegenerative Diseases and Toronto Western Hospital, Division of Neurology, Department of Medicine, University of Toronto (2011 from CiNii)

    Articles in CiNii:1

    • Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease (2011)
  • ST. GEORGE-HYSLOP Peter ID: 9000001068885

    Centre for Research in Neurodegenerative Diseases, University of Toronto (2002 from CiNii)

    Articles in CiNii:1

    • Aβ-degrading endopeptidase, neprilysin, in mouse brain : synaptic and axonal localization inversely correlating with Aβ pathology (2002)
  • ST.GEORGE-HYSLOP Peter ID: 9000000982651

    トロント大学神経変性疾患研究センター (2003 from CiNii)

    Articles in CiNii:1

    • ラット小脳・脊髄形成過程におけるプレセニリンNTF、CTF発現の変化 (2003)
  • St George-Hyslop Peter ID: 9000344810668

    Articles in CiNii:1

    • Random Mutagenesis of Presenilin-1 Identifies Novel Mutants Exclusively Generating Long Amyloid β-Peptides (2005)
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