Showing 1 - 3 results of 3 for search 'Mathuranath Pavagada' Skip to content
VuFind
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
高級檢索
  • 作者
  • Mathuranath Pavagada
Showing 1 - 3 results of 3 for search 'Mathuranath Pavagada', 查詢時間: 0.02s Refine Results
  1. 1
    Neuro-Bechet’s disease: a case series from India

    Neuro-Bechet’s disease: a case series from India 由 Rohan R. Mahale, Sneha Kamath, C. M. Ravindranadh, Hansashree Padmanabha, Pooja Mailankody, Mathuranath Pavagada

    出版 2022-12-01
    獲取全文
    Article
  2. 2
    Autosomal dominant cerebral small vessel disease in HTRA1 gene mutation

    Autosomal dominant cerebral small vessel disease in HTRA1 gene mutation 由 Rohan R Mahale, Aakash Agarwal, Jyothi Gautam, Nibu Varghese, Jennifer Kovoor, Pooja Mailankody, Hansashree Padmanabha, Mathuranath Pavagada

    出版 2021-01-01
    獲取全文
    Article
  3. 3
    A rare treatable cause for atypical frontotemporal dementia with multiple fractures in a young female

    A rare treatable cause for atypical frontotemporal dementia with multiple fractures in a young female 由 Sadanandavalli Retnaswami Chandra, Neeraja Koti, Ganaraja Valakunja Harikrishna, Pooja Mailankody, C Nitin Ramanujam, S Mathuranath Pavagada, Thomas Gregor Issac

    出版 2018-01-01
    獲取全文
    Article

檢索工具:

  • 得到RSS訂閱
  • 推薦此搜索

檢索選項

  • 檢索歷史
  • 高級檢索

查找更多

  • 瀏覽目錄
  • 按字母順序瀏覽
  • Explore Channels
  • 課程儲備
  • 新項目

需要幫助?

  • 檢索技巧
  • 咨詢台
  • 常見問題