Showing 21 - 40 results of 148 for search '"amyloidosis"', query time: 0.05s Refine Results
  1. 21

    From the Bone Marrow to the Heart by Dia A. Smiley, DO, Andrew J. Einstein, MD, PhD

    Published 2025-01-01
    Subjects: “…AL amyloidosis…”
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    Article
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    Epidemiology of transthyretin (ATTR) amyloidosis: a systematic literature review by Diego Delgado, Firas Dabbous, Nitin Shivappa, Faizan Mazhar, Eric Wittbrodt, Divya Shridharmurthy, Krister Järbrink

    Published 2025-01-01
    “…Abstract Introduction Significant advances in the treatment of transthyretin (ATTR) amyloidosis has led to an evolving understanding of the epidemiology of this condition. …”
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    Article
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    Histochemical Differential Diagnosis and Polarization Optical Analysis of Amyloid and Amyloidosis by M. Bély

    Published 2006-01-01
    “…Amyloidosis is characterized by extracellular deposition of protein fibrils of chemically heterogeneous composition. …”
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    Article
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    A Rare Case of Light Chain Amyloidosis of the Gastrointestinal Tract by Kathrin Dvir, Gliceida M. Galarza-Fortuna, Anna Willet, Christopher Febres-Aldana, Nathaly Cortez, Samuel Rapaka, Andre Coombs, Robert Goldberg, Michael Schwartz, Kfir Ben-David

    Published 2020-01-01
    “…Repeated intraoperative biopsies of the gastric mass and of liver parenchyma demonstrated diffuse hyalinized stroma consistent with amyloid deposition, and a bone marrow biopsy confirmed the diagnosis of primary light chain (AL) amyloidosis.…”
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    Article
  9. 29

    Diagnosing Cardiac Amyloidosis: From Heart Failure to Electrical Storm by Adithya T. Mathews, Abu-Sayeef Mirza, Chandrashekar Bohra, Akshay G. Mathews, Philip Ritucci-Chinni, Jamie L. Weber, William W. Bulkeley, Maqsood Siddique, David Whitaker, Richard Bowerman

    Published 2021-01-01
    “…Cardiac amyloidosis is a condition when amyloid fibers are deposited in the extracellular space of the heart causing tachyarrhythmias, heart failure, or sudden cardiac death. …”
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    Article
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    Systemic Amyloidosis and Cardiac Autonomic Neuropathy Associated with Waldenstrom’s Macroglobulinemia by Aasems Jacob, Rishi Raj, Warren Walkow

    Published 2017-01-01
    “…A 73-year-old male with long-standing Waldenstrom’s macroglobulinemia complicated with systemic amyloidosis presented with a witnessed syncopal episode. …”
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    Article
  12. 32

    Recurrent Pleural Effusions Occurring in Association with Primary Pulmonary Amyloidosis by Lauren Tada, Humayun Anjum, W. Kenneth Linville, Salim Surani

    Published 2015-01-01
    “…Recurrent pleural effusions occurring in association with immunoglobulin light chain amyloidosis and not associated with amyloid cardiomyopathy are rare. …”
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    Article
  13. 33

    Along for the Ride: Intrahepatic Cholangiocarcinoma with Concomitant LECT2 Amyloidosis by Phoenix D. Bell, Aaron R. Huber, Tom C. DeRoche

    Published 2020-01-01
    “…To our knowledge, this is the first documented case of intrahepatic cholangiocarcinoma arising in association with LECT2 amyloidosis.…”
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    Article
  14. 34

    Sjögren Syndrome Complicated with Cystic Lung Disease and Pulmonary Amyloidosis by Koichiro Takahashi, Hironori Sadamatsu, Shinsuke Ogusu, Kazutoshi Komiya, Tomomi Nakamura, Shinya Kimura, Naoko Sueoka-Aragane

    Published 2018-01-01
    “…Here, we report a rare case of Sjögren syndrome complicated with cystic lung disease and pulmonary amyloidosis.…”
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    Article
  15. 35

    Poor Outcomes in Hepatic Amyloidosis: A Report of 2 Cases by Brandon Yim, Elizabeth Kertowidjojo, Yue Zhang, Pruthvi Patel

    Published 2016-01-01
    “…Hepatic amyloidosis is a rare disease entity that results from insoluble amyloid protein deposition in the liver. …”
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    Article
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    Nonfluent/Agrammatic PPA with In-Vivo Cortical Amyloidosis and Pick’s Disease Pathology by Francesca Caso, Benno Gesierich, Maya Henry, Manu Sidhu, Amanda LaMarre, Miranda Babiak, Bruce L. Miller, Gil D. Rabinovici, Eric J. Huang, Giuseppe Magnani, Massimo Filippi, Giancarlo Comi, William W. Seeley, Maria Luisa Gorno-Tempini

    Published 2013-01-01
    “…This patient demonstrates that biomarkers indicating brain amyloidosis should not be considered conclusive evidence that AD pathology accounts for a typical FTD clinical/anatomical syndrome.…”
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    Article