Literature DB >> 15745733

Underdiagnosed amyloidosis: amyloidosis of lysozyme variant.

Brigitte Granel, Jacques Serratrice, Patrick Disdier, Pierre-Jean Weiller, Sophie Valleix, Gilles Grateau, Dominique Droz.   

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Year:  2005        PMID： 15745733     DOI： 10.1016/j.amjmed.2004.10.022

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  2 in total

Review 1.  Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review.

Authors:  Audrey Benyamine; Fanny Bernard-Guervilly; Céline Tummino; Nicolas Macagno; Laurent Daniel; Sophie Valleix; Brigitte Granel
Journal:  Clin Rheumatol       Date:  2017-09-30       Impact factor: 2.980

Review 2.  Hereditary renal amyloidosis with a variant lysozyme p.Trp82Arg in a Chinese family: case report and literature review.

Authors:  Zhenyu Li; Hui Xu; Dan Liu; Danyang Li; Gang Liu; Su-Xia Wang
Journal:  BMC Nephrol       Date:  2019-08-08       Impact factor: 2.388
  2 in total

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