Renal amyloidosis historical perspective: Difference between revisions

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===Discovery===
===Discovery===
*[Disease name] was first discovered by [name of scientist], a [nationality + occupation], in [year]/during/following [event].
*In 1969, Finnish-type familial amyloidosis (FAF) first described as one of the causes of renal amyloidosis.<ref name="pmid26019848">{{cite journal |vauthors=Yamanaka S, Miyazaki Y, Kasai K, Ikeda S, Kiuru-Enari S, Hosoya T |title=Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases |journal=Clin Kidney J |volume=6 |issue=2 |pages=189–93 |date=April 2013 |pmid=26019848 |pmc=4432447 |doi=10.1093/ckj/sft007 |url=}}</ref>
 
*The association between [important risk factor/cause] and [disease name] was made in/during [year/event].
*In [year], [scientist] was the first to discover the association between [risk factor] and the development of [disease name].
*In [year], [gene] mutations were first implicated in the pathogenesis of [disease name].


==References==
==References==

Revision as of 16:42, 21 June 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[2]

Overview

Historical Perspective

Discovery

  • In 1969, Finnish-type familial amyloidosis (FAF) first described as one of the causes of renal amyloidosis.[1]

References

  1. Yamanaka S, Miyazaki Y, Kasai K, Ikeda S, Kiuru-Enari S, Hosoya T (April 2013). "Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases". Clin Kidney J. 6 (2): 189–93. doi:10.1093/ckj/sft007. PMC 4432447. PMID 26019848.

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