Antithrombin III deficiency historical perspective: Difference between revisions

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===Discovery===
===Discovery===
* There is limited information about the historical perspective of [disease name].
* Antithrombin deficiency was first Described in 1965 Olav Egeberg.<ref name="pmid11301618">{{cite journal| author=Abildgaard U| title=[Olav Egeberg--hereditary antithrombin deficiency and thrombophilia]. | journal=Tidsskr Nor Laegeforen | year= 2001 | volume= 121 | issue= 5 | pages= 604-5 | pmid=11301618 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11301618  }}</ref>
OR
*it was observed in an Scandinavian family with multiple venous embolism.
*[Disease name] was first discovered by [name of scientist], a [nationality + occupation], in [year]/during/following [event].
 
*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].
 
===Landmark Events in the Development of Treatment Strategies===
 
===Impact on Cultural History===
 
===Famous Cases===
The following are a few famous cases of [disease name]:


==References==
==References==

Latest revision as of 22:46, 14 July 2020

Antithrombin III deficiency Microchapters

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

Overview

Historical Perspective

Discovery

  • Antithrombin deficiency was first Described in 1965 Olav Egeberg.[1]
  • it was observed in an Scandinavian family with multiple venous embolism.

References

  1. Abildgaard U (2001). "[Olav Egeberg--hereditary antithrombin deficiency and thrombophilia]". Tidsskr Nor Laegeforen. 121 (5): 604–5. PMID 11301618.

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