GENITOURINARY DISTURBANCES IN FAMILIAL AND SPORADIC CASES OF PRIMARY AMYLOIDOSIS WITH POLYNEUROPATHY-Reference-Cited by-同舟云学术

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GENITOURINARY DISTURBANCES IN FAMILIAL AND SPORADIC CASES OF PRIMARY AMYLOIDOSIS WITH POLYNEUROPATHY

Published:2009-04-24 Issue:1-6 Volume:195 Page:49-58
ISSN:0001-6101
Container-title:Acta Medica Scandinavica
language:en
Short-container-title:

Author:

Andersson R.,Hofer P.-Å.

Publisher

Wiley

Subject

Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.0954-6820.1974.tb08096.x/fullpdf

Reference25 articles.

1. Hereditary amyloidosis with polyneuropathy;Andersson;Acta med. scand.,1970

2. Neurophysiological studies in hereditary amyloidosis with polyneuropathy;Andersson;Acta med. scand.,1972

3. Vitreous opacities in primary familial amyloidosis;Andersson;Acta Ophthal. (Kbh.),1968

4. A peculiar form of peripheral neuropathy. Familiar atypical generalized amyloidosis with special involvement of the peripheral nerves;Andrade;Brain,1952

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