家族性腎澱粉樣變 (Chinese Wikipedia)
Analysis of information sources in references of the Wikipedia article "家族性腎澱粉樣變" in Chinese language version.
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doi.org
- Uemichi T, Liepnieks JJ, Gertz MA, Benson MD. Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis. Amyloid. September 1998, 5 (3): 188–92. PMID 9818055. doi:10.3109/13506129809003844.
- Soutar AK; Hawkins PN; Vigushin DM; et al. Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. Proc. Natl. Acad. Sci. U.S.A. August 1992, 89 (16): 7389–93 [2014-08-05]. PMC 49715
. PMID 1502149. doi:10.1073/pnas.89.16.7389. （原始内容存档于2019-09-25）. - Granel B; Serratrice J; Disdier P; et al. Underdiagnosed amyloidosis: amyloidosis of lysozyme variant. Am. J. Med. March 2005, 118 (3): 321–2 [2014-08-05]. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022. （原始内容存档于2019-09-25）.
- Granel B; Valleix S; Serratrice J; et al. Lysozyme amyloidosis: report of 4 cases and a review of the literature. Medicine (Baltimore). January 2006, 85 (1): 66–73 [2014-08-05]. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. （原始内容存档于2012-02-15）.
elsevier.com
linkinghub.elsevier.com
- Granel B; Serratrice J; Disdier P; et al. Underdiagnosed amyloidosis: amyloidosis of lysozyme variant. Am. J. Med. March 2005, 118 (3): 321–2 [2014-08-05]. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022. （原始内容存档于2019-09-25）.
nih.gov
ncbi.nlm.nih.gov
- Uemichi T, Liepnieks JJ, Gertz MA, Benson MD. Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis. Amyloid. September 1998, 5 (3): 188–92. PMID 9818055. doi:10.3109/13506129809003844.
- Soutar AK; Hawkins PN; Vigushin DM; et al. Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. Proc. Natl. Acad. Sci. U.S.A. August 1992, 89 (16): 7389–93 [2014-08-05]. PMC 49715 . PMID 1502149. doi:10.1073/pnas.89.16.7389. （原始内容存档于2019-09-25）.
- Granel B; Serratrice J; Disdier P; et al. Underdiagnosed amyloidosis: amyloidosis of lysozyme variant. Am. J. Med. March 2005, 118 (3): 321–2 [2014-08-05]. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022. （原始内容存档于2019-09-25）.
- Granel B; Valleix S; Serratrice J; et al. Lysozyme amyloidosis: report of 4 cases and a review of the literature. Medicine (Baltimore). January 2006, 85 (1): 66–73 [2014-08-05]. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. （原始内容存档于2012-02-15）.
pnas.org
- Soutar AK; Hawkins PN; Vigushin DM; et al. Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. Proc. Natl. Acad. Sci. U.S.A. August 1992, 89 (16): 7389–93 [2014-08-05]. PMC 49715 . PMID 1502149. doi:10.1073/pnas.89.16.7389. （原始内容存档于2019-09-25）.
web.archive.org
- Amyloid. （原始内容存档于2019-02-17）.
- Soutar AK; Hawkins PN; Vigushin DM; et al. Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. Proc. Natl. Acad. Sci. U.S.A. August 1992, 89 (16): 7389–93 [2014-08-05]. PMC 49715 . PMID 1502149. doi:10.1073/pnas.89.16.7389. （原始内容存档于2019-09-25）.
- Granel B; Serratrice J; Disdier P; et al. Underdiagnosed amyloidosis: amyloidosis of lysozyme variant. Am. J. Med. March 2005, 118 (3): 321–2 [2014-08-05]. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022. （原始内容存档于2019-09-25）.
- Granel B; Valleix S; Serratrice J; et al. Lysozyme amyloidosis: report of 4 cases and a review of the literature. Medicine (Baltimore). January 2006, 85 (1): 66–73 [2014-08-05]. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. （原始内容存档于2012-02-15）.
wkhealth.com
meta.wkhealth.com
- Granel B; Valleix S; Serratrice J; et al. Lysozyme amyloidosis: report of 4 cases and a review of the literature. Medicine (Baltimore). January 2006, 85 (1): 66–73 [2014-08-05]. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. （原始内容存档于2012-02-15）.