Amiloidose familiar renal (Galician Wikipedia)

Analysis of information sources in references of the Wikipedia article "Amiloidose familiar renal" in Galician language version.

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Uemichi T, Liepnieks JJ, Gertz MA, Benson MD (1998). "Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis". Amyloid 5 (3): 188–92. PMID 9818055. doi:10.3109/13506129809003844.
Soutar AK; Hawkins PN; Vigushin DM; et al. (1992). "Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis". Proc. Natl. Acad. Sci. U.S.A. 89 (16): 7389–93. PMC 49715. PMID 1502149. doi:10.1073/pnas.89.16.7389.
Granel B; Serratrice J; Disdier P; et al. (2005). "Underdiagnosed amyloidosis: amyloidosis of lysozyme variant". Am. J. Med. 118 (3): 321–2. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022.
Granel B; Valleix S; Serratrice J; et al. (2006). "Lysozyme amyloidosis: report of 4 cases and a review of the literature". Medicine (Baltimore) 85 (1): 66–73. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. Arquivado dende o orixinal o 15 de febreiro de 2012. Consultado o 31 de decembro de 2013.

elsevier.com

linkinghub.elsevier.com

Granel B; Serratrice J; Disdier P; et al. (2005). "Underdiagnosed amyloidosis: amyloidosis of lysozyme variant". Am. J. Med. 118 (3): 321–2. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022.

medscape.com

emedicine.medscape.com

Helen J Lachmann, MB. Familial Renal Amyloidosis Medscape

nih.gov

ncbi.nlm.nih.gov

Uemichi T, Liepnieks JJ, Gertz MA, Benson MD (1998). "Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis". Amyloid 5 (3): 188–92. PMID 9818055. doi:10.3109/13506129809003844.
Soutar AK; Hawkins PN; Vigushin DM; et al. (1992). "Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis". Proc. Natl. Acad. Sci. U.S.A. 89 (16): 7389–93. PMC 49715. PMID 1502149. doi:10.1073/pnas.89.16.7389.
Granel B; Serratrice J; Disdier P; et al. (2005). "Underdiagnosed amyloidosis: amyloidosis of lysozyme variant". Am. J. Med. 118 (3): 321–2. PMID 15745733. doi:10.1016/j.amjmed.2004.10.022.
Granel B; Valleix S; Serratrice J; et al. (2006). "Lysozyme amyloidosis: report of 4 cases and a review of the literature". Medicine (Baltimore) 85 (1): 66–73. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. Arquivado dende o orixinal o 15 de febreiro de 2012. Consultado o 31 de decembro de 2013.

orpha.net

Orphanet: Amiloidose familiar renal.

pnas.org

Soutar AK; Hawkins PN; Vigushin DM; et al. (1992). "Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis". Proc. Natl. Acad. Sci. U.S.A. 89 (16): 7389–93. PMC 49715. PMID 1502149. doi:10.1073/pnas.89.16.7389.

web.archive.org

Granel B; Valleix S; Serratrice J; et al. (2006). "Lysozyme amyloidosis: report of 4 cases and a review of the literature". Medicine (Baltimore) 85 (1): 66–73. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. Arquivado dende o orixinal o 15 de febreiro de 2012. Consultado o 31 de decembro de 2013.

wkhealth.com

meta.wkhealth.com

Granel B; Valleix S; Serratrice J; et al. (2006). "Lysozyme amyloidosis: report of 4 cases and a review of the literature". Medicine (Baltimore) 85 (1): 66–73. PMID 16523055. doi:10.1097/01.md.0000200467.51816.6d. Arquivado dende o orixinal o 15 de febreiro de 2012. Consultado o 31 de decembro de 2013.

wustl.edu

neuromuscular.wustl.edu

"Amyloid".