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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1977 2
1984 1
1992 1
1994 1
1996 1
1999 1
2001 1
2002 5
2003 1
2004 3
2005 3
2006 4
2007 4
2008 10
2009 5
2010 1
2011 1
2012 1
2015 1
2016 1
2017 2
2018 2
2019 3
2021 0
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Similar articles for PMID: 12068025

52 results
Results by year
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Page 1
Renal pathology in Fabry disease.
Alroy J, Sabnis S, Kopp JB. Alroy J, et al. J Am Soc Nephrol. 2002 Jun;13 Suppl 2:S134-8. J Am Soc Nephrol. 2002. PMID: 12068025 Free article. Review. No abstract available.
Natural history and treatment of renal involvement in Fabry disease.
Branton M, Schiffmann R, Kopp JB. Branton M, et al. J Am Soc Nephrol. 2002 Jun;13 Suppl 2:S139-43. J Am Soc Nephrol. 2002. PMID: 12068026 Free article. Review. No abstract available.
[Fabry disease].
Jakubowska E, Ryba M, Hruby Z. Jakubowska E, et al. Przegl Lek. 2006;63(4):218-9. Przegl Lek. 2006. PMID: 17080745 Review. Polish.
[Fabry disease - complex clinical picture, simple diagnosis procedure, causal treatment].
Hoffmann B, Beck M, Rolfs A, Neumann HP. Hoffmann B, et al. Dtsch Med Wochenschr. 2008 Sep;133(39):1965-72; quiz 1973-4. doi: 10.1055/s-0028-1085605. Epub 2008 Sep 16. Dtsch Med Wochenschr. 2008. PMID: 18798134 Review. German. No abstract available.
Cardiac microvascular pathology in Fabry disease: evaluation of endomyocardial biopsies before and after enzyme replacement therapy.
Thurberg BL, Fallon JT, Mitchell R, Aretz T, Gordon RE, O'Callaghan MW. Thurberg BL, et al. Circulation. 2009 May 19;119(19):2561-7. doi: 10.1161/CIRCULATIONAHA.108.841494. Epub 2009 May 4. Circulation. 2009. PMID: 19414635
New therapies for Fabry's disease.
Gahl WA. Gahl WA. N Engl J Med. 2001 Jul 5;345(1):55-7. doi: 10.1056/NEJM200107053450109. N Engl J Med. 2001. PMID: 11439950 No abstract available.
Proteinuria in a male adolescent with hearing loss: Answers.
Kaya Aksoy G, Çomak E, Akkaya B, Koyun M, Akman S. Kaya Aksoy G, et al. Pediatr Nephrol. 2018 Jul;33(7):1161-1163. doi: 10.1007/s00467-017-3825-y. Epub 2017 Nov 2. Pediatr Nephrol. 2018. PMID: 29098401 No abstract available.
Evaluation of recombinant alpha-galactosidase A therapy for amelioration of the cardiovascular manifestations of Fabry disease: an important role for endomyocardial biopsy.
Buja LM. Buja LM. Circulation. 2009 May 19;119(19):2539-41. doi: 10.1161/CIRCULATIONAHA.109.861534. Circulation. 2009. PMID: 19451361 No abstract available.
Partial correction of the alpha-galactosidase A deficiency and reduction of glycolipid storage in Fabry mice using synthetic vectors.
Przybylska M, Wu IH, Zhao H, Ziegler RJ, Tousignant JD, Desnick RJ, Scheule RK, Cheng SH, Yew NS. Przybylska M, et al. J Gene Med. 2004 Jan;6(1):85-92. doi: 10.1002/jgm.468. J Gene Med. 2004. PMID: 14716680
[Biochemical and pathological studies on a carrier of Fabry's disease manifesting bouts of pain in the extremities].
Katayama M, Kobayashi T, Ohnishi A, Goto I, Kuroiwa Y. Katayama M, et al. Rinsho Shinkeigaku. 1984 Jun;24(6):575-80. Rinsho Shinkeigaku. 1984. PMID: 6094070 Japanese. No abstract available.
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