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

Year Number of Results
1957 1
1975 1
1977 1
1979 3
1980 1
1981 1
1982 2
1983 1
1986 1
1988 2
1991 1
1993 1
1994 1
1995 1
1998 1
2001 1
2002 6
2003 4
2004 12
2005 16
2006 21
2007 21
2008 22
2009 22
2010 9
2011 12
2012 9
2013 12
2014 7
2015 8
2016 8
2017 9
2018 8
2019 10
2020 6
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Article type
Publication date

Similar Articles for PMID: 18003767

214 results
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Page 1
Screening for Fabry disease in patients with chronic kidney disease: limitations of plasma alpha-galactosidase assay as a screening test.
Andrade J, Waters PJ, Singh RS, Levin A, Toh BC, Vallance HD, Sirrs S. Andrade J, et al. Clin J Am Soc Nephrol. 2008 Jan;3(1):139-45. doi: 10.2215/CJN.02490607. Epub 2007 Nov 14. Clin J Am Soc Nephrol. 2008. PMID: 18003767 Free PMC article. Clinical Trial.
Screening of male dialysis patients for fabry disease by plasma globotriaosylsphingosine.
Maruyama H, Takata T, Tsubata Y, Tazawa R, Goto K, Tohyama J, Narita I, Yoshioka H, Ishii S. Maruyama H, et al. Clin J Am Soc Nephrol. 2013 Apr;8(4):629-36. doi: 10.2215/CJN.08780812. Epub 2013 Jan 10. Clin J Am Soc Nephrol. 2013. PMID: 23307880 Free PMC article.
Anderson-Fabry disease: a case-finding study among male kidney transplant recipients in Austria.
Kleinert J, Kotanko P, Spada M, Pagliardini S, Paschke E, Paul K, Voigtländer T, Wallner M, Kramar R, Stummvoll HK, Schwarz C, Horn S, Holzer H, Födinger M, Sunder-Plassmann G. Kleinert J, et al. Transpl Int. 2009 Mar;22(3):287-92. doi: 10.1111/j.1432-2277.2008.00791.x. Epub 2008 Oct 24. Transpl Int. 2009. PMID: 18954370 Free article.
Identification of a novel mutation and prevalence study for fabry disease in Japanese dialysis patients.
Nishino T, Obata Y, Furusu A, Hirose M, Shinzato K, Hattori K, Nakamura K, Matsumoto T, Endo F, Kohno S. Nishino T, et al. Ren Fail. 2012;34(5):566-70. doi: 10.3109/0886022X.2012.669300. Ren Fail. 2012. PMID: 22563919 Clinical Trial.
Fabry disease in hemodialysis patients in southern Brazil: prevalence study and clinical report.
Porsch DB, Nunes AC, Milani V, Rossato LB, Mattos CB, Tsao M, Netto C, Burin M, Pereira F, Matte U, Giugliani R, Barros EJ. Porsch DB, et al. Ren Fail. 2008;30(9):825-30. doi: 10.1080/08860220802353777. Ren Fail. 2008. PMID: 18925518 Clinical Trial.
High incidence of the cardiac variant of Fabry disease revealed by newborn screening in the Taiwan Chinese population.
Lin HY, Chong KW, Hsu JH, Yu HC, Shih CC, Huang CH, Lin SJ, Chen CH, Chiang CC, Ho HJ, Lee PC, Kao CH, Cheng KH, Hsueh C, Niu DM. Lin HY, et al. Circ Cardiovasc Genet. 2009 Oct;2(5):450-6. doi: 10.1161/CIRCGENETICS.109.862920. Epub 2009 Jul 24. Circ Cardiovasc Genet. 2009. PMID: 20031620
A nationwide blood spot screening study for Fabry disease in the Czech Republic haemodialysis patient population.
Merta M, Reiterova J, Ledvinova J, Poupetová H, Dobrovolny R, Rysavá R, Maixnerová D, Bultas J, Motán J, Slivkova J, Sobotova D, Smrzova J, Tesar V. Merta M, et al. Nephrol Dial Transplant. 2007 Jan;22(1):179-86. doi: 10.1093/ndt/gfl528. Epub 2006 Oct 13. Nephrol Dial Transplant. 2007. PMID: 17040996
Fabry disease in patients with end-stage renal failure: the potential benefits of screening.
Bekri S, Enica A, Ghafari T, Plaza G, Champenois I, Choukroun G, Unwin R, Jaeger P. Bekri S, et al. Nephron Clin Pract. 2005;101(1):c33-8. doi: 10.1159/000085709. Epub 2005 May 9. Nephron Clin Pract. 2005. PMID: 15886492
Screening for Fabry disease in patients undergoing dialysis for chronic renal failure in Turkey: identification of new case with novel mutation.
Okur I, Ezgu F, Biberoglu G, Tumer L, Erten Y, Isitman M, Eminoglu FT, Hasanoglu A. Okur I, et al. Gene. 2013 Sep 15;527(1):42-7. doi: 10.1016/j.gene.2013.05.050. Epub 2013 Jun 10. Gene. 2013. PMID: 23756194
Heterozygote detection in Fabry disease utilizing multiple enzyme activities.
Sheth KJ, Good TA, Murphy JV. Sheth KJ, et al. Am J Med Genet. 1981;10(2):141-6. doi: 10.1002/ajmg.1320100207. Am J Med Genet. 1981. PMID: 6274191
214 results
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