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- cjn.02210310 date "October 2010".
- cjn.02210310 displayauthors "3".
- cjn.02210310 doi "10.2215/CJN.02210310".
- cjn.02210310 first1 "M".
- cjn.02210310 first1 "M.".
- cjn.02210310 first10 "A.".
- cjn.02210310 first11 "R.".
- cjn.02210310 first12 "R.".
- cjn.02210310 first13 "R.".
- cjn.02210310 first14 "I.".
- cjn.02210310 first15 "E. M.".
- cjn.02210310 first16 "P. F.".
- cjn.02210310 first17 "T. H.".
- cjn.02210310 first18 "G.".
- cjn.02210310 first2 "J".
- cjn.02210310 first2 "J.".
- cjn.02210310 first3 "E".
- cjn.02210310 first3 "E.".
- cjn.02210310 first4 "C".
- cjn.02210310 first4 "C.".
- cjn.02210310 first5 "G".
- cjn.02210310 first5 "G.".
- cjn.02210310 first6 "S".
- cjn.02210310 first6 "S.".
- cjn.02210310 first7 "E".
- cjn.02210310 first7 "E.".
- cjn.02210310 first8 "C".
- cjn.02210310 first8 "C.".
- cjn.02210310 first9 "F".
- cjn.02210310 first9 "F.".
- cjn.02210310 isCitedBy Atypical_hemolytic_uremic_syndrome.
- cjn.02210310 isCitedBy Hemolytic-uremic_syndrome.
- cjn.02210310 isCitedBy Thrombotic_thrombocytopenic_purpura.
- cjn.02210310 issue "10".
- cjn.02210310 journal "Clin J Am Soc Nephrol".
- cjn.02210310 last1 "Noris".
- cjn.02210310 last10 "Sorosina".
- cjn.02210310 last11 "Piras".
- cjn.02210310 last12 "Donadelli".
- cjn.02210310 last13 "Maranta".
- cjn.02210310 last14 "Van Der Meer".
- cjn.02210310 last14 "van der Meer".
- cjn.02210310 last15 "Conway".
- cjn.02210310 last16 "Zipfel".
- cjn.02210310 last17 "Goodship".
- cjn.02210310 last18 "Remuzzi".
- cjn.02210310 last2 "Caprioli".
- cjn.02210310 last3 "Bresin".
- cjn.02210310 last4 "Mossali".
- cjn.02210310 last5 "Pianetti".
- cjn.02210310 last6 "Gamba".
- cjn.02210310 last7 "Daina".
- cjn.02210310 last8 "Fenili".
- cjn.02210310 last9 "Castelletti".
- cjn.02210310 pages "1844–1859".
- cjn.02210310 pages "1844–59".
- cjn.02210310 pmc "2974386".
- cjn.02210310 pmid "20595690".
- cjn.02210310 title "Relative role of genetic complement abnormalities in infrequent and familial aHUS and their impact on clinical phemotype".
- cjn.02210310 title "Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype".
- cjn.02210310 url pmidlookup?view=long&pmid=20595690.
- cjn.02210310 vauthors "Noris M, Caprioli J, Bresin E, etal".
- cjn.02210310 volume "5".
- cjn.02210310 year "2010".