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Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GN.
Wong EK, Anderson HE, Herbert AP, Challis RC, Brown P, Reis GS, Tellez JO, Strain L, Fluck N, Humphrey A, Macleod A, Richards A, Ahlert D, Santibanez-Koref M, Barlow PN, Marchbank KJ, Harris CL, Goodship TH, Kavanagh D. Wong EK, et al. Among authors: ahlert d. J Am Soc Nephrol. 2014 Nov;25(11):2425-33. doi: 10.1681/ASN.2013070732. Epub 2014 Apr 10. J Am Soc Nephrol. 2014. PMID: 24722444 Free PMC article.
Ring Y chromosome: molecular characterization by DNA probes.
Pohlschmidt M, Rappold G, Krause M, Ahlert D, Hosenfeld D, Weissenbach J, Gal A. Pohlschmidt M, et al. Among authors: ahlert d. Cytogenet Cell Genet. 1991;56(2):65-8. doi: 10.1159/000133051. Cytogenet Cell Genet. 1991. PMID: 2013232
Choroideremia-locus maps between DXS3 and DXS11 on Xq.
Gal A, Brunsmann F, Hogenkamp D, Rüther K, Ahlert D, Wienker TF, Hammerstein W, Pawlowitzki IH. Gal A, et al. Among authors: ahlert d. Hum Genet. 1986 Jun;73(2):123-6. doi: 10.1007/BF00291600. Hum Genet. 1986. PMID: 3755117
[Pericarditis in meningococcal meningitis (author's transl)].
Rupprath G, Vogt J, Ahlert D, Wolf H. Rupprath G, et al. Among authors: ahlert d. Klin Padiatr. 1981 Jul;193(4):322-4. doi: 10.1055/s-2008-1034486. Klin Padiatr. 1981. PMID: 7265802 German. No abstract available.