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Diagnosis of Alport syndrome--search for proteomic biomarkers in body fluids.
Pohl M, Danz K, Gross O, John U, Urban J, Patzer L, Habbig S, Feldkötter M, Witzke O, Walther M, Rhode H. Pohl M, et al. Among authors: john u. Pediatr Nephrol. 2013 Nov;28(11):2117-23. doi: 10.1007/s00467-013-2533-5. Epub 2013 Jun 23. Pediatr Nephrol. 2013. PMID: 23793922
Urinary tract effects of HPSE2 mutations.
Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ; UK VUR Study Group; Saggar A, Kinali M; 4C Study Group; Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Stuart HM, et al. J Am Soc Nephrol. 2015 Apr;26(4):797-804. doi: 10.1681/ASN.2013090961. Epub 2014 Aug 21. J Am Soc Nephrol. 2015. PMID: 25145936 Free PMC article.
697 results