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Clinical and molecular characterization of a family with a dominant renin gene mutation and response to treatment with fludrocortisone.
Bleyer AJ, Zivná M, Hulková H, Hodanová K, Vyletal P, Sikora J, Zivný J, Sovová J, Hart TC, Adams JN, Elleder M, Kapp K, Haws R, Cornell LD, Kmoch S, Hart PS. Bleyer AJ, et al. Among authors: hart ps, hart tc. Clin Nephrol. 2010 Dec;74(6):411-22. doi: 10.5414/cnp74411. Clin Nephrol. 2010. PMID: 21084044 Free PMC article.
Hereditary interstitial kidney disease.
Bleyer AJ, Hart PS, Kmoch S. Bleyer AJ, et al. Among authors: hart ps. Semin Nephrol. 2010 Jul;30(4):366-73. doi: 10.1016/j.semnephrol.2010.06.003. Semin Nephrol. 2010. PMID: 20807609 Free PMC article. Review.
Dominant renin gene mutations associated with early-onset hyperuricemia, anemia, and chronic kidney failure.
Zivná M, Hůlková H, Matignon M, Hodanová K, Vylet'al P, Kalbácová M, Baresová V, Sikora J, Blazková H, Zivný J, Ivánek R, Stránecký V, Sovová J, Claes K, Lerut E, Fryns JP, Hart PS, Hart TC, Adams JN, Pawtowski A, Clemessy M, Gasc JM, Gübler MC, Antignac C, Elleder M, Kapp K, Grimbert P, Bleyer AJ, Kmoch S. Zivná M, et al. Among authors: hart ps, hart tc. Am J Hum Genet. 2009 Aug;85(2):204-13. doi: 10.1016/j.ajhg.2009.07.010. Epub 2009 Aug 6. Am J Hum Genet. 2009. PMID: 19664745 Free PMC article.
Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1.
Bleyer AJ, Kmoch S, Antignac C, Robins V, Kidd K, Kelsoe JR, Hladik G, Klemmer P, Knohl SJ, Scheinman SJ, Vo N, Santi A, Harris A, Canaday O, Weller N, Hulick PJ, Vogel K, Rahbari-Oskoui FF, Tuazon J, Deltas C, Somers D, Megarbane A, Kimmel PL, Sperati CJ, Orr-Urtreger A, Ben-Shachar S, Waugh DA, McGinn S, Bleyer AJ Jr, Hodanová K, Vylet'al P, Živná M, Hart TC, Hart PS. Bleyer AJ, et al. Among authors: hart ps, hart tc. Clin J Am Soc Nephrol. 2014 Mar;9(3):527-35. doi: 10.2215/CJN.06380613. Epub 2014 Feb 7. Clin J Am Soc Nephrol. 2014. PMID: 24509297 Free PMC article.
Polymorphism (g2035C>T) in the amelogenin gene.
Hart PS, Vlaservich AC, Hart TC, Wright JT. Hart PS, et al. Among authors: hart tc. Hum Mutat. 2000 Mar;15(3):298. doi: 10.1002/(SICI)1098-1004(200003)15:3<298::AID-HUMU20>3.0.CO;2-D. Hum Mutat. 2000. PMID: 10679955 No abstract available.
Disorders of human dentin.
Hart PS, Hart TC. Hart PS, et al. Among authors: hart tc. Cells Tissues Organs. 2007;186(1):70-7. doi: 10.1159/000102682. Cells Tissues Organs. 2007. PMID: 17627120 Free PMC article.
98 results