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5. Hereditary nephritis associated with low-tone sensorineural hearing difficulty: a case report. Motoyama O, Ohshima M, Shigetomi Y, Ohara T, Nagai Y, Kawamura S, Iitaka K. Nihon Jinzo Gakkai Shi; 1996 May; 38(5):233-7. PubMed ID: 8699614 [Abstract] [Full Text] [Related]
7. [A case of Alport syndrome diagnosed by immunofluorescence using a newly defined monoclonal antibody]. Ohtomo Y, Yabuta K, Shirato I, Tomino Y, Shirai T. Nihon Jinzo Gakkai Shi; 1990 Jan; 32(1):105-10. PubMed ID: 2190029 [Abstract] [Full Text] [Related]
8. The glomerular basement membrane defect in Alport-type hereditary nephritis: absence of cationic antigenic components. van den Heuvel LP, Savage CO, Wong M, Price RG, Noel L, Grunfeld JP, Lockwood CM. Nephrol Dial Transplant; 1989 Jan; 4(9):770-5. PubMed ID: 2483255 [Abstract] [Full Text] [Related]
9. [Significance of family studies and kidney biopsies in children with renal hematuria]. Pistor K, Bachmann H, Rumpelt HJ, Olbing H. Monatsschr Kinderheilkd; 1985 May; 133(5):269-73. PubMed ID: 4010678 [Abstract] [Full Text] [Related]
10. [Alport syndrome or progressive hereditary nephritis with hearing loss]. Gubler MC, Heidet L, Antignac C. Nephrol Ther; 2007 Jun; 3(3):113-20. PubMed ID: 17540313 [Abstract] [Full Text] [Related]
19. Distribution of familial nephritis antigen in normal tissue and renal basement membranes of patients with homozygous and heterozygous Alport familial nephritis. Relationship of familial nephritis and Goodpasture antigens to novel collagen chains and type IV collagen. Kleppel MM, Kashtan C, Santi PA, Wieslander J, Michael AF. Lab Invest; 1989 Sep 02; 61(3):278-89. PubMed ID: 2671490 [Abstract] [Full Text] [Related]
20. [Macrothrombopenia, nephritis and hearing loss--a new case of Epstein syndrome]. Kóbor J, Túri S, Erdös A, Bodrogi T, Virág I. Orv Hetil; 1991 Aug 25; 132(34):1875-7. PubMed ID: 1881666 [Abstract] [Full Text] [Related] Page: [Next] [New Search]