These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
32. [Hereditary Alport nephropathy]. Koban F; Schröder HE; Rose W; Mank H Z Arztl Fortbild (Jena); 1986; 80(14):587-9. PubMed ID: 3532581 [No Abstract] [Full Text] [Related]
33. Familial juvenile hyperuricaemic nephropathy is not such a rare genetic metabolic purine disease in Britain. Simmonds HA; Cameron JS; Goldsmith DJ; Fairbanks LD; Raman GV Nucleosides Nucleotides Nucleic Acids; 2006; 25(9-11):1071-5. PubMed ID: 17065066 [TBL] [Abstract][Full Text] [Related]
34. [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 [TBL] [Abstract][Full Text] [Related]
37. Hereditary nephropathy with hematuria (Alport's syndrome). Chiricosta A; Jindal SL; Metuzals J; Koch B Can Med Assoc J; 1970 Feb; 102(4):396-401. PubMed ID: 4905862 [TBL] [Abstract][Full Text] [Related]
38. [The first experience in Russia of using DNA diagnosis in Alport's syndrome in a family with a unique morphological picture of the kidney lesion]. Tsalikova FD; Ignatova MS; Krasnopol'skaia KD; Tverskaia SM; Brydun AV Ter Arkh; 1995; 67(4):45-7. PubMed ID: 7784975 [TBL] [Abstract][Full Text] [Related]
39. Hereditary nephropathy. Bĕlobrádková J; Herout V; Kubes L Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove; 1978; 21(5):487-98. PubMed ID: 292128 [No Abstract] [Full Text] [Related]
40. [Diagnosis of Alport syndrome by immunohistochemical staining of type IV collagen alpha chains in paraffin-embedded renal sections]. Yu LX; Guan N; Wu GH Zhonghua Er Ke Za Zhi; 2008 Apr; 46(4):301. PubMed ID: 19099735 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]