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4. Familial IgA nephropathy and sensorineural deafness. Bizzarri D; Duranti E; Sasdelli M; Casanova S Contrib Nephrol; 1990; 80():113-7. PubMed ID: 2282808 [No Abstract] [Full Text] [Related]
5. Familial IgA nephropathy associated with bilateral sensorineural deafness. Trachtman H; Gauthier B Am J Kidney Dis; 1993 Mar; 21(3):344. PubMed ID: 8447315 [No Abstract] [Full Text] [Related]
6. Spastic paraplegia, glaucoma and mental retardation--in three siblings. A new genetic syndrome. Heijbel J; Jagell S Hereditas; 1981; 94(2):203-7. PubMed ID: 7298353 [No Abstract] [Full Text] [Related]
7. Four brothers with mental retardation, spastic paraplegia and palmoplantar hyperkeratosis. A new syndrome? Fitzsimmons JS; Fitzsimmons EM; McLachlan JI; Gilbert GB Clin Genet; 1983 Apr; 23(4):329-35. PubMed ID: 6221837 [TBL] [Abstract][Full Text] [Related]
8. Thin basement membrane disease in patients with familial IgA nephropathy. Frascá GM; Soverini L; Gharavi AG; Lifton RP; Canova C; Preda P; Vangelista A; Stefoni S J Nephrol; 2004; 17(6):778-85. PubMed ID: 15593051 [TBL] [Abstract][Full Text] [Related]
9. Hereditary glomerulonephritis of non-Alport type. Doherty CC; Middleton DT; Hill CM Proc Eur Dial Transplant Assoc; 1983; 19():575-81. PubMed ID: 6878256 [TBL] [Abstract][Full Text] [Related]
10. [Primary nephropathy due to mesangial deposits of IgA (Berger's disease)]. Rosenberg H Rev Med Chil; 1990 Feb; 118(2):125-33. PubMed ID: 2152710 [TBL] [Abstract][Full Text] [Related]
11. Slowly progressive autosomal dominant spastic paraplegia with late onset, variable expression and reduced penetrance: a basis for diagnosis and counseling. Burdick AB; Owens LA; Peterson CR Clin Genet; 1981 Jan; 19(1):1-7. PubMed ID: 7460376 [TBL] [Abstract][Full Text] [Related]
12. [Late hereditary degenerative sensorineural hearing loss associated with IgA mesangial glomerulonephritis of probable autosomal dominant heredity]. de Serdio JL; Chahin J; Gil-Curbelo JA; Perera A; Saavedra JA Acta Otorrinolaringol Esp; 1993; 44(6):447-54. PubMed ID: 8155361 [TBL] [Abstract][Full Text] [Related]
13. A case of IgA nephropathy in three sisters with thin basement membrane disease. Yoshida K; Suzuki J; Suzuki S; Kume K; Suzuki H; Hujiki T Am J Nephrol; 1998; 18(5):422-4. PubMed ID: 9730567 [TBL] [Abstract][Full Text] [Related]
14. Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or "new" syndrome. Neuhäuser G; Wiffler C; Opitz JM Clin Genet; 1976 Mar; 9(3):315-23. PubMed ID: 1261070 [TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant polycystic kidney disease associated with familial sensorineural deafness. Mora C; Navarro JF; García J; Gallego E; Macía M; Méndez ML; Chahin J; Rivero A Scand J Urol Nephrol; 1999 Feb; 33(1):63-5. PubMed ID: 10100367 [TBL] [Abstract][Full Text] [Related]
16. Familial haematuria due to thin basement membrane nephropathy. Bailey RR N Z Med J; 1990 Jul; 103(893):312-3. PubMed ID: 2371004 [TBL] [Abstract][Full Text] [Related]
17. An X-linked syndrome with microcephaly, severe mental retardation, spasticity, epilepsy and deafness. Renier WO; Gabreëls FJ; Jasper HH; Hustinx TW; Geelen JA; van Haelst UJ J Ment Defic Res; 1982 Mar; 26(Pt 1):27-40. PubMed ID: 7077653 [No Abstract] [Full Text] [Related]
18. Association of angiotensin-converting enzyme gene polymorphism and renal pathology in Japanese children with IgA nephropathy. Asano T; Tatsuma N; Yoshida J; Ohashi R; Ambo K; Tsuchiya M; Murakami M; Yamanaka N; Honda M; Yamamoto M Clin Nephrol; 1999 Jun; 51(6):335-40. PubMed ID: 10404693 [TBL] [Abstract][Full Text] [Related]
19. [Epidemiological study in 4 family units with Alport's syndrome]. García-Delgado C; Gordillo-Paniagua G Bol Med Hosp Infant Mex; 1981; 38(6):887-902. PubMed ID: 7317143 [TBL] [Abstract][Full Text] [Related]