138 related articles for article (PubMed ID: 2282807)
1. Heterogeneity of hereditary nephritis.
Pecoraro C; Carbonaro L; Saravo MT; Manese M; Borgia G; Usberti M
Contrib Nephrol; 1990; 80():107-12. PubMed ID: 2282807
[No Abstract] [Full Text] [Related]
2. The inheritance of Alport's and related syndromes.
Flinter FA; Bobrow M; Chantler C; Cameron JS
Nephrol Dial Transplant; 1990; 5(10):900. PubMed ID: 2128388
[No Abstract] [Full Text] [Related]
3. Hereditary progressive nephropathy with sensorineural deafness. Report on four kindreds.
Ferrari L; Bonforte G; Brambilla P; Cairo G
Contrib Nephrol; 1990; 80():135-9. PubMed ID: 2282812
[No Abstract] [Full Text] [Related]
4. Three new kindreds affected with Alport's syndrome.
Barbera G; Costanzi S; Sturniolo A; Passalacqua S; Splendiani G; Sangiorgi M; Attanasio A; Capria A; Federico F
Contrib Nephrol; 1990; 80():143-6. PubMed ID: 2282814
[No Abstract] [Full Text] [Related]
5. Recent advances in Alport syndrome: the cross-fertilisation between genetics and clinical medicine.
Pirson Y
Acta Clin Belg; 1997; 52(4):233-40. PubMed ID: 9351295
[No Abstract] [Full Text] [Related]
6. Hereditary nephropathy without deafness.
Dockhorn RJ
Am J Dis Child; 1967 Aug; 114(2):135-8. PubMed ID: 4951535
[No Abstract] [Full Text] [Related]
7. Hereditary nephritis: clinical evaluation of a pediatric series.
Piaggio G; Degl'Innocenti ML; Perfumo F; Gusmano R
Contrib Nephrol; 1990; 80():157-61. PubMed ID: 2282816
[No Abstract] [Full Text] [Related]
8. Hereditary nephropathy with nerve deafness (Alport's syndrome).
Ferguson AC; Rance CP
Am J Dis Child; 1972 Jul; 124(1):84-8. PubMed ID: 5033754
[No Abstract] [Full Text] [Related]
9. Hereditary nephritis. Clinical spectrum and mode of inheritance in five new kindreds.
Chazan JA; Zacks J; Cohen JJ; Garella S
Am J Med; 1971 Jun; 50(6):764-71. PubMed ID: 5089851
[No Abstract] [Full Text] [Related]
10. Chronic hereditary nephritis with nerve deafness. A Nebraska kindred.
Patton RB
Ann Otol Rhinol Laryngol; 1970 Feb; 79(1):194-202. PubMed ID: 5415602
[No Abstract] [Full Text] [Related]
11. [Alport's syndrome. Clinical and genetic study].
Beaudoing A; Gachon J; Gilbert Y; Dieterlen M; Bertolo J
Ann Pediatr (Paris); 1970 Apr; 17(4):271-8. PubMed ID: 5442472
[No Abstract] [Full Text] [Related]
12. Genetic features of Alport's syndrome.
Schröder CH; Brunner H; Monnens LA
Contrib Nephrol; 1990; 80():3-8. PubMed ID: 2282819
[No Abstract] [Full Text] [Related]
13. [Alport's syndrome (heredo-familial glomerulonephritis with deafness and eye abnormalities)].
Genova R
Clin Pediatr (Bologna); 1971 Sep; 53(9):301-13. PubMed ID: 5004353
[No Abstract] [Full Text] [Related]
14. [Alport's syndrome: hereditary nephropathy with hematuria and deafness].
Giger C; Guignard JP; Pelet B; Campiche M; Krstic R
Rev Med Suisse Romande; 1988 Apr; 108(4):349-55. PubMed ID: 3387770
[No Abstract] [Full Text] [Related]
15. A family showing hereditary nephropathy.
Pashayan H; Fraser FC; Goldbloom RB
Am J Hum Genet; 1971 Nov; 23(6):555-67. PubMed ID: 5132064
[No Abstract] [Full Text] [Related]
16. Making the diagnosis of Alport's syndrome.
Pirson Y
Kidney Int; 1999 Aug; 56(2):760-75. PubMed ID: 10432421
[No Abstract] [Full Text] [Related]
17. [Hereditary nephritis with deafness in one family].
Golev GD
Klin Med (Mosk); 1989 Nov; 67(11):128-30. PubMed ID: 2625948
[No Abstract] [Full Text] [Related]
18. 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]
19. Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies.
Ilan T; Shohat T; Tobar A; Magal N; Yahav M; Halpern GJ; Rechavi G; Shohat M
Isr Med Assoc J; 2001 Jul; 3(7):488-91. PubMed ID: 11791413
[TBL] [Abstract][Full Text] [Related]
20. [Chronic hereditary nephropathy with deafness and ocular lesions].
Hauser J
Schweiz Med Wochenschr; 1974 May; 104(20):724-8. PubMed ID: 4829630
[No Abstract] [Full Text] [Related]
[Next] [New Search]