189 related articles for article (PubMed ID: 5004890)
1. [Contribution to the study of Alport's syndrome. Apropos of a case].
Schneegans E; Rohmer A; Levy-Silagy J; el-Mejjati A; Sengel A; Stoebner P; Laforgue D
Ann Pediatr (Paris); 1971 Dec; 18(12):757-69. PubMed ID: 5004890
[No Abstract] [Full Text] [Related]
2. Alport's syndrome (progressive hereditary nephritis).
Gaboardi F; Edefonti A; Imbasciati E; Tarantino A; Mihatsch MJ; Zollinger HU
Clin Nephrol; 1974; 2(4):143-56. PubMed ID: 4603152
[No Abstract] [Full Text] [Related]
3. Recent developments in hereditary nephritis (Alport's syndrome).
Bubalo FS; Davidson DD
Indiana Med; 1991 Dec; 84(12):860-6. PubMed ID: 1774457
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Pathology of the kidney in Alport's syndrome.
Spear GS
Pathol Annu; 1974; 9(0):93-138. PubMed ID: 4422868
[No Abstract] [Full Text] [Related]
6. [Hereditary nephritis (Alport's syndrome). Description of a family].
Marcen Letosa R; Fdez Alonso J; Quereda Rguez navarro C; López Checa F; Castilla Jiménez J; Rodríguez Algarra G; Maceira Cruz B; Pereira Palomo P; Mateos Aguilar J
Rev Clin Esp; 1977 Nov; 147(3):291-6. PubMed ID: 605240
[No Abstract] [Full Text] [Related]
7. [Associated anterior lenticonus, deafness and familial nephropathy(Alport's syndrome)].
Ardouin M; Coutel Y; Bourguet J; Urvoy M; Thomet G
J Genet Hum; 1966; 15():Suppl:44-8. PubMed ID: 4968158
[No Abstract] [Full Text] [Related]
8. [3 cases of Alport's syndrome with different clinical and morphologic manifestations].
Bechcińska B; Danilewicz M; Kałuzyński A; Marek K; Wagrowska-Danilewicz M
Patol Pol; 1989; 40(1):123-8. PubMed ID: 2477788
[TBL] [Abstract][Full Text] [Related]
9. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).
Hinglais N; Grünfeld JP; Bois E
Lab Invest; 1972 Nov; 27(5):473-87. PubMed ID: 4653971
[No Abstract] [Full Text] [Related]
10. [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]
11. [Alport's syndrome in childhood - electron microscopic study of 2 patients].
Vlatković G; Belicza M; Subotić R; Uhlik Z; Batinić D; Ljubesić N
Acta Med Iugosl; 1976; 30(1):109-23. PubMed ID: 1258682
[No Abstract] [Full Text] [Related]
12. Alport's syndrome (familial nephropathy with deafness).
Srivastava RN; Mayekar G; Ghai OP
Indian Pediatr; 1971 Oct; 8(10):725-7. PubMed ID: 5160238
[No Abstract] [Full Text] [Related]
13. [A case of familial hematuria. (A contribution to Alport's syndrome)].
Jończyk K; Kobierska-Szczepańska A
Wiad Lek; 1970 Dec; 23(23):2139-42. PubMed ID: 5496021
[No Abstract] [Full Text] [Related]
14. [2 families with Alport's syndrome].
Cohen-Solal J; Delepierre M; Delepierre F; Herrault A
Ann Pediatr (Paris); 1970 Nov; 17(11):734-49. PubMed ID: 5484618
[No Abstract] [Full Text] [Related]
15. Auditory manifestations of Alport's disease syndrome.
Rintelmann W
Trans Sect Otolaryngol Am Acad Ophthalmol Otolaryngol; 1976; 82(3 Pt 1):375-87. PubMed ID: 960411
[No Abstract] [Full Text] [Related]
16. 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]
17. [Alport's syndrome].
Knotková V; Stejskal J; Voldrich L; Beran M; Straková M; Tomásek R
Sb Lek; 1973 Jun; 75(6):169-76. PubMed ID: 4709456
[No Abstract] [Full Text] [Related]
18. [Alport's syndrome].
Gaboardi F; Edefonti A; Chiccoli C; Imbasciati E; Tarantino A; Mihatsch MJ; Zollinger HU
Minerva Nefrol; 1976; 23(3):165-9. PubMed ID: 1018858
[No Abstract] [Full Text] [Related]
19. Hereditary hearing loss with nephropathy (Alport's syndrome).
Turner JS
Acta Otolaryngol Suppl; 1970; 271():1-26. PubMed ID: 5278250
[No Abstract] [Full Text] [Related]
20. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
Kharrat M; Makni S; Makni K; Kammoun K; Charfeddine K; Azaeiz H; Jarraya F; Ben Hmida M; Gubler MC; Ayadi H; Hachicha J
Saudi J Kidney Dis Transpl; 2006 Sep; 17(3):320-5. PubMed ID: 16970251
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]