202 related articles for article (PubMed ID: 16966065)
1. [Nephronophtisis].
Niaudet P; Salomon R
Nephrol Ther; 2006 Sep; 2(4):200-6. PubMed ID: 16966065
[TBL] [Abstract][Full Text] [Related]
2. The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin.
Mollet G; Salomon R; Gribouval O; Silbermann F; Bacq D; Landthaler G; Milford D; Nayir A; Rizzoni G; Antignac C; Saunier S
Nat Genet; 2002 Oct; 32(2):300-5. PubMed ID: 12244321
[TBL] [Abstract][Full Text] [Related]
3. [Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report].
Costet C; Betis F; Bérard E; Tsimaratos M; Sigaudy S; Antignac C; Gastaud P
J Fr Ophtalmol; 2000 Feb; 23(2):158-60. PubMed ID: 10705117
[TBL] [Abstract][Full Text] [Related]
4. Nephronophthisis.
Salomon R; Saunier S; Niaudet P
Pediatr Nephrol; 2009 Dec; 24(12):2333-44. PubMed ID: 18607645
[TBL] [Abstract][Full Text] [Related]
5. Familial interstitial nephritis with progressive renal failure.
Zhang H; Wada J; Nanba K; Kunitomi M; Hida K; Nagake Y; Shikata K; Makino H
Am J Kidney Dis; 2000 Oct; 36(4):E25. PubMed ID: 11007700
[TBL] [Abstract][Full Text] [Related]
6. Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: insights from molecular screening.
Caridi G; Dagnino M; Gusmano R; Ginevri F; Murer L; Ghio L; Piaggio G; Ciardi MR; Perfumo F; Ghiggeri GM
Am J Kidney Dis; 2000 Jan; 35(1):44-51. PubMed ID: 10620543
[TBL] [Abstract][Full Text] [Related]
7. [Nephronophthisis: study of 10 cases. Incidence, natural history and associated pathology (author's transl)].
Gómez Campderá FJ; Niembro E; López Gómez JM; Canals MJ; Bárcenas MC; Gómez JA; Rengel MA; Luque de Pablos A
Med Clin (Barc); 1981 Oct; 77(6):230-5. PubMed ID: 7321636
[TBL] [Abstract][Full Text] [Related]
8. Ehlers-Danlos syndrome coexisting with juvenile nephronophtisis.
Tarrass F; Benjelloun M; Hachim K; Benghanem MG; Ramdani B; Zaid D; Benkirane A; Sqalli S
Nephrology (Carlton); 2006 Apr; 11(2):117-9. PubMed ID: 16669972
[TBL] [Abstract][Full Text] [Related]
9. [Nephronophtisis in Senegal: first 3 cases].
Diouf B; Niang A; Ka MM; Ka EF; Diouf ML; Ba A; Droz D; Benessy F; Antignac C; Moreira Diop T; Bao O
Nephrologie; 1997; 18(7):299-302. PubMed ID: 9496571
[TBL] [Abstract][Full Text] [Related]
10. [Hereditary tubulo-interstitial nephropathy].
Horie S
Nihon Rinsho; 1995 Aug; 53(8):2064-7. PubMed ID: 7563651
[TBL] [Abstract][Full Text] [Related]
11. [Nephronophthisis].
Loirat C
Rev Prat; 1997 Sep; 47(14):1541-4. PubMed ID: 9366111
[TBL] [Abstract][Full Text] [Related]
12. Nephronophthisis-associated ciliopathies.
Hildebrandt F; Zhou W
J Am Soc Nephrol; 2007 Jun; 18(6):1855-71. PubMed ID: 17513324
[TBL] [Abstract][Full Text] [Related]
13. [Chronic tubulo-interstitial nephropathy and tapetal-retinal degeneration. Senior's syndrome?].
André JL; Afflalo G; Duprez A; Kifffer B; Neimann N
Sem Hop; 1975 Dec; 51(49):2995-3000. PubMed ID: 174219
[TBL] [Abstract][Full Text] [Related]
14. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
15. [Nephronophtisis in a child whose father has isolated ocular involvement].
Blanc P; Sinnassamy P; Brackman D; Bensman A
Arch Fr Pediatr; 1989 Mar; 46(3):203-4. PubMed ID: 2660768
[TBL] [Abstract][Full Text] [Related]
16. [Jeune's syndrome (3 case reports)].
Novaković I; Kostić M; Popović-Rolović M; Sindjić M; Peco-Antić A; Jovanović O; Krscić D
Srp Arh Celok Lek; 1996; 124 Suppl 1():244-6. PubMed ID: 9102920
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus.
Scolari F; Ghiggeri GM; Casari G; Amoroso A; Puzzer D; Caridi GL; Valzorio B; Tardanico R; Vizzardi V; Savoldi S; Viola BF; Bossini N; Prati E; Gusmano R; Maiorca R
Nephrol Dial Transplant; 1998 Oct; 13(10):2536-46. PubMed ID: 9794556
[TBL] [Abstract][Full Text] [Related]
18. [Cystic kidney disease--genetics, pathogenesis and clinical aspects in children].
Popović-Rolović M; Marsenić O; Kostić M; Peco-Antić A; Jovanović O; Kruscić D; Pejcić I
Srp Arh Celok Lek; 1996; 124 Suppl 1():222-8. PubMed ID: 9102915
[TBL] [Abstract][Full Text] [Related]
19. High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations.
Tory K; Lacoste T; Burglen L; Morinière V; Boddaert N; Macher MA; Llanas B; Nivet H; Bensman A; Niaudet P; Antignac C; Salomon R; Saunier S
J Am Soc Nephrol; 2007 May; 18(5):1566-75. PubMed ID: 17409309
[TBL] [Abstract][Full Text] [Related]
20. Nephronophthisis.
Saunier S; Salomon R; Antignac C
Curr Opin Genet Dev; 2005 Jun; 15(3):324-31. PubMed ID: 15917209
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]