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2. [Hereditary chorioretinal degeneration and nephronophthisis. The role of Senior-Löken syndrome]. Orssaud C; Kleinknecht C; Habib R; Broyer M Ophtalmologie; 1989; 3(4):270-2. PubMed ID: 2641132 [TBL] [Abstract][Full Text] [Related]
3. Senior-Loken syndrome in an Iranian family. Roozbeh J; Sharifian M; Hosseini H; Sagheb MM; Behzadi S; Raeisjalali GA; Iraniparast A; Afshariani R; Tohidi M; Sharifian M Saudi J Kidney Dis Transpl; 2010 Jul; 21(4):735-7. PubMed ID: 20587883 [TBL] [Abstract][Full Text] [Related]
4. [Electroretinography in nephronophthisis. Role of the Senior-Loken syndrome]. Puech JF; Renard G; Dufier JL; Blanck MF; Polliot L Arch Ophtalmol (Paris); 1976 Apr; 36(4):313-20. PubMed ID: 135546 [TBL] [Abstract][Full Text] [Related]
5. [Contribution of an ophthalmologic test to the diagnosis of familial nephropathies. Apropos of 10 cases]. Marrakchi S; Lasram L; Bouguila H; Barbirou I; Ouertani A; Ayed S J Fr Ophtalmol; 1994; 17(4):238-41. PubMed ID: 8089404 [TBL] [Abstract][Full Text] [Related]
6. Phenotypic variations in renal-retinal dysplasia. Godel V; Iaina A; Nemet P; Lazar M Metab Pediatr Ophthalmol; 1980; 4(3):161-3. PubMed ID: 7453281 [No Abstract] [Full Text] [Related]
7. Senior's syndrome (hereditary renal retinal dysplasia) associated with cataracts. Rosenthal G; Biedner B; Yassur Y Ann Ophthalmol; 1992 Mar; 24(3):104-5. PubMed ID: 1570923 [TBL] [Abstract][Full Text] [Related]
8. Twins with senior-Loken syndrome. Giridhar S; Padmaraj R; Senguttuvan P Indian J Pediatr; 2006 Nov; 73(11):1041-3. PubMed ID: 17127790 [TBL] [Abstract][Full Text] [Related]
9. Senior-Loken syndrome secondary to IQCB1 mutation in association with retinitis pigmentosa. Rishi E; Goel S; Rishi P Can J Ophthalmol; 2021 Aug; 56(4):e112-e114. PubMed ID: 33535056 [No Abstract] [Full Text] [Related]
10. [Familial interstitial chronic nephropathy (nephronophthisis and tapeto-retiniana degeneration (Senior-Loken syndrome)]. Arias M; Zubimendi JA; Val F; de Castro S; Llamazares C Rev Clin Esp; 1975 Sep; 138(5):481-5. PubMed ID: 1178997 [No Abstract] [Full Text] [Related]
11. Hereditary renal disease,retinitis pigmentosa and other anomalies. Asmal AC S Afr Med J; 1969 Aug; 43(33):1033-6. PubMed ID: 5822933 [No Abstract] [Full Text] [Related]
13. A Japanese child with Senior-Loken syndrome. Sekiya K; Nakazawa M; Tanaka H Jpn J Ophthalmol; 2001; 45(6):636-9. PubMed ID: 11754908 [TBL] [Abstract][Full Text] [Related]
14. [Progressive nuclear ophthalmoplegic myopathy with retinitis pigmentosa, scrotal tongue and intellectual deterioration--a nosologically independent syndrome?]. Badalian LO; Temin PA; Arkhipov BA; Mukhin KIu; Maergoĭz SN Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(3):321-3. PubMed ID: 3577522 [TBL] [Abstract][Full Text] [Related]
17. Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing. Otto EA; Helou J; Allen SJ; O'Toole JF; Wise EL; Ashraf S; Attanasio M; Zhou W; Wolf MT; Hildebrandt F Hum Mutat; 2008 Mar; 29(3):418-26. PubMed ID: 18076122 [TBL] [Abstract][Full Text] [Related]
18. [The Senior-Loken syndrome. Description of a case]. Penza R; Armenio L; Schena FP; Bellizzi M; Marzullo F; Falcone G; Loprieno AM Minerva Nefrol; 1976; 23(3):194-200. PubMed ID: 1018861 [No Abstract] [Full Text] [Related]
19. Retinitis pigmentosa and renal failure in a patient with mutations in INVS. O'Toole JF; Otto EA; Frishberg Y; Hildebrandt F Nephrol Dial Transplant; 2006 Jul; 21(7):1989-91. PubMed ID: 16522655 [TBL] [Abstract][Full Text] [Related]
20. [Familial nephropathy with retinitis pigmentosa and peripheral dysostosis]. Diekmann L; Louis C; Schulte-Kemna E Helv Paediatr Acta; 1977 Nov; 32(4-5):375-82. PubMed ID: 617982 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]