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Items: 1 to 20 of 87

1.

The Senior-Loken syndrome: Two cases from the State of Qatar.

Othman M, Rashed A, Bakr A.

J Clin Diagn Res. 2012 Oct;6(8):1411-3. doi: 10.7860/JCDR/2012/4131.2372.

2.

Senior-loken syndrome with rare manifestations: a case report.

Aggarwal HK, Jain D, Yadav S, Kaverappa V, Gupta A.

Eurasian J Med. 2013 Jun;45(2):128-31. doi: 10.5152/eajm.2013.25.

3.

Senior- loken syndrome - a ciliopathy.

R H.

J Clin Diagn Res. 2014 Nov;8(11):MD04-5. doi: 10.7860/JCDR/2014/9688.5120. Epub 2014 Nov 20.

4.

Senior-Loken syndrome (nephronophthisis and tapeto-retinal degeneration): a study of 8 cases from 5 families.

Fillastre JP, Guenel J, Riberi P, Marx P, Whitworth JA, Kunh JM.

Clin Nephrol. 1976 Jan;5(1):14-9.

PMID:
1248184
5.

Senior-Loken syndrome (familial renal-retinal dystrophy) and Coats' disease.

Schuman JS, Lieberman KV, Friedman AH, Berger M, Schoeneman MJ.

Am J Ophthalmol. 1985 Dec 15;100(6):822-7.

PMID:
4073180
6.

Clinical features and mutation of NPHP5 in two Chinese siblings with Senior-Løken syndrome.

Tong H, Yue Z, Sun L, Chen H, Wang W, Wang H.

Nephrology (Carlton). 2013 Dec;18(12):838-42. doi: 10.1111/nep.12156.

PMID:
24674142
7.

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.

8.

Twins with senior-Loken syndrome.

Giridhar S, Padmaraj R, Senguttuvan P.

Indian J Pediatr. 2006 Nov;73(11):1041-3.

PMID:
17127790
9.

Senior-Loken syndrome with unusual manifestations.

Singh NP, Anuradha S, Gupta S, Rizvi SN, Arora R.

J Assoc Physicians India. 1998 Aug;46(8):740-2.

PMID:
11229290
10.

A Japanese child with Senior-Loken syndrome.

Sekiya K, Nakazawa M, Tanaka H.

Jpn J Ophthalmol. 2001 Nov-Dec;45(6):636-9.

PMID:
11754908
11.

Senior-loken syndrome complicated with severe coats disease-like exudative retinopathy.

Sato T, Mimura M, Sugiyama T, Maeno T, Ishizaki E, Minami M, Sugasawa J, Ikeda T.

Retin Cases Brief Rep. 2007 Summer;1(3):172-4. doi: 10.1097/01.ICB.0000279653.16358.ce.

PMID:
25390787
12.

[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. French.

PMID:
135546
13.

Senior-Loken syndrome in a Saudi child.

AlFadhel M, AlAmir A.

Saudi J Kidney Dis Transpl. 2008 May;19(3):443-5.

14.

Late-onset renal failure in Senior-Loken syndrome.

Georges B, Cosyns JP, Dahan K, Snyers B, Carlier B, Loute G, Pirson Y.

Am J Kidney Dis. 2000 Dec;36(6):1271-5.

PMID:
11096053
15.

Leber's congenital amaurosis associated with familial juvenile nephronophthisis and cone-shaped epiphyses of the hands (the Saldino-Mainzer syndrome).

Ellis DS, Heckenlively JR, Martin CL, Lachman RS, Sakati NA, Rimoin DL.

Am J Ophthalmol. 1984 Feb;97(2):233-9.

PMID:
6696034
16.
17.

Senior-Loken syndrome (nephronophthisis and pigmentary retinopathy) associated to liver fibrosis: a family study.

Fernández-Rodriguez R, Morales JM, Martínez R, Lizasoaín M, Colina F, Martínez MA, Praga M, Prieto C, Rodicio JL.

Nephron. 1990;55(1):74-7. Review.

PMID:
2191234
18.

Nephronophthisis: a genetically diverse ciliopathy.

Simms RJ, Hynes AM, Eley L, Sayer JA.

Int J Nephrol. 2011;2011:527137. doi: 10.4061/2011/527137. Epub 2011 May 15.

19.

[Ocular manifestations associated with nephronophthisis and genetic study in three Tunisian families].

Sellami D, Makni K, Chaker H, Kharrat M, Hentati N, Kammoun K, Chabouni F, Ben Hamida M, Hachicha J, Salomon R, Antignac C, Ayadi H, Feki J.

J Fr Ophtalmol. 2006 Nov;29(9):1019-23. French.

20.

Mapping of gene loci for nephronophthisis type 4 and Senior-Løken syndrome, to chromosome 1p36.

Schuermann MJ, Otto E, Becker A, Saar K, Rüschendorf F, Polak BC, Ala-Mello S, Hoefele J, Wiedensohler A, Haller M, Omran H, Nürnberg P, Hildebrandt F.

Am J Hum Genet. 2002 May;70(5):1240-6. Epub 2002 Mar 27.

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