197 related articles for article (PubMed ID: 17646750)
1. [Two cases of Wolfram syndrome].
Sayouti A; Benhaddou R; Khoumiri R; Gaboune L; Guelzim H; Benfdil N; Moutaoukil A
J Fr Ophtalmol; 2007 Jun; 30(6):607-9. PubMed ID: 17646750
[TBL] [Abstract][Full Text] [Related]
2. [Wolfram syndrome. Three case reports].
Hajji Z; Halhal M; Chaoui Z; Chefchaouni M; Agnaou L; Berraho A
J Fr Ophtalmol; 1998 Dec; 21(10):734-40. PubMed ID: 10052046
[TBL] [Abstract][Full Text] [Related]
3. [Familial Wolfram syndrome].
Bessahraoui M; Paquis V; Rouzier C; Bouziane-Nedjadi K; Naceur M; Niar S; Zennaki A; Boudraa G; Touhami M
Arch Pediatr; 2014 Nov; 21(11):1229-32. PubMed ID: 25282462
[TBL] [Abstract][Full Text] [Related]
4. [Bilateral progressive optic atrophy and without diabetic retinopathy in a young diabetic patient. Wolfram syndrome: diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD)].
Meyer CH; Rodrigues EB; Schmidt JC
Ophthalmologe; 2004 Apr; 101(4):394-6. PubMed ID: 15067422
[No Abstract] [Full Text] [Related]
5. Optic atrophy as a sign of wolfram syndrome.
Dedes W; Wildberger H; Landau K
Klin Monbl Augenheilkd; 2005 Mar; 222(3):248-51. PubMed ID: 15785992
[TBL] [Abstract][Full Text] [Related]
6. Four cases of Wolfram syndrome: ophthalmologic findings and complications.
Seynaeve H; Vermeiren A; Leys A; Dralands L
Bull Soc Belge Ophtalmol; 1994; 252():75-80. PubMed ID: 7894760
[TBL] [Abstract][Full Text] [Related]
7. Wolfram Syndrome: a rare optic neuropathy in youth with type 1 diabetes.
Bucca BC; Klingensmith G; Bennett JL
Optom Vis Sci; 2011 Nov; 88(11):E1383-90. PubMed ID: 21892113
[TBL] [Abstract][Full Text] [Related]
8. [Wolfram syndrome: clinical and genetic analysis in two sisters].
Conart JB; Maalouf T; Jonveaux P; Guerci B; Angioi K
J Fr Ophtalmol; 2011 Oct; 34(8):543-6. PubMed ID: 21632151
[TBL] [Abstract][Full Text] [Related]
9. Ophthalmic, systemic, and genetic characteristics of patients with Wolfram syndrome.
Ustaoglu M; Onder F; Karapapak M; Taslidere H; Guven D
Eur J Ophthalmol; 2020 Sep; 30(5):1099-1105. PubMed ID: 30957632
[TBL] [Abstract][Full Text] [Related]
10. Wolfram (DIDMOAD) syndrome: report of two patients.
Lin CH; Lee YJ; Huang CY; Shieh JW; Lin HC; Wang AM; Shih BF
J Pediatr Endocrinol Metab; 2004 Oct; 17(10):1461-4. PubMed ID: 15526727
[TBL] [Abstract][Full Text] [Related]
11. Three cases of Wolfram syndrome with different clinical aspects.
Çamtosun E; Şıklar Z; Kocaay P; Ceylaner S; Flanagan SE; Ellard S; Berberoğlu M
J Pediatr Endocrinol Metab; 2015 Mar; 28(3-4):433-8. PubMed ID: 25210753
[TBL] [Abstract][Full Text] [Related]
12. [From gene to disease; mutations in the WFS1-gene as the cause of juvenile type I diabetes mellitus with optic atrophy (Wolfram syndrome)].
Pennings RJ; Dikkeschei LD; Cremers CW; van den Ouweland JM
Ned Tijdschr Geneeskd; 2002 May; 146(21):985-7. PubMed ID: 12058630
[TBL] [Abstract][Full Text] [Related]
13. Wolfram syndrome 1 and Wolfram syndrome 2.
Rigoli L; Di Bella C
Curr Opin Pediatr; 2012 Aug; 24(4):512-7. PubMed ID: 22790102
[TBL] [Abstract][Full Text] [Related]
14. Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome gene.
Titah SM; Meunier I; Blanchet C; Lopez S; Rondouin G; Lenaers G; Amati-Bonneau P; Reynier P; Paquis-Flucklinger V; Hamel CP
Eur J Ophthalmol; 2012; 22(2):254-8. PubMed ID: 21623591
[TBL] [Abstract][Full Text] [Related]
15. Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?
Ghirardello S; Dusi E; Castiglione B; Fumagalli M; Mosca F
Ital J Pediatr; 2014 Sep; 40():76. PubMed ID: 25255707
[TBL] [Abstract][Full Text] [Related]
16. Wolfram syndrome.
Megighian D; Savastano M
Int J Pediatr Otorhinolaryngol; 2004 Feb; 68(2):243-7. PubMed ID: 14725994
[TBL] [Abstract][Full Text] [Related]
17. A novel mutation of WFS1 gene in a Chinese patient with Wolfram syndrome: a case report.
Li M; Liu J; Yi H; Xu L; Zhong X; Peng F
BMC Pediatr; 2018 Mar; 18(1):116. PubMed ID: 29549887
[TBL] [Abstract][Full Text] [Related]
18. Ophthalmologic Manifestations of Wolfram Syndrome: Report of 14 Cases.
Soares A; Mota Á; Fonseca S; Faria O; Brandão E; Falcão Dos Reis F; Gentil R; Guimarães S; Mendonça L
Ophthalmologica; 2019; 241(2):116-119. PubMed ID: 30056456
[TBL] [Abstract][Full Text] [Related]
19. Congenital cataracts in two siblings with Wolfram syndrome.
Mets RB; Emery SB; Lesperance MM; Mets MB
Ophthalmic Genet; 2010 Dec; 31(4):227-9. PubMed ID: 21067485
[TBL] [Abstract][Full Text] [Related]
20. Wolfram/DIDMOAD syndrome, a heterogenic and molecularly complex neurodegenerative disease.
Domenech E; Gomez-Zaera M; Nunes V
Pediatr Endocrinol Rev; 2006 Mar; 3(3):249-57. PubMed ID: 16639390
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
