343 related articles for article (PubMed ID: 9537152)
21. Progressive visual loss, diabetes mellitus, and associated abnormalities (DIDMOAD syndrome).
Kocher GA; Spoor TC; Ferguson JG
J Clin Neuroophthalmol; 1982 Dec; 2(4):241-4. PubMed ID: 6226706
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. [Diabetes mellitus, diabetes insipidus, optic atrophy and deafness].
Labrune B; Benichou JJ
Ann Pediatr (Paris); 1991 Apr; 38(4):249-54. PubMed ID: 2069360
[TBL] [Abstract][Full Text] [Related]
24. [Neurologic manifestations in Wolfram's syndrome].
Leiva-Santana C; Carro-Martinez A; Monge-Argiles A; Palao-Sanchez A
Rev Neurol (Paris); 1993; 149(1):26-9. PubMed ID: 8337558
[TBL] [Abstract][Full Text] [Related]
25. Rapidly progressive renal disease as part of Wolfram syndrome in a large inbred Turkish family due to a novel WFS1 mutation (p.Leu511Pro).
Yuca SA; Rendtorff ND; Boulahbel H; Lodahl M; Tranebjærg L; Cesur Y; Dogan M; Yilmaz C; Akgun C; Acikgoz M
Eur J Med Genet; 2012 Jan; 55(1):37-42. PubMed ID: 21968327
[TBL] [Abstract][Full Text] [Related]
26. Coexistence of diabetes mellitus, optic atrophy, and sensorineural deafness: case report.
Osei K; Weber PA; Falko JM
Ann Ophthalmol; 1986 May; 18(5):196-8. PubMed ID: 3717843
[TBL] [Abstract][Full Text] [Related]
27. Imaging characteristics of familial Wolfram syndrome.
Yang MS; Chen CC; Cheng YY; Tyan YS; Wang YF; Lee SK
J Formos Med Assoc; 2005 Feb; 104(2):129-32. PubMed ID: 15765170
[TBL] [Abstract][Full Text] [Related]
28. [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]
29. [Early symptoms and findings in optic nerve meningiomas].
Wilhelm H; Dörr S; Paulsen F; Becker G; Classen J
Klin Monbl Augenheilkd; 2009 Nov; 226(11):869-74. PubMed ID: 19916145
[TBL] [Abstract][Full Text] [Related]
30. Diabetes mellitus, diabetes insipidus, optic atrophy and deafness (DIDMOAD syndrome).
Saatçi U; Söylemezoğlu O; Ozen S; Yordam N; Saatçi O
Turk J Pediatr; 1990; 32(3):211-5. PubMed ID: 2093258
[TBL] [Abstract][Full Text] [Related]
31. [Description of Wolfram syndrome (DIDMOAD) on the basis of a new case].
Bernabeau Morón I; Cámara Gómez R; Araujo Ayala R; Díez Alvarez S; Estrada García J; Lucas Morante T; Barceló Lucerga B
Rev Clin Esp; 1989 May; 184(8):418-20. PubMed ID: 2781075
[TBL] [Abstract][Full Text] [Related]
32. [DIDMOAD syndrome].
Alicanoğlu R; Canbakan B; Yildiz N; Arikan E; Kundur H; Bahtiyar K; Sayali E
Wien Med Wochenschr; 1994; 144(4):78-81. PubMed ID: 8023526
[TBL] [Abstract][Full Text] [Related]
33. Association of diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. The Wolfram or DIDMOAD syndrome.
Najjar SS; Saikaly MG; Zaytoun GM; Abdelnoor A
Arch Dis Child; 1985 Sep; 60(9):823-8. PubMed ID: 4051539
[TBL] [Abstract][Full Text] [Related]
34. [DIDMOAD syndrome (diabetes insipidus, diabetes mellitus, optic atrophy, deafness) with cerebello-pontine atrophy].
Kehl O; Keller U
Schweiz Med Wochenschr; 1982 Mar; 112(10):348-52. PubMed ID: 7079680
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. 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]
37. Optic atrophy in Wolfram syndrome.
Mtanda AT; Cruysberg JR; Pinckers AJ
Ophthalmic Paediatr Genet; 1986 Dec; 7(3):159-65. PubMed ID: 3561950
[TBL] [Abstract][Full Text] [Related]
38. Teaching NeuroImages: a neuroendocrine rarity: Wolfram syndrome.
Vale TC; Perpétuo FO
Neurology; 2013 Nov; 81(20):e153. PubMed ID: 24218323
[TBL] [Abstract][Full Text] [Related]
39. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
Smith PR; Bain SC; Good PA; Hattersley AT; Barnett AH; Gibson JM; Dodson PM
Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077
[TBL] [Abstract][Full Text] [Related]
40. Wolfram (DIDMOAD) syndrome.
Barrett TG; Bundey SE
J Med Genet; 1997 Oct; 34(10):838-41. PubMed ID: 9350817
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
