81 related articles for article (PubMed ID: 9543772)
1. [Diabetes mellitus in connection with a hereditary disorder].
Boomsma LJ
Ned Tijdschr Geneeskd; 1997 Aug; 141(33):1632. PubMed ID: 9543772
[No Abstract] [Full Text] [Related]
2. [Optic atrophy, type I diabetes and neurosensory hearing loss: a family syndrome].
Bujara K; Burck U; Dreyer M; Koepp P; Herberhold C
Klin Monbl Augenheilkd; 1982 Jun; 180(6):559-62. PubMed ID: 6890123
[No Abstract] [Full Text] [Related]
3. Sensorineural hearing loss, diabetes, and mitochondrial DNA mutation in Taiwan.
Tseng FY
Laryngoscope; 2006 Mar; 116(3):506. PubMed ID: 16540924
[No Abstract] [Full Text] [Related]
4. [Involvement of neuromuscular disorders in maternally inherited diabetes with deafness (MIDD)].
Hirayama T; Kaneshige Y; Okahara S; Adachi Y; Suzuki A; Aoki S; Nakagawa N; Yabana T; Imai T; Matsumoto H
Nihon Naika Gakkai Zasshi; 2003 Apr; 92(4):668-70. PubMed ID: 12746969
[No Abstract] [Full Text] [Related]
5. Diabetes, sensorineural deafness, and mitochondrial DNA mutation.
Prisco F; Iafusco D
Laryngoscope; 2006 Mar; 116(3):505-6; author reply 506. PubMed ID: 16540920
[No Abstract] [Full Text] [Related]
6. Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics.
Nagata H; Kumahara K; Tomemori T; Arimoto Y; Isoyama K; Yoshida K; Konno A
J Hum Genet; 2001; 46(10):595-9. PubMed ID: 11587074
[TBL] [Abstract][Full Text] [Related]
7. [Maternally inherited diabetes and deafness: a case report].
Maseda E; Sampedro A; Ablanedo A; Alonso JR
Acta Otorrinolaringol Esp; 2008 Nov; 59(9):472-3. PubMed ID: 19080780
[TBL] [Abstract][Full Text] [Related]
8. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation].
Xiu L; Zhang Q; Yu B
Zhonghua Yi Xue Za Zhi; 1997 Jun; 77(6):418-21. PubMed ID: 9772504
[TBL] [Abstract][Full Text] [Related]
9. Role of mitochondrial variation in maternally inherited diabetes and deafness syndrome.
Howes T; Madden C; Dasgupta S; Saeed S; Das V
J Laryngol Otol; 2008 Nov; 122(11):1249-52. PubMed ID: 18950542
[TBL] [Abstract][Full Text] [Related]
10. [Wolfram syndrome or DIDMOAD syndrome].
Sarría A; Legido A; Garagorri JM; Palomar T; González I; Bueno M
Arch Fr Pediatr; 1983 Dec; 40(10):795-7. PubMed ID: 6673684
[TBL] [Abstract][Full Text] [Related]
11. Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.
Cryns K; Sivakumaran TA; Van den Ouweland JM; Pennings RJ; Cremers CW; Flothmann K; Young TL; Smith RJ; Lesperance MM; Van Camp G
Hum Mutat; 2003 Oct; 22(4):275-87. PubMed ID: 12955714
[TBL] [Abstract][Full Text] [Related]
12. Thiamine-responsive megaloblastic anemia syndrome: long term follow-up.
Borgna-Pignatti C; Azzalli M; Pedretti S
J Pediatr; 2009 Aug; 155(2):295-7. PubMed ID: 19619756
[TBL] [Abstract][Full Text] [Related]
13. Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD).
Hendrickx JJ; Mudde AH; 't Hart LM; Huygen PL; Cremers CW
Otol Neurotol; 2006 Sep; 27(6):802-8. PubMed ID: 16788417
[TBL] [Abstract][Full Text] [Related]
14. A novel mutation in the SLC19A2 gene in a Turkish female with thiamine-responsive megaloblastic anemia syndrome.
Yeşilkaya E; Bideci A; Temizkan M; Kaya Z; Camurdan O; Koç A; Bozkaya D; Koçak U; Cinaz P
J Trop Pediatr; 2009 Aug; 55(4):265-7. PubMed ID: 18614593
[TBL] [Abstract][Full Text] [Related]
15. [Loss of hearing and vision in diabetes mellitus].
Krasheninnikov VF
Zh Ushn Nos Gorl Bolezn; 1979; (5):71-2. PubMed ID: 494772
[No Abstract] [Full Text] [Related]
16. A pedigree with Pendred syndrome: case report and discussion on hereditary hearing loss.
Hiyoshi M; Yamane H
Acta Otolaryngol Suppl; 2004 Oct; (554):45-6. PubMed ID: 15513511
[TBL] [Abstract][Full Text] [Related]
17. Three new cases of Alström syndrome.
Benso C; Hadjadj E; Conrath J; Denis D
Graefes Arch Clin Exp Ophthalmol; 2002 Aug; 240(8):622-7. PubMed ID: 12192455
[TBL] [Abstract][Full Text] [Related]
18. [Hearing loss in Turner syndrome].
Hultcrantz M; Sylvén L
Lakartidningen; 1996 May; 93(22):2150, 2155-7. PubMed ID: 8667849
[No Abstract] [Full Text] [Related]
19. Thiamine-responsive megaloblastic anaemia: a cause of syndromic diabetes in childhood.
Olsen BS; Hahnemann JM; Schwartz M; Østergaard E
Pediatr Diabetes; 2007 Aug; 8(4):239-41. PubMed ID: 17659067
[TBL] [Abstract][Full Text] [Related]
20. Dystonia in the Woodhouse Sakati syndrome: A new family and literature review.
Schneider SA; Bhatia KP
Mov Disord; 2008 Mar; 23(4):592-6. PubMed ID: 18175354
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]