119 related articles for article (PubMed ID: 7342395)
21. Cockayne syndrome: MRI correlates of hypomyelination.
Dabbagh O; Swaiman KF
Pediatr Neurol; 1988; 4(2):113-6. PubMed ID: 3242508
[TBL] [Abstract][Full Text] [Related]
22. [Cockayne syndrome: a new mutation in the ERCC8 gene].
Conchello-Monleón R; Peña-Segura JL; Tello-Martín Á; Monge-Galindo L; Cabrejas-Lalmolda A; Miramar MD; López-Pisón J
Rev Neurol; 2012 Aug; 55(4):250-1. PubMed ID: 22829088
[No Abstract] [Full Text] [Related]
23. CAMFAK syndrome: a demyelinating inherited disease similar to Cockayne syndrome.
Talwar D; Smith SA
Am J Med Genet; 1989 Oct; 34(2):194-8. PubMed ID: 2554729
[TBL] [Abstract][Full Text] [Related]
24. Severe form of Cockayne syndrome with varying clinical presentation and no photosensitivity in a family.
Sonmez FM; Celep F; Ugur SA; Tolun A
J Child Neurol; 2006 Apr; 21(4):333-7. PubMed ID: 16900932
[TBL] [Abstract][Full Text] [Related]
25. Cockayne syndrome--a case report, and a review of the premature aging syndromes in paediatrics.
Loke KY
J Singapore Paediatr Soc; 1991; 33(1-2):49-54. PubMed ID: 1784111
[TBL] [Abstract][Full Text] [Related]
26. What syndrome is this? Cockayne syndrome.
Bender MM; Potocki L; Metry DW
Pediatr Dermatol; 2003; 20(6):538-40. PubMed ID: 14651579
[No Abstract] [Full Text] [Related]
27. Peripheral neuropathy in Cockayne syndrome.
Schenone A; Rolando S; Ferrari M; Romagnoli P; Tabaton M; Mancardi GL
Ital J Neurol Sci; 1986 Aug; 7(4):447-52. PubMed ID: 3019920
[TBL] [Abstract][Full Text] [Related]
28. [UV or X-ray sensitivity of cells from Cockayne syndrome].
Sugita K; Arima M; Iai M; Tamai K; Aihara M
No To Hattatsu; 1986 Jul; 18(4):286-91. PubMed ID: 2425830
[No Abstract] [Full Text] [Related]
29. Dental findings in a child with Cockayne's syndrome.
Schneider PE
ASDC J Dent Child; 1983; 50(1):58-64. PubMed ID: 6572201
[No Abstract] [Full Text] [Related]
30. Host cell reactivation of ultraviolet light irradiated adenovirus 5 in fibroblasts from patients with Cockayne syndrome: a study with six Japanese cases.
Watatani M; Ohtani H; Takai S; Ikenaga M
J Radiat Res; 1984 Jun; 25(2):150-9. PubMed ID: 6481688
[No Abstract] [Full Text] [Related]
31. Rapid procedures for prenatal diagnosis of Cockayne syndrome.
Kawai K; Ikenaga M; Ohtani H; Fukuchi K; Yamamura K; Kumahara Y
Jinrui Idengaku Zasshi; 1983 Sep; 28(3):223-9. PubMed ID: 6672367
[No Abstract] [Full Text] [Related]
32. Ultrastructure and electrodiagnosis of peripheral neuropathy in Cockayne's syndrome.
Grunnet ML; Zimmerman AW; Lewis RA
Neurology; 1983 Dec; 33(12):1606-9. PubMed ID: 6316205
[TBL] [Abstract][Full Text] [Related]
33. The current evidence for defective repair of oxidatively damaged DNA in Cockayne syndrome.
Frosina G
Free Radic Biol Med; 2007 Jul; 43(2):165-77. PubMed ID: 17603927
[TBL] [Abstract][Full Text] [Related]
34. Renal lesions in Cockayne syndrome.
Hirooka M; Hirota M; Kamada M
Pediatr Nephrol; 1988 Apr; 2(2):239-43. PubMed ID: 3153017
[TBL] [Abstract][Full Text] [Related]
35. Cranial nerve and cauda equina contrast enhancement in Cockayne syndrome.
Biancheri R; Mancardi MM; Celle ME; Nardo T; Morana G
Neurology; 2014 Oct; 83(17):1581. PubMed ID: 25332446
[No Abstract] [Full Text] [Related]
36. [Cockayne syndrome].
Dumić M; Jasenka I; Silahić A; Kordić R
Lijec Vjesn; 1995; 117(9-10):232-5. PubMed ID: 8643015
[TBL] [Abstract][Full Text] [Related]
37. Cockayne's syndrome.
Neetens A; Van Acker K; Smets RM
Bull Soc Belge Ophtalmol; 1982; 203():85-92. PubMed ID: 7187624
[No Abstract] [Full Text] [Related]
38. A novel splice site mutation in the Cockayne syndrome group A gene in two siblings with Cockayne syndrome.
Kleppa L; Kanavin ØJ; Klungland A; Strømme P
Neuroscience; 2007 Apr; 145(4):1397-406. PubMed ID: 17084038
[TBL] [Abstract][Full Text] [Related]
39. An adult case of Cockayne syndrome without sclerotic angiopathy.
Inoue T; Sano N; Ito Y; Matsuzaki Y; Okauchi Y; Kondo H; Horiuchi N; Nakao K; Iwata M
Intern Med; 1997 Aug; 36(8):565-70. PubMed ID: 9260774
[TBL] [Abstract][Full Text] [Related]
40. Cockayne syndrome in three sisters with varying clinical presentation.
Mahmoud AA; Yousef GM; Al-Hifzi I; Diamandis EP
Am J Med Genet; 2002 Jul; 111(1):81-5. PubMed ID: 12124741
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]