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43. Association between common genetic variation in Cockayne syndrome A and B genes and nucleotide excision repair capacity among smokers. Leng S; Bernauer A; Stidley CA; Picchi MA; Sheng X; Frasco MA; Van Den Berg D; Gilliland FD; Crowell RE; Belinsky SA Cancer Epidemiol Biomarkers Prev; 2008 Aug; 17(8):2062-9. PubMed ID: 18708399 [TBL] [Abstract][Full Text] [Related]
46. Rare syndromes. I. Cockayne syndrome: a review of the 129 cases so far reported in the literature. Cantani A; Bamonte G; Bellioni P; Tucci Bamonte M; Ceccoli D; Tacconi ML Riv Eur Sci Med Farmacol; 1987 Mar; 9(1):9-17. PubMed ID: 3334173 [No Abstract] [Full Text] [Related]
47. Embryonal sarcoma of the liver in a girl with Cockayne syndrome. Thorbinson C; Penn A; Nicola P; Hardcastle C; Waller S; Ramsden S; Coorens THH; Tang V; Cheesman E; Douzgou S; Meyer S Clin Genet; 2022 Mar; 101(3):375-376. PubMed ID: 34878179 [TBL] [Abstract][Full Text] [Related]
49. 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]
51. [Premature aging syndromes : From phenotype to gene]. Dereure O; Marque M; Guillot B Ann Dermatol Venereol; 2008; 135(6-7):466-78. PubMed ID: 18598796 [TBL] [Abstract][Full Text] [Related]
52. [Cockayne syndrome: a case with thymic hormone deficiency]. Julien T; Rejou F; Clot J; Eliaou JF; Dumas R; Jean R Ann Pediatr (Paris); 1986 Apr; 33(4):345-8. PubMed ID: 3729245 [No Abstract] [Full Text] [Related]
53. [Chromosome studies in Cockayne syndrome (author's transl)]. Kim MA; Lenz W; Maaser R Arch Genet (Zur); 1976-1977; 49-50(2-3):127-33. PubMed ID: 1053151 [No Abstract] [Full Text] [Related]
54. 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]
55. Response of motor complications in Cockayne syndrome to carbidopa-levodopa. Neilan EG; Delgado MR; Donovan MA; Kim SY; Jou RL; Wu BL; Kang PB Arch Neurol; 2008 Aug; 65(8):1117-21. PubMed ID: 18695064 [TBL] [Abstract][Full Text] [Related]
56. Non-radioisotope method for diagnosing photosensitive genodermatoses and a new marker for xeroderma pigmentosum variant. Hashimoto S; Egawa K; Ihn H; Tateishi S J Dermatol; 2009 Mar; 36(3):138-43. PubMed ID: 19335687 [TBL] [Abstract][Full Text] [Related]
57. What syndrome is this? Wiedemann-Rautenstrauch syndrome. Almeida P; Hernández J; Marti M; Hernández B Pediatr Dermatol; 2005; 22(1):75-8. PubMed ID: 15660904 [No Abstract] [Full Text] [Related]
58. Deep brain stimulation to treat hyperkinetic symptoms of Cockayne syndrome. Hebb MO; Gaudet P; Mendez I Mov Disord; 2006 Jan; 21(1):112-5. PubMed ID: 16108029 [TBL] [Abstract][Full Text] [Related]
59. Review of cases presenting with microcephaly and bilateral congenital cataract in a paediatric cataract clinic. Goyal R; Thompson D; Timms C; Wilson LC; Russell-Eggitt I Eye (Lond); 2008 Feb; 22(2):273-81. PubMed ID: 17975563 [TBL] [Abstract][Full Text] [Related]
60. Infantile onset of Cockayne syndrome in two siblings. Batra P; Saha A; Kumar A Indian J Dermatol Venereol Leprol; 2008; 74(1):65-7. PubMed ID: 18187833 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]