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26. [Anesthesia for a patient with Cockayne's syndrome]. Shimizu T; Inomata S; Miyabe M; Toyooka H Masui; 2002 Jan; 51(1):39-41. PubMed ID: 11840661 [TBL] [Abstract][Full Text] [Related]
27. Cockayne syndrome with early onset of manifestations. Moyer DB; Marquis P; Shertzer ME; Burton BK Am J Med Genet; 1982 Oct; 13(2):225-30. PubMed ID: 7137233 [TBL] [Abstract][Full Text] [Related]
28. [Cockayne's syndrome with unusual retinal involvement (report of one family)]. Hamdani M; El Kettani A; Rais L; Benhaddou M; Hda N; Rachid R; El Belhadji M; Laouissi N; Zaghloul K; Benslimane A; Amraoui A J Fr Ophtalmol; 2000 Jan; 23(1):52-6. PubMed ID: 10660649 [TBL] [Abstract][Full Text] [Related]
29. Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome. Mohammadi-Asl J; Hajjari M; Tahmasebi Birgani M; Riahi K; Nasiri H; Kollaee A Ann Hum Genet; 2018 Sep; 82(5):304-308. PubMed ID: 30039856 [TBL] [Abstract][Full Text] [Related]
30. Deep intronic variation in splicing regulatory element of the ERCC8 gene associated with severe but long-term survival Cockayne syndrome. Schalk A; Greff G; Drouot N; Obringer C; Dollfus H; Laugel V; Chelly J; Calmels N Eur J Hum Genet; 2018 Apr; 26(4):527-536. PubMed ID: 29422660 [TBL] [Abstract][Full Text] [Related]
31. Cockayne Syndrome due to a maternally-inherited whole gene deletion of ERCC8 and a paternally-inherited ERCC8 exon 4 deletion. Ting TW; Brett MS; Tan ES; Shen Y; Lee SP; Lim EC; Vasanwala RF; Lek N; Thomas T; Lim KW; Tan EC Gene; 2015 Nov; 572(2):274-8. PubMed ID: 26210811 [TBL] [Abstract][Full Text] [Related]
32. Infantile onset of Cockayne syndrome without photosensitivity in a Tunisian girl. Tinsa F; Bellalah M; Brini I; Bousnina D; Lehmann A; Boussetta K; Bousnina S Tunis Med; 2009 Dec; 87(12):877-9. PubMed ID: 20209858 [TBL] [Abstract][Full Text] [Related]
33. Atypical features and de novo heterozygous mutations in two siblings with Cockayne syndrome. Wu S; Liu Y; Zhang Q; Meng X; Huang L; Xu Z; Zhang C; Li Y; Chen T; Bai Z Mol Genet Genomic Med; 2020 May; 8(5):e1204. PubMed ID: 32160415 [TBL] [Abstract][Full Text] [Related]
34. Central motor pathways conduction after magnetic stimulation of the brain in Cockayne's syndrome. Cruz Martínez A; Anciones B Acta Neurol Scand; 1991 Oct; 84(4):291-4. PubMed ID: 1663306 [TBL] [Abstract][Full Text] [Related]
35. Early onset Cockayne's syndrome: case reports with neuropathological and fibroblast studies. Patton MA; Giannelli F; Francis AJ; Baraitser M; Harding B; Williams AJ J Med Genet; 1989 Mar; 26(3):154-9. PubMed ID: 2468771 [TBL] [Abstract][Full Text] [Related]
36. Identification of two novel homozygous mutations in ERCC8 gene in two unrelated consanguineous families with Cockayne syndrome from Iran. Yousefipour F; Mahjoobi F Clin Chim Acta; 2021 Dec; 523():65-71. PubMed ID: 34461059 [TBL] [Abstract][Full Text] [Related]
37. Chronological changes of auditory brainstem responses in Cockayne's syndrome. Iwasaki S; Kaga K Int J Pediatr Otorhinolaryngol; 1994 Nov; 30(3):211-21. PubMed ID: 7836034 [TBL] [Abstract][Full Text] [Related]
38. Cockayne syndrome--a primary defect in DNA repair, transcription, both or neither? Friedberg EC Bioessays; 1996 Sep; 18(9):731-8. PubMed ID: 8831289 [TBL] [Abstract][Full Text] [Related]
39. Prenatal diagnosis of Cockayne's syndrome. Lehmann AR; Francis AJ; Giannelli F Lancet; 1985 Mar; 1(8427):486-8. PubMed ID: 2579301 [TBL] [Abstract][Full Text] [Related]