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7. 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]
8. Cockayne syndrome in siblings (Clinico-pathological study). Ozdirim E; Tinaztepe B; Pirnar T Turk J Pediatr; 1981; 23(1):47-56. PubMed ID: 7342395 [No Abstract] [Full Text] [Related]
9. 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]
11. 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]
12. [Cockayne syndrome in Lebanon. Description of 3 cases and review of the literature]. Jabre P; Mezzina M; Megarbane A J Med Liban; 1999; 47(2):144-7. PubMed ID: 10410472 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Children with 4q-syndrome: the parents' perspective. Strehle EM; Middlemiss PM Genet Couns; 2007; 18(2):189-99. PubMed ID: 17710871 [TBL] [Abstract][Full Text] [Related]
15. [Morphofunctional characteristics of fibroblasts in basal cell nevus and Cockayne syndrome]. Barenfel'd LS; Kalmykova NV; Andreeva LF; Pleskach NM; Prokof'ev VV; Mikhel'son VM Tsitologiia; 1999; 41(11):927-31. PubMed ID: 10643049 [TBL] [Abstract][Full Text] [Related]
16. A painful legacy. Mahony C Nurs Times; 1999 Oct 20-26; 95(42):26-7. PubMed ID: 10788879 [No Abstract] [Full Text] [Related]
17. Counseling parents and prospective parents with epilepsy. Shafer PO; Santilli N Clin Nurs Pract Epilepsy; 1996 Jan; 3(1):10. PubMed ID: 8696568 [No Abstract] [Full Text] [Related]
18. Cockayne syndrome type III with high intelligence. Czeizel AE; Marchalkó M Clin Genet; 1995 Dec; 48(6):331-3. PubMed ID: 8835332 [TBL] [Abstract][Full Text] [Related]
19. Adequacy and pitfalls of G6PD deficiency counseling in Hong Kong. Li KC; Lai SS; Lam ST Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():79-83. PubMed ID: 11400793 [TBL] [Abstract][Full Text] [Related]
20. Cockayne's syndrome: a case report. Literature review. Arenas-Sordo Mde L; Hernández-Zamora E; Montoya-Pérez LA; Aldape-Barrios BC Med Oral Patol Oral Cir Bucal; 2006 May; 11(3):E236-8. PubMed ID: 16648759 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]