These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
339 related articles for article (PubMed ID: 23435289)
41. 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]
43. Cockayne syndrome: the developing phenotype. Tan WH; Baris H; Robson CD; Kimonis VE Am J Med Genet A; 2005 Jun; 135(2):214-6. PubMed ID: 15887300 [TBL] [Abstract][Full Text] [Related]
44. Mitochondria in Ageing and Diseases: The Super Trouper of the Cell. Coppotelli G; Ross JM Int J Mol Sci; 2016 May; 17(5):. PubMed ID: 27187361 [TBL] [Abstract][Full Text] [Related]
45. [The metabolic and molecular bases of Cockayne syndrome]. Flores-Alvarado LJ; Ramirez-Garcia SA; Núñez-Reveles NY Rev Invest Clin; 2010; 62(5):480-90. PubMed ID: 21416736 [TBL] [Abstract][Full Text] [Related]
46. Clinical trials in mitochondrial disorders, an update. Almannai M; El-Hattab AW; Ali M; Soler-Alfonso C; Scaglia F Mol Genet Metab; 2020; 131(1-2):1-13. PubMed ID: 33129691 [TBL] [Abstract][Full Text] [Related]
47. 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]
48. Mitochondrial disorders as windows into an ancient organelle. Vafai SB; Mootha VK Nature; 2012 Nov; 491(7424):374-83. PubMed ID: 23151580 [TBL] [Abstract][Full Text] [Related]
49. The coordination of nuclear and mitochondrial communication during aging and calorie restriction. Finley LW; Haigis MC Ageing Res Rev; 2009 Jul; 8(3):173-88. PubMed ID: 19491041 [TBL] [Abstract][Full Text] [Related]
51. Insights into the Pathogenesis of Neurodegenerative Diseases: Focus on Mitochondrial Dysfunction and Oxidative Stress. Jurcau A Int J Mol Sci; 2021 Oct; 22(21):. PubMed ID: 34769277 [TBL] [Abstract][Full Text] [Related]
52. Mitochondrial Heteroplasmy. Stefano GB; Bjenning C; Wang F; Wang N; Kream RM Adv Exp Med Biol; 2017; 982():577-594. PubMed ID: 28551808 [TBL] [Abstract][Full Text] [Related]
53. Collagen synthesis by fibroblasts in a patient with the Cockayne syndrome. Keren G; Duksin D; Cohen BE; Goodman RM Eur J Pediatr; 1981 Nov; 137(3):339-42. PubMed ID: 7318848 [No Abstract] [Full Text] [Related]
54. Eccrine sweat gland anatomy in cockayne syndrome: a possible diagnostic aid. Landing BH; Sugarman G; Dixon LG Pediatr Pathol; 1983; 1(3):349-53. PubMed ID: 6687286 [TBL] [Abstract][Full Text] [Related]
55. A clinical and radiological study of two brothers affected by Cockayne syndrome type II. Colabucci F; Rossodivita A; Parigi A; Colavita N Rays; 1987; 12(2):57-63, 106-7. PubMed ID: 3444914 [No Abstract] [Full Text] [Related]
56. Mitochondrial medicine for aging and neurodegenerative diseases. Reddy PH Neuromolecular Med; 2008; 10(4):291-315. PubMed ID: 18566920 [TBL] [Abstract][Full Text] [Related]
57. Altered Metabolic Flexibility in Inherited Metabolic Diseases of Mitochondrial Fatty Acid Metabolism. Tucci S; Alatibi KI; Wehbe Z Int J Mol Sci; 2021 Apr; 22(7):. PubMed ID: 33917608 [TBL] [Abstract][Full Text] [Related]
58. Two Novel Heterozygous Mutations in ERCC8 Cause Cockayne Syndrome in a Chinese Patient. Cui YP; Chen YY; Wang XM; Wang XL; Nan X; Zhao H Pediatr Neurol; 2015 Sep; 53(3):262-5. PubMed ID: 26173784 [TBL] [Abstract][Full Text] [Related]
60. [Cockayne syndrome: siblings with different ultraviolet sensitivity and early onset of manifestations]. Okamoto N; Otani K; Abe J; Futagi Y; Nishida M No To Hattatsu; 1989 May; 21(3):265-70. PubMed ID: 2736126 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]