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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1990 3
1991 1
1993 1
1994 1
1995 3
1996 2
1997 1
1998 3
1999 6
2000 3
2001 9
2002 6
2003 5
2004 3
2005 5
2006 6
2007 5
2008 5
2009 8
2010 5
2011 2
2012 4
2013 4
2014 7
2015 5
2016 5
2017 4
2018 8
2019 3
2020 4
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Publication date

Similar Articles for PMID: 12169463

117 results
Results by year
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Page 1
MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations.
Farina L, Chiapparini L, Uziel G, Bugiani M, Zeviani M, Savoiardo M. Farina L, et al. AJNR Am J Neuroradiol. 2002 Aug;23(7):1095-100. AJNR Am J Neuroradiol. 2002. PMID: 12169463 Free article.
Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findings.
Rossi A, Biancheri R, Bruno C, Di Rocco M, Calvi A, Pessagno A, Tortori-Donati P. Rossi A, et al. AJNR Am J Neuroradiol. 2003 Jun-Jul;24(6):1188-91. AJNR Am J Neuroradiol. 2003. PMID: 12812953 Free article.
Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochrome c oxidase deficiency.
Tiranti V, Jaksch M, Hofmann S, Galimberti C, Hoertnagel K, Lulli L, Freisinger P, Bindoff L, Gerbitz KD, Comi GP, Uziel G, Zeviani M, Meitinger T. Tiranti V, et al. Ann Neurol. 1999 Aug;46(2):161-6. doi: 10.1002/1531-8249(199908)46:2<161::aid-ana4>;2-o. Ann Neurol. 1999. PMID: 10443880
Facial dysmorphism in Leigh syndrome with SURF-1 mutation and COX deficiency.
Yüksel A, Seven M, Cetincelik U, Yeşil G, Köksal V. Yüksel A, et al. Pediatr Neurol. 2006 Jun;34(6):486-9. doi: 10.1016/j.pediatrneurol.2005.10.020. Pediatr Neurol. 2006. PMID: 16765830
Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
Yang YL, Sun F, Zhang Y, Qian N, Yuan Y, Wang ZX, Qi Y, Xiao JX, Wang XY, Qi ZY, Zhang YH, Jiang YW, Bao XH, Qin J, Wu XR. Yang YL, et al. Chin Med J (Engl). 2006 Mar 5;119(5):373-7. Chin Med J (Engl). 2006. PMID: 16542579
SURF1 gene mutations in three cases with Leigh syndrome and cytochrome c oxidase deficiency.
Moslemi AR, Tulinius M, Darin N, Aman P, Holme E, Oldfors A. Moslemi AR, et al. Neurology. 2003 Oct 14;61(7):991-3. doi: 10.1212/01.wnl.0000082391.98672.0a. Neurology. 2003. PMID: 14557577
[Cytochrome c oxidase deficiency--SURF1 mutations].
Naito E, Ogawa Y. Naito E, et al. Nihon Rinsho. 2002 Apr;60 Suppl 4:446-9. Nihon Rinsho. 2002. PMID: 12013909 Review. Japanese. No abstract available.
Maternal segmental disomy in Leigh syndrome with cytochrome c oxidase deficiency caused by homozygous SURF1 mutation.
van Riesen AK, Antonicka H, Ohlenbusch A, Shoubridge EA, Wilichowski EK. van Riesen AK, et al. Neuropediatrics. 2006 Apr;37(2):88-94. doi: 10.1055/s-2006-924227. Neuropediatrics. 2006. PMID: 16773507
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2.
Sue CM, Karadimas C, Checcarelli N, Tanji K, Papadopoulou LC, Pallotti F, Guo FL, Shanske S, Hirano M, De Vivo DC, Van Coster R, Kaplan P, Bonilla E, DiMauro S. Sue CM, et al. Ann Neurol. 2000 May;47(5):589-95. Ann Neurol. 2000. PMID: 10805329
Heterogeneity of magnetic resonance imaging in Leigh syndrome with SURF1 gene 604G-->C mutation.
Xie S, Xiao JX, Qi ZY, Yang YL, Jiang XX. Xie S, et al. Clin Imaging. 2009 Jan-Feb;33(1):1-6. doi: 10.1016/j.clinimag.2008.08.001. Clin Imaging. 2009. PMID: 19135921
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