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

Year Number of Results
1978 1
1980 1
1982 1
1986 1
1988 1
1990 2
1991 1
1992 1
1993 8
1994 8
1995 5
1996 17
1997 13
1998 11
1999 14
2000 10
2001 15
2002 15
2003 13
2004 11
2005 22
2006 18
2007 19
2008 24
2009 15
2010 8
2011 10
2012 11
2013 7
2014 4
2015 4
2016 5
2017 8
2018 11
2019 3
2020 3
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Similar Articles for PMID: 16091512

300 results
Results by year
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Page 1
Predominant cerebellar volume loss as a neuroradiologic feature of pediatric respiratory chain defects.
Scaglia F, Wong LJ, Vladutiu GD, Hunter JV. Scaglia F, et al. AJNR Am J Neuroradiol. 2005 Aug;26(7):1675-80. AJNR Am J Neuroradiol. 2005. PMID: 16091512 Free article.
Neuroradiologic findings in children with mitochondrial disorders.
Valanne L, Ketonen L, Majander A, Suomalainen A, Pihko H. Valanne L, et al. AJNR Am J Neuroradiol. 1998 Feb;19(2):369-77. AJNR Am J Neuroradiol. 1998. PMID: 9504497 Free article.
Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease.
Scaglia F, Towbin JA, Craigen WJ, Belmont JW, Smith EO, Neish SR, Ware SM, Hunter JV, Fernbach SD, Vladutiu GD, Wong LJ, Vogel H. Scaglia F, et al. Pediatrics. 2004 Oct;114(4):925-31. doi: 10.1542/peds.2004-0718. Pediatrics. 2004. PMID: 15466086
Proton MR spectroscopy in the diagnostic evaluation of suspected mitochondrial disease.
Lin DD, Crawford TO, Barker PB. Lin DD, et al. AJNR Am J Neuroradiol. 2003 Jan;24(1):33-41. AJNR Am J Neuroradiol. 2003. PMID: 12533324 Free article.
Cerebellar hypoplasia in respiratory chain dysfunction.
Lincke CR, van den Bogert C, Nijtmans LG, Wanders RJ, Tamminga P, Barth PG. Lincke CR, et al. Neuropediatrics. 1996 Aug;27(4):216-8. doi: 10.1055/s-2007-973792. Neuropediatrics. 1996. PMID: 8892374
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chain.
Birch-Machin MA, Marsac C, Ponsot G, Parfait B, Taylor RW, Rustin P, Munnich A. Birch-Machin MA, et al. Biochem Biophys Res Commun. 1996 Mar 7;220(1):57-62. doi: 10.1006/bbrc.1996.0356. Biochem Biophys Res Commun. 1996. PMID: 8602857
Value of brain magnetic resonance imaging in mitochondrial respiratory chain disorders.
Diogo L, Cordeiro M, Garcia P, Fineza I, Moura C, Oliveira CR, Veiga M, Garcia T, Grazina M. Diogo L, et al. Pediatr Neurol. 2010 Mar;42(3):196-200. doi: 10.1016/j.pediatrneurol.2009.09.010. Pediatr Neurol. 2010. PMID: 20159429
[Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases].
Castro-Gago M, González-Conde V, Fernández-Seara MJ, Rodrigo-Sáez E, Fernández-Cebrián S, Alonso-Martín A, Campos Y, Arenas J, Eirís-Puñal J. Castro-Gago M, et al. Rev Neurol. 1999 Nov 16-30;29(10):912-7. Rev Neurol. 1999. PMID: 10637838 Spanish.
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.
Carrozzo R, Dionisi-Vici C, Steuerwald U, Lucioli S, Deodato F, Di Giandomenico S, Bertini E, Franke B, Kluijtmans LA, Meschini MC, Rizzo C, Piemonte F, Rodenburg R, Santer R, Santorelli FM, van Rooij A, Vermunt-de Koning D, Morava E, Wevers RA. Carrozzo R, et al. Brain. 2007 Mar;130(Pt 3):862-74. doi: 10.1093/brain/awl389. Epub 2007 Feb 14. Brain. 2007. PMID: 17301081
Stroke due to mitochondrial disorders in Saudi children.
Salih MA, Abdel-Gader AG, Zahraa JN, Al-Rayess MM, Alorainy IA, Hassan HH, Ruitenbeek W, Zeviani M. Salih MA, et al. Saudi Med J. 2006 Mar;27 Suppl 1:S81-90. Saudi Med J. 2006. PMID: 16532135
300 results
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