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

Year Number of Results
1996 1
1997 2
2001 3
2002 4
2003 1
2004 3
2006 1
2007 2
2008 1
2009 2
2010 4
2012 1
2024 0

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24 results

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Page 1
Metabolic myopathies.
DiMauro S, Garone C, Naini A. DiMauro S, et al. Curr Rheumatol Rep. 2010 Oct;12(5):386-93. doi: 10.1007/s11926-010-0119-9. Curr Rheumatol Rep. 2010. PMID: 20676808
Lessons from mitochondrial DNA mutations.
DiMauro S. DiMauro S. Semin Cell Dev Biol. 2001 Dec;12(6):397-405. doi: 10.1006/scdb.2001.0277. Semin Cell Dev Biol. 2001. PMID: 11735374 Review.
Neuronal degeneration and mitochondrial dysfunction.
Schon EA, Manfredi G. Schon EA, et al. J Clin Invest. 2003 Feb;111(3):303-12. doi: 10.1172/JCI17741. J Clin Invest. 2003. PMID: 12569152 Free PMC article. Review. No abstract available.
Historical perspective on mitochondrial medicine.
DiMauro S, Garone C. DiMauro S, et al. Dev Disabil Res Rev. 2010;16(2):106-13. doi: 10.1002/ddrr.102. Dev Disabil Res Rev. 2010. PMID: 20818724 Free PMC article.
Coenzyme Q-responsive Leigh's encephalopathy in two sisters.
Van Maldergem L, Trijbels F, DiMauro S, Sindelar PJ, Musumeci O, Janssen A, Delberghe X, Martin JJ, Gillerot Y. Van Maldergem L, et al. Ann Neurol. 2002 Dec;52(6):750-4. doi: 10.1002/ana.10371. Ann Neurol. 2002. PMID: 12447928
Mitochondrial DNA abnormalities and autistic spectrum disorders.
Pons R, Andreu AL, Checcarelli N, Vilà MR, Engelstad K, Sue CM, Shungu D, Haggerty R, de Vivo DC, DiMauro S. Pons R, et al. J Pediatr. 2004 Jan;144(1):81-5. doi: 10.1016/j.jpeds.2003.10.023. J Pediatr. 2004. PMID: 14722523
24 results