Lezza AM - Search Results

1

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2nd, Nikoskelainen EK. Wallace DC, et al. Among authors: lezza am. Science. 1988 Dec 9;242(4884):1427-30. doi: 10.1126/science.3201231. Science. 1988. PMID: 3201231

2

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation.

Shoffner JM, Lott MT, Lezza AM, Seibel P, Ballinger SW, Wallace DC. Shoffner JM, et al. Among authors: lezza am. Cell. 1990 Jun 15;61(6):931-7. doi: 10.1016/0092-8674(90)90059-n. Cell. 1990. PMID: 2112427

3

Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction.

Wallace DC, Lott MT, Lezza AM, Seibel P, Voljavec AS, Shoffner JM. Wallace DC, et al. Among authors: lezza am. Pediatr Res. 1990 Nov;28(5):525-8. doi: 10.1203/00006450-199011000-00023. Pediatr Res. 1990. PMID: 2123980

4

Mitochondrial DNA deletions in oculopharyngeal muscular dystrophy.

Lezza AM, Cormio A, Gerardi P, Silvestri G, Servidei S, Serlenga L, Cantatore P, Gadaleta MN. Lezza AM, et al. FEBS Lett. 1997 Nov 24;418(1-2):167-70. doi: 10.1016/s0014-5793(97)01374-4. FEBS Lett. 1997. PMID: 9414119 Free article.

5

MtDNA deletions in aging and in nonmitochondrial pathologies.

Cormio A, Lezza AM, Vecchiet J, Felzani G, Marangi L, Guglielmi FW, Francavilla A, Cantatore P, Gadaleta MN. Cormio A, et al. Among authors: lezza am. Ann N Y Acad Sci. 2000 Jun;908:299-301. doi: 10.1111/j.1749-6632.2000.tb06658.x. Ann N Y Acad Sci. 2000. PMID: 10911970 No abstract available.

6

Correlation between mitochondrial DNA 4977-bp deletion and respiratory chain enzyme activities in aging human skeletal muscles.

Lezza AM, Boffoli D, Scacco S, Cantatore P, Gadaleta MN. Lezza AM, et al. Biochem Biophys Res Commun. 1994 Nov 30;205(1):772-9. doi: 10.1006/bbrc.1994.2732. Biochem Biophys Res Commun. 1994. PMID: 7999111

7

Mitochondrial DNA copy number and mitochondrial DNA deletion in adult and senescent rats.

Gadaleta MN, Rainaldi G, Lezza AM, Milella F, Fracasso F, Cantatore P. Gadaleta MN, et al. Among authors: lezza am. Mutat Res. 1992 Sep;275(3-6):181-93. doi: 10.1016/0921-8734(92)90022-h. Mutat Res. 1992. PMID: 1383760 Review.

8

Mitochondrial DNA 4977 bp deletion and OH8dG levels correlate in the brain of aged subjects but not Alzheimer's disease patients.

Lezza AM, Mecocci P, Cormio A, Beal MF, Cherubini A, Cantatore P, Senin U, Gadaleta MN. Lezza AM, et al. FASEB J. 1999 Jun;13(9):1083-8. doi: 10.1096/fasebj.13.9.1083. FASEB J. 1999. PMID: 10336891

9

Variations at the H-strand replication origins of mitochondrial DNA and mitochondrial DNA content in the blood of type 2 diabetes patients.

Cormio A, Milella F, Marra M, Pala M, Lezza AM, Bonfigli AR, Franceschi C, Cantatore P, Gadaleta MN. Cormio A, et al. Among authors: lezza am. Biochim Biophys Acta. 2009 May;1787(5):547-52. doi: 10.1016/j.bbabio.2009.01.008. Epub 2009 Jan 22. Biochim Biophys Acta. 2009. PMID: 19344660 Free article.

10

Age-related mitochondrial genotypic and phenotypic alterations in human skeletal muscle.

Pesce V, Cormio A, Fracasso F, Vecchiet J, Felzani G, Lezza AM, Cantatore P, Gadaleta MN. Pesce V, et al. Among authors: lezza am. Free Radic Biol Med. 2001 Jun 1;30(11):1223-33. doi: 10.1016/s0891-5849(01)00517-2. Free Radic Biol Med. 2001. PMID: 11368920

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