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Combined cyclic vomiting and Kearns-Sayre syndromes.
Boles RG, Baldwin EE, Prezant TR. Boles RG, et al. Among authors: prezant tr. Pediatr Neurol. 2007 Feb;36(2):135-6. doi: 10.1016/j.pediatrneurol.2006.09.008. Pediatr Neurol. 2007. PMID: 17275670
Mitochondrial mutation associated with nonsyndromic deafness.
Fischel-Ghodsian N, Prezant TR, Fournier P, Stewart IA, Maw M. Fischel-Ghodsian N, et al. Among authors: prezant tr. Am J Otolaryngol. 1995 Nov-Dec;16(6):403-8. doi: 10.1016/0196-0709(95)90078-0. Am J Otolaryngol. 1995. PMID: 8572257
Screening for mtDNA diabetes mutations in Pima Indians with NIDDM.
Sepehrnia B, Prezant TR, Rotter JI, Pettitt DJ, Knowler WC, Fischel-Ghodsian N. Sepehrnia B, et al. Among authors: prezant tr. Am J Med Genet. 1995 Mar 27;56(2):198-202. doi: 10.1002/ajmg.1320560217. Am J Med Genet. 1995. PMID: 7625445
Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome.
Fischel-Ghodsian N, Bohlman MC, Prezant TR, Graham JM Jr, Cederbaum SD, Edwards MJ. Fischel-Ghodsian N, et al. Among authors: prezant tr. Pediatr Res. 1992 Jun;31(6):557-60. doi: 10.1203/00006450-199206000-00004. Pediatr Res. 1992. PMID: 1635816
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