Prezant TR - Search Results

1

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

2

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

3

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

4

Corrections to the human mitochondrial ribosomal RNA sequences.

Prezant TR, Agapian JV, Fischel-Ghodsian N. Prezant TR, et al. Hum Genet. 1994 Jan;93(1):87-8. doi: 10.1007/BF00218923. Hum Genet. 1994. PMID: 8270263

5

Trapped-oligonucleotide nucleotide incorporation (TONI) assay, a simple method for screening point mutations.

Prezant TR, Fischel-Ghodsian N. Prezant TR, et al. Hum Mutat. 1992;1(2):159-64. doi: 10.1002/humu.1380010212. Hum Mutat. 1992. PMID: 1301203

6

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.

Prezant TR, Agapian JV, Bohlman MC, Bu X, Oztas S, Qiu WQ, Arnos KS, Cortopassi GA, Jaber L, Rotter JI, et al. Prezant TR, et al. Nat Genet. 1993 Jul;4(3):289-94. doi: 10.1038/ng0793-289. Nat Genet. 1993. PMID: 7689389

7

Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.

Fischel-Ghodsian N, Prezant TR, Bu X, Oztas S. Fischel-Ghodsian N, et al. Among authors: prezant tr. Am J Otolaryngol. 1993 Nov-Dec;14(6):399-403. doi: 10.1016/0196-0709(93)90113-l. Am J Otolaryngol. 1993. PMID: 8285309

8

Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome.

Bernes SM, Bacino C, Prezant TR, Pearson MA, Wood TS, Fournier P, Fischel-Ghodsian N. Bernes SM, et al. Among authors: prezant tr. J Pediatr. 1993 Oct;123(4):598-602. doi: 10.1016/s0022-3476(05)80962-x. J Pediatr. 1993. PMID: 8410517

9

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

10

Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness.

Bacino C, Prezant TR, Bu X, Fournier P, Fischel-Ghodsian N. Bacino C, et al. Among authors: prezant tr. Pharmacogenetics. 1995 Jun;5(3):165-72. doi: 10.1097/00008571-199506000-00005. Pharmacogenetics. 1995. PMID: 7550368

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