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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. J Pediatr. 1993 Oct;123(4):598-602. doi: 10.1016/s0022-3476(05)80962-x. J Pediatr. 1993. PMID: 8410517
Mitochondrial mutation associated with nonsyndromic deafness.
Fischel-Ghodsian N, Prezant TR, Fournier P, Stewart IA, Maw M. Fischel-Ghodsian N, et al. Am J Otolaryngol. 1995 Nov-Dec;16(6):403-8. doi: 10.1016/0196-0709(95)90078-0. Am J Otolaryngol. 1995. PMID: 8572257
Regional mapping of the gene for familial Mediterranean fever on human chromosome 16p13.
Fischel-Ghodsian N, Bu X, Prezant TR, Oeztas S, Huang ZS, Bohlman MC, Rotter JI, Shohat M. Fischel-Ghodsian N, et al. Am J Med Genet. 1993 Jul 1;46(6):689-93. doi: 10.1002/ajmg.1320460619. Am J Med Genet. 1993. PMID: 8362911
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
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. 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. Pediatr Res. 1992 Jun;31(6):557-60. doi: 10.1203/00006450-199206000-00004. Pediatr Res. 1992. PMID: 1635816
Identification of an overexpressed yeast gene which prevents aminoglycoside toxicity.
Prezant TR, Chaltraw WE Jr, Fischel-Ghodsian N. Prezant TR, et al. Microbiology (Reading). 1996 Dec;142 ( Pt 12):3407-14. doi: 10.1099/13500872-142-12-3407. Microbiology (Reading). 1996. PMID: 9004503
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