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Items: 27

1.

Revisiting the prevalence of nonclassic congenital adrenal hyperplasia in US Ashkenazi Jews and Caucasians.

Hannah-Shmouni F, Morissette R, Sinaii N, Elman M, Prezant TR, Chen W, Pulver A, Merke DP.

Genet Med. 2017 Nov;19(11):1276-1279. doi: 10.1038/gim.2017.46. Epub 2017 May 25.

2.

Combined cyclic vomiting and Kearns-Sayre syndromes.

Boles RG, Baldwin EE, Prezant TR.

Pediatr Neurol. 2007 Feb;36(2):135-6.

PMID:
17275670
3.

Isolated familial somatotropinomas: clinical features and analysis of the MEN1 gene.

De Menis E, Prezant TR.

Pituitary. 2002 Jan;5(1):11-5.

PMID:
12638720
4.

PRKAR1A, one of the Carney complex genes, and its locus (17q22-24) are rarely altered in pituitary tumours outside the Carney complex.

Sandrini F, Kirschner LS, Bei T, Farmakidis C, Yasufuku-Takano J, Takano K, Prezant TR, Marx SJ, Farrell WE, Clayton RN, Groussin L, Bertherat J, Stratakis CA.

J Med Genet. 2002 Dec;39(12):e78. No abstract available.

5.

Long-acting peptidomimergic control of gigantism caused by pituitary acidophilic stem cell adenoma.

Maheshwari HG, Prezant TR, Herman-Bonert V, Shahinian H, Kovacs K, Melmed S.

J Clin Endocrinol Metab. 2000 Sep;85(9):3409-16.

PMID:
10999842
6.

An intronless homolog of human proto-oncogene hPTTG is expressed in pituitary tumors: evidence for hPTTG family.

Prezant TR, Kadioglu P, Melmed S.

J Clin Endocrinol Metab. 1999 Mar;84(3):1149-52.

PMID:
10084610
7.

Pituitary tumor transforming gene (PTTG) expression in pituitary adenomas.

Zhang X, Horwitz GA, Heaney AP, Nakashima M, Prezant TR, Bronstein MD, Melmed S.

J Clin Endocrinol Metab. 1999 Feb;84(2):761-7.

PMID:
10022450
8.

Loss of heterozygosity on chromosome 11q13 in two families with acromegaly/gigantism is independent of mutations of the multiple endocrine neoplasia type I gene.

Gadelha MR, Prezant TR, Une KN, Glick RP, Moskal SF 2nd, Vaisman M, Melmed S, Kineman RD, Frohman LA.

J Clin Endocrinol Metab. 1999 Jan;84(1):249-56.

PMID:
9920092
9.

Structure, expression, and function of human pituitary tumor-transforming gene (PTTG).

Zhang X, Horwitz GA, Prezant TR, Valentini A, Nakashima M, Bronstein MD, Melmed S.

Mol Endocrinol. 1999 Jan;13(1):156-66.

PMID:
9892021
10.

Isolation of overexpressed yeast genes which prevent aminoglycoside toxicity.

Johnson DF, Prezant TR, Lubavin B, Chaltraw WE, Fischel-Ghodsian N.

Hear Res. 1998 Jun;120(1-2):62-8.

PMID:
9667431
11.

Molecular characterization of the men1 tumor suppressor gene in sporadic pituitary tumors.

Prezant TR, Levine J, Melmed S.

J Clin Endocrinol Metab. 1998 Apr;83(4):1388-91.

PMID:
9543172
12.

Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity.

Fischel-Ghodsian N, Prezant TR, Chaltraw WE, Wendt KA, Nelson RA, Arnos KS, Falk RE.

Am J Otolaryngol. 1997 May-Jun;18(3):173-8.

PMID:
9164619
13.

Identification of an overexpressed yeast gene which prevents aminoglycoside toxicity.

Prezant TR, Chaltraw WE Jr, Fischel-Ghodsian N.

Microbiology. 1996 Dec;142 ( Pt 12):3407-14.

PMID:
9004503
14.

Mitochondrial mutation associated with nonsyndromic deafness.

Fischel-Ghodsian N, Prezant TR, Fournier P, Stewart IA, Maw M.

Am J Otolaryngol. 1995 Nov-Dec;16(6):403-8.

PMID:
8572257
15.

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

Bacino C, Prezant TR, Bu X, Fournier P, Fischel-Ghodsian N.

Pharmacogenetics. 1995 Jun;5(3):165-72.

PMID:
7550368
16.

Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literature.

Bacino CA, Schreck R, Fischel-Ghodsian N, Pepkowitz S, Prezant TR, Graham JM Jr.

Am J Med Genet. 1995 May 8;56(4):359-65. Review.

PMID:
7604844
17.

Screening for mtDNA diabetes mutations in Pima Indians with NIDDM.

Sepehrnia B, Prezant TR, Rotter JI, Pettitt DJ, Knowler WC, Fischel-Ghodsian N.

Am J Med Genet. 1995 Mar 27;56(2):198-202.

PMID:
7625445
18.

Corrections to the human mitochondrial ribosomal RNA sequences.

Prezant TR, Agapian JV, Fischel-Ghodsian N.

Hum Genet. 1994 Jan;93(1):87-8.

PMID:
8270263
19.

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

Fischel-Ghodsian N, Prezant TR, Bu X, Oztas S.

Am J Otolaryngol. 1993 Nov-Dec;14(6):399-403.

PMID:
8285309
20.

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.

J Pediatr. 1993 Oct;123(4):598-602.

PMID:
8410517
21.

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.

Am J Med Genet. 1993 Jul 1;46(6):689-93.

PMID:
8362911
22.

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.

Nat Genet. 1993 Jul;4(3):289-94.

PMID:
7689389
23.

Deletion in blood mitochondrial DNA in Kearns-Sayre syndrome.

Fischel-Ghodsian N, Bohlman MC, Prezant TR, Graham JM Jr, Cederbaum SD, Edwards MJ.

Pediatr Res. 1992 Jun;31(6):557-60.

PMID:
1635816
24.
25.

Expression of human lysosomal beta-hexosaminidase in yeast vacuoles.

Prezant TR.

Biochem Biophys Res Commun. 1990 Jul 16;170(1):383-90.

PMID:
2142595
26.
27.

Yeast HAP1 activator binds to two upstream activation sites of different sequence.

Pfeifer K, Prezant T, Guarente L.

Cell. 1987 Apr 10;49(1):19-27.

PMID:
3030565

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