Pass K - Search Results

1

Decline in perinatal HIV transmission in New York State (1997-2000).

Wade NA, Zielinski MA, Butsashvili M, McNutt LA, Warren BL, Glaros R, Cheku B, Pulver W, Pass K, Fox K, Novello AC, Birkhead GS. Wade NA, et al. Among authors: pass k. J Acquir Immune Defic Syndr. 2004 Aug 15;36(5):1075-82. doi: 10.1097/00126334-200408150-00011. J Acquir Immune Defic Syndr. 2004. PMID: 15247561

2

Consented testing of newborns and childbearing women for human immunodeficiency virus through a newborn metabolic screening program.

Birkhead GS, Chang HG, Smith PF, Warren BL, Glaros R, Pass KA, DeBuono BA. Birkhead GS, et al. Among authors: pass ka. Am J Obstet Gynecol. 2000 Jul;183(1):245-51. doi: 10.1067/mob.2000.105937. Am J Obstet Gynecol. 2000. PMID: 10920339

3

Plasma and cellular markers of 3'-azido-3'-dideoxythymidine (AZT) metabolism as indicators of DNA damage in cord blood mononuclear cells from infants receiving prepartum NRTIs.

Meng Q, Olivero OA, Fasco MJ, Bellisario R, Kaminsky L, Pass KA, Wade NA, Abrams EJ, Nesel CJ, Ness RB, Bigbee WL, O'Neill JP, Walker DM, Poirier MC, Walker VE. Meng Q, et al. Environ Mol Mutagen. 2007 Apr-May;48(3-4):307-21. doi: 10.1002/em.20298. Environ Mol Mutagen. 2007. PMID: 17358024 Clinical Trial.

4

HIV seroprevalence in newborns in New York State.

Novick LF, Berns D, Stricof R, Stevens R, Pass K, Wethers J. Novick LF, et al. Among authors: pass k. JAMA. 1989 Mar 24-31;261(12):1745-50. JAMA. 1989. PMID: 2918672

5

Increase in congenital hypothyroidism in New York State and in the United States.

Harris KB, Pass KA. Harris KB, et al. Mol Genet Metab. 2007 Jul;91(3):268-77. doi: 10.1016/j.ymgme.2007.03.012. Epub 2007 May 23. Mol Genet Metab. 2007. PMID: 17512233

6

Use of newborn screening program blood spots for exposure assessment: declining levels of perluorinated compounds in New York State infants.

Spliethoff HM, Tao L, Shaver SM, Aldous KM, Pass KA, Kannan K, Eadon GA. Spliethoff HM, et al. Among authors: pass ka. Environ Sci Technol. 2008 Jul 15;42(14):5361-7. doi: 10.1021/es8006244. Environ Sci Technol. 2008. PMID: 18754394

7

Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: under-representation of the common c.985 A > G mutation in the New York state population.

Nichols MJ, Saavedra-Matiz CA, Pass KA, Caggana M. Nichols MJ, et al. Am J Med Genet A. 2008 Mar 1;146A(5):610-9. doi: 10.1002/ajmg.a.32192. Am J Med Genet A. 2008. PMID: 18241067

8

The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects.

Fitzgerald T, Duva S, Ostrer H, Pass K, Oddoux C, Ruben R, Caggana M. Fitzgerald T, et al. Among authors: pass k. Clin Genet. 2004 Apr;65(4):338-42. doi: 10.1111/j.1399-0004.2004.00233.x. Clin Genet. 2004. PMID: 15025729

9

Multivariate discrimination for phenylketonuria (PKU) and non-PKU hyperphenylalaninemia after analysis of newborns' dried blood-spot specimens for six amino acids by ion-exchange chromatography.

Reilly AA, Bellisario R, Pass KA. Reilly AA, et al. Among authors: pass ka. Clin Chem. 1998 Feb;44(2):317-26. Clin Chem. 1998. PMID: 9474031

10

How reliable is newborn screening for congenital adrenal hyperplasia?

Pass KA. Pass KA. Nat Clin Pract Endocrinol Metab. 2006 Feb;2(2):74-5. doi: 10.1038/ncpendmet0095. Nat Clin Pract Endocrinol Metab. 2006. PMID: 16932259 No abstract available.

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