Orvisky E - Search Results

1

Enrichment of low molecular weight fraction of serum for MS analysis of peptides associated with hepatocellular carcinoma.

Orvisky E, Drake SK, Martin BM, Abdel-Hamid M, Ressom HW, Varghese RS, An Y, Saha D, Hortin GL, Loffredo CA, Goldman R. Orvisky E, et al. Proteomics. 2006 May;6(9):2895-902. doi: 10.1002/pmic.200500443. Proteomics. 2006. PMID: 16586431

2

Ant colony optimization for biomarker identification from MALDI-TOF mass spectra.

Ressom HW, Varghese RS, Orvisky E, Drake SK, Hortin GL, Abdel-Hamid M, Loffredo CA, Goldman R. Ressom HW, et al. Among authors: orvisky e. Conf Proc IEEE Eng Med Biol Soc. 2006;2006:4560-3. doi: 10.1109/IEMBS.2006.260707. Conf Proc IEEE Eng Med Biol Soc. 2006. PMID: 17946638

3

Gustin from human parotid saliva is carbonic anhydrase VI.

Thatcher BJ, Doherty AE, Orvisky E, Martin BM, Henkin RI. Thatcher BJ, et al. Among authors: orvisky e. Biochem Biophys Res Commun. 1998 Sep 29;250(3):635-41. doi: 10.1006/bbrc.1998.9356. Biochem Biophys Res Commun. 1998. PMID: 9784398

4

Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: correlation with phenotype and genotype.

Orvisky E, Park JK, LaMarca ME, Ginns EI, Martin BM, Tayebi N, Sidransky E. Orvisky E, et al. Mol Genet Metab. 2002 Aug;76(4):262-70. doi: 10.1016/s1096-7192(02)00117-8. Mol Genet Metab. 2002. PMID: 12208131

5

Phosphomannomutase activity in congenital disorders of glycosylation type Ia determined by direct analysis of the interconversion of mannose-1-phosphate to mannose-6-phosphate by high-pH anion-exchange chromatography with pulsed amperometric detection.

Orvisky E, Stubblefield B, Long RT, Martin BM, Sidransky E, Krasnewich D. Orvisky E, et al. Anal Biochem. 2003 Jun 1;317(1):12-8. doi: 10.1016/s0003-2697(03)00109-x. Anal Biochem. 2003. PMID: 12729595

6

Myoclonic epilepsy in Gaucher disease: genotype-phenotype insights from a rare patient subgroup.

Park JK, Orvisky E, Tayebi N, Kaneski C, Lamarca ME, Stubblefield BK, Martin BM, Schiffmann R, Sidransky E. Park JK, et al. Among authors: orvisky e. Pediatr Res. 2003 Mar;53(3):387-95. doi: 10.1203/01.PDR.0000049515.79882.94. Pediatr Res. 2003. PMID: 12595585

7

The identification of eight novel glucocerebrosidase (GBA) mutations in patients with Gaucher disease.

Orvisky E, Park JK, Parker A, Walker JM, Martin BM, Stubblefield BK, Uyama E, Tayebi N, Sidransky E. Orvisky E, et al. Hum Mutat. 2002 Apr;19(4):458-9. doi: 10.1002/humu.9024. Hum Mutat. 2002. PMID: 11933202

8

Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestation.

Orvisky E, Sidransky E, McKinney CE, Lamarca ME, Samimi R, Krasnewich D, Martin BM, Ginns EI. Orvisky E, et al. Pediatr Res. 2000 Aug;48(2):233-7. doi: 10.1203/00006450-200008000-00018. Pediatr Res. 2000. PMID: 10926300

9

Reciprocal and nonreciprocal recombination at the glucocerebrosidase gene region: implications for complexity in Gaucher disease.

Tayebi N, Stubblefield BK, Park JK, Orvisky E, Walker JM, LaMarca ME, Sidransky E. Tayebi N, et al. Among authors: orvisky e. Am J Hum Genet. 2003 Mar;72(3):519-34. doi: 10.1086/367850. Epub 2003 Feb 13. Am J Hum Genet. 2003. PMID: 12587096 Free PMC article.

10

Glucocerebrosidase mutations in subjects with parkinsonism.

Lwin A, Orvisky E, Goker-Alpan O, LaMarca ME, Sidransky E. Lwin A, et al. Among authors: orvisky e. Mol Genet Metab. 2004 Jan;81(1):70-3. doi: 10.1016/j.ymgme.2003.11.004. Mol Genet Metab. 2004. PMID: 14728994

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