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Eduard Orvisky

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Orvisky Eduard; Drake Steven K; Martin Brian M; Abdel-Hamid Mohamed; Ressom Habtom W; Varghese Rency S; An Yanming; Saha Daniel; Hortin Glen L; Loffredo Christopher A; Goldman Radoslav
Enrichment of low molecular weight fraction of serum for MS analysis of peptides associated with hepatocellular carcinoma.
Ressom Habtom W; Varghese Rency S; Orvisky Eduard; Drake Steven K; Hortin Glen L; Abdel-Hamid Mohamed; Loffredo Christopher A; Goldman Radoslav
Ant colony optimization for biomarker identification from MALDI-TOF mass spectra.
Sparks Susan E; Ciccone Carla; Lalor Molly; Orvisky Eduard; Klootwijk Riko; Savelkoul Paul J; Dalakas Marinos C; Krasnewich Donna M; Gahl William A; Huizing Marjan
Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.

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All Publications

2006: Orvisky Eduard; Drake Steven K; Martin Brian M; Abdel-Hamid Mohamed; Ressom Habtom W; Varghese Rency S; An Yanming; Saha Daniel; Hortin Glen L; Loffredo Christopher A; Goldman Radoslav
Enrichment of low molecular weight fraction of serum for MS analysis of peptides associated with hepatocellular carcinoma.
Proteomics 2006;6(9):2895-902.
2006: Ressom Habtom W; Varghese Rency S; Orvisky Eduard; Drake Steven K; Hortin Glen L; Abdel-Hamid Mohamed; Loffredo Christopher A; Goldman Radoslav
Ant colony optimization for biomarker identification from MALDI-TOF mass spectra.
Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Conference 2006;1():4560-3.
2005: Sparks Susan E; Ciccone Carla; Lalor Molly; Orvisky Eduard; Klootwijk Riko; Savelkoul Paul J; Dalakas Marinos C; Krasnewich Donna M; Gahl William A; Huizing Marjan
Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy.
Glycobiology 2005;15(11):1102-10.
2005: Goker-Alpan O; Hruska K S; Orvisky E; Kishnani P S; Stubblefield B K; Schiffmann R; Sidransky E
Divergent phenotypes in Gaucher disease implicate the role of modifiers.
Journal of medical genetics 2005;42(6):e37.
2004: Kleta Robert; Morse Richard P; Orvisky Eduard; Krasnewich Donna; Alroy Joseph; Ucci Angelo A; Bernardini Isa; Wenger David A; Gahl William A
Clinical, biochemical, and molecular diagnosis of a free sialic acid storage disease patient of moderate severity.
Molecular genetics and metabolism 2004;82(2):137-43.
2004: Lwin Alicia; Orvisky Eduard; Goker-Alpan Ozlem; LaMarca Mary E; Sidransky Ellen
Glucocerebrosidase mutations in subjects with parkinsonism.
Molecular genetics and metabolism 2004;81(1):70-3.
2003: Kleta Robert; Aughton David J; Rivkin Michael J; Huizing Marjan; Strovel Erin; Anikster Yair; Orvisky Eduard; Natowicz Marvin; Krasnewich Donna; Gahl William A
Biochemical and molecular analyses of infantile free sialic acid storage disease in North American children.
American journal of medical genetics. Part A 2003;120A(1):28-33.
2003: Martin Rick A; Slaugh Rachel; Natowicz Marvin; Pearlman Kayla; Orvisky Eduard; Krasnewich Donna; Kleta Robert; Huizing Marjan; Gahl William A
Sialic acid storage disease of the Salla phenotype in American monozygous twin female sibs.
American journal of medical genetics. Part A 2003;120A(1):23-7.
2003: Tayebi N; Walker J; Stubblefield B; Orvisky E; LaMarca M E; Wong K; Rosenbaum H; Schiffmann R; Bembi B; Sidransky E
Gaucher disease with parkinsonian manifestations: does glucocerebrosidase deficiency contribute to a vulnerability to parkinsonism?
Molecular genetics and metabolism 2003;79(2):104-9.
2003: Orvisky E; Stubblefield B; Long R T; Martin B M; Sidransky E; Krasnewich D
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.
Analytical biochemistry 2003;317(1):12-8.
2003: Walker J M; Lwin A; Tayebi N; LaMarca M E; Orvisky E; Sidransky E
Glucocerebrosidase mutation T369M appears to be another polymorphism.
Clinical genetics 2003;63(3):237-8.
2003: Park Joseph K; Orvisky Eduard; Tayebi Nahid; Kaneski Christine; Lamarca Mary E; Stubblefield Barbara K; Martin Brian M; Schiffmann Raphael; Sidransky Ellen
Myoclonic epilepsy in Gaucher disease: genotype-phenotype insights from a rare patient subgroup.
Pediatric research 2003;53(3):387-95.
2003: Tayebi Nahid; Stubblefield Barbara K; Park Joseph K; Orvisky Eduard; Walker Jamie M; LaMarca Mary E; Sidransky Ellen
Reciprocal and nonreciprocal recombination at the glucocerebrosidase gene region: implications for complexity in Gaucher disease.
American journal of human genetics 2003;72(3):519-34.
2002: Orvisky Eduard; Park Joseph K; LaMarca Mary E; Ginns Edward I; Martin Brian M; Tayebi Nahid; Sidransky Ellen
Glucosylsphingosine accumulation in tissues from patients with Gaucher disease: correlation with phenotype and genotype.
Molecular genetics and metabolism 2002;76(4):262-70.
2002: Orvisky E; Park J K; Parker A; Walker J M; Martin B M; Stubblefield B K; Uyama E; Tayebi N; Sidransky E
The identification of eight novel glucocerebrosidase (GBA) mutations in patients with Gaucher disease.
Human mutation 2002;19(4):458-9.
2002: Tayebi Nahid; Andrews David Q; Park Joseph K; Orvisky Eduard; McReynolds John; Sidransky Ellen; Krasnewich Donna M
A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia.
American journal of medical genetics 2002;108(3):241-6.
2001: Tayebi N; Callahan M; Madike V; Stubblefield B K; Orvisky E; Krasnewich D; Fillano J J; Sidransky E
Gaucher disease and parkinsonism: a phenotypic and genotypic characterization.
Molecular genetics and metabolism 2001;73(4):313-21.
2001: Leroy J G; Seppala R; Huizing M; Dacremont G; De Simpel H; Van Coster R N; Orvisky E; Krasnewich D M; Gahl W A
Dominant inheritance of sialuria, an inborn error of feedback inhibition.
American journal of human genetics 2001;68(6):1419-27.
2000: Orvisky E; Sidransky E; McKinney C E; Lamarca M E; Samimi R; Krasnewich D; Martin B M; Ginns E I
Glucosylsphingosine accumulation in mice and patients with type 2 Gaucher disease begins early in gestation.
Pediatric research 2000;48(2):233-7.
2000: Stone D L; Tayebi N; Orvisky E; Stubblefield B; Madike V; Sidransky E
Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease.
Human mutation 2000;15(2):181-8.
1998: Thatcher B J; Doherty A E; Orvisky E; Martin B M; Henkin R I
Gustin from human parotid saliva is carbonic anhydrase VI.
Biochemical and biophysical research communications 1998;250(3):635-41.

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Eduard Orvisky

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