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Demonstrating the Stability of Albinterferon Alfa-2b in the Presence of Silicone Oil

Journal of pharmaceutical sciences, 2011-12, Vol.100 (12), p.5100-5114

2011

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Reciprocal and Nonreciprocal Recombination at the Glucocerebrosidase Gene Region: Implications for Complexity in Gaucher Disease

American journal of human genetics, 2003-03, Vol.72 (3), p.519-534

2003

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

Pediatric research, 2003-03, Vol.53 (3), p.387-395

2003

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Glucocerebrosidase mutations in subjects with parkinsonism

Molecular genetics and metabolism, 2004, Vol.81 (1), p.70-73

2004

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

Proteomics (Weinheim), 2006-05, Vol.6 (9), p.2895-2902

2006

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Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease

Human mutation, 2000-02, Vol.15 (2), p.181-188

2000

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

Molecular genetics and metabolism, 2002-08, Vol.76 (4), p.262-270

2002

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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 (Oxford), 2005-11, Vol.15 (11), p.1102-1110

2005

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Clinical, biochemical, and molecular diagnosis of a free sialic acid storage disease patient of moderate severity

Molecular genetics and metabolism, 2004-06, Vol.82 (2), p.137-143

2004

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Biochemical and molecular analyses of infantile free sialic acid storage disease in North American children

American journal of medical genetics, 2003-07, Vol.120A (1), p.28-33

2003

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Sialic acid storage disease of the Salla phenotype in American monozygous twin female sibs

American journal of medical genetics, 2003-07, Vol.120A (1), p.23-27

2003

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Comparative depolymerization of sodium hyaluronate by ultrasonic and enzymatic treatments

Journal of applied polymer science, 1991, Vol.48, p.233-241

1991

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Ant Colony Optimization for Biomarker Identification from MALDI-TOF Mass Spectra

2006 International Conference of the IEEE Engineering in Medicine and Biology Society, 2006, Vol.2006, p.4560-4563

2006

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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, 2002-03, Vol.108 (3), p.241-246

2002

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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, Vol.108 (3), p.241-246

2002

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Microplate Assay for Hyaluronan Useful in Clinical Practice

Collection of Czechoslovak chemical communications, 1994-10, Vol.59 (10), p.2331-2342

1994

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Rapid determination of immobilized ConA lectin activity

Applied biochemistry and biotechnology, 1992, Vol.32 (1-3), p.127-134

1992

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Preparation and Characterization of the High Molecular Weight [3H]Hyaluronic Acid

Collection of Czechoslovak chemical communications, 1992-10, Vol.57 (10), p.2151-2156

1992

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Demonstrating the Stability of Albinterferon Alfa-2b in the Presence of Silicone Oil

Reciprocal and Nonreciprocal Recombination at the Glucocerebrosidase Gene Region: Implications for Complexity in Gaucher Disease

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

Glucocerebrosidase mutations in subjects with parkinsonism

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

Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease

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

Use of a cell-free system to determine UDP-N-acetylglucosamine 2-epimerase and N-acetylmannosamine kinase activities in human hereditary inclusion body myopathy

Clinical, biochemical, and molecular diagnosis of a free sialic acid storage disease patient of moderate severity

Biochemical and molecular analyses of infantile free sialic acid storage disease in North American children

Sialic acid storage disease of the Salla phenotype in American monozygous twin female sibs

Comparative depolymerization of sodium hyaluronate by ultrasonic and enzymatic treatments

Ant Colony Optimization for Biomarker Identification from MALDI-TOF Mass Spectra

A deletion–insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation‐Ia

A deletion-insertion mutation in the phosphomannomutase 2 gene in an African American patient with congenital disorders of glycosylation-Ia

Microplate Assay for Hyaluronan Useful in Clinical Practice

Rapid determination of immobilized ConA lectin activity

Preparation and Characterization of the High Molecular Weight [3H]Hyaluronic Acid

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