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Glycoengineered Acid α-Glucosidase With Improved Efficacy at Correcting the Metabolic Aberrations and Motor Function Deficits in a Mouse Model of Pompe Disease

Molecular therapy, 2009-06, Vol.17 (6), p.954-963

2009

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104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07)

Journal of neurology, 2024-05, Vol.271 (5), p.2810-2823

2024

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Inhibition mechanism of ferulic acid against α-amylase and α-glucosidase

Food chemistry, 2020-07, Vol.317, p.126346-126346, Article 126346

2020

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A Randomized Study of Alglucosidase Alfa in Late-Onset Pompe's Disease

The New England journal of medicine, 2010-04, Vol.362 (15), p.1396-1406

2010

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An overview on the role of bioactive α-glucosidase inhibitors in ameliorating diabetic complications

Food and chemical toxicology, 2020-11, Vol.145, p.111738-111738, Article 111738

2020

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Enzyme replacement therapy for infantile-onset Pompe disease

Cochrane database of systematic reviews, 2017-11, Vol.11 (12), p.CD011539

2017

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Inhibition of α-glucosidase and α-amylase by Spanish extra virgin olive oils: The involvement of bioactive compounds other than oleuropein and hydroxytyrosol

Food chemistry, 2017-11, Vol.235, p.298-307

2017

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Galangin inhibits α-glucosidase activity and formation of non-enzymatic glycation products

Food chemistry, 2019-01, Vol.271, p.70-79

2019

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Identification and characterization of novel transglycosylating α‐glucosidase from Aspergillus neoniger

Journal of applied microbiology, 2020-12, Vol.129 (6), p.1644-1656

2020

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Immunodominant liver-specific expression suppresses transgene-directed immune responses in murine pompe disease

Human gene therapy, 2012-05, Vol.23 (5), p.460

2012

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Insight into the glycosylation and hydrolysis kinetics of alpha-glucosidase in the synthesis of glycosides

Applied microbiology and biotechnology, 2019-12, Vol.103 (23-24), p.9423-9432

2019

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Response to Comments on "Increasing Enzyme Mannose-6-Phosphate Levels but Not Miglustat Coadministration Enhances the Efficacy of Enzyme Replacement Therapy in Pompe Mice"

The Journal of pharmacology and experimental therapeutics, 2024-05, Vol.389 (3), p.313-314

2024

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Efficient therapy for refractory Pompe disease by mannose 6-phosphate analogue grafting on acid α-glucosidase

Journal of controlled release, 2018-01, Vol.269, p.15-23

2018

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Inhibitory kinetics and mechanism of kaempferol on α-glucosidase

Food chemistry, 2016-01, Vol.190, p.207-215

2016

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Characterization of novel thermophilic alpha-glucosidase from Bifidobacterium longum

International journal of biological macromolecules, 2017-06, Vol.99, p.594-599

2017

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5‑C‑Branched Deoxynojirimycin: Strategy for Designing a 1‑Deoxynojirimycin-Based Pharmacological Chaperone with a Nanomolar Affinity for Pompe Disease

Journal of medicinal chemistry, 2022-02, Vol.65 (3), p.2329-2341

2022

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Comparative study of inhibition mechanisms of structurally different flavonoid compounds on α-glucosidase and synergistic effect with acarbose

Food chemistry, 2021-06, Vol.347, p.129056, Article 129056

2021

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Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in Austria

The Lancet (British edition), 2012-01, Vol.379 (9813), p.335-341

2012

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Enzyme therapy and immune response in relation to CRIM status: the Dutch experience in classic infantile Pompe disease

Journal of inherited metabolic disease, 2015-03, Vol.38 (2), p.305-314

2015

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C-glucosidic ellagitannins and galloylated glucoses as potential functional food ingredients with anti-diabetic properties: a study of α-glucosidase and α-amylase inhibition

Food chemistry, 2020-05, Vol.313, p.126099-126099, Article 126099

2020

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Pompe disease in adulthood: effects of antibody formation on enzyme replacement therapy

Genetics in medicine, 2017-01, Vol.19 (1), p.90-97

2017

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Biochemical properties and substrate recognition mechanism of GH31 α-glucosidase from Bacillus sp. AHU 2001 with broad substrate specificity

Biochimie, 2015-01, Vol.108, p.140-148

2015

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Dynamical origins of heat capacity changes in enzyme-catalysed reactions

Nature communications, 2018-03, Vol.9 (1), p.1177-7, Article 1177

2018

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Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness

Neurology, 2016-07, Vol.87 (3), p.295-298

2016

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Characterization of selenized polysaccharides from Ribes nigrum L. and its inhibitory effects on α-amylase and α-glucosidase

Carbohydrate polymers, 2021-05, Vol.259, p.117729-117729, Article 117729

2021

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Glycoengineered Acid α-Glucosidase With Improved Efficacy at Correcting the Metabolic Aberrations and Motor Function Deficits in a Mouse Model of Pompe Disease

104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07)

Inhibition mechanism of ferulic acid against α-amylase and α-glucosidase

A Randomized Study of Alglucosidase Alfa in Late-Onset Pompe's Disease

An overview on the role of bioactive α-glucosidase inhibitors in ameliorating diabetic complications

Enzyme replacement therapy for infantile-onset Pompe disease

Inhibition of α-glucosidase and α-amylase by Spanish extra virgin olive oils: The involvement of bioactive compounds other than oleuropein and hydroxytyrosol

Galangin inhibits α-glucosidase activity and formation of non-enzymatic glycation products

Identification and characterization of novel transglycosylating α‐glucosidase from Aspergillus neoniger

Immunodominant liver-specific expression suppresses transgene-directed immune responses in murine pompe disease

Insight into the glycosylation and hydrolysis kinetics of alpha-glucosidase in the synthesis of glycosides

Response to Comments on "Increasing Enzyme Mannose-6-Phosphate Levels but Not Miglustat Coadministration Enhances the Efficacy of Enzyme Replacement Therapy in Pompe Mice"

Efficient therapy for refractory Pompe disease by mannose 6-phosphate analogue grafting on acid α-glucosidase

Inhibitory kinetics and mechanism of kaempferol on α-glucosidase

Characterization of novel thermophilic alpha-glucosidase from Bifidobacterium longum

5‑C‑Branched Deoxynojirimycin: Strategy for Designing a 1‑Deoxynojirimycin-Based Pharmacological Chaperone with a Nanomolar Affinity for Pompe Disease

Comparative study of inhibition mechanisms of structurally different flavonoid compounds on α-glucosidase and synergistic effect with acarbose

Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in Austria

Enzyme therapy and immune response in relation to CRIM status: the Dutch experience in classic infantile Pompe disease

C-glucosidic ellagitannins and galloylated glucoses as potential functional food ingredients with anti-diabetic properties: a study of α-glucosidase and α-amylase inhibition

Pompe disease in adulthood: effects of antibody formation on enzyme replacement therapy

Biochemical properties and substrate recognition mechanism of GH31 α-glucosidase from Bacillus sp. AHU 2001 with broad substrate specificity

Dynamical origins of heat capacity changes in enzyme-catalysed reactions

Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness

Characterization of selenized polysaccharides from Ribes nigrum L. and its inhibitory effects on α-amylase and α-glucosidase

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