Alglucosidase alfa enzyme replacement therapy as a therapeutic approach for glycogen storage disease type III

Molecular Genetics and Metabolism ◽

10.1016/j.ymgme.2012.12.002 ◽

2013 ◽

Vol 108 (2) ◽

pp. 145-147 ◽

Author(s):

Baodong Sun ◽

Keri Fredrickson ◽

Stephanie Austin ◽

Adviye A. Tolun ◽

Beth L. Thurberg ◽

...

Keyword(s):

Enzyme Replacement Therapy ◽

Replacement Therapy ◽

Glycogen Storage Disease ◽

Therapeutic Approach ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Enzyme Replacement ◽

Alglucosidase Alfa

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Faculty Opinions recommendation of Alglucosidase alfa enzyme replacement therapy as a therapeutic approach for glycogen storage disease type III.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.717982893.793471770 ◽

2013 ◽

Author(s):

Janice Fletcher ◽

Shanti Balasubramaniam

Keyword(s):

Enzyme Replacement Therapy ◽

Replacement Therapy ◽

Glycogen Storage Disease ◽

Therapeutic Approach ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Enzyme Replacement ◽

Alglucosidase Alfa

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Glycogen storage disease type II (Pompe disease) - influence of enzyme replacement therapy in adults

European Journal of Neurology ◽

10.1111/j.1468-1331.2008.02377.x ◽

2009 ◽

Vol 16 (2) ◽

pp. 274-277 ◽

Author(s):

T. Merk ◽

T. Wibmer ◽

C. Schumann ◽

S. Krüger

Keyword(s):

Enzyme Replacement Therapy ◽

Replacement Therapy ◽

Glycogen Storage Disease ◽

Pompe Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Enzyme Replacement

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Enzyme replacement therapy in severe adult-onset glycogen storage disease type II

Advances in Therapy ◽

10.1007/s12325-008-0086-y ◽

2008 ◽

Vol 25 (8) ◽

pp. 820-829 ◽

Author(s):

Sabrina Ravaglia ◽

Cesare Danesino ◽

Anna Pichiecchio ◽

Alessandra Repetto ◽

Guy Umberto Poloni ◽

...

Keyword(s):

Enzyme Replacement Therapy ◽

Replacement Therapy ◽

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Adult Onset ◽

Enzyme Replacement

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Progress in enzyme replacement therapy in glycogen storage disease type II

Therapeutic Advances in Neurological Disorders ◽

10.1177/1756285609103324 ◽

2009 ◽

Vol 2 (3) ◽

pp. 143-153 ◽

Author(s):

Corrado Angelini ◽

Claudio Semplicini ◽

Paola Tonin ◽

Massimiliano Filosto ◽

Elena Pegoraro ◽

...

Keyword(s):

Enzyme Replacement Therapy ◽

Replacement Therapy ◽

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Enzyme Replacement

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Enzyme replacement therapy with alglucosidase alfa in 44 patients with late-onset glycogen storage disease type 2: 12-month results of an observational clinical trial

Journal of Neurology ◽

10.1007/s00415-009-5275-3 ◽

2009 ◽

Vol 257 (1) ◽

pp. 91-97 ◽

Author(s):

S. Strothotte ◽

N. Strigl-Pill ◽

B. Grunert ◽

C. Kornblum ◽

K. Eger ◽

...

Keyword(s):

Clinical Trial ◽

Enzyme Replacement Therapy ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Enzyme Replacement ◽

Alglucosidase Alfa

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Exercise testing in late-onset glycogen storage disease type II patients undergoing enzyme replacement therapy

Neuromuscular Disorders ◽

10.1016/j.nmd.2012.10.017 ◽

2012 ◽

Vol 22 ◽

pp. S230-S234 ◽

Author(s):

Mauro Marzorati ◽

Simone Porcelli ◽

Giuseppe Bellistri ◽

Lucia Morandi ◽

Bruno Grassi

Keyword(s):

Enzyme Replacement Therapy ◽

Replacement Therapy ◽

Exercise Testing ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Enzyme Replacement

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Pregnancy and associated events in women receiving enzyme replacement therapy for late-onset glycogen storage disease type II (Pompe disease)

Journal of Obstetrics and Gynaecology Research ◽

10.1111/jog.13055 ◽

2016 ◽

Vol 42 (10) ◽

pp. 1263-1271 ◽

Author(s):

Philippa J. Rohman ◽

Elaine Scott ◽

Linda Richfield ◽

Uma Ramaswami ◽

Derralynn A. Hughes

Keyword(s):

Enzyme Replacement Therapy ◽

Replacement Therapy ◽

Pompe Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Enzyme Replacement

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Impaired autophagy affects acid α-glucosidase processing and enzyme replacement therapy efficacy in late-onset glycogen storage disease type II

Neuropathology and Applied Neurobiology ◽

10.1111/nan.12214 ◽

2015 ◽

Vol 41 (5) ◽

pp. 672-675 ◽

Author(s):

Anna Chiara Nascimbeni ◽

Marina Fanin ◽

Elisabetta Tasca ◽

Corrado Angelini ◽

Marco Sandri

Keyword(s):

Enzyme Replacement Therapy ◽

Replacement Therapy ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Enzyme Replacement ◽

Therapy Efficacy

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Alglucosidase alfa effectively improves functional aspects of late-onset glycogen storage disease type II

Inpharma Weekly ◽

10.2165/00128413-200816190-00039 ◽

2008 ◽

Vol &NA; (1619) ◽

pp. 15

Author(s):

&NA;

Keyword(s):

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Ii ◽

Functional Aspects ◽

Alglucosidase Alfa

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Alglucosidase alfa treatment alleviates liver disease in a mouse model of glycogen storage disease type IV

Molecular Genetics and Metabolism Reports ◽

10.1016/j.ymgmr.2016.09.008 ◽

2016 ◽

Vol 9 ◽

pp. 31-33 ◽

Author(s):

Haiqing Yi ◽

Fengqin Gao ◽

Stephanie Austin ◽

Priya S Kishnani ◽

Baodong Sun

Keyword(s):

Liver Disease ◽

Mouse Model ◽

Glycogen Storage Disease ◽

Storage Disease ◽

Glycogen Storage Disease Type ◽

Glycogen Storage ◽

Disease Type ◽

Type Iv ◽

Alglucosidase Alfa

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