(Q42670886)

4 November 2017

title

Open-label extension study following the Late-Onset Treatment Study (LOTS) of alglucosidase alfa (English)

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4 November 2017

Robert J Hopkin

6

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author name string

Ans T van der Ploeg

1

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4 November 2017

Richard Barohn

2

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4 November 2017

Lisa Carlson

3

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4 November 2017

Joel Charrow

4

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4 November 2017

Paula R Clemens

5

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4 November 2017

Priya S Kishnani

7

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4 November 2017

Pascal Laforêt

8

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4 November 2017

Claire Morgan

9

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4 November 2017

Sharon Nations

10

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4 November 2017

Alan Pestronk

11

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4 November 2017

Horacio Plotkin

12

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4 November 2017

Barry E Rosenbloom

13

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4 November 2017

Katherine B Sims

14

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4 November 2017

Elisa Tsao

15

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4 November 2017

language of work or name

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17 September 2012

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Molecular Genetics and Metabolism

4 November 2017

published in

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4 November 2017

volume

107

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4 November 2017

issue

3

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4 November 2017

page(s)

456-461

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Course of disability and respiratory function in untreated late-onset Pompe disease

4 November 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

Late onset Pompe disease: Clinical and neurophysiological spectrum of 38 patients including long-term follow-up in 18 patients

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

Clinical features of late-onset Pompe disease: a prospective cohort study

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

A randomized study of alglucosidase alfa in late-onset Pompe's disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

Desensitization of an adult patient with Pompe disease and a history of anaphylaxis to alglucosidase alfa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

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.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

Long-term observational, non-randomized study of enzyme replacement therapy in late-onset glycogenosis type II

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

Disease severity in children and adults with Pompe disease related to age and disease duration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2012.09.015

10.1016/J.YMGME.2012.09.015

7 January 2021

Identifiers

DOI

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4 November 2017

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