(Q64042342)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20838899%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

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

1 reference

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13 February 2020

2

1 reference

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13 February 2020

Marco Confalonieri

3

1 reference

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13 February 2020

Alfredo Costa

9

1 reference

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13 February 2020

author name string

Bruno Bembi

1

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13 February 2020

Giovanni Ciana

4

1 reference

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13 February 2020

Agata Fiumara

5

1 reference

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13 February 2020

Rossella Parini

6

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13 February 2020

Miriam Rigoldi

7

1 reference

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13 February 2020

Annalisa Carlucci

10

1 reference

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13 February 2020

Cesare Danesino

11

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13 February 2020

Maria Gabriela Pittis

12

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13 February 2020

Andrea Dardis

13

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13 February 2020

Sabrina Ravaglia

14

1 reference

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13 February 2020

Arrigo Moglia

8

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13 February 2020

language of work or name

English

0 references

publication date

14 September 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20838899%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

13 February 2020

published in

1 reference

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13 February 2020

volume

33

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13 February 2020

issue

6

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13 February 2020

page(s)

727-735

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https://scigraph.springernature.com/pub.10.1007/s10545-010-9201-8

13 February 2020

exact match

0 references

cites work

Six-minute walk test in children and adolescents.

1 reference

12 December 2020

Interpreting small differences in functional status: the Six Minute Walk test in chronic lung disease patients

1 reference

12 December 2020

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

1 reference

12 December 2020

The natural course of non-classic Pompe's disease; a review of 225 published cases

1 reference

12 December 2020

Enzyme reconstitution/replacement therapy for lysosomal storage diseases

1 reference

12 December 2020

1 reference

12 December 2020

Reference equations for the six-minute walk in healthy adults

1 reference

12 December 2020

Enzyme replacement therapy in late-onset type II glycogenosis.

1 reference

12 December 2020

[Neuromuscular disorders - assessment of the respiratory muscles]

1 reference

12 December 2020

The clinical effectiveness and cost-effectiveness of enzyme replacement therapy for Gaucher's disease: a systematic review

1 reference

12 December 2020

Long-term intravenous treatment of Pompe disease with recombinant human alpha-glucosidase from milk

1 reference

12 December 2020

Neural deficits contribute to respiratory insufficiency in Pompe disease

1 reference

12 December 2020

Management and treatment of glycogenosis type II.

1 reference

12 December 2020

Mutation profile of the GAA gene in 40 Italian patients with late onset glycogen storage disease type II

1 reference

12 December 2020

Conditional tissue-specific expression of the acid alpha-glucosidase (GAA) gene in the GAA knockout mice: implications for therapy

1 reference

12 December 2020

The value of multiple tests of respiratory muscle strength

1 reference

12 December 2020

Clinical manifestation and natural course of late-onset Pompe's disease in 54 Dutch patients

1 reference

12 December 2020

Autophagy and mistargeting of therapeutic enzyme in skeletal muscle in Pompe disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Respiratory insufficiency and limb muscle weakness in adults with Pompe's disease

1 reference

12 December 2020

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.

1 reference

12 December 2020

Molecular diagnosis of German patients with late-onset glycogen storage disease type II

1 reference

12 December 2020

Modification of the natural history of adult-onset acid maltase deficiency by nutrition and exercise therapy

1 reference

12 December 2020

Treatment of lysosomal storage disorders : progress with enzyme replacement therapy

1 reference

12 December 2020

Chinese hamster ovary cell-derived recombinant human acid alpha-glucosidase in infantile-onset Pompe disease

1 reference

12 December 2020