(Q42629452)

English

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.

scientific article published on August 2009

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19649685%20AND%20SRC:MED&resulttype=core&format=json

4 February 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 (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19649685%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

enzyme replacement therapy

0 references

alglucosidase alfa

1 reference

based on heuristic

inferred from title

glycogen storage disease

1 reference

based on heuristic

inferred from title

Benedikt Schoser

17

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19649685%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

Karlheinz Reiners

13

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19649685%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

author name string

S Strothotte

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19649685%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

N Strigl-Pill

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19649685%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

B Grunert

3

1 reference

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4 February 2020

C Kornblum

4

1 reference

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4 February 2020

K Eger

5

1 reference

Europe PubMed Central

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4 February 2020

C Wessig

6

1 reference

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4 February 2020

M Deschauer

7

1 reference

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4 February 2020

F Breunig

8

1 reference

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4 February 2020

F X Glocker

9

1 reference

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4 February 2020

S Vielhaber

10

1 reference

Europe PubMed Central

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4 February 2020

A Brejova

11

1 reference

Europe PubMed Central

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4 February 2020

M Hilz

12

1 reference

Europe PubMed Central

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4 February 2020

W Müller-Felber

14

1 reference

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4 February 2020

E Mengel

15

1 reference

Europe PubMed Central

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4 February 2020

M Spranger

16

1 reference

Europe PubMed Central

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4 February 2020

publication date

1 August 2009

1 reference

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4 February 2020

Journal of Neurology

1 reference

Europe PubMed Central

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4 February 2020

257

1 reference

Europe PubMed Central

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4 February 2020

1

1 reference

Europe PubMed Central

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4 February 2020

91-97

1 reference

Europe PubMed Central

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4 February 2020

https://scigraph.springernature.com/pub.10.1007/s00415-009-5275-3

0 references

Carrier frequency for glycogen storage disease type II in New York and estimates of affected individuals born with the disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pompe's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure and function of the mannose 6-phosphate/insulinlike growth factor II receptors

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme replacement therapy in late-onset Pompe's disease: a three-year follow-up

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adult-onset glycogen storage disease type 2: clinico-pathological phenotype revisited

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term enzyme replacement therapy for pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Therapeutic approaches in glycogen storage disease type II/Pompe Disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural and functional changes of lysosomal acid alpha-glucosidase during intracellular transport and maturation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mannose 6-phosphate receptors: new twists in the tale

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improvement with ongoing Enzyme Replacement Therapy in advanced late-onset Pompe disease: A case study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lysosomal acid alpha-glucosidase consists of four different peptides processed from a single chain precursor

1 reference

https://pubmed.ncbi.nlm.nih.gov/19649685

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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