(Q34281037)

English

Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milk

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milk (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

author name string

Van den Hout JM

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Reuser AJ

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

de Klerk JB

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Arts WF

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Smeitink JA

5

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Van der Ploeg AT

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

1 April 2001

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

24

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

266-274

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Glycogenosis type II (acid maltase deficiency)

2 references

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

https://api.crossref.org/works/10.1023%2FA%3A1010383421286

7 January 2021

based on heuristic

inferred from DOI database lookup

AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycogen-storage disease of the myocardium with obstruction to left ventricular outflow

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombinant human alpha-glucosidase from rabbit milk in Pompe patients.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lysosomes in type II glycogenosis. Changes during administration of extract from Aspergillus niger

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme therapy in type 1 Gaucher disease: comparative efficacy of mannose-terminated glucocerebrosidase from natural and recombinant sources

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical, immunological, and cell genetic studies in glycogenosis type II

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Left ventricular myocardial mass determined by cross-sectional echocardiography in normal newborns, infants, and children

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Three hypotonic neonates with hypertrophic cardiomyopathy: Pompe's disease]

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombinant human acid alpha-glucosidase: high level production in mouse milk, biochemical characteristics, correction of enzyme deficiency in GSDII KO mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/11405345

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1010383421286

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34281037&oldid=2196457096"