A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studies (Q28348809)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11179018%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11179018%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

main subject

phase I clinical trial

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phase II clinical trial

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1 reference

10

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4 November 2019

17

R J Desnick

1 reference

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4 November 2019

author name string

C M Eng

1

1 reference

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4 November 2019

M Banikazemi

2

1 reference

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4 November 2019

R E Gordon

3

1 reference

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4 November 2019

M Goldman

4

1 reference

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4 November 2019

R Phelps

5

1 reference

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4 November 2019

L Kim

6

1 reference

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4 November 2019

A Gass

7

1 reference

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4 November 2019

J Winston

8

1 reference

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4 November 2019

S Dikman

9

1 reference

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4 November 2019

S Brodie

11

1 reference

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4 November 2019

C B Stacy

12

1 reference

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4 November 2019

D Mehta

13

1 reference

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4 November 2019

R Parsons

14

1 reference

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4 November 2019

K Norton

15

1 reference

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4 November 2019

M O'Callaghan

16

1 reference

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4 November 2019

language of work or name

English

0 references

publication date

1 February 2001

1 reference

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American Journal of Human Genetics

4 November 2019

published in

1 reference

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4 November 2019

volume

68

1 reference

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4 November 2019

page(s)

711-722

1 reference

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4 November 2019

issue

3

1 reference

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Fabry disease: preclinical studies demonstrate the effectiveness of alpha-galactosidase A replacement in enzyme-deficient mice

4 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Human alpha-galactosidase A: nucleotide sequence of a cDNA clone encoding the mature enzyme

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

An Atypical Variant of Fabry's Disease with Manifestations Confined to the Myocardium

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Overexpression of human alpha-galactosidase A results in its intracellular aggregation, crystallization in lysosomes, and selective secretion

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Nature and frequency of mutations in the alpha-galactosidase A gene that cause Fabry disease

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease

20 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Gaucher's disease: a model for modern management of a genetic disease.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Angiokeratoma corporis diffusum--Fabry's disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Enzyme therapy in Fabry disease: differential in vivo plasma clearance and metabolic effectiveness of plasma and splenic alpha-galactosidase A isozymes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Enzyme therapy for Gaucher disease: the first 5 years.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Enzyme Replacement in Fabry's Disease, an Inborn Error of Metabolism

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease. Report on a case simulating hypertrophic non-obstructive cardiomyopathy

2 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274483

Enzyme therapy XVII: metabolic and immunologic evaluation of alpha- galactosidase A replacement in Fabry disease

27 November 2018

1 reference

12 December 2020

Replacement Therapy for Inherited Enzyme Deficiency

1 reference

12 December 2020

The short-form McGill Pain Questionnaire

1 reference

12 December 2020

Human alpha-galactosidase A: characterization of the N-linked oligosaccharides on the intracellular and secreted glycoforms overexpressed by Chinese hamster ovary cells

1 reference

12 December 2020

Quantitative determination of globotriaosylceramide by immunodetection of glycolipid-bound recombinant verotoxin B subunit

1 reference

12 December 2020

Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. Alpha-galactosidase activities in plasma, serum, urine, and leukocytes

1 reference

12 December 2020

Identifiers

DOI

10.1086/318809

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11179018%20AND%20SRC:MED&resulttype=core&format=json

OpenCitations bibliographic resource ID

4 November 2019

5028483

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11179018%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference