(Q38644464)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26597321%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

title

Immune response to enzyme replacement therapies in lysosomal storage diseases and the role of immune tolerance induction (English)

1 reference

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1 March 2020

20

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1 March 2020

author name string

Priya S Kishnani

1

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1 March 2020

Patricia I Dickson

2

1 reference

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1 March 2020

Laurie Muldowney

3

1 reference

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1 March 2020

Jessica J Lee

4

1 reference

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1 March 2020

Amy Rosenberg

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26597321%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

Rekha Abichandani

6

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1 March 2020

Jeffrey A Bluestone

7

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1 March 2020

Barbara K Burton

8

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1 March 2020

Maureen Dewey

9

1 reference

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1 March 2020

Alexandra Freitas

10

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1 March 2020

Derek Gavin

11

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1 March 2020

Donna Griebel

12

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1 March 2020

Melissa Hogan

13

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1 March 2020

Stephen Holland

14

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1 March 2020

Pranoot Tanpaiboon

15

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1 March 2020

Laurence A Turka

16

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1 March 2020

Jeanine J Utz

17

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1 March 2020

Yow-Ming Wang

18

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1 March 2020

Chester B Whitley

19

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1 March 2020

Anne R Pariser

21

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1 March 2020

publication date

10 November 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26597321%20AND%20SRC:MED&resulttype=core&format=json

Molecular Genetics and Metabolism

1 March 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26597321%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

volume

117

1 reference

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1 March 2020

issue

2

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1 March 2020

page(s)

66-83

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26597321%20AND%20SRC:MED&resulttype=core&format=json

Measuring relative lysosomal volume for monitoring lysosomal storage diseases

1 March 2020

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Clarifying lysosomal storage diseases

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Lysosomal disorders: from storage to cellular damage

7 January 2021

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Common and uncommon pathogenic cascades in lysosomal storage diseases

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Prevalence of lysosomal storage disorders

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Newborn screening for lysosomal storage disorders

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Newborn screening for lysosomal storage disorders and other neuronopathic conditions

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IgE-mediated anaphylaxis and allergic reactions to idursulfase in patients with Hunter syndrome

7 January 2021

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Significance of immune response to enzyme-replacement therapy for patients with a lysosomal storage disorder.

7 January 2021

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Incidence and timing of infusion-related reactions in patients with mucopolysaccharidosis type II (Hunter syndrome) on idursulfase therapy in the real-world setting: A perspective from the Hunter Outcome Survey (HOS)

7 January 2021

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Successful management of difficult infusion-associated reactions in a young patient with mucopolysaccharidosis type VI receiving recombinant human arylsulfatase B (galsulfase [Naglazyme])

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7 January 2021

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Bortezomib in the rapid reduction of high sustained antibody titers in disorders treated with therapeutic protein: lessons learned from Pompe disease

7 January 2021

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Successful immune tolerance induction to enzyme replacement therapy in CRIM-negative infantile Pompe disease.

7 January 2021

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7 January 2021

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Enzyme replacement therapy in patients who have mucopolysaccharidosis I and are younger than 5 years: results of a multinational study of recombinant human alpha-L-iduronidase (laronidase).

7 January 2021

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Cross-reactive immunologic material status affects treatment outcomes in Pompe disease infants

7 January 2021

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Genetic risk factors for inhibitors to factors VIII and IX.

7 January 2021

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Considering Fabry, but Diagnosing MPS I: Difficulties in the Diagnostic Process

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7 January 2021

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7 January 2021

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Reduced alpha-Gal A enzyme activity in Fabry fibroblast cells and Fabry mice tissues induced by serum from antibody positive patients with Fabry disease

7 January 2021

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A retrospective analysis of the potential impact of IgG antibodies to agalsidase beta on efficacy during enzyme replacement therapy for Fabry disease

7 January 2021

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Enzyme therapy for Fabry disease: neutralizing antibodies toward agalsidase alpha and beta

7 January 2021

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Immune response to enzyme replacement therapy in Fabry disease: impact on clinical outcome?

7 January 2021

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Long-term effect of antibodies against infused alpha-galactosidase A in Fabry disease on plasma and urinary (lyso)Gb3 reduction and treatment outcome

7 January 2021

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The relationship between anti-idursulfase antibody status and safety and efficacy outcomes in attenuated mucopolysaccharidosis II patients aged 5 years and older treated with intravenous idursulfase.

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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10.1016/J.YMGME.2015.11.001

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26597321%20AND%20SRC:MED&resulttype=core&format=json

1 March 2020

1 reference