Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase. (Q33995906)

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English	Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase.	scientific article

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7 February 2020

Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase (English)

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7 February 2020

enzyme replacement therapy

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mucopolysaccharidosis VI

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Robert D. Steiner

15

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7 February 2020

Ida Vanessa D Schwartz

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Ida Vanessa D Schwartz

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7 February 2020

Roberto Giugliani

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Roberto Giugliani

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7 February 2020

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Paul Harmatz

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7 February 2020

David Ketteridge

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David Ketteridge

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7 February 2020

Nathalie Guffon

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Nathalie Guffon

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7 February 2020

Elisa Leão Teles

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Elisa Leão Teles

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7 February 2020

Stuart J Swiedler

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Stuart J Swiedler

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7 February 2020

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J Edmond Wraith

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7 February 2020

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Laila Arash

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7 February 2020

Maurizio Scarpa

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Maurizio Scarpa

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7 February 2020

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Barbara Plecko

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7 February 2020

Chester B Whitley

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Chester B Whitley

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7 February 2020

17

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Paige Kaplan

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7 February 2020

1

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Celeste Decker

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7 February 2020

13

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John J Hopwood

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7 February 2020

author name string

Zi-Fan Yu

2

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7 February 2020

M Clara Sá Miranda

7

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7 February 2020

Michael Beck

9

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7 February 2020

Susan Conrad

19

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7 February 2020

publication date

1 January 2010

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7 February 2020

Journal of pediatric rehabilitation medicine

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7 February 2020

3

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7 February 2020

2

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7 February 2020

89-100

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20634905%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Age-appropriate body mass index in children with achondroplasia: interpretation in relation to indexes of height

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5 July 2018

Examination of US puberty-timing data from 1940 to 1994 for secular trends: panel findings

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5 July 2018

Mechanism of glycosaminoglycan-mediated bone and joint disease: implications for the mucopolysaccharidoses and other connective tissue diseases

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5 July 2018

Management guidelines for mucopolysaccharidosis VI.

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5 July 2018

Growth and normal puberty.

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5 July 2018

Use of segmental measures to estimate stature in children with cerebral palsy

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5 July 2018

Variations in pattern of pubertal changes in girls

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5 July 2018

Variations in the Pattern of Pubertal Changes in Boys

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5 July 2018

Clinical longitudinal standards for height and height velocity for North American children

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5 July 2018

A biologically-oriented mathematical model (ICP) for human growth.

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5 July 2018

Pituitary function studies in a case of mild Hunter's syndrome (MPS IIB).

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On the construction of the infancy-childhood-puberty growth standard

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5 July 2018

Serum growth hormone levels in Hunter's syndrome

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5 July 2018

Physical growth: National Center for Health Statistics percentiles

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5 July 2018

Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.

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29 October 2018

Precocious puberty in Sanfilippo IIIA disease: diagnosis and follow-up of two new cases

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29 October 2018

Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase

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29 October 2018

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29 October 2018

Growth and endocrine function in patients with Hurler syndrome after hematopoietic stem cell transplantation.

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29 October 2018

A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years

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29 October 2018

Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human N-ac

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29 October 2018

Joint and bone disease in mucopolysaccharidoses VI and VII: identification of new therapeutic targets and biomarkers using animal models

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Early diagnosis of Maroteaux-Lamy syndrome in two patients with accelerated growth and advanced bone maturation.

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29 October 2018

Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome).

1 reference

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29 October 2018

Maroteaux-Lamy syndrome associated with growth hormone deficiency

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Articular chondrocytes from animals with a dermatan sulfate storage disease undergo a high rate of apoptosis and release nitric oxide and inflammatory cytokines: a possible mechanism underlying degenerative joint disease in the mucopolysaccharidoses

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enzyme replacement therapy for mucopolysaccharidosis VI: A phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, o

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Threshold effect of urinary glycosaminoglycans and the walk test as indicators of disease progression in a survey of subjects with Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/20634905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of enzyme replacement therapy on bone formation in a feline model of mucopolysaccharidosis type VI

1 reference

https://pubmed.ncbi.nlm.nih.gov/20634905

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3233/PRM-2010-0113

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Europe PubMed Central

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7 February 2020

PMC publication ID

1 reference

Europe PubMed Central

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7 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

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7 February 2020

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