(Q70442208)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6410119%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

title

A clinical trial of fibroblast transplantation for the treatment of mucopolysaccharidoses (English)

1 reference

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11 October 2019

author name string

D A Gibbs

1

1 reference

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11 October 2019

E Spellacy

2

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11 October 2019

R Tompkins

3

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11 October 2019

R W Watts

4

1 reference

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11 October 2019

J F Mowbray

5

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11 October 2019

publication date

1 January 1983

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Journal of Inherited Metabolic Disease

11 October 2019

published in

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11 October 2019

volume

6

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11 October 2019

issue

2

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11 October 2019

page(s)

62-81

1 reference

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Glaucoma in a case of Hurler disease

11 October 2019

cites work

1 reference

12 December 2020

A newly recognized syndrome of connective tissue dysplasia in siblings (previously described as a variant of Morquio disease).

1 reference

12 December 2020

Enzyme replacement therapy by transplantation of HLA-compatible fibroblasts in Sanfilippo A syndrome

1 reference

12 December 2020

Cellular distribution, purification, and molecular nature of human Ia antigens

1 reference

12 December 2020

Enzyme replacement therapy--an experiment of nature in a chimeric mannosidosis calf

1 reference

12 December 2020

Induced degradation of glycosaminoglycans in Hurler's and Hunter's syndromes by plasma infusion

1 reference

12 December 2020

Lack of relationship between blood and urine levels of glycosaminoglycans and lysomal enzymes

1 reference

12 December 2020

Genetic heterogeneity and allelic variation in the mucopolysaccharidoses. Introduction

1 reference

12 December 2020

Recognition and receptor-mediated uptake of a lysosomal enzyme, alpha-l-iduronidase, by cultured human fibroblasts

1 reference

12 December 2020

Effect of prednisolone on urinary acid mucopolysaccharides excretion in genetic mucopolysaccharidoses.

1 reference

12 December 2020

Effect of leukocyte transfusion in a child with type II mucopolysaccharidosis

1 reference

12 December 2020

Computed tomography studies on patients with mucopolysaccharidoses

1 reference

12 December 2020

Allelism, non-allelism and genetic compounds among the mucopolysaccharidoses: corrective factors in nosology, genetics and therapy.

1 reference

12 December 2020

The treatment of lysosomal storage diseases by fibroblast transplantation: some preliminary observations

1 reference

12 December 2020

The measurement of creatinine in plasma and urine

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12 December 2020

Bone marrow transplantation for inborn errors

1 reference

12 December 2020

A review and selection of simple laboratory methods used for the study of glycosaminoglycan excretion and the diagnosis of the mucopolysaccharidoses

1 reference

12 December 2020

The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase

1 reference

12 December 2020

Modification of the blood-brain barrier: increased concentration and fate of enzymes entering the brain

1 reference

12 December 2020

Increased breakdown of glycosaminoglycans and appearance of corrective enzyme after skin transplants in Hunter syndrome

1 reference

12 December 2020

Effects of fresh plasma or whole blood transfusions on patients with various types of mucopolysaccharidosis.

1 reference

12 December 2020

The nomenclature of mucopolysaccharides

1 reference

12 December 2020

Estimation of liver size by the multiple cut off scintillation scanning technique.

1 reference

12 December 2020

Pre- and postnatal pathology, enzyme treatment, and unresolved issues in five lysosomal disorders

1 reference

12 December 2020

Tissue typing of cells in culture. II. Histocompatibility typing of diploid fibroblastic cultures by the mixed hemadsorption (MH) test

1 reference

12 December 2020

Enzyme replacement therapy by fibroblast transplantation in a case of Hunter syndrome

1 reference

12 December 2020

Proteoglycans: Their structure, interactions and molecular organization in cartilage

1 reference

12 December 2020

The Hurler corrective factor. Purification and some properties

1 reference

12 December 2020

Modification of urinary mucopolysaccharide excretion in patients with Hurler's syndrome

1 reference

12 December 2020

The transport of lysosomal enzymes

1 reference

12 December 2020

Direct demonstration of binding of a lysosomal enzyme, alpha-L-iduronidase, to receptors on cultured fibroblasts

1 reference

12 December 2020

46 Enzymic diagnosis of the genetic mucopolysaccharide storage disorders

1 reference

12 December 2020

Reversible osmotic blood-brain barrier disruption in humans: implications for the chemotherapy of malignant brain tumors.

1 reference

12 December 2020

Metabolic co-operation between biochemically marked mammalian cells in tissue culture

1 reference

12 December 2020

Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.

1 reference

12 December 2020

Prospects for enzyme replacement for lysosomal storage diseases

1 reference

12 December 2020

Inefficacy of fresh frozen plasma therapy of mucopolysaccharidosis II

1 reference

12 December 2020

The correction of Hunter fibroblasts by exogenous iduronate sulfate sulfatase: biochemical and ultrastructural studies.

1 reference

12 December 2020

Protein filtration and secretion at human body fluid barriers

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Enzyme replacement therapy by fibroblast transplantation: long-term biochemical study in three cases of Hunter's syndrome

1 reference

12 December 2020

Liver volume determination by ultrasound: a feasibility study

1 reference

12 December 2020

Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation

1 reference

12 December 2020

Direct transfer of a lysosomal enzyme from lymphoid cells to deficient fibroblasts

1 reference

12 December 2020

Treatment of mucopolysaccharidosis: clinical and biochemical aspects of leucocyte transfusion as compared with plasma infusion in patients with Hurler's and Scheie's syndromes

1 reference

12 December 2020

The variation of urinary oxalate excretion with age

1 reference

12 December 2020

Sequential thin layer chromatography of urinary acidic glycosaminglycans

1 reference

12 December 2020

Treatment of Hurler syndrome

1 reference

12 December 2020

Microdroplet Assay of Human Serum Cytotoxins

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF02338973

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6410119%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

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