(Q39094468)

English

Mannosidosis: Phenotype of a severely affected child and characterization of α-mannosidase activity in cultured fibroblasts from the patient and his parents

scientific article published on May 1, 1976

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scholarly article

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Europe PubMed Central

PubMed publication ID

9 September 2017

Mannosidosis: phenotype of a severely affected child and characterization of alpha-mannosidase activity in cultured fibroblasts from the patient and his parents (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5584

5 October 2022

Mannosidosis: Phenotype of a severely affected child and characterization of α-mannosidase activity in cultured fibroblasts from the patient and his parents (English)

1 reference

10.1016/S0022-3476(76)81120-1

https://api.crossref.org/works/10.1016/S0022-3476(76)81120-1

11 October 2022

author name string

A. S. Aylsworth

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5584

5 October 2022

H. A. Taylor

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5584

5 October 2022

C. M. Stuart

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5584

5 October 2022

G. H. Thomas

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5584

5 October 2022

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publication date

1 May 1976

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Europe PubMed Central

PubMed publication ID

9 September 2017

full work available at URL

https://api.elsevier.com/content/article/PII:S0022347676811201?httpAccept=text/xml

1 reference

10.1016/S0022-3476(76)81120-1

https://api.crossref.org/works/10.1016/S0022-3476(76)81120-1

11 October 2022

https://api.elsevier.com/content/article/PII:S0022347676811201?httpAccept=text/plain

1 reference

10.1016/S0022-3476(76)81120-1

https://api.crossref.org/works/10.1016/S0022-3476(76)81120-1

11 October 2022

The Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

88

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

814-818

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

A GENERALISED STORAGE DISORDER RESEMBLING HURLER'S SYNDROME

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

Urinary mannose in mannosidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

Mannosidosis: clinical, fine-structural and biochemical findings in three cases

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

Excretion of mannose-rich complex carbohydrates by a patient with α-mannosidase deficiency (mannosidosis)

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

Mannosidosis: Deficiency of a specific α-mannosidase component in cultured fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

Mannosidosis: isolation of oligosaccharide storage material from brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

A modified screening test for glycosaminoglycan excretion

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

Mucolipidosis 3 (pseudo-Hurler polydystrophy): cytological and ultrastructural observations of cultured fibroblast cells

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2876%2981120-1

7 January 2021

Identifiers

10.1016/S0022-3476(76)81120-1

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 September 2017

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