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English
Congenital disorders of glycosylation (CDG): update and new developments
scientific article
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instance of
scholarly article
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review article
1 reference
stated in
Europe PubMed Central
title
Congenital disorders of glycosylation (CDG): update and new developments
(English)
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main subject
congenital disorder
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glycosylation
1 reference
based on heuristic
inferred from title
author name string
J Jaeken
series ordinal
1
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language of work or name
English
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publication date
2004
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published in
Journal of Inherited Metabolic Disease
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volume
27
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issue
3
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page(s)
423-6
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cites work
Diagnosis of congenital disorders of glycosylation by capillary zone electrophoresis of serum transferrin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031221.44647.9E
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carbohydrate-deficient glycoprotein syndrome: beyond the screen
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031221.44647.9E
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031221.44647.9E
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carbohydrate-deficient glycoprotein syndrome 1b: a new answer to an old diagnostic dilemma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031221.44647.9E
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031221.44647.9E
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital disorders of glycosylation type Ia and IIa are associated with different primary haemostatic complications.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031221.44647.9E
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phosphomannomutase deficiency is a cause of carbohydrate-deficient glycoprotein syndrome type I
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1023%2FB%3ABOLI.0000031221.44647.9E
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1023/B:BOLI.0000031221.44647.9E
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Dimensions Publication ID
1020970751
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PubMed publication ID
15272470
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