Cited by 284Glycosylation and Glycoproteins ResearchLysosomal Storage Disorders ResearchIron Metabolism and Disorders

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome

Jaeken, J., van Eijk, H.G., van der Heul, C., Corbeel, L., Eeckels, R., Eggermont, E.·1984·Clinica Chimica Acta

Abstract

Identical twin-sisters with evidence of a demyelinating disease showed multiple serum glycoprotein abnormalities. The association of a low serum iron level and a normal blood haemoglobin suggested an abnormality of transferrin too. This was confirmed by finding a sialic acid-deficiency of this glycoprotein in serum as well as in cerebrospinal fluid.

Overview

Integrity signals

Registry

Crossref · 10.1016/0009-8981(84)90059-7

Cites

7 of 7 references verified0 citation errors · 0 not checkable

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Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Citations

Cites

Research works printed but not linked: 1

  1. Heath, 1981, The biosynthesis and turnover of glycoproteins, Vol. 3

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Metadata

Authors
Jaeken, J., van Eijk, H. G., van der Heul, C., Corbeel, L., Eeckels, R., & Eggermont, E.
Affiliations
KU Leuven (BE)
Corresponding author
Jaeken, J.
Venue
Clinica Chimica Acta
Publisher
Elsevier BV
Published
1984-12
Volume
144
Issue
2-3
Pages
245-247
ISSN
0009-8981 (ISSN-L)
OpenAlex
W1985413330
Cited by
280
References
7
Citations by year
2026: 3 · 2025: 7 · 2024: 10 · 2023: 8 · 2022: 7 · 2021: 14 · 2020: 13 · 2019: 8 · 2018: 6 · 2017: 6 · 2016: 9 · 2015: 1 · 2014: 4 · 2013: 4 · 2012: 8
FWCI
0.61
Type
journal article
Language
en
Open access
closed
Locations
  • Clinica Chimica Acta (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
  • Health Sciences › Medicine › Genetics (clinical) › Lysosomal Storage Disorders Research
  • Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
Keywords
sialic acid deficiency, transferrin, demyelinating disease, serum glycoproteins, cerebrospinal fluid, monozygotic twins, genetic syndromes
MeSH terms
Child, Child, Preschool, Demyelinating Diseases, Diseases in Twins, Female, Humans, Immunoelectrophoresis, Two-Dimensional, Pregnancy, Sialic Acids, Transferrin, Twins, Monozygotic, N-Acetylneuraminic Acid

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