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
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.
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Cites
Jaeken, J., Vanderschueren‐Lodeweyckx, M., Casaer, P., Snoeck, L., Corbeel, L., Eggermont, E., & Eeckels, R. (1980) · Pediatric Research · doi:10.1203/00006450-198002000-00117 · Cited by 287
Self-citationThe microheterogeneity of human transferrins in biological fluids
van Eijk, H. G., van Noort, W. L., Dubelaar, M., & Heul, C. V. D. (1983) · Clinica Chimica Acta · doi:10.1016/0009-8981(83)90244-9 · Cited by 80
Bezkorovainy, A. (1981) · Springer eBooks · doi:10.1007/978-1-4684-3779-9 · Cited by 72
Hepatic recognition and catabolism of serum glycoproteins.
Ashwell, G., & Steer, C. J. (1981) · PubMed · Cited by 66
Chemistry and Metabolism of the Transferrins
Bezkorovainy, A. (1980) · Springer eBooks · doi:10.1007/978-1-4684-3779-9_4 · Cited by 13
Hepatic recognition and catabolism of serum glycoproteins
Ashwell, G. (1981) · JAMA · doi:10.1001/jama.246.20.2358 · Cited by 12
Iron uptake from sialo transferrins by rat reticulocytes
Dekker, C. J., Kroos, M. J., Heul, C. V. D., & van Eijk, H. G. (1984) · International Journal of Biochemistry · doi:10.1016/0020-711x(84)90190-3 · Cited by 5
Research works printed but not linked: 1
- Heath, 1981, The biosynthesis and turnover of glycoproteins, Vol. 3
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Sorted by citations
Glycobiology: Toward Understanding the Function of Sugars
Dwek, R. A. (1996) · Chemical Reviews · doi:10.1021/cr940283b · Cited by 2,800
Varki, A. (2017) · Glycobiology · doi:10.1093/glycob/cww086 · Cited by 2,635
de Jong, G., van Dijk, J. P., & van Eijk, H. G. (1990) · Clinica Chimica Acta · doi:10.1016/0009-8981(90)90278-z · Cited by 360
Matthijs, G., Schollen, E., Pardon, E., Veiga‐da‐Cunha, M., Jaeken, J., Cassiman, J., & SCHAFTINGEN, E. V. (1997) · Nature Genetics · doi:10.1038/ng0597-88 · Cited by 357
Self-citationBeard, J. L., Connor, J. R., & Jones, B. C. (2009) · Nutrition Reviews · doi:10.1111/j.1753-4887.1993.tb03096.x · Cited by 341
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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- The paper
- Jaeken, J., van Eijk, H. G., van der Heul, C., Corbeel, L., Eeckels, R., & Eggermont, E. (1984). Sialic acid-deficient serum and cerebrospinal fluid transferrin in a newly recognized genetic syndrome. Clinica Chimica Acta. https://doi.org/10.1016/0009-8981(84)90059-7