Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome.

Author:

Stibler H,Jaeken J

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference27 articles.

1. An apparent homozygous X-linked disorder with carbohydrate-deficient serum glycoproteins;Jaeken, J.; Eggermont, E.; Stibler, H.;Lancet,1987

2. A newly recognized inherited neurological disease with carbohydrate-deficient secretory glycoproteins;Jaeken, J.; Stibler, H.,1989

3. Micro anion exchange chromatography of carbohydrate-deficient transferrin in serum in relation to alcohol consumption;Stibler, H.; Borg, S.; Joustra, M.;Alcoholism: Clinical and Experimental Research,1986

4. The normal cerebrospinal fluid proteins identified by means of isoelectric focusing and crossed immunoelectrofocusing;Stibler, H.;J Neurol Sci,1978

5. Silver-staining of oligoclonal IgG subfractions in cerebrospinal fluid after isoelectric focusing in thin-layer polyacrylamide gels;Schipper, H.; Kruse, H.; Reiber, H.;Science Tools,1984

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