DOI: 10.1007/978-1-349-10729-2_7. A Newly Recognized Inherited Neurological Disease with Carbohydrate Deficient Secretory Glycoproteins

A Newly Recognized Inherited Neurological Disease with Carbohydrate Deficient Secretory Glycoproteins

10.1007/978-1-349-10729-2_7

Crossref book-chapter

Macmillan Education UK

Genetics of Neuropsychiatric Diseases (297)

Bibliography

Jaeken, J., & Stibler, H. (1989). A Newly Recognized Inherited Neurological Disease with Carbohydrate Deficient Secretory Glycoproteins. Genetics of Neuropsychiatric Diseases, 69â80.

Authors 2

J. Jaeken (first)
H. Stibler (additional)

References 24 Referenced 27

Fairbanks, G., Steck, T., Wallach, D. (1971). Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry, 10, 2606–2617. (10.1021/bi00789a030) / Biochemistry by G Fairbanks (1971)
Finch, P., Yuen, R., Schachter, H., Moscarello, M. (1969). Enzymic methods for the micro-assay of D-mannose, D-glucose, D-galactose and L-fucose from acid hydrolyzates of glycoproteins. Anal. Biochem., 31, 296–305. (10.1016/0003-2697(69)90269-3) / Anal. Biochem. by P Finch (1969)
Fukuda, M.N., Dell, A., Scartezzini, P. (1987). Primary defect of congenital dyserythropoietic anemia type II. J. Biol. Chem., 262, 7195–7206. (10.1016/S0021-9258(18)48223-3) / J. Biol. Chem. by MN Fukuda (1987)
Gregoriadis, G., Putman, D., Louis, L., Neerunjun, D. (1974). Comparative effect and fate of non-entrapped and liposome-entrapped neuraminidase injected into rats. Biochem. J., 140, 323–330. (10.1042/bj1400323) / Biochem. J. by G Gregoriadis (1974)
Jaeken, J., Eggermont, E., Stibler, H. (1987). An apparent homozygous X-linked disorder with carbohydrate-deficient serum glycoproteins. Lancet, 2, 1938. / Lancet by J Jaeken (1987)
Jaeken, J., Eggermont, E., Stibler, H. (1988). An apparently homozygous X-linked neurological disease with carbohydrate deficient serum glycoproteins. In: Modern trends in Neurology and Neurological Emergencies. Proceedings from 1st European Congress of Neurology, Prague, pp. 175–176. / In: Modern trends in Neurology and Neurological Emergencies. Proceedings from 1st European Congress of Neurology by J Jaeken (1988)
Jaeken, J., Kint, J. (1987). Abnormal serum lysosomal isoenzymes in leukodystrophy with sialic acid deficient glycoproteins. Proceedings of the 25th Symposium of the Society for the Study of Inborn Errors of Metabolism, Sheffield. / Abnormal serum lysosomal isoenzymes in leukodystrophy with sialic acid deficient glycoproteins. Proceedings of the 25th Symposium of the Society for the Study of Inborn Errors of Metabolism by J Jaeken (1987)
Kim, Y., Perdomo, J., Bella, A., Nordberg, J. (1971). Properties of a CMP-N-acetylneuraminic acid: glycoprotein sialyltransferase in human serum and erythrocyte membranes. Biochim. Biophys. Acta, 244, 505–512. (10.1016/0304-4165(71)90067-5) / Biochim. Biophys. Acta by Y Kim (1971)
Kim, Y., Perdomo, J., Whitehead, J. (1972). Galactosyltransferase in human serum and erythrocyte membranes. J. Clin. Invest., 51, 2024–2032. (10.1172/JCI107008) / J. Clin. Invest. by Y Kim (1972)
Lowry, O., Rosebrough, N., Farr, A., Randall, R. (1951). Protein measurements with the Folin phenol reagent. J. Biol. Chem., 193, 265–275. (10.1016/S0021-9258(19)52451-6) / J. Biol. Chem. by O Lowry (1951)
Mookerjea, S., Chow, A., Hudgin, R. (1971). Occurrence of UDP-N-acetylglucosamine: glycoprotein N-acetylglucosaminyltransferase activity in human and rat sera. Can. J. Biochem., 49, 297–299. (10.1139/o71-042) / Can. J. Biochem. by S Mookerjea (1971)
Schachter, H. (1984). Glycoproteins: their structure, biosynthesis and possible clinical implications. Clin. Biochem., 17, 3–14. (10.1016/S0009-9120(84)90360-6) / Clin. Biochem. by H Schachter (1984)
Schipper, H., Kruse, H., Reiber, H. (1984). Silver-staining of oligoclonal Ig G subfractions in cerebrospinal fluid after isoelectric focusing in thin-layer Polyacrylamide gels. Sci. Tools, 31, 5–6. / Sci. Tools by H Schipper (1984)
Spik, G., Bayard, B., Strecker, G., Bouquelet, S., Montreuil, J. (1975). Studies on Glycoconjugates. LXIV. Complete structure of two carbohydrate units of human serotransferrin. FEBS Lett., 50, 296–299. (10.1016/0014-5793(75)80513-8) / FEBS Lett. by G Spik (1975)
Stibler, H. (1978). The normal cerebrospinal fluid proteins identified by means of isoelectric focusing and crossed immunoelectro-focusing. J. Neurol. Sci., 36, 273–288. (10.1016/0022-510X(78)90088-6) / J. Neurol. Sci. by H Stibler (1978)
Stibler, H. (1979). Direct immunofixation after isoelectric focusing. J. Neurol. Sci., 42, 275–281. (10.1016/0022-510X(79)90059-5) / J. Neurol. Sci. by H Stibler (1979)
Stibler, H., Beaugé, F., Borg, S. (1984). Changes in (Na K)ATPase and the composition of surface carbohydrates in erythrocyte membranes in alcoholics. Alcohol. Clin. Exp. Res., 8, 522–527. (10.1111/j.1530-0277.1984.tb05722.x) / Alcohol. Clin. Exp. Res. by H Stibler (1984)
Stibler, H., Borg, S. (1986). Carbohydrate composition of serum transferrin in alcoholic patients. Alcohol. Clin. Exp. Res., 10, 61–64. (10.1111/j.1530-0277.1986.tb05616.x) / Alcohol. Clin. Exp. Res. by H Stibler (1986)
Stibler, H., Borg, S. (1986). Glycoprotein sialyl- and galactosyl-transferase activities in erythrocyte membranes in alcoholic patients and controls. Drug Alc. Dep., 16, 331–340. (10.1016/0376-8716(86)90067-0) / Drug Alc. Dep. by H Stibler (1986)
Stibler, H., Borg, S., Joustra, M. (1986). Micro anion exchange chromatography of carbohydrate-deficient transferrin in serum in relation to alcohol consumption. Alcohol. Clin. Exp. Res., 10, 535–544. (10.1111/j.1530-0277.1986.tb05138.x) / Alcohol. Clin. Exp. Res. by H Stibler (1986)
Stibler, H., Sydow, O. (1984). Carbohydrate composition of erythrocyte membranes and glycosidase activities in serum in patients with myotonic dystrophy, limb-girdle dystrophy and congenital myotonia. J. Neurol. Sci., 63, 285–298. (10.1016/0022-510X(84)90151-5) / J. Neurol. Sci. by H Stibler (1984)
Troost, J., van der Heijden, M., Staal, G. (1976). Characterization of α-L-fucosidase from two different families with fucosidosis. Clin. Chim. Acta, 73, 329–346. (10.1016/0009-8981(76)90180-7) / Clin. Chim. Acta by J Troost (1976)
Von Figura, K., Hasilik, A. (1986). Lysosomal enzymes and their receptors. Ann. Rev. Biochem., 55, 167–193. (10.1146/annurev.bi.55.070186.001123) / Ann. Rev. Biochem. by K Figura Von (1986)
West, C.M. (1986). Current ideas on the significance of protein glycosylation. Mol. Cell. Biochem., 72, 3–20. (10.1007/BF00230632) / Mol. Cell. Biochem. by CM West (1986)

Dates

Type	When
Created	9 years, 8 months ago (Dec. 17, 2015, 8:29 p.m.)
Deposited	3 years, 3 months ago (May 29, 2022, 11:25 a.m.)
Indexed	11 months, 3 weeks ago (Sept. 15, 2024, 6:32 a.m.)
Issued	36 years, 8 months ago (Jan. 1, 1989)
Published	36 years, 8 months ago (Jan. 1, 1989)
Published Print	36 years, 8 months ago (Jan. 1, 1989)

Funders 0

None

BibTeX

@inbook{Jaeken_1989, title={A Newly Recognized Inherited Neurological Disease with Carbohydrate Deficient Secretory Glycoproteins}, ISBN={9781349107292}, url={http://dx.doi.org/10.1007/978-1-349-10729-2_7}, DOI={10.1007/978-1-349-10729-2_7}, booktitle={Genetics of Neuropsychiatric Diseases}, publisher={Macmillan Education UK}, author={Jaeken, J. and Stibler, H.}, year={1989}, pages={69–80} }

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