-
1
-
-
0025279652
-
The biology of transferrin
-
G. de Jong, J.P. van Dijk and H.G. van Eijk, The biology of transferrin, Clin. Chim. Acta, 190, 1-46 (1990).
-
(1990)
Clin. Chim. Acta
, vol.190
, pp. 1-46
-
-
De Jong, G.1
Van Dijk, J.P.2
Van Eijk, H.G.3
-
2
-
-
0035152278
-
Carbohydrate-deficient transferrin as a marker of chronic alcohol abuse:a critical review of preanalysis analysis, and interpretation
-
T. Arndt, Carbohydrate-deficient transferrin as a marker of chronic alcohol abuse:a critical review of preanalysis, analysis, and interpretation, Clin. Chem., 47, 13-27 (2001).
-
(2001)
Clin. Chem.
, vol.47
, pp. 13-27
-
-
Arndt, T.1
-
3
-
-
0029020045
-
Transferrin microheterogeneity as a probe in normal and disease states
-
G. de Jong, R. Feelders, W.L. van Noort and H.G. van Eijk, Transferrin microheterogeneity as a probe in normal and disease states, Glycoconj. J., 12, 219-226 (1995).
-
(1995)
Glycoconj. J.
, vol.12
, pp. 219-226
-
-
De Jong, G.1
Feelders, R.2
Van Noort, W.L.3
Van Eijk, H.G.4
-
4
-
-
0026331891
-
Carbohydrate-deficient transferrin in serum:a new marker of potentially harmful alcohol consumption reviewed
-
H. Stibler, Carbohydrate-deficient transferrin in serum:a new marker of potentially harmful alcohol consumption reviewed, Clin. Chem., 37, 2029-2037 (1991).
-
(1991)
Clin. Chem.
, vol.37
, pp. 2029-2037
-
-
Stibler, H.1
-
5
-
-
0037605951
-
Congenital disorders of glycosylation:review of their molecular bases clinical presentations and specific therapies
-
T. Marquardt and J. Denecke, Congenital disorders of glycosylation:review of their molecular bases, clinical presentations and specific therapies, Eur. J. Pediatr., 162, 359-379 (2003).
-
(2003)
Eur. J. Pediatr.
, vol.162
, pp. 359-379
-
-
Marquardt, T.1
Denecke, J.2
-
6
-
-
0344784414
-
Transferrin isoform distribution:gender and alcohol consumption
-
O. Ma°rtensson, A. Härlin, R. Brandt, K. Seppä and P. Sillanaukee, Transferrin isoform distribution:gender and alcohol consumption, Alcohol. Clin. Exp. Res., 21, 1710-1715 (1997).
-
(1997)
Alcohol. Clin. Exp. Res.
, vol.21
, pp. 1710-1715
-
-
Ma°rtensson, O.1
Härlin, A.2
Brandt, R.3
Seppä, K.4
Sillanaukee, P.5
-
7
-
-
0242267940
-
Improved HPLC method for carbohydrate-deficient transferrin in serum
-
A. Helander, A. Husa and J.-O. Jeppsson, Improved HPLC method for carbohydrate-deficient transferrin in serum, Clin. Chem., 49, 1881-1890 (2003).
-
(2003)
Clin. Chem.
, vol.49
, pp. 1881-1890
-
-
Helander, A.1
Husa, A.2
Jeppsson, J.-O.3
-
8
-
-
0023090641
-
Human transferrin polymorphism
-
M.I. Kamboh and R.E. Ferrell, Human transferrin polymorphism, Hum. Hered., 37, 65-81 (1987).
-
(1987)
Hum. Hered.
, vol.37
, pp. 65-81
-
-
Kamboh, M.I.1
Ferrell, R.E.2
-
9
-
-
0642276878
-
Biological markers in alcoholism
-
A. Helander, Biological markers in alcoholism, J. Neural Transm. Suppl., 15-32 (2003).
-
(2003)
J. Neural Transm
, Issue.SUPPL.
, pp. 15-32
-
-
Helander, A.1
-
10
-
-
0032742686
-
Carbohydrate deficient transferrin in alcoholic liver disease:mechanisms and clinical implications
-
C.S. Lieber, Carbohydrate deficient transferrin in alcoholic liver disease:mechanisms and clinical implications, Alcohol, 19, 249-254 (1999).
-
(1999)
Alcohol
, vol.19
, pp. 249-254
-
-
Lieber, C.S.1
-
11
-
-
0035125082
-
Possible reasons why heavy drinking increases carbohydrate-deficient transferrin
-
P. Sillanaukee, N. Strid, J.P. Allen and R.Z. Litten, Possible reasons why heavy drinking increases carbohydrate-deficient transferrin, Alcohol. Clin. Exp. Res., 25, 34-40 (2001).
-
(2001)
Alcohol. Clin. Exp. Res.
, vol.25
, pp. 34-40
-
-
Sillanaukee, P.1
Strid, N.2
Allen, J.P.3
Litten, R.Z.4
-
12
-
-
0027429940
-
Carbohydrate-deficient transferrin quantified by HPLC to determine heavy consumption of alcohol
-
J.O. Jeppsson, H. Kristensson and C. Fimiani, Carbohydrate-deficient transferrin quantified by HPLC to determine heavy consumption of alcohol, Clin. Chem., 39, 2115-2120 (1993).
-
(1993)
Clin. Chem.
, vol.39
, pp. 2115-2120
-
-
Jeppsson, J.O.1
Kristensson, H.2
Fimiani, C.3
-
13
-
-
0029858953
-
Carbohydrate-deficient transferrin and gamma-glutamyl transferase levels during disulfiram therapy
-
A. Helander and S. Carlsson, Carbohydrate-deficient transferrin and gamma-glutamyl transferase levels during disulfiram therapy, Alcohol. Clin. Exp. Res., 20, 1202-1205 (1996).
-
(1996)
Alcohol. Clin. Exp. Res.
, vol.20
, pp. 1202-1205
-
-
Helander, A.1
Carlsson, S.2
-
14
-
-
0029005170
-
Carbohydrate composition of serum transferrin isoforms from patients with high alcohol consumption
-
E. Landberg, P. Pa°hlsson, A. Lundblad, A. Arnetorp and J.-O. Jeppsson, Carbohydrate composition of serum transferrin isoforms from patients with high alcohol consumption, Biochem. Biophys. Res. Commun., 210, 267-274 (1995).
-
(1995)
Biochem. Biophys. Res. Commun.
, vol.210
, pp. 267-274
-
-
Landberg, E.1
Pa°hlsson, P.2
Lundblad, A.3
Arnetorp, A.4
Jeppsson, J.-O.5
-
15
-
-
0032510424
-
Identification of carbohydrate deficient transferrin forms by MALDI-TOF mass spectrometry and lectin ELISA
-
J. Peter, C. Unverzagt, W.D. Engel, D. Renauer, C. Seidel and W. Hösel, Identification of carbohydrate deficient transferrin forms by MALDI-TOF mass spectrometry and lectin ELISA, Biochim. Biophys. Acta, 1380, 93-101 (1998).
-
(1998)
Biochim. Biophys. Acta
, vol.1380
, pp. 93-101
-
-
Peter, J.1
Unverzagt, C.2
Engel, W.D.3
Renauer, D.4
Seidel, C.5
Hösel, W.6
-
16
-
-
0032823845
-
Microheterogeneity of serum glycoproteins in patients with chronic alcohol abuse compared with carbohydrate-deficient glycoprotein syndrome type I
-
H. Henry, F. Froehlich, R. Perret, J.D. Tissot, B. Eilers-Messerli, D. Lavanchy, C. Dionisi-Vici, J.J. Gonvers and C. Bachmann, Microheterogeneity of serum glycoproteins in patients with chronic alcohol abuse compared with carbohydrate-deficient glycoprotein syndrome type I, Clin. Chem., 45, 1408-1413 (1999).
-
(1999)
Clin. Chem.
, vol.45
, pp. 1408-1413
-
-
Henry, H.1
Froehlich, F.2
Perret, R.3
Tissot, J.D.4
Eilers-Messerli, B.5
Lavanchy, D.6
Dionisi-Vici, C.7
Gonvers, J.J.8
Bachmann, C.9
-
17
-
-
0037368601
-
The effects of ethanol on the glycosylation of human transferrin
-
C. Flahaut, J.C. Michalski, T. Danel, M.H. Humbert and A. Klein, The effects of ethanol on the glycosylation of human transferrin, Glycobiology, 13, 191-198 (2003).
-
(2003)
Glycobiology
, vol.13
, pp. 191-198
-
-
Flahaut, C.1
Michalski, J.C.2
Danel, T.3
Humbert, M.H.4
Klein, A.5
-
18
-
-
0347989232
-
Mass spectrometric analysis of human transferrin in different body fluids
-
P. Kleinert, T. Kuster, S. Durka, D. Ballhausen, N.U. Bosshard, B. Steinmann, E. Hanseler, J. Jaeken, C.W. Heizmann and H. Troxler, Mass spectrometric analysis of human transferrin in different body fluids, Clin. Chem. Lab. Med., 41, 1580-1588 (2003).
-
(2003)
Clin. Chem. Lab. Med.
, vol.41
, pp. 1580-1588
-
-
Kleinert, P.1
Kuster, T.2
Durka, S.3
Ballhausen, D.4
Bosshard, N.U.5
Steinmann, B.6
Hanseler, E.7
Jaeken, J.8
Heizmann, C.W.9
Troxler, H.10
-
19
-
-
0023020154
-
Micro anion exchange chromatography of carbohydrate-deficient transferrin in serum in relation to alcohol consumption (Swedish Patent 8400587-5)
-
H. Stibler, S. Borg and M. Joustra, Micro anion exchange chromatography of carbohydrate-deficient transferrin in serum in relation to alcohol consumption (Swedish Patent 8400587-5), Alcohol. Clin. Exp. Res., 10, 535-544 (1986).
-
(1986)
Alcohol. Clin. Exp. Res.
, vol.10
, pp. 535-544
-
-
Stibler, H.1
Borg, S.2
Joustra, M.3
-
20
-
-
0033023879
-
Comparing the diagnostic accuracy of carbohydrate-deficient transferrin gamma-glutamyltransferase, and mean cell volume in a general practice population
-
G.J. Meerkerk, K.H. Njoo, I.M. Bongers, P. Trienekens and J.A. van Oers, Comparing the diagnostic accuracy of carbohydrate-deficient transferrin, gamma-glutamyltransferase, and mean cell volume in a general practice population, Alcohol Clin. Exp. Res., 23, 1052-1059 (1999).
-
(1999)
Alcohol Clin. Exp. Res.
, vol.23
, pp. 1052-1059
-
-
Meerkerk, G.J.1
Njoo, K.H.2
Bongers, I.M.3
Trienekens, P.4
Van Oers, J.A.5
-
21
-
-
0032948087
-
Absolute or relative measurement of carbohydrate-deficient transferrin in serum? Experiences with three immunological assays
-
A. Helander, Absolute or relative measurement of carbohydrate-deficient transferrin in serum? Experiences with three immunological assays, Clin. Chem., 45, 131-135 (1999).
-
(1999)
Clin. Chem.
, vol.45
, pp. 131-135
-
-
Helander, A.1
-
22
-
-
0034960523
-
Interference of transferrin isoform types with carbohydrate-deficient transferrin quantification in the identification of alcohol abuse
-
A. Helander, G. Eriksson, H. Stibler and J.-O. Jeppsson, Interference of transferrin isoform types with carbohydrate-deficient transferrin quantification in the identification of alcohol abuse, Clin. Chem., 47, 1225-1233 (2001).
-
(2001)
Clin. Chem.
, vol.47
, pp. 1225-1233
-
-
Helander, A.1
Eriksson, G.2
Stibler, H.3
Jeppsson, J.-O.4
-
23
-
-
0037137478
-
Human disorders in N-glycosylation and animal models
-
H.H. Freeze, Human disorders in N-glycosylation and animal models, Biochim. Biophys. Acta, 1573, 388-393 (2002).
-
(2002)
Biochim. Biophys. Acta
, vol.1573
, pp. 388-393
-
-
Freeze, H.H.1
-
24
-
-
0038042511
-
Komrower Lecture. Congenital disorders of glycosylation (CDG):it's all in it!
-
J. Jaeken, Komrower Lecture. Congenital disorders of glycosylation (CDG):it's all in it!, J. Inherit. Metab. Dis., 26, 99-118 (2003).
-
(2003)
J. Inherit. Metab. Dis.
, vol.26
, pp. 99-118
-
-
Jaeken, J.1
-
25
-
-
0035937499
-
Chemical glycobiology
-
C.R. Bertozzi and L.L. Kiessling, Chemical glycobiology, Science, 291, 2357-2364 (2001).
-
(2001)
Science
, vol.291
, pp. 2357-2364
-
-
Bertozzi, C.R.1
Kiessling, L.L.2
-
26
-
-
3442881366
-
Congenital disorders of glycosylation:a booming chapter of pediatrics
-
J. Jaeken and H. Carchon, Congenital disorders of glycosylation:a booming chapter of pediatrics, Curr. Opin. Pediatr., 16, 434-439 (2004).
-
(2004)
Curr. Opin. Pediatr.
, vol.16
, pp. 434-439
-
-
Jaeken, J.1
Carchon, H.2
-
27
-
-
3042684546
-
Identification and functional analysis of a defect in the human ALG9 gene:definition of congenital disorder of glycosylation type IL
-
C.G. Frank, C.E. Grubenmann, W. Eyaid, E.G. Berger, M. Aebi and T. Hennet, Identification and functional analysis of a defect in the human ALG9 gene:definition of congenital disorder of glycosylation type IL, Am. J. Hum. Genet., 75, 146-150 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 146-150
-
-
Frank, C.G.1
Grubenmann, C.E.2
Eyaid, W.3
Berger, E.G.4
Aebi, M.5
Hennet, T.6
-
28
-
-
0035204777
-
Congenital disorders of glycosylation and the pediatric liver
-
H.H. Freeze, Congenital disorders of glycosylation and the pediatric liver, Semin. Liver Dis., 21, 501-515 (2001).
-
(2001)
Semin. Liver Dis.
, vol.21
, pp. 501-515
-
-
Freeze, H.H.1
-
29
-
-
0034921209
-
Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease
-
P. Briones, M.A. Vilaseca, M.T. Garcia-Silva, M. Pineda, J. Colomer, I. Ferrer, J. Artigas, J. Jaeken and A. Chabas, Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease, Eur. J. Paediatr. Neurol., 5, 127-131 (2001).
-
(2001)
Eur. J. Paediatr. Neurol.
, vol.5
, pp. 127-131
-
-
Briones, P.1
Vilaseca, M.A.2
Garcia-Silva, M.T.3
Pineda, M.4
Colomer, J.5
Ferrer, I.6
Artigas, J.7
Jaeken, J.8
Chabas, A.9
-
30
-
-
0036842354
-
Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins
-
G.M. Enns, R.D. Steiner, N. Buist, C. Cowan, K.A. Leppig, M.F. McCracken, V. Westphal, H.H. Freeze, F. O'Brien J, J. Jaeken, G. Matthijs, S. Behera and L. Hudgins, Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins, J. Pediatr., 141, 695-700 (2002).
-
(2002)
J. Pediatr.
, vol.141
, pp. 695-700
-
-
Enns, G.M.1
Steiner, R.D.2
Buist, N.3
Cowan, C.4
Leppig, K.A.5
McCracken, M.F.6
Westphal, V.7
Freeze, H.H.8
O'Brien, F.J.9
Jaeken, J.10
Matthijs, G.11
Behera, S.12
Hudgins, L.13
-
31
-
-
2142759526
-
Testing for congenital disorders of glycosylation by HPLC measurement of serum transferrin glycoforms
-
A. Helander, J. Bergström and H.H. Freeze, Testing for congenital disorders of glycosylation by HPLC measurement of serum transferrin glycoforms, Clin. Chem., 50, 954-958 (2004).
-
(2004)
Clin. Chem.
, vol.50
, pp. 954-958
-
-
Helander, A.1
Bergström, J.2
Freeze, H.H.3
-
32
-
-
4644364677
-
Improvement of CDG diagnosis by combined examination of several glycoproteins
-
J. Fang, V. Peters, B. Assmann, C. Korner and G.F. Hoffmann, Improvement of CDG diagnosis by combined examination of several glycoproteins, J. Inherit. Metab. Dis., 27, 581-590 (2004).
-
(2004)
J. Inherit. Metab. Dis.
, vol.27
, pp. 581-590
-
-
Fang, J.1
Peters, V.2
Assmann, B.3
Korner, C.4
Hoffmann, G.F.5
-
33
-
-
1542291044
-
The prenatal diagnosis of congenital disorders of glycosylation (CDG)
-
G. Matthijs, E. Schollen and E. Van Schaftingen, The prenatal diagnosis of congenital disorders of glycosylation (CDG), Prenat. Diagn., 24, 114-116 (2004).
-
(2004)
Prenat. Diagn.
, vol.24
, pp. 114-116
-
-
Matthijs, G.1
Schollen, E.2
Van Schaftingen, E.3
-
34
-
-
0029875278
-
Sensitivity and specificity of carbohydratedeficient transferrin as a marker of alcohol abuse are significantly influenced by alterations in serum transferrin:comparison of two methods
-
K. Sorvajärvi, J.E. Blake, Y. Israel and O. Niemelä, Sensitivity and specificity of carbohydratedeficient transferrin as a marker of alcohol abuse are significantly influenced by alterations in serum transferrin:comparison of two methods, Alcohol. Clin. Exp. Res., 20, 449-454 (1996).
-
(1996)
Alcohol. Clin. Exp. Res.
, vol.20
, pp. 449-454
-
-
Sorvajärvi, K.1
Blake, J.E.2
Israel, Y.3
Niemelä, O.4
-
35
-
-
0032571783
-
Carbohydrate deficient transferrin in the assessment of alcohol misuse:absolute or relative measurements?
-
J. Keating, C. Cheung, T.J. Peters and R.A. Sherwood, Carbohydrate deficient transferrin in the assessment of alcohol misuse:absolute or relative measurements? A comparison of two methods with regard to total transferrin concentration, Clin. Chim. Acta, 272, 159-169 (1998).
-
(1998)
A comparison of two methods with regard to total transferrin concentration, Clin. Chim. Acta
, vol.272
, pp. 159-169
-
-
Keating, J.1
Cheung, C.2
Peters, T.J.3
Sherwood, R.A.4
-
36
-
-
0033880511
-
Does trisialo-transferrin provide valuable information for the laboratory diagnosis of chronically increased alcohol consumption by determination of carbohydrate-deficient transferrin?
-
L. Dibbelt, Does trisialo-transferrin provide valuable information for the laboratory diagnosis of chronically increased alcohol consumption by determination of carbohydrate-deficient transferrin?, Clin. Chem., 46, 1203-1205 (2000).
-
(2000)
Clin. Chem.
, vol.46
, pp. 1203-1205
-
-
Dibbelt, L.1
-
37
-
-
0030869940
-
Capillary electrophoresis-based separation of transferrin sialoforms in patients with carbohydratedeficient glycoprotein syndrome
-
R.P. Oda, R. Prasad, R.L. Stout, D. Coffin, W.P. Patton, D.L. Kraft, J.F. O'Brien and J.P. Landers, Capillary electrophoresis-based separation of transferrin sialoforms in patients with carbohydratedeficient glycoprotein syndrome, Electrophoresis, 18, 1819-1826 (1997).
-
(1997)
Electrophoresis
, vol.18
, pp. 1819-1826
-
-
Oda, R.P.1
Prasad, R.2
Stout, R.L.3
Coffin, D.4
Patton, W.P.5
Kraft, D.L.6
O'Brien, J.F.7
Landers, J.P.8
-
38
-
-
0033652951
-
Personal experience with the application of carbohydrate-deficient transferrin (CDT) assays to the detection of congenital disorders of glycosylation
-
C. Colome, I. Ferrer, R. Artuch, M.A. Vilaseca, M. Pineda and P. Briones, Personal experience with the application of carbohydrate-deficient transferrin (CDT) assays to the detection of congenital disorders of glycosylation, Clin. Chem. Lab. Med., 38, 965-969 (2000).
-
(2000)
Clin. Chem. Lab. Med.
, vol.38
, pp. 965-969
-
-
Colome, C.1
Ferrer, I.2
Artuch, R.3
Vilaseca, M.A.4
Pineda, M.5
Briones, P.6
-
39
-
-
0035107128
-
Rapid determination of transferrin isoforms by immunoaffinity liquid chromatography and electrospray mass spectrometry
-
J.M. Lacey, H.R. Bergen, M.J. Magera, S. Naylor and J.F. O'Brien, Rapid determination of transferrin isoforms by immunoaffinity liquid chromatography and electrospray mass spectrometry, Clin. Chem., 47, 513-518 (2001).
-
(2001)
Clin. Chem.
, vol.47
, pp. 513-518
-
-
Lacey, J.M.1
Bergen, H.R.2
Magera, M.J.3
Naylor, S.4
O'Brien, J.F.5
-
40
-
-
0038238795
-
Western blotting with diaminobenzidine detection for the diagnosis of congenital disorders of glycosylation
-
R. Artuch, I. Ferrer, J. Pineda, J. Moreno, C. Busquets, P. Briones and M.A. Vilaseca, Western blotting with diaminobenzidine detection for the diagnosis of congenital disorders of glycosylation, J. Neurosci. Methods., 125, 167-171 (2003).
-
(2003)
J. Neurosci. Methods.
, vol.125
, pp. 167-171
-
-
Artuch, R.1
Ferrer, I.2
Pineda, J.3
Moreno, J.4
Busquets, C.5
Briones, P.6
Vilaseca, M.A.7
-
41
-
-
0027768796
-
Electrospray ionization-mass spectrometric analysis of serum transferrin isoforms in patients with carbohydrate-deficient glycoprotein syndrome
-
K. Yamashita, T. Ohkura, H. Ideo, K. Ohno and M. Kanai, Electrospray ionization-mass spectrometric analysis of serum transferrin isoforms in patients with carbohydrate-deficient glycoprotein syndrome, J. Biochem. (Tokyo), 114, 766-769 (1993).
-
(1993)
J. Biochem. (Tokyo)
, vol.114
, pp. 766-769
-
-
Yamashita, K.1
Ohkura, T.2
Ideo, H.3
Ohno, K.4
Kanai, M.5
-
42
-
-
0035042973
-
Lectin analyses of glycoprotein hormones in patients with congenital disorders of glycosylation
-
M.C. Ferrari, R. Parini, M.D. Di Rocco, G. Radetti, P. Beck-Peccoz and L. Persani, Lectin analyses of glycoprotein hormones in patients with congenital disorders of glycosylation, Eur. J. Endocrinol., 144, 409-416 (2001).
-
(2001)
Eur. J. Endocrinol.
, vol.144
, pp. 409-416
-
-
Ferrari, M.C.1
Parini, R.2
Di Rocco, M.D.3
Radetti, G.4
Beck-Peccoz, P.5
Persani, L.6
-
43
-
-
0034855738
-
Study of Axis-Shield new %CDT immunoassay for quantification of carbohydrate-deficient transferrin (CDT) in serum
-
A. Helander, M. Fors and B. Zakrisson, Study of Axis-Shield new %CDT immunoassay for quantification of carbohydrate-deficient transferrin (CDT) in serum, Alcohol Alcohol., 36, 406-412 (2001).
-
(2001)
Alcohol Alcohol.
, vol.36
, pp. 406-412
-
-
Helander, A.1
Fors, M.2
Zakrisson, B.3
-
44
-
-
0029743406
-
Carbohydrate-deficient transferrin measured by highperformance liquid chromatography and CDTect immunoassay
-
P. Simonsson, S. Lindberg and C. Alling, Carbohydrate-deficient transferrin measured by highperformance liquid chromatography and CDTect immunoassay, Alcohol Alcohol., 31, 397-402 (1996).
-
(1996)
Alcohol Alcohol.
, vol.31
, pp. 397-402
-
-
Simonsson, P.1
Lindberg, S.2
Alling, C.3
-
45
-
-
0030829912
-
Determination of carbohydrate-deficient transferrin and total transferrin by HPLC:diagnostic evaluation
-
F. Renner, K. Stratmann, R.D. Kanitz and T. Wetterling, Determination of carbohydrate-deficient transferrin and total transferrin by HPLC:diagnostic evaluation, Clin. Lab., 43, 955-964 (1997).
-
(1997)
Clin. Lab.
, vol.43
, pp. 955-964
-
-
Renner, F.1
Stratmann, K.2
Kanitz, R.D.3
Wetterling, T.4
-
46
-
-
0031057660
-
Quantification of carbohydrate-deficient transferrin by ion-exchange chromatography with an enzymatically prepared calibrator
-
F. Renner and R.D. Kanitz, Quantification of carbohydrate-deficient transferrin by ion-exchange chromatography with an enzymatically prepared calibrator, Clin. Chem., 43, 485-490 (1997).
-
(1997)
Clin. Chem.
, vol.43
, pp. 485-490
-
-
Renner, F.1
Kanitz, R.D.2
-
47
-
-
0031058920
-
High-performance liquid chromatography improves diagnostic efficiency of carbohydrate-deficient transferrin
-
E. Werle, G.E. Seitz, B. Kohl, W. Fiehn and H.K. Seitz, High-performance liquid chromatography improves diagnostic efficiency of carbohydrate-deficient transferrin, Alcohol Alcohol., 32, 71-77 (1997).
-
(1997)
Alcohol Alcohol.
, vol.32
, pp. 71-77
-
-
Werle, E.1
Seitz, G.E.2
Kohl, B.3
Fiehn, W.4
Seitz, H.K.5
-
48
-
-
0034833683
-
Comparison of HPLCand small column(CDTect) methods for disialotransferrin
-
U. Turpeinen, T. Methuen, H. Alfthan, K. Laitinen, M. Salaspuro and U.H. Stenman, Comparison of HPLCand small column(CDTect) methods for disialotransferrin, Clin.Chem., 47, 1782-1787 (2001).
-
(2001)
Clin.Chem.
, vol.47
, pp. 1782-1787
-
-
Turpeinen, U.1
Methuen, T.2
Alfthan, H.3
Laitinen, K.4
Salaspuro, M.5
Stenman, U.H.6
-
49
-
-
33746736849
-
-
A. Helander, J.P. Bergström, Determination of carbohydrate-deficient transferrin in human serum using the Bio-Rad% CDT by HPLC test, Clin Chim. Acta, 187-190 (2006).
-
-
-
Helander, A.1
Bergström, J.P.2
-
50
-
-
0014206038
-
Isolation and partial characterization of three human transferrin variants
-
J.O. Jeppsson, Isolation and partial characterization of three human transferrin variants, Biochim. Biophys. Acta, 140, 468-476 (1967).
-
(1967)
Biochim. Biophys. Acta
, vol.140
, pp. 468-476
-
-
Jeppsson, J.O.1
-
51
-
-
18744399543
-
Carbohydrate-deficient transferrin isoforms measured by capillary zone electrophoresis for detection of alcohol abuse
-
F.J. Legros, V. Nuyens, E. Minet, P. Emonts, K.Z. Boudjeltia, A. Courbe, J.L. Ruelle, J. Colicis, F. de L'Escaille and J.P. Henry, Carbohydrate-deficient transferrin isoforms measured by capillary zone electrophoresis for detection of alcohol abuse, Clin. Chem., 48, 2177-2186 (2002).
-
(2002)
Clin. Chem.
, vol.48
, pp. 2177-2186
-
-
Legros, F.J.1
Nuyens, V.2
Minet, E.3
Emonts, P.4
Boudjeltia, K.Z.5
Courbe, A.6
Ruelle, J.L.7
Colicis, J.8
L'Escaille De, F.9
Henry, J.P.10
-
52
-
-
0018086057
-
Analysis of the iron-binding sites of transferrin by isoelectric focussing
-
H.G. van Eijk,W.L. van Noort, M.J. Kroos and C. van der Heul, Analysis of the iron-binding sites of transferrin by isoelectric focussing, J. Clin. Chem. Clin. Biochem., 16, 557-560 (1978).
-
(1978)
J. Clin. Chem. Clin. Biochem.
, vol.16
, pp. 557-560
-
-
Van Eijk, H.G.1
Van Noort, W.L.2
Kroos, M.J.3
Van Der Heul, C.4
-
53
-
-
1642533464
-
Diagnosis of congenital disorders of glycosylation by capillary zone electrophoresis of serum transferrin
-
H.A. Carchon, R. Chevigne, J.B. Falmagne and J. Jaeken, Diagnosis of congenital disorders of glycosylation by capillary zone electrophoresis of serum transferrin, Clin. Chem., 50, 101-111 (2004).
-
(2004)
Clin. Chem.
, vol.50
, pp. 101-111
-
-
Carchon, H.A.1
Chevigne, R.2
Falmagne, J.B.3
Jaeken, J.4
-
54
-
-
0038732507
-
Increased fucosylation and reduced branching of serum glycoprotein N-glycans in all known subtypes of congenital disorder of glycosylation I
-
N. Callewaert, E. Schollen, A. Vanhecke, J. Jaeken, G. Matthijs and R. Contreras, Increased fucosylation and reduced branching of serum glycoprotein N-glycans in all known subtypes of congenital disorder of glycosylation I, Glycobiology, 13, 367-375 (2003).
-
(2003)
Glycobiology
, vol.13
, pp. 367-375
-
-
Callewaert, N.1
Schollen, E.2
Vanhecke, A.3
Jaeken, J.4
Matthijs, G.5
Contreras, R.6
-
55
-
-
0027930443
-
Carbohydrate deficient glycoprotein syndrome type II:a deficiency in Golgi localised N-acetyl-glucosaminyltransferase II
-
J. Jaeken, H. Schachter, H. Carchon, P. De Cock, B. Coddeville and G. Spik, Carbohydrate deficient glycoprotein syndrome type II:a deficiency in Golgi localised N-acetyl-glucosaminyltransferase II, Arch. Dis. Child., 71, 123-127 (1994).
-
(1994)
Arch. Dis. Child.
, vol.71
, pp. 123-127
-
-
Jaeken, J.1
Schachter, H.2
Carchon, H.3
De Cock, P.4
Coddeville, B.5
Spik, G.6
-
56
-
-
0036200383
-
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId
-
B. Hansske, C. Thiel, T. Lubke, M. Hasilik, S. Honing, V. Peters, P.H. Heidemann, G.F. Hoffmann, E.G. Berger, K. von Figura and C. Korner, Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId, J. Clin. Invest., 109, 725-733 (2002).
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 725-733
-
-
Hansske, B.1
Thiel, C.2
Lubke, T.3
Hasilik, M.4
Honing, S.5
Peters, V.6
Heidemann, P.H.7
Hoffmann, G.F.8
Berger, E.G.9
Von Figura, K.10
Korner, C.11
-
57
-
-
0036208301
-
Congenital disorder of glycosylation IId (CDG-IId)-a new entity:clinical presentation with Dandy-Walker malformation and myopathy
-
V. Peters, J.M. Penzien, G. Reiter, C. Korner, R. Hackler, B. Assmann, J. Fang, J.R. Schaefer, G.F. Hoffmann and P.H. Heidemann, Congenital disorder of glycosylation IId (CDG-IId)-a new entity:clinical presentation with Dandy-Walker malformation and myopathy, Neuropediatrics, 33, 27-32 (2002).
-
(2002)
Neuropediatrics
, vol.33
, pp. 27-32
-
-
Peters, V.1
Penzien, J.M.2
Reiter, G.3
Korner, C.4
Hackler, R.5
Assmann, B.6
Fang, J.7
Schaefer, J.R.8
Hoffmann, G.F.9
Heidemann, P.H.10
-
58
-
-
0035718934
-
Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib:long-term outcome and effects of mannose supplementation
-
V. Westphal, S. Kjaergaard, J.A. Davis, S.M. Peterson, F. Skovby and H.H. Freeze, Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib:long-term outcome and effects of mannose supplementation, Mol. Genet. Metab., 73, 77-85 (2001).
-
(2001)
Mol. Genet. Metab.
, vol.73
, pp. 77-85
-
-
Westphal, V.1
Kjaergaard, S.2
Davis, J.A.3
Peterson, S.M.4
Skovby, F.5
Freeze, H.H.6
|