| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abnormal glycosylation of dystroglycan in human genetic disease
|
Hewitt, Jane E.
|
|
2009
|
1792 |
9 |
p. 853-861
9 p.
|
artikel
|
| 2 |
CDG nomenclature: Time for a change!
|
Jaeken, Jaak
|
|
2009
|
1792 |
9 |
p. 825-826
2 p.
|
artikel
|
| 3 |
COG defects, birth and rise!
|
Foulquier, François
|
|
2009
|
1792 |
9 |
p. 896-902
7 p.
|
artikel
|
| 4 |
Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): Where are we now?
|
Denecke, Jonas
|
|
2009
|
1792 |
9 |
p. 915-920
6 p.
|
artikel
|
| 5 |
Editorial Board
|
|
|
2009
|
1792 |
9 |
p. i-
1 p.
|
artikel
|
| 6 |
Familial tumoral calcinosis and the role of O-glycosylation in the maintenance of phosphate homeostasis
|
Chefetz, Ilana
|
|
2009
|
1792 |
9 |
p. 847-852
6 p.
|
artikel
|
| 7 |
From glycosylation disorders back to glycosylation: What have we learned?
|
Hennet, Thierry
|
|
2009
|
1792 |
9 |
p. 921-924
4 p.
|
artikel
|
| 8 |
From glycosylation to glycosylation diseases
|
Jaeken, Jaak
|
|
2009
|
1792 |
9 |
p. 823-
1 p.
|
artikel
|
| 9 |
Glycosylation diseases: Quo vadis?
|
Schachter, Harry
|
|
2009
|
1792 |
9 |
p. 925-930
6 p.
|
artikel
|
| 10 |
Hereditary Inclusion Body Myopathy: A decade of progress
|
Huizing, Marjan
|
|
2009
|
1792 |
9 |
p. 881-887
7 p.
|
artikel
|
| 11 |
How does a medical doctor become a glycobiologist
|
Hennet, Thierry
|
|
2009
|
1792 |
9 |
p. 824-
1 p.
|
artikel
|
| 12 |
Hypoglycosylation due to dolichol metabolism defects
|
Denecke, Jonas
|
|
2009
|
1792 |
9 |
p. 888-895
8 p.
|
artikel
|
| 13 |
Inherited glycosylphosphatidyl inositol deficiency: A treatable CDG
|
Almeida, Antonio
|
|
2009
|
1792 |
9 |
p. 874-880
7 p.
|
artikel
|
| 14 |
MGAT2 deficiency (CDG-IIa): The Life of J.
|
de Cock, Paul
|
|
2009
|
1792 |
9 |
p. 844-846
3 p.
|
artikel
|
| 15 |
The clinical spectrum of phosphomannomutase 2 deficiency (CDG-Ia)
|
Grünewald, Stephanie
|
|
2009
|
1792 |
9 |
p. 827-834
8 p.
|
artikel
|
| 16 |
The clinical spectrum of phosphomannose isomerase deficiency, with an evaluation of mannose treatment for CDG-Ib
|
de Lonlay, P.
|
|
2009
|
1792 |
9 |
p. 841-843
3 p.
|
artikel
|
| 17 |
Towards a therapy for phosphomannomutase 2 deficiency, the defect in CDG-Ia patients
|
Freeze, Hudson H.
|
|
2009
|
1792 |
9 |
p. 835-840
6 p.
|
artikel
|
| 18 |
Vacuolar H+-ATPase meets glycosylation in patients with cutis laxa
|
Guillard, Mailys
|
|
2009
|
1792 |
9 |
p. 903-914
12 p.
|
artikel
|
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