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Journal of Inherited Metabolic Disease
|
January 1, 1991
A new variant of the carbohydrate deficient glycoproteins syndrome
V T Ramaekers, H Stibler, J Kint, et al.
Lancet (London, England)
|
May 13, 1989
Vigabatrin in GABA metabolism disorders
J Jaeken, P Casaer, P de Cock, et al.
Journal of Inherited Metabolic Disease
|
June 1, 1997
Inborn errors of the purine nucleotide cycle: adenylosuccinase deficiency
G Van den Berghe, M F Vincent, J Jaeken
Biochimica Et Biophysica Acta
|
November 26, 1999
Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency)
H Carchon, E Van Schaftingen, G Matthijs, et al.
Journal of Inherited Metabolic Disease
|
October 25, 2008
On the nomenclature of congenital disorders of glycosylation (CDG)
J Jaeken, T Hennet, H H Freeze, et al.
Annales De Genetique
|
January 1, 1979
Partial trisomy 22q with elevated arylsulfatase-A activity
J P Fryns, J Jaeken, H van den Berghe
Glycoconjugate Journal
|
May 14, 1998
Determination of glycan structures and molecular masses of the glycovariants of serum transferrin from a patient with carbohydrate deficient syndrome type II
B Coddeville, H Carchon, J Jaeken, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1994
Genetic and clinical heterogeneity in hypoxanthine phosphoribosyltransferase deficiencies
R Burgemeister, W Gutensohn, G Van den Berghe, et al.
Tijdschrift Voor Kindergeneeskunde
|
June 1, 1983
[Neonatal hyperammonemia]
J Jaeken, H Devlieger, M Evens, et al.
The British Journal of Ophthalmology
|
October 1, 1996
Evolution of ophthalmic and electrophysiological findings in identical twin sisters with the carbohydrate deficient glycoprotein syndrome type 1 over a period of 14 years
I Casteels, W Spileers, A Leys, et al.
Page
of 26
Search research articles
Search
Showing results (61-70 of 257) with videos related to
Sort By:
Page
of 26
Journal of Inherited Metabolic Disease
|
January 1, 1991
A new variant of the carbohydrate deficient glycoproteins syndrome
V T Ramaekers, H Stibler, J Kint, et al.
Lancet (London, England)
|
May 13, 1989
Vigabatrin in GABA metabolism disorders
J Jaeken, P Casaer, P de Cock, et al.
Journal of Inherited Metabolic Disease
|
June 1, 1997
Inborn errors of the purine nucleotide cycle: adenylosuccinase deficiency
G Van den Berghe, M F Vincent, J Jaeken
Biochimica Et Biophysica Acta
|
November 26, 1999
Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency)
H Carchon, E Van Schaftingen, G Matthijs, et al.
Journal of Inherited Metabolic Disease
|
October 25, 2008
On the nomenclature of congenital disorders of glycosylation (CDG)
J Jaeken, T Hennet, H H Freeze, et al.
Annales De Genetique
|
January 1, 1979
Partial trisomy 22q with elevated arylsulfatase-A activity
J P Fryns, J Jaeken, H van den Berghe
Glycoconjugate Journal
|
May 14, 1998
Determination of glycan structures and molecular masses of the glycovariants of serum transferrin from a patient with carbohydrate deficient syndrome type II
B Coddeville, H Carchon, J Jaeken, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1994
Genetic and clinical heterogeneity in hypoxanthine phosphoribosyltransferase deficiencies
R Burgemeister, W Gutensohn, G Van den Berghe, et al.
Tijdschrift Voor Kindergeneeskunde
|
June 1, 1983
[Neonatal hyperammonemia]
J Jaeken, H Devlieger, M Evens, et al.
The British Journal of Ophthalmology
|
October 1, 1996
Evolution of ophthalmic and electrophysiological findings in identical twin sisters with the carbohydrate deficient glycoprotein syndrome type 1 over a period of 14 years
I Casteels, W Spileers, A Leys, et al.
Page
of 26