Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J Jaeken

Showing results (61-70 of 257) with videos related to

Pageof 26
Sort By:
Journal of Inherited Metabolic Disease|January 1, 1991
A new variant of the carbohydrate deficient glycoproteins syndromeV T Ramaekers, H Stibler, J Kint, et al.
Lancet (London, England)|May 13, 1989
Vigabatrin in GABA metabolism disordersJ Jaeken, P Casaer, P de Cock, et al.
Journal of Inherited Metabolic Disease|June 1, 1997
Inborn errors of the purine nucleotide cycle: adenylosuccinase deficiencyG 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 activityJ 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 IIB Coddeville, H Carchon, J Jaeken, et al.
Advances in Experimental Medicine and Biology|January 1, 1994
Genetic and clinical heterogeneity in hypoxanthine phosphoribosyltransferase deficienciesR 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 yearsI Casteels, W Spileers, A Leys, et al.
Pageof 26

Showing results (61-70 of 257) with videos related to

Sort By:
Pageof 26
Journal of Inherited Metabolic Disease|January 1, 1991
A new variant of the carbohydrate deficient glycoproteins syndromeV T Ramaekers, H Stibler, J Kint, et al.
Lancet (London, England)|May 13, 1989
Vigabatrin in GABA metabolism disordersJ Jaeken, P Casaer, P de Cock, et al.
Journal of Inherited Metabolic Disease|June 1, 1997
Inborn errors of the purine nucleotide cycle: adenylosuccinase deficiencyG 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 activityJ 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 IIB Coddeville, H Carchon, J Jaeken, et al.
Advances in Experimental Medicine and Biology|January 1, 1994
Genetic and clinical heterogeneity in hypoxanthine phosphoribosyltransferase deficienciesR 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 yearsI Casteels, W Spileers, A Leys, et al.
Pageof 26