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 (41-50 of 257) with videos related to

Pageof 26
Sort By:
Lancet (London, England)|December 12, 1992
Serum lysosomal enzyme abnormalities in galactosaemiaJ Jaeken, J Kint, L Spaapen
Lancet (London, England)|October 9, 1976
D-penicillamine-induced IgA deficiency in Wilson's diseaseW Proesmans, J Jaeken, R Eeckels
European Journal of Pediatrics|May 2, 2000
Long-term follow-up of portacaval shunt in glycogen storage disease type 1BL Corbeel, S Van Lierde, J Jaeken
Journal of Inherited Metabolic Disease|January 1, 1993
Inherited disorders of GABA metabolismC Jakobs, J Jaeken, K M Gibson
Lancet (London, England)|December 21, 1991
Vigabatrin as spasmolytic drugJ Jaeken, P De Cock, P Casaer
Journal of Inherited Metabolic Disease|January 19, 2026
CDG due to Defective Membrane Transporters: UpdateD Quelhas, C R Ferreira, J Jaeken
Journal of Inherited Metabolic Disease|July 23, 2003
Abnormal lysosomal inclusions in liver hepatocytes but not in fibroblasts in congenital disorders of glycosylation (CDG)S Grünewald, R De Vos, J Jaeken
American Journal of Human Genetics|October 1, 1996
Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain developmentJ Tan, J Dunn, J Jaeken, et al.
Bulletin De La Societe Belge D'Ophtalmologie|January 5, 2002
Sudden development of bilateral cataract in a child with Dubowitz syndrome: a case reportI Annemans, B Foets, J Jaeken, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1995
Does a mutation of the glycine receptor modify GABA metabolism in startle disease?M Berthier, D Oriot, D Bonneau, et al.
Pageof 26

Showing results (41-50 of 257) with videos related to

Sort By:
Pageof 26
Lancet (London, England)|December 12, 1992
Serum lysosomal enzyme abnormalities in galactosaemiaJ Jaeken, J Kint, L Spaapen
Lancet (London, England)|October 9, 1976
D-penicillamine-induced IgA deficiency in Wilson's diseaseW Proesmans, J Jaeken, R Eeckels
European Journal of Pediatrics|May 2, 2000
Long-term follow-up of portacaval shunt in glycogen storage disease type 1BL Corbeel, S Van Lierde, J Jaeken
Journal of Inherited Metabolic Disease|January 1, 1993
Inherited disorders of GABA metabolismC Jakobs, J Jaeken, K M Gibson
Lancet (London, England)|December 21, 1991
Vigabatrin as spasmolytic drugJ Jaeken, P De Cock, P Casaer
Journal of Inherited Metabolic Disease|January 19, 2026
CDG due to Defective Membrane Transporters: UpdateD Quelhas, C R Ferreira, J Jaeken
Journal of Inherited Metabolic Disease|July 23, 2003
Abnormal lysosomal inclusions in liver hepatocytes but not in fibroblasts in congenital disorders of glycosylation (CDG)S Grünewald, R De Vos, J Jaeken
American Journal of Human Genetics|October 1, 1996
Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain developmentJ Tan, J Dunn, J Jaeken, et al.
Bulletin De La Societe Belge D'Ophtalmologie|January 5, 2002
Sudden development of bilateral cataract in a child with Dubowitz syndrome: a case reportI Annemans, B Foets, J Jaeken, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1995
Does a mutation of the glycine receptor modify GABA metabolism in startle disease?M Berthier, D Oriot, D Bonneau, et al.
Pageof 26