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J Jaeken

Showing results (1-10 of 257) with videos related to

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Verhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|January 1, 1989
[A not-previously described hereditary neurological disease with a deficiency of sialic acid, galactose and N-acetylglucosamine of plasma glycoproteins]J Jaeken
European Journal of Pediatrics|January 1, 1994
Cerebrospinal fluid as a tool in the diagnosis of neurometabolic diseases: amino acid analysis before and after acid hydrolysisJ Jaeken
Handbook of Clinical Neurology|April 30, 2013
Congenital disorders of glycosylationJ Jaeken
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 6, 2001
Alexander disease and intermediate filaments in astrocytes: a fatal gain of functionJ Jaeken
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Disturbances in aminoglycan synthesis]J Jaeken
Archives of Disease in Childhood|May 1, 1989
Disialotransferrin developmental deficiency syndrome and olivopontocerebellar atrophyJ Jaeken
Journal of Inherited Metabolic Disease|August 2, 2003
Komrower Lecture. Congenital disorders of glycosylation (CDG): it's all in it!J Jaeken
Journal of Inherited Metabolic Disease|July 27, 2004
Congenital disorders of glycosylation (CDG): update and new developmentsJ Jaeken
Verhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|January 1, 1990
[Metabolic diseases: a challenge for pediatrics]J Jaeken
Acta Paediatrica Belgica|January 1, 1977
Metabolic homoiostasis and its disorders in the new-born infant. Recent acquisitionsJ Jaeken, E Eggermont
Pageof 26

Showing results (1-10 of 257) with videos related to

Sort By:
Pageof 26
Verhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|January 1, 1989
[A not-previously described hereditary neurological disease with a deficiency of sialic acid, galactose and N-acetylglucosamine of plasma glycoproteins]J Jaeken
European Journal of Pediatrics|January 1, 1994
Cerebrospinal fluid as a tool in the diagnosis of neurometabolic diseases: amino acid analysis before and after acid hydrolysisJ Jaeken
Handbook of Clinical Neurology|April 30, 2013
Congenital disorders of glycosylationJ Jaeken
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 6, 2001
Alexander disease and intermediate filaments in astrocytes: a fatal gain of functionJ Jaeken
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 17, 1999
[Disturbances in aminoglycan synthesis]J Jaeken
Archives of Disease in Childhood|May 1, 1989
Disialotransferrin developmental deficiency syndrome and olivopontocerebellar atrophyJ Jaeken
Journal of Inherited Metabolic Disease|August 2, 2003
Komrower Lecture. Congenital disorders of glycosylation (CDG): it's all in it!J Jaeken
Journal of Inherited Metabolic Disease|July 27, 2004
Congenital disorders of glycosylation (CDG): update and new developmentsJ Jaeken
Verhandelingen - Koninklijke Academie Voor Geneeskunde Van Belgie|January 1, 1990
[Metabolic diseases: a challenge for pediatrics]J Jaeken
Acta Paediatrica Belgica|January 1, 1977
Metabolic homoiostasis and its disorders in the new-born infant. Recent acquisitionsJ Jaeken, E Eggermont
Pageof 26