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Jaak Jaeken

Showing results (11-20 of 177) with videos related to

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Annual Review of Genomics and Human Genetics|May 18, 2007
Congenital disorders of glycosylation: a rapidly expanding disease familyJaak Jaeken, Gert Matthijs
Journal of Inherited Metabolic Disease|June 28, 2017
Erratum to: What is new in CDG?Jaak Jaeken, Romain Péanne
Journal of Inherited Metabolic Disease|May 10, 2017
What is new in CDG?Jaak Jaeken, Romain Péanne
Biochimica Et Biophysica Acta|May 8, 2009
MGAT2 deficiency (CDG-IIa): the Life of JPaul de Cock, Jaak Jaeken
Seminars in Neurology|September 6, 2014
Congenital disorders of glycosylation with emphasis on cerebellar involvementRita Barone, Agata Fiumara, Jaak Jaeken
Developmental Medicine and Child Neurology|January 4, 2012
Evaluation of the pediatric patient with hypotonia: don't forget the hypotonia-cystinuria syndrome!Jaak Jaeken, John Creemers, Luc Régal
Journal of Child Neurology|October 1, 2011
Distinct features of congenital disorder of glycosylation type IIx in Kuwait: a case reportNawal Makhseed, Gursev Dhaunsi, Jaak Jaeken
European Journal of Human Genetics : EJHG|August 1, 2013
Congenital disorders of glycosylation: other causes of ichthyosisJaak Jaeken, Daisy Rymen, Gert Matthijs
European Journal of Human Genetics : EJHG|August 6, 2015
Clinical utility gene card for: DPAGT1 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|February 5, 2015
Clinical utility gene card for: ALG1 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
Pageof 18

Showing results (11-20 of 177) with videos related to

Sort By:
Pageof 18
Annual Review of Genomics and Human Genetics|May 18, 2007
Congenital disorders of glycosylation: a rapidly expanding disease familyJaak Jaeken, Gert Matthijs
Journal of Inherited Metabolic Disease|June 28, 2017
Erratum to: What is new in CDG?Jaak Jaeken, Romain Péanne
Journal of Inherited Metabolic Disease|May 10, 2017
What is new in CDG?Jaak Jaeken, Romain Péanne
Biochimica Et Biophysica Acta|May 8, 2009
MGAT2 deficiency (CDG-IIa): the Life of JPaul de Cock, Jaak Jaeken
Seminars in Neurology|September 6, 2014
Congenital disorders of glycosylation with emphasis on cerebellar involvementRita Barone, Agata Fiumara, Jaak Jaeken
Developmental Medicine and Child Neurology|January 4, 2012
Evaluation of the pediatric patient with hypotonia: don't forget the hypotonia-cystinuria syndrome!Jaak Jaeken, John Creemers, Luc Régal
Journal of Child Neurology|October 1, 2011
Distinct features of congenital disorder of glycosylation type IIx in Kuwait: a case reportNawal Makhseed, Gursev Dhaunsi, Jaak Jaeken
European Journal of Human Genetics : EJHG|August 1, 2013
Congenital disorders of glycosylation: other causes of ichthyosisJaak Jaeken, Daisy Rymen, Gert Matthijs
European Journal of Human Genetics : EJHG|August 6, 2015
Clinical utility gene card for: DPAGT1 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
European Journal of Human Genetics : EJHG|February 5, 2015
Clinical utility gene card for: ALG1 defective congenital disorder of glycosylationJaak Jaeken, Dirk Lefeber, Gert Matthijs
Pageof 18