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Gert Van Goethem

Showing results (1-10 of 21) with videos related to

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Acta Neurologica Belgica|August 11, 2006
Autosomal disorders of mitochondrial DNA maintenanceGert Van Goethem
Movement Disorders Clinical Practice|February 13, 2019
Spectrum of Movement Disorders in 18p Deletion SyndromeDavid Crosiers, Bettina Blaumeiser, Gert Van Goethem
Acta Neurologica Belgica|July 4, 2002
Progressive external ophthalmoplegia and multiple mitochondrial DNA deletionsGert Van Goethem, Jean-Jacques Martin, Christine Van Broeckhoven
Neuromolecular Medicine|July 2, 2003
Progressive external ophthalmoplegia characterized by multiple deletions of mitochondrial DNA: unraveling the pathogenesis of human mitochondrial DNA instability and the initiation of a genetic classificationGert Van Goethem, Jean-Jacques Martin, Christine Van Broeckhoven
European Journal of Medical Genetics|February 7, 2015
3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variabilityElfi Vergaelen, Ann Swillen, Hilde Van Esch, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathyGert Van Goethem, Marianne Schwartz, Ann Löfgren, et al.
International Journal of Colorectal Disease|March 23, 2010
Colonic transit time in mentally retarded personsSaskia Vande Velde, Stephanie Van Biervliet, Gert Van Goethem, et al.
Nucleic Acids Research|June 8, 2004
Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNASjoerd Wanrooij, Petri Luoma, Gert van Goethem, et al.
Acta Neurologica Belgica|June 25, 2015
The spectrum of epilepsy caused by POLG mutationsWouter Janssen, Annelies Quaegebeur, Gert Van Goethem, et al.
Pediatric Neurology|October 11, 2014
Basal ganglia calcification in a patient with beta-propeller protein-associated neurodegenerationGert Van Goethem, John H Livingston, Daniel Warren, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Acta Neurologica Belgica|August 11, 2006
Autosomal disorders of mitochondrial DNA maintenanceGert Van Goethem
Movement Disorders Clinical Practice|February 13, 2019
Spectrum of Movement Disorders in 18p Deletion SyndromeDavid Crosiers, Bettina Blaumeiser, Gert Van Goethem
Acta Neurologica Belgica|July 4, 2002
Progressive external ophthalmoplegia and multiple mitochondrial DNA deletionsGert Van Goethem, Jean-Jacques Martin, Christine Van Broeckhoven
Neuromolecular Medicine|July 2, 2003
Progressive external ophthalmoplegia characterized by multiple deletions of mitochondrial DNA: unraveling the pathogenesis of human mitochondrial DNA instability and the initiation of a genetic classificationGert Van Goethem, Jean-Jacques Martin, Christine Van Broeckhoven
European Journal of Medical Genetics|February 7, 2015
3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variabilityElfi Vergaelen, Ann Swillen, Hilde Van Esch, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathyGert Van Goethem, Marianne Schwartz, Ann Löfgren, et al.
International Journal of Colorectal Disease|March 23, 2010
Colonic transit time in mentally retarded personsSaskia Vande Velde, Stephanie Van Biervliet, Gert Van Goethem, et al.
Nucleic Acids Research|June 8, 2004
Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNASjoerd Wanrooij, Petri Luoma, Gert van Goethem, et al.
Acta Neurologica Belgica|June 25, 2015
The spectrum of epilepsy caused by POLG mutationsWouter Janssen, Annelies Quaegebeur, Gert Van Goethem, et al.
Pediatric Neurology|October 11, 2014
Basal ganglia calcification in a patient with beta-propeller protein-associated neurodegenerationGert Van Goethem, John H Livingston, Daniel Warren, et al.
Pageof 3