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

Renske Oegema

Showing results (1-10 of 69) with videos related to

Pageof 7
Sort By:
Brain : a Journal of Neurology|July 11, 2023
When brain size matters: novel insights into brain volume controlRenske Oegema
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 19, 2021
Genetic causes underlying grey matter heterotopiaIlona Vriend, Renske Oegema
Nederlands Tijdschrift Voor Geneeskunde|March 31, 2011
[Diabetes treatment in children: intensive therapy is not always best]Renske Oegema, Petra Schram, Roos Nuboer
Brain : a Journal of Neurology|August 8, 2013
A single strand that links multiple neuropathologies in human diseaseRenske Oegema, Cathryn J Poulton, Grazia M S Mancini
Neurology|September 6, 2019
Subcortical heterotopic gray matter brain malformations: Classification study of 107 individualsRenske Oegema, A James Barkovich, Grazia M S Mancini, et al.
Clinical Genetics|October 28, 2024
Recognisable Neuroradiological Findings in Five Neurogenetic DisordersJessica Rosenblum, Marije Meuwissen, Anna C Jansen, et al.
European Journal of Medical Genetics|December 5, 2020
Deep intronic TIMMDC1 variant delays diagnosis of rapidly progressive complex I deficiencyMyrthe Naber, Debby Hellebrekers, Rutger A J Nievelstein, et al.
European Journal of Medical Genetics|March 13, 2012
Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20pRenske Oegema, Laura J C M van Zutven, Daniella A C M van Hassel, et al.
Clinical Dysmorphology|April 1, 2010
KBG syndrome associated with periventricular nodular heterotopiaRenske Oegema, Rachel Schot, Marie Claire Y de Wit, et al.
Neurogenetics|December 11, 2012
Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutationsCathryn Poulton, Renske Oegema, Daphne Heijsman, et al.
Pageof 7

Showing results (1-10 of 69) with videos related to

Sort By:
Pageof 7
Brain : a Journal of Neurology|July 11, 2023
When brain size matters: novel insights into brain volume controlRenske Oegema
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 19, 2021
Genetic causes underlying grey matter heterotopiaIlona Vriend, Renske Oegema
Nederlands Tijdschrift Voor Geneeskunde|March 31, 2011
[Diabetes treatment in children: intensive therapy is not always best]Renske Oegema, Petra Schram, Roos Nuboer
Brain : a Journal of Neurology|August 8, 2013
A single strand that links multiple neuropathologies in human diseaseRenske Oegema, Cathryn J Poulton, Grazia M S Mancini
Neurology|September 6, 2019
Subcortical heterotopic gray matter brain malformations: Classification study of 107 individualsRenske Oegema, A James Barkovich, Grazia M S Mancini, et al.
Clinical Genetics|October 28, 2024
Recognisable Neuroradiological Findings in Five Neurogenetic DisordersJessica Rosenblum, Marije Meuwissen, Anna C Jansen, et al.
European Journal of Medical Genetics|December 5, 2020
Deep intronic TIMMDC1 variant delays diagnosis of rapidly progressive complex I deficiencyMyrthe Naber, Debby Hellebrekers, Rutger A J Nievelstein, et al.
European Journal of Medical Genetics|March 13, 2012
Unbalanced three-way chromosomal translocation leading to deletion 18q and duplication 20pRenske Oegema, Laura J C M van Zutven, Daniella A C M van Hassel, et al.
Clinical Dysmorphology|April 1, 2010
KBG syndrome associated with periventricular nodular heterotopiaRenske Oegema, Rachel Schot, Marie Claire Y de Wit, et al.
Neurogenetics|December 11, 2012
Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutationsCathryn Poulton, Renske Oegema, Daphne Heijsman, et al.
Pageof 7