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

R N Van Coster

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2000
A family with X-linked dominant Charcot-Marie-Tooth caused by a connexin32 mutationH E Verhelst, A Lofgren, R N Van Coster
AJNR. American Journal of Neuroradiology|April 29, 1999
Neurocutaneous melanosis presenting with intracranial amelanotic melanomaB D Vanzieleghem, M M Lemmerling, R N Van Coster
Pediatric Research|July 1, 1991
Pyruvate carboxylase deficiency: a benign variant with normal developmentR N Van Coster, P M Fernhoff, D C De Vivo
European Journal of Pediatrics|August 13, 1999
Fungal intracranial aneurysm in a child with familial chronic mucocutaneous candidiasisB L Loeys, R N Van Coster, L R Defreyne, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samplesR N Van Coster, S Janssens, J P Misson, et al.
Pediatric Neurology|September 23, 1998
MRI findings in a neonate with cerebellar agenesisR N Van Coster, C M De Praeter, P J Vanhaesebrouck, et al.
Neurology|November 1, 1991
Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processingR N Van Coster, D C De Vivo, D Blake, et al.
American Journal of Medical Genetics|October 28, 1996
Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: a new example of the Chitty syndromeS G Van Daele, R N Van Coster, F Meire, et al.
American Journal of Human Genetics|April 28, 2001
Dominant inheritance of sialuria, an inborn error of feedback inhibitionJ G Leroy, R Seppala, M Huizing, et al.
Annals of Neurology|July 1, 1994
Pyruvate dehydrogenase deficiency: molecular basis for intrafamilial heterogeneityT Fujii, R N Van Coster, S E Old, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2000
A family with X-linked dominant Charcot-Marie-Tooth caused by a connexin32 mutationH E Verhelst, A Lofgren, R N Van Coster
AJNR. American Journal of Neuroradiology|April 29, 1999
Neurocutaneous melanosis presenting with intracranial amelanotic melanomaB D Vanzieleghem, M M Lemmerling, R N Van Coster
Pediatric Research|July 1, 1991
Pyruvate carboxylase deficiency: a benign variant with normal developmentR N Van Coster, P M Fernhoff, D C De Vivo
European Journal of Pediatrics|August 13, 1999
Fungal intracranial aneurysm in a child with familial chronic mucocutaneous candidiasisB L Loeys, R N Van Coster, L R Defreyne, et al.
Prenatal Diagnosis|November 25, 1998
Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samplesR N Van Coster, S Janssens, J P Misson, et al.
Pediatric Neurology|September 23, 1998
MRI findings in a neonate with cerebellar agenesisR N Van Coster, C M De Praeter, P J Vanhaesebrouck, et al.
Neurology|November 1, 1991
Adult Reye's syndrome: a review with new evidence for a generalized defect in intramitochondrial enzyme processingR N Van Coster, D C De Vivo, D Blake, et al.
American Journal of Medical Genetics|October 28, 1996
Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: a new example of the Chitty syndromeS G Van Daele, R N Van Coster, F Meire, et al.
American Journal of Human Genetics|April 28, 2001
Dominant inheritance of sialuria, an inborn error of feedback inhibitionJ G Leroy, R Seppala, M Huizing, et al.
Annals of Neurology|July 1, 1994
Pyruvate dehydrogenase deficiency: molecular basis for intrafamilial heterogeneityT Fujii, R N Van Coster, S E Old, et al.
Pageof 2