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Luc Régal

Showing results (1-10 of 22) with videos related to

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Brain Pathology (Zurich, Switzerland)|July 24, 2015
Peroxisomal Disorders: A Review on Cerebellar PathologiesStephanie De Munter, Simon Verheijden, Luc Régal, et al.
CNS & Neurological Disorders Drug Targets|January 13, 2011
PREPL, a prolyl endopeptidase-like enzyme by name only?--Lessons from patientsKurt Boonen, Luc Régal, Jaak Jaeken, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2010
Neuromyelitis optica-IgG+ optic neuritis associated with celiac disease and dysgammaglobulinemia: a role for tacrolimus?Isabelle Meyts, Katrien Jansen, Marleen Renard, et al.
Archives of Neurology|February 16, 2006
The G93C mutation in superoxide dismutase 1: clinicopathologic phenotype and prognosisLuc Régal, Ludo Vanopdenbosch, Petra Tilkin, et al.
Journal of Inherited Metabolic Disease|October 6, 2017
Isolated sulfite oxidase deficiencyHelena Claerhout, Peter Witters, Luc Régal, et al.
Neurology|March 11, 2014
PREPL deficiency with or without cystinuria causes a novel myasthenic syndromeLuc Régal, Xin-Ming Shen, Duygu Selcen, et al.
Frontiers in Genetics|March 3, 2020
Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and SyndactylyKatrien Stouffs, Patrick Verloo, Stefanie Brock, et al.
Human Molecular Genetics|September 27, 2012
NPC1 defect results in abnormal platelet formation and function: studies in Niemann-Pick disease type C1 patients and zebrafishSophie Louwette, Luc Régal, Christine Wittevrongel, et al.
Annals of Neurology|August 10, 2010
Mutations in PEX10 are a cause of autosomal recessive ataxiaLuc Régal, Merel S Ebberink, Nathalie Goemans, et al.
Orphanet Journal of Rare Diseases|December 12, 2012
COG5-CDG: expanding the clinical spectrumDaisy Rymen, Liesbeth Keldermans, Valérie Race, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Brain Pathology (Zurich, Switzerland)|July 24, 2015
Peroxisomal Disorders: A Review on Cerebellar PathologiesStephanie De Munter, Simon Verheijden, Luc Régal, et al.
CNS & Neurological Disorders Drug Targets|January 13, 2011
PREPL, a prolyl endopeptidase-like enzyme by name only?--Lessons from patientsKurt Boonen, Luc Régal, Jaak Jaeken, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2010
Neuromyelitis optica-IgG+ optic neuritis associated with celiac disease and dysgammaglobulinemia: a role for tacrolimus?Isabelle Meyts, Katrien Jansen, Marleen Renard, et al.
Archives of Neurology|February 16, 2006
The G93C mutation in superoxide dismutase 1: clinicopathologic phenotype and prognosisLuc Régal, Ludo Vanopdenbosch, Petra Tilkin, et al.
Journal of Inherited Metabolic Disease|October 6, 2017
Isolated sulfite oxidase deficiencyHelena Claerhout, Peter Witters, Luc Régal, et al.
Neurology|March 11, 2014
PREPL deficiency with or without cystinuria causes a novel myasthenic syndromeLuc Régal, Xin-Ming Shen, Duygu Selcen, et al.
Frontiers in Genetics|March 3, 2020
Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and SyndactylyKatrien Stouffs, Patrick Verloo, Stefanie Brock, et al.
Human Molecular Genetics|September 27, 2012
NPC1 defect results in abnormal platelet formation and function: studies in Niemann-Pick disease type C1 patients and zebrafishSophie Louwette, Luc Régal, Christine Wittevrongel, et al.
Annals of Neurology|August 10, 2010
Mutations in PEX10 are a cause of autosomal recessive ataxiaLuc Régal, Merel S Ebberink, Nathalie Goemans, et al.
Orphanet Journal of Rare Diseases|December 12, 2012
COG5-CDG: expanding the clinical spectrumDaisy Rymen, Liesbeth Keldermans, Valérie Race, et al.
Pageof 3