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

Stephan Kemp

Showing results (31-40 of 107) with videos related to

Pageof 11
Sort By:
Molecular Genetics and Metabolism|November 28, 2020
The variability conundrum in neurometabolic degenerative diseasesClara D M van Karnebeek, Phillip A Richmond, Frans van der Kloet, et al.
Molecular Neurodegeneration|November 20, 2024
Stearoyl-CoA desaturase-1: a potential therapeutic target for neurological disordersMelanie Loix, Sam Vanherle, Marta Turri, et al.
Histochemistry and Cell Biology|March 31, 2019
Peroxisomes: new insights into protein sorting, dynamics, quality control, signalling and roles in health and diseaseJoseph L Costello, Einat Zalckvar, Stephan Kemp, et al.
Clinical Neurology and Neurosurgery|September 11, 2013
Comment on the paper "Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: a revisit"Marc Engelen, Rob Ofman, Marcel Dijkgraaf, et al.
Molecular Genetics and Metabolism|January 27, 2005
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophyStephan Kemp, Fredoen Valianpour, Simone Denis, et al.
Experimental Cell Research|August 9, 2005
Gene expression profiling in response to the histone deacetylase inhibitor BL1521 in neuroblastomaAnnemieke J M de Ruijter, Rutger J Meinsma, Peter Bosma, et al.
Brain : a Journal of Neurology|December 12, 2018
Progression of myelopathy in males with adrenoleukodystrophy: towards clinical trial readinessIrene C Huffnagel, Wouter J C van Ballegoij, Björn M van Geel, et al.
Orphanet Journal of Rare Diseases|August 15, 2012
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and managementMarc Engelen, Stephan Kemp, Marianne de Visser, et al.
Molecular Genetics and Metabolism|July 12, 2003
Analysis of very long-chain fatty acids using electrospray ionization mass spectrometryFredoen Valianpour, Jacqueline J M Selhorst, Lia E M van Lint, et al.
American Journal of Medical Genetics. Part A|April 5, 2013
Intellectual disability and hemizygous GPD2 mutationDaniela Q C M Barge-Schaapveld, Rob Ofman, Alida C Knegt, et al.
Pageof 11

Showing results (31-40 of 107) with videos related to

Sort By:
Pageof 11
Molecular Genetics and Metabolism|November 28, 2020
The variability conundrum in neurometabolic degenerative diseasesClara D M van Karnebeek, Phillip A Richmond, Frans van der Kloet, et al.
Molecular Neurodegeneration|November 20, 2024
Stearoyl-CoA desaturase-1: a potential therapeutic target for neurological disordersMelanie Loix, Sam Vanherle, Marta Turri, et al.
Histochemistry and Cell Biology|March 31, 2019
Peroxisomes: new insights into protein sorting, dynamics, quality control, signalling and roles in health and diseaseJoseph L Costello, Einat Zalckvar, Stephan Kemp, et al.
Clinical Neurology and Neurosurgery|September 11, 2013
Comment on the paper "Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: a revisit"Marc Engelen, Rob Ofman, Marcel Dijkgraaf, et al.
Molecular Genetics and Metabolism|January 27, 2005
Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophyStephan Kemp, Fredoen Valianpour, Simone Denis, et al.
Experimental Cell Research|August 9, 2005
Gene expression profiling in response to the histone deacetylase inhibitor BL1521 in neuroblastomaAnnemieke J M de Ruijter, Rutger J Meinsma, Peter Bosma, et al.
Brain : a Journal of Neurology|December 12, 2018
Progression of myelopathy in males with adrenoleukodystrophy: towards clinical trial readinessIrene C Huffnagel, Wouter J C van Ballegoij, Björn M van Geel, et al.
Orphanet Journal of Rare Diseases|August 15, 2012
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and managementMarc Engelen, Stephan Kemp, Marianne de Visser, et al.
Molecular Genetics and Metabolism|July 12, 2003
Analysis of very long-chain fatty acids using electrospray ionization mass spectrometryFredoen Valianpour, Jacqueline J M Selhorst, Lia E M van Lint, et al.
American Journal of Medical Genetics. Part A|April 5, 2013
Intellectual disability and hemizygous GPD2 mutationDaniela Q C M Barge-Schaapveld, Rob Ofman, Alida C Knegt, et al.
Pageof 11