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

P G Barth

Showing results (161-170 of 177) with videos related to

Pageof 18
Sort By:
Neurology|March 29, 2006
MRI of the brain and cervical spinal cord in rhizomelic chondrodysplasia punctataA M Bams-Mengerink, C B L M Majoie, M Duran, et al.
Biochimica Et Biophysica Acta|April 24, 1995
Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathyL G Nijtmans, P G Barth, C R Lincke, et al.
Platelets|June 24, 2006
Lorenzo's oil and platelet activation in adrenomyeloneuropathy and asymptomatic X-linked adrenoleukodystrophyA Konijnenberg, B M van Geel, A Sturk, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1G J Jöbsis, J W Weber, P G Barth, et al.
Biochemical and Biophysical Research Communications|July 29, 1994
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutationsS Kemp, M J Ligtenberg, B M van Geel, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
A sibship with a mild variant of Zellweger syndromeP G Barth, R B Schutgens, R J Wanders, et al.
Neurology|February 12, 2004
Neuroimaging of peroxisome biogenesis disorders (Zellweger spectrum) with prolonged survivalP G Barth, C B L M Majoie, J Gootjes, et al.
AJNR. American Journal of Neuroradiology|March 10, 2001
Alexander disease: diagnosis with MR imagingM S van der Knaap, S Naidu, S N Breiter, et al.
Neuropediatrics|June 10, 2005
Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruptionH L M van Straaten, J P van Tintelen, J M F Trijbels, et al.
Human Mutation|July 17, 1999
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disordersZ Zhang, Y Suzuki, N Shimozawa, et al.
Pageof 18

Showing results (161-170 of 177) with videos related to

Sort By:
Pageof 18
Neurology|March 29, 2006
MRI of the brain and cervical spinal cord in rhizomelic chondrodysplasia punctataA M Bams-Mengerink, C B L M Majoie, M Duran, et al.
Biochimica Et Biophysica Acta|April 24, 1995
Altered kinetics of cytochrome c oxidase in a patient with severe mitochondrial encephalomyopathyL G Nijtmans, P G Barth, C R Lincke, et al.
Platelets|June 24, 2006
Lorenzo's oil and platelet activation in adrenomyeloneuropathy and asymptomatic X-linked adrenoleukodystrophyA Konijnenberg, B M van Geel, A Sturk, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1G J Jöbsis, J W Weber, P G Barth, et al.
Biochemical and Biophysical Research Communications|July 29, 1994
Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutationsS Kemp, M J Ligtenberg, B M van Geel, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
A sibship with a mild variant of Zellweger syndromeP G Barth, R B Schutgens, R J Wanders, et al.
Neurology|February 12, 2004
Neuroimaging of peroxisome biogenesis disorders (Zellweger spectrum) with prolonged survivalP G Barth, C B L M Majoie, J Gootjes, et al.
AJNR. American Journal of Neuroradiology|March 10, 2001
Alexander disease: diagnosis with MR imagingM S van der Knaap, S Naidu, S N Breiter, et al.
Neuropediatrics|June 10, 2005
Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruptionH L M van Straaten, J P van Tintelen, J M F Trijbels, et al.
Human Mutation|July 17, 1999
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disordersZ Zhang, Y Suzuki, N Shimozawa, et al.
Pageof 18