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 (91-100 of 177) with videos related to

Pageof 18
Sort By:
Journal of the Neurological Sciences|December 1, 1990
Metallothionein in Menkes' disease: induction in cultured muscle cellsN H Herzberg, R A Wolterman, G J van den Berg, et al.
American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Familial mitochondrial complex I deficiency with an abnormal mitochondrial encoded proteinP G Barth, P A Bolhuis, F A Wijburg, et al.
European Journal of Pediatrics|January 1, 1985
An infant with Marfanoid phenotype and congenital contractures associated with ocular and cardiovascular anomalies, cerebral white matter hypoplasia and spinal axonopathyP Tamminga, F G Jennekens, P G Barth, et al.
Neurology|August 26, 1998
Phenotypic variation in leukoencephalopathy with vanishing white matterM S van der Knaap, W Kamphorst, P G Barth, et al.
Neuropediatrics|May 6, 2004
The spectrum of cranial ultrasound and magnetic resonance imaging abnormalities in congenital cytomegalovirus infectionL S de Vries, H Gunardi, P G Barth, et al.
Neuropediatrics|August 1, 1996
Cerebellar hypoplasia in respiratory chain dysfunctionC R Lincke, C van den Bogert, L G Nijtmans, et al.
Journal of Lipid Research|February 4, 2003
Linoleic acid supplementation of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatmentF Valianpour, R J A Wanders, H Overmars, et al.
Biochemical and Biophysical Research Communications|December 19, 2000
Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndromeP Vreken, F Valianpour, L G Nijtmans, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Aromatic L-amino acid decarboxylase deficiency: a new case with a mild clinical presentation and unexpected laboratory findingsN G Abeling, A H van Gennip, P G Barth, et al.
Pageof 18

Showing results (91-100 of 177) with videos related to

Sort By:
Pageof 18
Journal of the Neurological Sciences|December 1, 1990
Metallothionein in Menkes' disease: induction in cultured muscle cellsN H Herzberg, R A Wolterman, G J van den Berg, et al.
American Journal of Medical Genetics|July 1, 1991
Joubert syndrome: a clinical and pathological description of an affected male and a female fetus from the same sibshipD B van Dorp, A Palan, M L Kwee, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Familial mitochondrial complex I deficiency with an abnormal mitochondrial encoded proteinP G Barth, P A Bolhuis, F A Wijburg, et al.
European Journal of Pediatrics|January 1, 1985
An infant with Marfanoid phenotype and congenital contractures associated with ocular and cardiovascular anomalies, cerebral white matter hypoplasia and spinal axonopathyP Tamminga, F G Jennekens, P G Barth, et al.
Neurology|August 26, 1998
Phenotypic variation in leukoencephalopathy with vanishing white matterM S van der Knaap, W Kamphorst, P G Barth, et al.
Neuropediatrics|May 6, 2004
The spectrum of cranial ultrasound and magnetic resonance imaging abnormalities in congenital cytomegalovirus infectionL S de Vries, H Gunardi, P G Barth, et al.
Neuropediatrics|August 1, 1996
Cerebellar hypoplasia in respiratory chain dysfunctionC R Lincke, C van den Bogert, L G Nijtmans, et al.
Journal of Lipid Research|February 4, 2003
Linoleic acid supplementation of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatmentF Valianpour, R J A Wanders, H Overmars, et al.
Biochemical and Biophysical Research Communications|December 19, 2000
Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndromeP Vreken, F Valianpour, L G Nijtmans, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Aromatic L-amino acid decarboxylase deficiency: a new case with a mild clinical presentation and unexpected laboratory findingsN G Abeling, A H van Gennip, P G Barth, et al.
Pageof 18