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

Frank Roels

Showing results (11-20 of 24) with videos related to

Pageof 3
Sort By:
Biochemical Pharmacology|December 31, 2002
Inhibition of cytokine production by the herbicide atrazine. Search for nuclear receptor targetsSabrina Devos, Karolien De Bosscher, Bart Staels, et al.
Orphanet Journal of Rare Diseases|May 23, 2018
Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiencyElise Vantroys, Joél Smet, Arnaud V Vanlander, et al.
American Journal of Nephrology|June 18, 2005
Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in IsraelYaacov Frishberg, Choni Rinat, Adel Shalata, et al.
Advances in Experimental Medicine and Biology|January 10, 2004
Pharmacological induction of redundant genes for a therapy of X-ALD: phenylbutyrate and other compoundsMaurice Bugaut, Stephane Fourcade, Catherine Gondcaille, et al.
Journal of Inherited Metabolic Disease|June 1, 2019
Hepatic symptoms and histology in 13 patients with a Zellweger spectrum disorderKevin Berendse, Bart G P Koot, Femke C C Klouwer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 21, 2012
Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathyEmmanuel Scalais, Baudouin Francois, Patrick Schlesser, et al.
BMC Clinical Pathology|June 9, 2009
Mitochondrial mosaics in the liver of 3 infants with mtDNA defectsFrank Roels, Patrick Verloo, François Eyskens, et al.
BMC Cancer|August 28, 2004
No evidence for involvement of SDHD in neuroblastoma pathogenesisKatleen De Preter, Jo Vandesompele, Jasmien Hoebeeck, et al.
American Journal of Human Genetics|March 2, 2002
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parentsAnnick Raas-Rothschild, Ronald J A Wanders, Petra A W Mooijer, et al.
Kidney International|December 5, 2008
Hepatocellular transport and gastrointestinal absorption of lanthanum in chronic renal failureAn R J Bervoets, Geert J Behets, Dominick Schryvers, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Biochemical Pharmacology|December 31, 2002
Inhibition of cytokine production by the herbicide atrazine. Search for nuclear receptor targetsSabrina Devos, Karolien De Bosscher, Bart Staels, et al.
Orphanet Journal of Rare Diseases|May 23, 2018
Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiencyElise Vantroys, Joél Smet, Arnaud V Vanlander, et al.
American Journal of Nephrology|June 18, 2005
Intra-familial clinical heterogeneity: absence of genotype-phenotype correlation in primary hyperoxaluria type 1 in IsraelYaacov Frishberg, Choni Rinat, Adel Shalata, et al.
Advances in Experimental Medicine and Biology|January 10, 2004
Pharmacological induction of redundant genes for a therapy of X-ALD: phenylbutyrate and other compoundsMaurice Bugaut, Stephane Fourcade, Catherine Gondcaille, et al.
Journal of Inherited Metabolic Disease|June 1, 2019
Hepatic symptoms and histology in 13 patients with a Zellweger spectrum disorderKevin Berendse, Bart G P Koot, Femke C C Klouwer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 21, 2012
Polymerase gamma deficiency (POLG): clinical course in a child with a two stage evolution from infantile myocerebrohepatopathy spectrum to an Alpers syndrome and neuropathological findings of Leigh's encephalopathyEmmanuel Scalais, Baudouin Francois, Patrick Schlesser, et al.
BMC Clinical Pathology|June 9, 2009
Mitochondrial mosaics in the liver of 3 infants with mtDNA defectsFrank Roels, Patrick Verloo, François Eyskens, et al.
BMC Cancer|August 28, 2004
No evidence for involvement of SDHD in neuroblastoma pathogenesisKatleen De Preter, Jo Vandesompele, Jasmien Hoebeeck, et al.
American Journal of Human Genetics|March 2, 2002
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parentsAnnick Raas-Rothschild, Ronald J A Wanders, Petra A W Mooijer, et al.
Kidney International|December 5, 2008
Hepatocellular transport and gastrointestinal absorption of lanthanum in chronic renal failureAn R J Bervoets, Geert J Behets, Dominick Schryvers, et al.
Pageof 3