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

H Wiebusch

Showing results (1-10 of 68) with videos related to

Pageof 7
Sort By:
Microscopy Research and Technique|August 11, 2000
Roles for lipoprotein lipase in Alzheimer's disease: an association studyL Baum, H Wiebusch, C P Pang
Human Genetics|April 6, 1999
Further evidence for a synergistic association between APOE epsilon4 and BCHE-K in confirmed Alzheimer's diseaseH Wiebusch, J Poirier, P Sévigny, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Fatal genetic defect causing Wolman diseaseE Mayatepek, U Seedorf, H Wiebusch, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
Mutational analysis of two frequently observed lipoprotein lipase gene variants in the Japanese populationH Wiebusch, H Funke, K Saku, et al.
Human Mutation|January 1, 1996
A novel missense (E163G) mutation in the catalytic subunit of lipoprotein lipase causes familial chylomicronemiaH Wiebusch, H Funke, R Santer, et al.
European Journal of Pediatrics|August 1, 1996
Dyslipidaemia in a boy with recurrent abdominal pain, hypersalivation and decreased lipoprotein lipase activityD Matern, H Seydewitz, H Niederhoff, et al.
Clinical Genetics|June 1, 1996
Four frequently observed polymorphisms in the 3'-UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypesP Young, H Wiebusch, F Stögbauer, et al.
Neurology|February 1, 1997
A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsiesP Young, H Wiebusch, F Stögbauer, et al.
Human Genetics|May 1, 1995
Homozygosity for a splice junction mutation in exon 8 of the gene encoding lysosomal acid lipase in a Spanish kindred with cholesterol ester storage disease (CESD)S Muntoni, H Wiebusch, H Funke, et al.
Circulation|November 1, 1996
ECG repolarization patterns in chromosome 7-linked QT syndrome (LQTS 2)E Schulze-Bahr, W Haverkamp, G Breithardt, et al.
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Microscopy Research and Technique|August 11, 2000
Roles for lipoprotein lipase in Alzheimer's disease: an association studyL Baum, H Wiebusch, C P Pang
Human Genetics|April 6, 1999
Further evidence for a synergistic association between APOE epsilon4 and BCHE-K in confirmed Alzheimer's diseaseH Wiebusch, J Poirier, P Sévigny, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
Fatal genetic defect causing Wolman diseaseE Mayatepek, U Seedorf, H Wiebusch, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
Mutational analysis of two frequently observed lipoprotein lipase gene variants in the Japanese populationH Wiebusch, H Funke, K Saku, et al.
Human Mutation|January 1, 1996
A novel missense (E163G) mutation in the catalytic subunit of lipoprotein lipase causes familial chylomicronemiaH Wiebusch, H Funke, R Santer, et al.
European Journal of Pediatrics|August 1, 1996
Dyslipidaemia in a boy with recurrent abdominal pain, hypersalivation and decreased lipoprotein lipase activityD Matern, H Seydewitz, H Niederhoff, et al.
Clinical Genetics|June 1, 1996
Four frequently observed polymorphisms in the 3'-UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypesP Young, H Wiebusch, F Stögbauer, et al.
Neurology|February 1, 1997
A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsiesP Young, H Wiebusch, F Stögbauer, et al.
Human Genetics|May 1, 1995
Homozygosity for a splice junction mutation in exon 8 of the gene encoding lysosomal acid lipase in a Spanish kindred with cholesterol ester storage disease (CESD)S Muntoni, H Wiebusch, H Funke, et al.
Circulation|November 1, 1996
ECG repolarization patterns in chromosome 7-linked QT syndrome (LQTS 2)E Schulze-Bahr, W Haverkamp, G Breithardt, et al.
Pageof 7