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

K Wulff

Showing results (91-100 of 118) with videos related to

Pageof 12
Sort By:
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1988
[Modified treatment of DNA preparation for cultured amniotic fluid cells and chorionic tissue]M Wehnert, U Kiessling, M Schütz, et al.
Ugeskrift for Laeger|May 2, 1977
[Sodium di-n-propylacetate: evaluation of its so-called psychotropic effect. A controlled study]K W Sommerbeck, A Theilgaard, K E Rasmussen, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 21, 2011
Factor X deficiency and intracranial bleeding: who is at risk?R Rauch, M Girisch, G Wiegand, et al.
Pediatric Hematology and Oncology|May 3, 2006
Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4+1G-->AU Hennewig, S Eisert, K Wulff, et al.
Epilepsia|June 1, 1977
Valproate sodium: evaluation of so-called psychotropic effect. A controlled studyK W Sommerbeck, A Theilgaard, K E Rasmussen, et al.
Neurobiology of Learning and Memory|July 14, 2020
Sleep-related memory consolidation in the psychosis spectrum phenotypeR J Purple, J Cosgrave, V Vyazovskiy, et al.
Clinical Genetics|January 1, 1994
Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10;17) may indicate candidate gene regionsA M Gerdes, M B Petersen, H D Schrøder, et al.
Neuropediatrics|May 1, 1990
Intravenous immunoglobulin: a single-blind trial in children with Lennox-Gastaut syndromeN Illum, K Taudorf, C Heilmann, et al.
Journal of Dental Research|July 5, 2002
Expression of N-acetyltransferases in periodontal granulation tissueP Meisel, J Giebel, M Peters, et al.
Allergy|August 11, 2017
Hereditary angioedema with a mutation in the plasminogen geneK Bork, K Wulff, L Steinmüller-Magin, et al.
Pageof 12

Showing results (91-100 of 118) with videos related to

Sort By:
Pageof 12
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik|January 1, 1988
[Modified treatment of DNA preparation for cultured amniotic fluid cells and chorionic tissue]M Wehnert, U Kiessling, M Schütz, et al.
Ugeskrift for Laeger|May 2, 1977
[Sodium di-n-propylacetate: evaluation of its so-called psychotropic effect. A controlled study]K W Sommerbeck, A Theilgaard, K E Rasmussen, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|June 21, 2011
Factor X deficiency and intracranial bleeding: who is at risk?R Rauch, M Girisch, G Wiegand, et al.
Pediatric Hematology and Oncology|May 3, 2006
Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4+1G-->AU Hennewig, S Eisert, K Wulff, et al.
Epilepsia|June 1, 1977
Valproate sodium: evaluation of so-called psychotropic effect. A controlled studyK W Sommerbeck, A Theilgaard, K E Rasmussen, et al.
Neurobiology of Learning and Memory|July 14, 2020
Sleep-related memory consolidation in the psychosis spectrum phenotypeR J Purple, J Cosgrave, V Vyazovskiy, et al.
Clinical Genetics|January 1, 1994
Congenital myopathy with fiber type disproportion: a family with a chromosomal translocation t(10;17) may indicate candidate gene regionsA M Gerdes, M B Petersen, H D Schrøder, et al.
Neuropediatrics|May 1, 1990
Intravenous immunoglobulin: a single-blind trial in children with Lennox-Gastaut syndromeN Illum, K Taudorf, C Heilmann, et al.
Journal of Dental Research|July 5, 2002
Expression of N-acetyltransferases in periodontal granulation tissueP Meisel, J Giebel, M Peters, et al.
Allergy|August 11, 2017
Hereditary angioedema with a mutation in the plasminogen geneK Bork, K Wulff, L Steinmüller-Magin, et al.
Pageof 12