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

F HOFFMANN

Showing results (551-560 of 1,073) with videos related to

Pageof 108
Sort By:
Neurology|June 30, 2005
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiencyS Külkens, I Harting, S Sauer, et al.
Sleep|March 24, 2006
Sex and age differences in sleep macroarchitecture in childhood and adolescent depressionJennifer J T Robert, Robert F Hoffmann, Graham J Emslie, et al.
Glycobiology|July 11, 2006
Gender-specific expression of complex-type N-glycans in schistosomesManfred Wuhrer, Carolien A M Koeleman, Jennifer M Fitzpatrick, et al.
Pediatric Neurology|November 1, 2006
Sepiapterin reductase deficiency: clinical presentation and evaluation of long-term therapyBernard Echenne, Agathe Roubertie, Birgit Assmann, et al.
European Journal of Medicinal Chemistry|April 27, 2018
Design, synthesis and anthelmintic activity of 7-keto-sempervirol analoguesAlessandra Crusco, Cinzia Bordoni, Anand Chakroborty, et al.
Orphanet Journal of Rare Diseases|December 5, 2024
Systematic quantitative modeling of the natural history of Aicardi syndrome: A cross sectional study of 245 published casesOliver Y Urban, Jan H Driedger, Sven F Garbade, et al.
Pediatric Pulmonology|November 29, 2022
German newborn screening for Cystic fibrosis: Parental perspectives and suggestions for improvementsSimon Gapp, Sven F Garbade, Patrik Feyh, et al.
Neuropediatrics|March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestationsB Assmann, R Hackler, V Peters, et al.
Plos Neglected Tropical Diseases|October 23, 2008
Use of genomic DNA as an indirect reference for identifying gender-associated transcripts in morphologically identical, but chromosomally distinct, Schistosoma mansoni cercariaeJennifer M Fitzpatrick, Anna V Protasio, Andrew J McArdle, et al.
Molecular Genetics and Metabolism|November 17, 2022
Detection of early cardiac disease manifestation in propionic acidemia - Results of a monocentric cross-sectional studyAlexander Kovacevic, Sven F Garbade, Friederike Hörster, et al.
Pageof 108

Showing results (551-560 of 1,073) with videos related to

Sort By:
Pageof 108
Neurology|June 30, 2005
Late-onset neurologic disease in glutaryl-CoA dehydrogenase deficiencyS Külkens, I Harting, S Sauer, et al.
Sleep|March 24, 2006
Sex and age differences in sleep macroarchitecture in childhood and adolescent depressionJennifer J T Robert, Robert F Hoffmann, Graham J Emslie, et al.
Glycobiology|July 11, 2006
Gender-specific expression of complex-type N-glycans in schistosomesManfred Wuhrer, Carolien A M Koeleman, Jennifer M Fitzpatrick, et al.
Pediatric Neurology|November 1, 2006
Sepiapterin reductase deficiency: clinical presentation and evaluation of long-term therapyBernard Echenne, Agathe Roubertie, Birgit Assmann, et al.
European Journal of Medicinal Chemistry|April 27, 2018
Design, synthesis and anthelmintic activity of 7-keto-sempervirol analoguesAlessandra Crusco, Cinzia Bordoni, Anand Chakroborty, et al.
Orphanet Journal of Rare Diseases|December 5, 2024
Systematic quantitative modeling of the natural history of Aicardi syndrome: A cross sectional study of 245 published casesOliver Y Urban, Jan H Driedger, Sven F Garbade, et al.
Pediatric Pulmonology|November 29, 2022
German newborn screening for Cystic fibrosis: Parental perspectives and suggestions for improvementsSimon Gapp, Sven F Garbade, Patrik Feyh, et al.
Neuropediatrics|March 1, 2002
A new subtype of a congenital disorder of glycosylation (CDG) with mild clinical manifestationsB Assmann, R Hackler, V Peters, et al.
Plos Neglected Tropical Diseases|October 23, 2008
Use of genomic DNA as an indirect reference for identifying gender-associated transcripts in morphologically identical, but chromosomally distinct, Schistosoma mansoni cercariaeJennifer M Fitzpatrick, Anna V Protasio, Andrew J McArdle, et al.
Molecular Genetics and Metabolism|November 17, 2022
Detection of early cardiac disease manifestation in propionic acidemia - Results of a monocentric cross-sectional studyAlexander Kovacevic, Sven F Garbade, Friederike Hörster, et al.
Pageof 108