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

Rolfs

Showing results (421-430 of 632) with videos related to

Pageof 64
Sort By:
Folia Neuropathologica|January 16, 2013
Diagnostic difficulties in Krabbe disease: a report of two cases and review of literatureKrystyna Szymańska, Agnieszka Ługowska, Milena Laure-Kamionowska, et al.
Journal of Proteomics|December 11, 2020
Feasibility of phosphoproteomics to uncover oncogenic signalling in secreted extracellular vesicles using glioblastoma-EGFRVIII cells as a modelIrene V Bijnsdorp, Tim Schelfhorst, Mark Luinenburg, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|February 13, 2019
Assessment of Cardiac Involvement in Fabry Disease (FD) with Native T1 MappingFritz Christian Roller, Sven Fuest, Marco Meyer, et al.
Fortschritte Der Neurologie-Psychiatrie|March 12, 2014
[The Rostock Headache Questionnaire ("Rokoko")--validation of a tool to screen and to qualify primary headaches]B Müller, A Baum, M Holzhausen, et al.
Archives of Toxicology|June 1, 2017
Conditional loss of hepatocellular Hedgehog signaling in female mice leads to the persistence of hepatic steroidogenesis, androgenization and infertilityChristiane Rennert, Franziska Eplinius, Ute Hofmann, et al.
Clinical Genetics|July 31, 2018
A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab childrenH Yavuz, A M Bertoli-Avella, M Alfadhel, et al.
International Heart Journal|May 13, 2017
Identification of a Novel GLA Gene Mutation, p.Ile239Met, in Fabry Disease With a Predominant Cardiac PhenotypeBeáta Csányi, Lidia Hategan, Viktória Nagy, et al.
International Journal of Molecular Sciences|February 7, 2020
Assessment of Gene Variant Amenability for Pharmacological Chaperone Therapy with 1-Deoxygalactonojirimycin in Fabry DiseaseJan Lukas, Chiara Cimmaruta, Ludovica Liguori, et al.
Human Molecular Genetics|May 27, 2005
Identification of quantitative trait loci controlling cortical motor evoked potentials in experimental autoimmune encephalomyelitis: correlation with incidence, onset and severity of diseaseIgnacio Mazón Peláez, Susanne Vogler, Ulf Strauss, et al.
Life Science Alliance|January 12, 2023
Secondary findings in a large Pakistani cohort tested with whole genome sequencingAliaksandr Skrahin, Huma Arshad Cheema, Maqbool Hussain, et al.
Pageof 64

Showing results (421-430 of 632) with videos related to

Sort By:
Pageof 64
Folia Neuropathologica|January 16, 2013
Diagnostic difficulties in Krabbe disease: a report of two cases and review of literatureKrystyna Szymańska, Agnieszka Ługowska, Milena Laure-Kamionowska, et al.
Journal of Proteomics|December 11, 2020
Feasibility of phosphoproteomics to uncover oncogenic signalling in secreted extracellular vesicles using glioblastoma-EGFRVIII cells as a modelIrene V Bijnsdorp, Tim Schelfhorst, Mark Luinenburg, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|February 13, 2019
Assessment of Cardiac Involvement in Fabry Disease (FD) with Native T1 MappingFritz Christian Roller, Sven Fuest, Marco Meyer, et al.
Fortschritte Der Neurologie-Psychiatrie|March 12, 2014
[The Rostock Headache Questionnaire ("Rokoko")--validation of a tool to screen and to qualify primary headaches]B Müller, A Baum, M Holzhausen, et al.
Archives of Toxicology|June 1, 2017
Conditional loss of hepatocellular Hedgehog signaling in female mice leads to the persistence of hepatic steroidogenesis, androgenization and infertilityChristiane Rennert, Franziska Eplinius, Ute Hofmann, et al.
Clinical Genetics|July 31, 2018
A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab childrenH Yavuz, A M Bertoli-Avella, M Alfadhel, et al.
International Heart Journal|May 13, 2017
Identification of a Novel GLA Gene Mutation, p.Ile239Met, in Fabry Disease With a Predominant Cardiac PhenotypeBeáta Csányi, Lidia Hategan, Viktória Nagy, et al.
International Journal of Molecular Sciences|February 7, 2020
Assessment of Gene Variant Amenability for Pharmacological Chaperone Therapy with 1-Deoxygalactonojirimycin in Fabry DiseaseJan Lukas, Chiara Cimmaruta, Ludovica Liguori, et al.
Human Molecular Genetics|May 27, 2005
Identification of quantitative trait loci controlling cortical motor evoked potentials in experimental autoimmune encephalomyelitis: correlation with incidence, onset and severity of diseaseIgnacio Mazón Peláez, Susanne Vogler, Ulf Strauss, et al.
Life Science Alliance|January 12, 2023
Secondary findings in a large Pakistani cohort tested with whole genome sequencingAliaksandr Skrahin, Huma Arshad Cheema, Maqbool Hussain, et al.
Pageof 64