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

Andreas Hahn

Showing results (501-510 of 559) with videos related to

Pageof 56
Sort By:
Annals of Neurology|March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhoodDennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Ecological Applications : a Publication of the Ecological Society of America|May 22, 2023
Trait-mediated responses of caterpillar communities to spongy moth outbreaks and subsequent tebufenozide treatmentsBenjamin M L Leroy, Dominik Rabl, Marcel Püls, et al.
Brain & Development|October 24, 2015
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugsSaskia M Herbst, Christiane R Proepper, Tobias Geis, et al.
Human Mutation|July 1, 2015
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney DiseaseJulia Vodopiutz, Rainer Seidl, Daniela Prayer, et al.
Human Mutation|May 26, 2020
ASAH1 pathogenic variants associated with acid ceramidase deficiency: Farber disease and spinal muscular atrophy with progressive myoclonic epilepsySarah H Elsea, Alexander Solyom, Kirt Martin, et al.
Orphanet Journal of Rare Diseases|October 17, 2015
47 patients with FLNA associated periventricular nodular heterotopiaMax Lange, Burkhard Kasper, Axel Bohring, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|April 2, 2022
Red blood cell fatty acid patterns from 7 countries: Focus on the Omega-3 indexJan Philipp Schuchardt, Marianna Cerrato, Martina Ceseri, et al.
Nature Communications|September 8, 2024
Non-invasive optoacoustic imaging of glycogen-storage and muscle degeneration in late-onset Pompe diseaseLina Tan, Jana Zschüntzsch, Stefanie Meyer, et al.
Orphanet Journal of Rare Diseases|May 5, 2019
Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age - a multicenter retrospective studyAfshin Saffari, Ines Brösse, Adelheid Wiemer-Kruel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 22, 2016
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutationKarim Kouz, Christina Lissewski, Stephanie Spranger, et al.
Pageof 56

Showing results (501-510 of 559) with videos related to

Sort By:
Pageof 56
Annals of Neurology|March 5, 2014
DEPDC5 mutations in genetic focal epilepsies of childhoodDennis Lal, Eva M Reinthaler, Julian Schubert, et al.
Ecological Applications : a Publication of the Ecological Society of America|May 22, 2023
Trait-mediated responses of caterpillar communities to spongy moth outbreaks and subsequent tebufenozide treatmentsBenjamin M L Leroy, Dominik Rabl, Marcel Püls, et al.
Brain & Development|October 24, 2015
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugsSaskia M Herbst, Christiane R Proepper, Tobias Geis, et al.
Human Mutation|July 1, 2015
WDR73 Mutations Cause Infantile Neurodegeneration and Variable Glomerular Kidney DiseaseJulia Vodopiutz, Rainer Seidl, Daniela Prayer, et al.
Human Mutation|May 26, 2020
ASAH1 pathogenic variants associated with acid ceramidase deficiency: Farber disease and spinal muscular atrophy with progressive myoclonic epilepsySarah H Elsea, Alexander Solyom, Kirt Martin, et al.
Orphanet Journal of Rare Diseases|October 17, 2015
47 patients with FLNA associated periventricular nodular heterotopiaMax Lange, Burkhard Kasper, Axel Bohring, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids|April 2, 2022
Red blood cell fatty acid patterns from 7 countries: Focus on the Omega-3 indexJan Philipp Schuchardt, Marianna Cerrato, Martina Ceseri, et al.
Nature Communications|September 8, 2024
Non-invasive optoacoustic imaging of glycogen-storage and muscle degeneration in late-onset Pompe diseaseLina Tan, Jana Zschüntzsch, Stefanie Meyer, et al.
Orphanet Journal of Rare Diseases|May 5, 2019
Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age - a multicenter retrospective studyAfshin Saffari, Ines Brösse, Adelheid Wiemer-Kruel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 22, 2016
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutationKarim Kouz, Christina Lissewski, Stephanie Spranger, et al.
Pageof 56