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

Ilka Schneider

Showing results (1-10 of 30) with videos related to

Pageof 3
Sort By:
Der Nervenarzt|February 21, 2020
[Gene-specific treatment approaches in muscle diseases]Diana Lehmann Urban, Ilka Schneider
Molecular Genetics and Metabolism|June 3, 2019
White matter lesions in treated late onset Pompe disease are not different to matched controlsIlka Schneider, Ole Hensel, Stephan Zierz
Journal of Medical Case Reports|April 18, 2015
Long-term observation of incremental response and antibodies to voltage-gated calcium channels in patients with Lambert-Eaton myasthenic syndrome: two case reportsIlka Schneider, Malte E Kornhuber, Frank Hanisch
Wiener Medizinische Wochenschrift (1946)|November 20, 2012
Respiratory function in late-onset Pompe disease patients receiving long-term enzyme replacement therapy for more than 48 monthsIlka Schneider, Frank Hanisch, Tobias Müller, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 21, 2014
Limb girdle muscular dystrophy type 2L presenting as necrotizing myopathyIlka Schneider, Gisela Stoltenburg, Marcus Deschauer, et al.
Journal of Neuroscience Research|September 21, 2004
Characterization of retinoic acid neuromodulation in the carp retinaPetra Dirks, Silke Tieding, Ilka Schneider, et al.
Orphanet Journal of Rare Diseases|April 15, 2018
Decreased outlet angle of the superior cerebellar artery as indicator for dolichoectasia in late onset Pompe diseaseOle Hensel, Ilka Schneider, Mathias Wieprecht, et al.
Brain and Behavior|August 30, 2020
Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathiesHans-Jonas Meyer, Ilka Schneider, Alexander Emmer, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 8, 2014
Eosinophils in hereditary and inflammatory myopathiesThomas Schröder, Johann Fuchss, Ilka Schneider, et al.
Parasitology Research|October 19, 2004
Molecular genetic characterization and subcellular localization of a putative Theileria annulata membrane proteinIlka Schneider, Daniel Haller, Ulrike Seitzer, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Der Nervenarzt|February 21, 2020
[Gene-specific treatment approaches in muscle diseases]Diana Lehmann Urban, Ilka Schneider
Molecular Genetics and Metabolism|June 3, 2019
White matter lesions in treated late onset Pompe disease are not different to matched controlsIlka Schneider, Ole Hensel, Stephan Zierz
Journal of Medical Case Reports|April 18, 2015
Long-term observation of incremental response and antibodies to voltage-gated calcium channels in patients with Lambert-Eaton myasthenic syndrome: two case reportsIlka Schneider, Malte E Kornhuber, Frank Hanisch
Wiener Medizinische Wochenschrift (1946)|November 20, 2012
Respiratory function in late-onset Pompe disease patients receiving long-term enzyme replacement therapy for more than 48 monthsIlka Schneider, Frank Hanisch, Tobias Müller, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 21, 2014
Limb girdle muscular dystrophy type 2L presenting as necrotizing myopathyIlka Schneider, Gisela Stoltenburg, Marcus Deschauer, et al.
Journal of Neuroscience Research|September 21, 2004
Characterization of retinoic acid neuromodulation in the carp retinaPetra Dirks, Silke Tieding, Ilka Schneider, et al.
Orphanet Journal of Rare Diseases|April 15, 2018
Decreased outlet angle of the superior cerebellar artery as indicator for dolichoectasia in late onset Pompe diseaseOle Hensel, Ilka Schneider, Mathias Wieprecht, et al.
Brain and Behavior|August 30, 2020
Associations between apparent diffusion coefficient values and histopathological tissue alterations in myopathiesHans-Jonas Meyer, Ilka Schneider, Alexander Emmer, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 8, 2014
Eosinophils in hereditary and inflammatory myopathiesThomas Schröder, Johann Fuchss, Ilka Schneider, et al.
Parasitology Research|October 19, 2004
Molecular genetic characterization and subcellular localization of a putative Theileria annulata membrane proteinIlka Schneider, Daniel Haller, Ulrike Seitzer, et al.
Pageof 3