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

Julia Wanschitz

Showing results (31-40 of 58) with videos related to

Pageof 6
Sort By:
Human Molecular Genetics|May 27, 2005
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndromePetri T Luoma, Ningguang Luo, Wolfgang N Löscher, et al.
Diagnostics (Basel, Switzerland)|January 8, 2025
A Prospective Comparison of Subjective Symptoms and Neurophysiological Findings in the Assessment of Neuropathy in Cancer PatientsVera Elisabeth Adreana Kleinveld, Miriam Emmelheinz, Daniel Egle, et al.
Journal of Neurology|May 11, 2015
Associations between co-medications and survival in ALS-a cohort study from AustriaHakan Cetin, Uros Klickovic, Jakob Rath, et al.
Plos One|October 27, 2015
Involvement of Peripheral Nerves in the Transgenic PLP-α-Syn Model of Multiple System Atrophy: Extending the PhenotypeDaniela Kuzdas-Wood, Regina Irschick, Markus Theurl, et al.
Journal of Neurology|February 27, 2026
Autonomic dysfunction in patients with wild-type transthyretin amyloidosisVera E A Kleinveld, Julia Wanschitz, Anna Hotter, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|February 14, 2018
Autonomic function testing in spinocerebellar ataxia type 2Elisabetta Indelicato, Alessandra Fanciulli, Jean Pierre Ndayisaba, et al.
Human Molecular Genetics|April 7, 2023
Skeletal muscle transcriptomics dissects the pathogenesis of Friedreich's ataxiaElisabetta Indelicato, Alexander Kirchmair, Matthias Amprosi, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 9, 2011
Abnormalities of satellite cells function in amyotrophic lateral sclerosisPierre-François Pradat, Aude Barani, Julia Wanschitz, et al.
Scientific Reports|October 1, 2016
Bisphosphonates in multicentric osteolysis, nodulosis and arthropathy (MONA) spectrum disorder - an alternative therapeutic approachKarin Pichler, Daniela Karall, Dieter Kotzot, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|March 15, 2016
Guidelines on dermatomyositis--excerpt from the interdisciplinary S2k guidelines on myositis syndromes by the German Society of NeurologyCord Sunderkötter, Alexander Nast, Margitta Worm, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|May 27, 2005
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndromePetri T Luoma, Ningguang Luo, Wolfgang N Löscher, et al.
Diagnostics (Basel, Switzerland)|January 8, 2025
A Prospective Comparison of Subjective Symptoms and Neurophysiological Findings in the Assessment of Neuropathy in Cancer PatientsVera Elisabeth Adreana Kleinveld, Miriam Emmelheinz, Daniel Egle, et al.
Journal of Neurology|May 11, 2015
Associations between co-medications and survival in ALS-a cohort study from AustriaHakan Cetin, Uros Klickovic, Jakob Rath, et al.
Plos One|October 27, 2015
Involvement of Peripheral Nerves in the Transgenic PLP-α-Syn Model of Multiple System Atrophy: Extending the PhenotypeDaniela Kuzdas-Wood, Regina Irschick, Markus Theurl, et al.
Journal of Neurology|February 27, 2026
Autonomic dysfunction in patients with wild-type transthyretin amyloidosisVera E A Kleinveld, Julia Wanschitz, Anna Hotter, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|February 14, 2018
Autonomic function testing in spinocerebellar ataxia type 2Elisabetta Indelicato, Alessandra Fanciulli, Jean Pierre Ndayisaba, et al.
Human Molecular Genetics|April 7, 2023
Skeletal muscle transcriptomics dissects the pathogenesis of Friedreich's ataxiaElisabetta Indelicato, Alexander Kirchmair, Matthias Amprosi, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 9, 2011
Abnormalities of satellite cells function in amyotrophic lateral sclerosisPierre-François Pradat, Aude Barani, Julia Wanschitz, et al.
Scientific Reports|October 1, 2016
Bisphosphonates in multicentric osteolysis, nodulosis and arthropathy (MONA) spectrum disorder - an alternative therapeutic approachKarin Pichler, Daniela Karall, Dieter Kotzot, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|March 15, 2016
Guidelines on dermatomyositis--excerpt from the interdisciplinary S2k guidelines on myositis syndromes by the German Society of NeurologyCord Sunderkötter, Alexander Nast, Margitta Worm, et al.
Pageof 6