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

A D Sperfeld

Showing results (11-20 of 23) with videos related to

Pageof 3
Sort By:
European Journal of Neurology|August 2, 2006
Brain atrophy in pure and complicated hereditary spastic paraparesis: a quantitative 3D MRI studyJ Kassubek, A-D Sperfeld, A Baumgartner, et al.
Neurology|March 24, 2010
CSF glial markers correlate with survival in amyotrophic lateral sclerosisS D Süssmuth, A D Sperfeld, A Hinz, et al.
Journal of Neurochemistry|June 15, 2000
Protein binding of NADH on chemical preconditioningR Huber, M Büchner, H Li, et al.
European Journal of Medical Research|August 14, 2008
Granulomatous myositis mimicking slowly progressive lower motor neuron diseaseHans-Jürgen Gdynia, N Osterfeld, J Dorst, et al.
Der Nervenarzt|January 23, 2008
[Diagnosis and differential diagnosis of granulomatous myositis]H-J Gdynia, H Mogel, P Kühnlein, et al.
Neurology|June 8, 2011
Small-fiber neuropathy in patients with ALSJ Weis, I Katona, G Müller-Newen, et al.
European Journal of Medical Research|December 22, 2006
Benign symmetric lipomatosis with axonal neuropathy and abnormalities in specific mitochondrial tRNA regionsHans-Jürgen Gdynia, A-D Sperfeld, U Knirsch, et al.
Neurology|August 25, 2004
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALSC Münch, R Sedlmeier, T Meyer, et al.
Annals of Neurology|November 30, 1999
FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutationA D Sperfeld, M B Collatz, H Baier, et al.
Neurology|April 10, 2009
Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24R Schüle, M Bonin, A Dürr, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
European Journal of Neurology|August 2, 2006
Brain atrophy in pure and complicated hereditary spastic paraparesis: a quantitative 3D MRI studyJ Kassubek, A-D Sperfeld, A Baumgartner, et al.
Neurology|March 24, 2010
CSF glial markers correlate with survival in amyotrophic lateral sclerosisS D Süssmuth, A D Sperfeld, A Hinz, et al.
Journal of Neurochemistry|June 15, 2000
Protein binding of NADH on chemical preconditioningR Huber, M Büchner, H Li, et al.
European Journal of Medical Research|August 14, 2008
Granulomatous myositis mimicking slowly progressive lower motor neuron diseaseHans-Jürgen Gdynia, N Osterfeld, J Dorst, et al.
Der Nervenarzt|January 23, 2008
[Diagnosis and differential diagnosis of granulomatous myositis]H-J Gdynia, H Mogel, P Kühnlein, et al.
Neurology|June 8, 2011
Small-fiber neuropathy in patients with ALSJ Weis, I Katona, G Müller-Newen, et al.
European Journal of Medical Research|December 22, 2006
Benign symmetric lipomatosis with axonal neuropathy and abnormalities in specific mitochondrial tRNA regionsHans-Jürgen Gdynia, A-D Sperfeld, U Knirsch, et al.
Neurology|August 25, 2004
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALSC Münch, R Sedlmeier, T Meyer, et al.
Annals of Neurology|November 30, 1999
FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutationA D Sperfeld, M B Collatz, H Baier, et al.
Neurology|April 10, 2009
Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24R Schüle, M Bonin, A Dürr, et al.
Pageof 3