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H Appel

Showing results (341-350 of 455) with videos related to

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Nature Genetics|December 24, 2002
Mutations in NR4A2 associated with familial Parkinson diseaseWei-Dong Le, Pingyi Xu, Joseph Jankovic, et al.
Glia|August 13, 2009
Extracellular mutant SOD1 induces microglial-mediated motoneuron injuryWeihua Zhao, David R Beers, Jenny S Henkel, et al.
Acta Neuropathologica|August 4, 2019
Dipeptide repeat (DPR) pathology in the skeletal muscle of ALS patients with C9ORF72 repeat expansionMatthew D Cykowski, Dennis W Dickson, Suzanne Z Powell, et al.
Muscle & Nerve|February 22, 2008
ALSFRS and appel ALS scores: discordance with disease progressionAndrei Voustianiouk, Gregory Seidel, Janki Panchal, et al.
Current Medical Research and Opinion|July 26, 2014
An open-label multicenter study to assess the safety of dextromethorphan/quinidine in patients with pseudobulbar affect associated with a range of underlying neurological conditionsGary L Pattee, James P Wymer, Catherine Lomen-Hoerth, et al.
Acta Neuropathologica Communications|April 15, 2018
Phosphorylated TDP-43 (pTDP-43) aggregates in the axial skeletal muscle of patients with sporadic and familial amyotrophic lateral sclerosisMatthew D Cykowski, Suzanne Z Powell, Joan W Appel, et al.
Annals of Neurology|December 1, 1994
The role of calcium-binding proteins in selective motoneuron vulnerability in amyotrophic lateral sclerosisM E Alexianu, B K Ho, A H Mohamed, et al.
The New England Journal of Medicine|December 10, 1992
Serum antibodies to L-type calcium channels in patients with amyotrophic lateral sclerosisR G Smith, S Hamilton, F Hofmann, et al.
Acta Neuropathologica|May 11, 2000
Altered calcium homeostasis in spinal motoneurons but not in oculomotor neurons of SOD-1 knockout miceL Siklós, J I Engelhardt, A G Reaume, et al.
Annals of Neurology|January 1, 1995
Amyotrophic lateral sclerosis immunoglobulins increase Ca2+ currents in a motoneuron cell lineD R Mosier, P Baldelli, O Delbono, et al.
Pageof 46

Showing results (341-350 of 455) with videos related to

Sort By:
Pageof 46
Nature Genetics|December 24, 2002
Mutations in NR4A2 associated with familial Parkinson diseaseWei-Dong Le, Pingyi Xu, Joseph Jankovic, et al.
Glia|August 13, 2009
Extracellular mutant SOD1 induces microglial-mediated motoneuron injuryWeihua Zhao, David R Beers, Jenny S Henkel, et al.
Acta Neuropathologica|August 4, 2019
Dipeptide repeat (DPR) pathology in the skeletal muscle of ALS patients with C9ORF72 repeat expansionMatthew D Cykowski, Dennis W Dickson, Suzanne Z Powell, et al.
Muscle & Nerve|February 22, 2008
ALSFRS and appel ALS scores: discordance with disease progressionAndrei Voustianiouk, Gregory Seidel, Janki Panchal, et al.
Current Medical Research and Opinion|July 26, 2014
An open-label multicenter study to assess the safety of dextromethorphan/quinidine in patients with pseudobulbar affect associated with a range of underlying neurological conditionsGary L Pattee, James P Wymer, Catherine Lomen-Hoerth, et al.
Acta Neuropathologica Communications|April 15, 2018
Phosphorylated TDP-43 (pTDP-43) aggregates in the axial skeletal muscle of patients with sporadic and familial amyotrophic lateral sclerosisMatthew D Cykowski, Suzanne Z Powell, Joan W Appel, et al.
Annals of Neurology|December 1, 1994
The role of calcium-binding proteins in selective motoneuron vulnerability in amyotrophic lateral sclerosisM E Alexianu, B K Ho, A H Mohamed, et al.
The New England Journal of Medicine|December 10, 1992
Serum antibodies to L-type calcium channels in patients with amyotrophic lateral sclerosisR G Smith, S Hamilton, F Hofmann, et al.
Acta Neuropathologica|May 11, 2000
Altered calcium homeostasis in spinal motoneurons but not in oculomotor neurons of SOD-1 knockout miceL Siklós, J I Engelhardt, A G Reaume, et al.
Annals of Neurology|January 1, 1995
Amyotrophic lateral sclerosis immunoglobulins increase Ca2+ currents in a motoneuron cell lineD R Mosier, P Baldelli, O Delbono, et al.
Pageof 46