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D Heiman

Showing results (41-50 of 61) with videos related to

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Electromyography and Clinical Neurophysiology|December 1, 1991
Clinical and electrophysiological assessments in ALS patientsA J Tahmoush, J A Gillespie, J F Hulihan, et al.
Neurology|June 1, 1991
Factors influencing outcome of prednisone dose reduction in myasthenia gravisM A Miano, T M Bosley, T D Heiman-Patterson, et al.
Brain Research. Molecular Brain Research|November 3, 2004
Effect of transgene copy number on survival in the G93A SOD1 transgenic mouse model of ALSGuillermo M Alexander, Kirsten L Erwin, Nathaniel Byers, et al.
The American Journal of Medicine|August 1, 1984
Neuroleptic malignant syndrome. Patient with unique clinical and physiologic featuresG P Downey, M Rosenberg, S Caroff, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 19, 2011
Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: a window of opportunity in the search for genetic modifiersTerry D Heiman-Patterson, Roger B Sher, Elizabeth A Blankenhorn, et al.
Journal of the Neurological Sciences|July 19, 2005
Background and gender effects on survival in the TgN(SOD1-G93A)1Gur mouse model of ALST D Heiman-Patterson, J S Deitch, E P Blankenhorn, et al.
Plos One|September 15, 2022
Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron diseaseGuillermo M Alexander, Terry D Heiman-Patterson, Frank Bearoff, et al.
Plos One|March 13, 2015
Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron diseaseTerry D Heiman-Patterson, Elizabeth P Blankenhorn, Roger B Sher, et al.
Neurogenetics|September 7, 2014
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathySenda Ajroud-Driss, Faisal Fecto, Kaouther Ajroud, et al.
Annals of Neurology|October 1, 1990
Peripheral neuropathy associated with eosinophilia-myalgia syndromeT D Heiman-Patterson, S J Bird, G J Parry, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Electromyography and Clinical Neurophysiology|December 1, 1991
Clinical and electrophysiological assessments in ALS patientsA J Tahmoush, J A Gillespie, J F Hulihan, et al.
Neurology|June 1, 1991
Factors influencing outcome of prednisone dose reduction in myasthenia gravisM A Miano, T M Bosley, T D Heiman-Patterson, et al.
Brain Research. Molecular Brain Research|November 3, 2004
Effect of transgene copy number on survival in the G93A SOD1 transgenic mouse model of ALSGuillermo M Alexander, Kirsten L Erwin, Nathaniel Byers, et al.
The American Journal of Medicine|August 1, 1984
Neuroleptic malignant syndrome. Patient with unique clinical and physiologic featuresG P Downey, M Rosenberg, S Caroff, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|January 19, 2011
Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: a window of opportunity in the search for genetic modifiersTerry D Heiman-Patterson, Roger B Sher, Elizabeth A Blankenhorn, et al.
Journal of the Neurological Sciences|July 19, 2005
Background and gender effects on survival in the TgN(SOD1-G93A)1Gur mouse model of ALST D Heiman-Patterson, J S Deitch, E P Blankenhorn, et al.
Plos One|September 15, 2022
Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron diseaseGuillermo M Alexander, Terry D Heiman-Patterson, Frank Bearoff, et al.
Plos One|March 13, 2015
Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron diseaseTerry D Heiman-Patterson, Elizabeth P Blankenhorn, Roger B Sher, et al.
Neurogenetics|September 7, 2014
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathySenda Ajroud-Driss, Faisal Fecto, Kaouther Ajroud, et al.
Annals of Neurology|October 1, 1990
Peripheral neuropathy associated with eosinophilia-myalgia syndromeT D Heiman-Patterson, S J Bird, G J Parry, et al.
Pageof 7