Search Results - "SHEFNER, J"

Refine Results
  1. 1

    Multipoint incremental motor unit number estimation as an outcome measure in ALS by SHEFNER, J. M, WATSON, M. L, SIMIONESCU, L, CARESS, J. B, BURNS, T. M, MARAGAKIS, N. J, BENATAR, M, DAVID, W. S, SHARMA, K. R, RUTKOVE, S. B

    Published in Neurology (19-07-2011)
    “…Improved outcome measures are necessary to reduce sample size and increase power in amyotrophic lateral sclerosis (ALS) clinical trials. Motor unit number…”
    Get full text
    Journal Article
  2. 2

    Assessment of bulbar function in amyotrophic lateral sclerosis: validation of a self‐report scale (Center for Neurologic Study Bulbar Function Scale) by Smith, R. A., Macklin, E. A., Myers, K. J., Pattee, G. L., Goslin, K. L., Meekins, G. D., Green, J. R., Shefner, J. M., Pioro, E. P.

    Published in European journal of neurology (01-07-2018)
    “…Background and purpose Impaired bulbar functions of speech and swallowing are among the most serious consequences of amyotrophic lateral sclerosis (ALS)…”
    Get full text
    Journal Article
  3. 3

    A clinical trial of creatine in ALS by SHEFNER, J. M, CUDKOWICZ, M. E, CARESS, J, DONOFRIO, P, SORENSON, E, BRADLEY, W, LOMEN-HOERTH, C, PIORO, E, REZANIA, K, ROSS, M, PASCUZZI, R, HEIMAN-PATTERSON, T, SCHOENFELD, D, TANDAN, R, MITSUMOTO, H, ROTHSTEIN, J, SMITH-PALMER, T, MACDONALD, D, BURKE, D, CONRAD, T, TAFT, J, CHILTON, M, URBINELLI, L, QURESHI, M, ZHANG, H, PESTRONK, A

    Published in Neurology (09-11-2004)
    “…Mitochondrial dysfunction occurs early in the course of ALS, and the mitochondria may be an important site for therapeutic intervention. Creatine stabilizes…”
    Get full text
    Journal Article
  4. 4

    The use of statistical MUNE in a multicenter clinical trial by Shefner, J. M., Cudkowicz, M. E., Zhang, H., Schoenfeld, D., Jillapalli, D.

    Published in Muscle & nerve (01-10-2004)
    “…Techniques to estimate motor unit number (MUNE) measure the number of functioning motor units in a muscle. In diseases characterized by progressive motor unit…”
    Get full text
    Journal Article
  5. 5

    Functional outcome measures as clinical trial endpoints in ALS by Traynor, B J, Zhang, H, Shefner, J M, Schoenfeld, D, Cudkowicz, M E

    Published in Neurology (23-11-2004)
    “…The topiramate study was a 12-month randomized placebo-controlled trial in patients with ALS. Follow-up evaluation of the placebo group (n = 97) constituted a…”
    Get full text
    Journal Article
  6. 6

    Tolerance of high-dose (3,000 mg/day) coenzyme Q10 in ALS by FERRANTE, K. L, SHEFNER, J, NEWHALL, K, DONOFRIO, P, CARESS, J, ASHBURN, C, FREIBERG, B, O'NEILL, C, PALADENECH, C, WALKER, T, PESTRONK, A, ABRAMS, B, ZHANG, H, FLORENCE, J, RENNA, R, SCHIERBECKER, J, MALKUS, B, CUDKOWICZ, M, BETENSKY, R, O'BRIEN, M, YU, H, FANTASIA, M, TAFT, J, BEAL, M. F, TRAYNOR, B

    Published in Neurology (13-12-2005)
    “…An open-label dose-escalation trial was performed to assess the safety and tolerability of high doses of coenzyme Q10 (CoQ10) in ALS. CoQ10, a cofactor in…”
    Get full text
    Journal Article
  7. 7

    Revised statistical motor unit number estimation in the Celecoxib/ALS trial by Shefner, J. M., Cudkowicz, M. E., Zhang, H., Schoenfeld, D., Jillapalli, D.

    Published in Muscle & nerve (01-02-2007)
    “…Techniques to estimate motor unit number (MUNE) measure the number of functioning motor units in a muscle. As amyotrophic lateral sclerosis (ALS) is…”
    Get full text
    Journal Article
  8. 8

    Monkey median nerve repaired by nerve graft or collagen nerve guide tube by Archibald, SJ, Shefner, J, Krarup, C, Madison, RD

    Published in The Journal of neuroscience (01-05-1995)
    “…Nerve regeneration was followed in 15 median and 1 ulnar nerve of eight Macaca fascicularis monkeys by serial electrophysiological assessments over a period of…”
    Get full text
    Journal Article
  9. 9

    Mice lacking cytosolic copper/zinc superoxide dismutase display a distinctive motor axonopathy by SHEFNER, J. M, REAUME, A. G, FLOOD, D. G, SCOTT, R. W, KOWALL, N. W, FERRANTE, R. J, SIWEK, D. F, UPTON-RICE, M, BROWN, R. H

    Published in Neurology (12-10-1999)
    “…To characterize the motor neuron dysfunction in two models by performing physiologic and morphometric studies. Mutations in the gene encoding cytosolic…”
    Get full text
    Journal Article
  10. 10

    Motor unit number estimation in human neurological diseases and animal models by Shefner, Jeremy M.

    Published in Clinical Neurophysiology (01-06-2001)
    “…Motor unit number estimation (MUNE) was introduced in 1971 as a way of providing an objective and meaningful estimate of axon loss in diseases affecting the…”
    Get full text
    Book Review Conference Proceeding Journal Article
  11. 11

    Lead exposure as a risk factor for amyotrophic lateral sclerosis by Kamel, F, Umbach, D M, Hu, H, Munsat, T L, Shefner, J M, Taylor, J A, Sandler, D P

    Published in Neuro-degenerative diseases (01-01-2005)
    “…The etiology of amyotrophic lateral sclerosis (ALS) likely involves an environmental component. We qualitatively assessed literature on ALS and lead exposure…”
    Get more information
    Journal Article
  12. 12
  13. 13

    Effect of neurophilin ligands on motor units in mice with SOD1 ALS mutations by SHEFNER, J. M, BROWN, R. H, COLE, D, CHATURVEDI, P, SCHOENFELD, D, PASTUSZAK, K, MATTHEWS, R, UPTON-RICE, M, CUDKOWICZ, M. E

    Published in Neurology (27-11-2001)
    “…Mice with trangenes that express mutations in the gene for cytosolic copper/zinc superoxide dismutase (SOD1) develop motor neuron degeneration resembling human…”
    Get full text
    Journal Article
  14. 14

    Reducing intersubject variability in motor unit number estimation by Shefner, Jeremy M., Jillapalli, Devanand, Bradshaw, Deborah Y.

    Published in Muscle & nerve (01-10-1999)
    “…Motor unit number estimation (MUNE) attempts to directly assess the number of functioning motor units present in a muscle. It is an important addition to the…”
    Get full text
    Journal Article
  15. 15

    Ulnar neuropathy at the elbow by Bradshaw, D Y, Shefner, J M

    Published in Neurologic clinics (01-08-1999)
    “…Among the entrapment neuropathies, ulnar neuropathy at the elbow is second only to carpal tunnel syndrome in frequency; however, diagnosis and management are…”
    Get more information
    Journal Article
  16. 16

    Ulnar neuropathy and dystonic flexion of the fourth and fifth digits: Clinical correlation in musicians by Charness, Michael E., Ross, Marjorie H., Shefner, Jeremy M.

    Published in Muscle & nerve (01-04-1996)
    “…Peripheral nerve lesions are sometimes associated with focal dystonia. We diagnosed ulnar neuropathy in 28 of 73 (40%) cases of occupational cramp in…”
    Get full text
    Journal Article
  17. 17

    Recurrent inhibition is decreased in patients with amyotrophic lateral sclerosis by RAYNOR, E. M, SHEFNER, J. M

    Published in Neurology (01-11-1994)
    “…Recurrent inhibitory pathways are powerful modulators of motor neuron excitability. Renshaw cell activation can both inhibit homologous motor neurons and…”
    Get full text
    Journal Article
  18. 18

    Immunotoxin therapy of small-cell lung cancer: a phase I study of N901-blocked ricin by Lynch, Jr, T J, Lambert, J M, Coral, F, Shefner, J, Wen, P, Blattler, W A, Collinson, A R, Ariniello, P D, Braman, G, Cook, S, Esseltine, D, Elias, A, Skarin, A, Ritz, J

    Published in Journal of clinical oncology (01-02-1997)
    “…Immunotoxins could improve outcome in small-cell lung cancer (SCLC) by targeting tumor cells that are resistant to chemotherapy and radiation. N901 is a murine…”
    Get more information
    Journal Article
  19. 19

    The cutaneous silent period is mediated by spinal inhibitory reflex by Logigian, Eric L., Plotkin, George M., Shefner, Jeremy M.

    Published in Muscle & nerve (01-04-1999)
    “…High‐intensity cutaneous stimuli inhibit tonically firing motor neurons resulting in a silent period (CSP) in EMG activity. To determine the central nervous…”
    Get full text
    Journal Article
  20. 20

    Dietary intake of calcium, magnesium and antioxidants in relation to risk of amyotrophic lateral sclerosis by Longnecker, M P, Kamel, F, Umbach, D M, Munsat, T L, Shefner, J M, Lansdell, L W, Sandler, D P

    Published in Neuroepidemiology (01-07-2000)
    “…Dietary factors have long been suspected of being risk factors for amyotrophic lateral sclerosis (ALS), but few human studies have been reported. To address…”
    Get more information
    Journal Article