Zobrazeno 1 - 10
of 156
pro vyhledávání: '"L, Dimberg"'
Autor:
Abhisek Swaika, Nicole J. Boczek, Neha Sood, Kimberly Guthrie, Eric W. Klee, Ankit Agrawal, Elliot L. Dimberg, Sikander Ailawadhi
Publikováno v:
Case Reports in Genetics, Vol 2016 (2016)
Dysferlinopathy is an uncommon, progressive muscular dystrophy that has a wide phenotypic variability and primarily supportive management (Nguyen et al., 2007; Narayanaswami et al., 2014). Amyloid myopathy is a distinct, rare disorder that can presen
Externí odkaz:
https://doaj.org/article/4e6fe1a1a8ed4093aa8cd50d70c18d18
Autor:
Gleydiane De Oliveira, Devon I. Rubin, Angelica R. Gicalone, Jaimin S. Shah, Christina R. Owens, Elliot L. Dimberg, Bjorn Oskarsson
Publikováno v:
The Neurologist. 25:141-143
Introduction Nusinersen antisense oligonucleotide infusions have been shown to be effective in the treatment spinal muscular atrophy. The majority of the evidence has been collected in young type 1 and type 2 patients, and evidence of efficacy in adu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79bde234467f0563efb631c0eec57d46
https://doi.org/10.1097/nrl.0000000000000284
https://doi.org/10.1097/nrl.0000000000000284
Autor:
Elliot L. Dimberg
Publikováno v:
Clinical Neurophysiology ISBN: 0190067853
Electrodiagnostic studies are essential to the evaluation of both brachial and lumbosacral plexus neuropathies. They not only can confirm a suspected diagnosis but also exclude alternative or additional possibilities, such as radiculopathy or mononeu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e85b798dd0ffc56c83aeb0b93aa2b1d
https://doi.org/10.1093/med/9780190067854.003.0031
https://doi.org/10.1093/med/9780190067854.003.0031
Autor:
Charles D. Kassardjian, Shahar Shelly, James D. Triplett, Margherita Milone, Elie Naddaf, Divanshu Dubey, Cecilia Kelly, Guy Livne, Christopher J. Lamb, Ruple S. Laughlin, John Mills, Devon I. Rubin, Jay Mandrekar, Teerin Liewluck, Elliot L. Dimberg, Christopher J. Klein
Publikováno v:
Brain Communications
Delayed diagnosis of immune-mediated necrotizing myopathy leads to increased morbidity. Patients with the chronic course without 3-hydroxy-3-methylglutaryl-coenzyme-A reductase-IgG or signal recognition particle-IgG are often challenging to diagnose.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c6854ea39bf0f7103ba468d14a201a1
https://doi.org/10.1093/braincomms/fcaa191
https://doi.org/10.1093/braincomms/fcaa191
Autor:
Ugur Sener, Devon I. Rubin, Jennifer M. Martinez-Thompson, Ruple S. Laughlin, Elliot L. Dimberg
Publikováno v:
Muscle & Nerve. 59:315-320
Introduction Needle electromyography (EMG) findings help confirm myopathy and may indicate specific pathologic changes on muscle biopsy. Methods We conducted a retrospective chart review of 218 consecutive patients referred for muscle biopsy. Presenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcb36753b2fc37ad1c5e4c0a8050b097
https://doi.org/10.1002/mus.26381
https://doi.org/10.1002/mus.26381
Akademický článek
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Autor:
Elliot L Dimberg
Publikováno v:
CONTINUUM: Lifelong Learning in Neurology. 23:691-721
This article reviews the various rheumatologic disorders that have neurologic complications and manifestations.Recent advances have improved the understanding of the true epidemiology of many rheumatologic diseases and their complications. Many years
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa17100c9348f816b6fdc41c2b3ba02
https://doi.org/10.1212/con.0000000000000474
https://doi.org/10.1212/con.0000000000000474
Publikováno v:
Neurology. 88:e185-e189
A 45-year-old man underwent rotator cuff surgery and developed fatigue and generalized myalgia postoperatively. After 4 weeks of mild symptoms, he experienced severe muscle aches and bilateral leg weakness after walking 1.5 miles, prompting him to se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4550a3ebab9e8b47be1b0d755abe3b5
https://doi.org/10.1212/wnl.0000000000003914
https://doi.org/10.1212/wnl.0000000000003914
Publikováno v:
Muscle & Nerve. 56:525-529
Introduction Eosinophilic fasciitis (EF) is a rare disorder that can present with muscle symptoms that mimic other neuromuscular diseases. Methods We report a 43-year-old woman with chronic muscle aches, tightness, and stiffness with hypertrophied, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::121167f7b9007112fed25d641b26e682
https://doi.org/10.1002/mus.25492
https://doi.org/10.1002/mus.25492
Autor:
Jennifer Gass, Duygu Selcen, Kimberly J. Harris, Elliot L. Dimberg, Jessica Jackson, Paldeep S. Atwal, Patrick R. Blackburn
Publikováno v:
Journal of Clinical Neuromuscular Disease
Welander distal myopathy is a rare autosomal dominant disorder characterized by muscle weakness in the hands and feet. Exome sequencing of affected families discovered a segregating p.Glu384Lys pathogenic variant in TIA-1 as the main genetic cause of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b918172c88cee0757fc097c66a854dc
https://doi.org/10.1097/cnd.0000000000000164
https://doi.org/10.1097/cnd.0000000000000164