Publication Venue For
Rasagiline for amyotrophic lateral sclerosis: A randomized, controlled trial.
Alterations in mitochondrial fission, fusion, and mitophagic protein expression in the gastrocnemius of mice after a sciatic nerve transection.
Needle electromyography practice patterns in patients taking novel oral anticoagulants: A survey-based study.
Gender and quality of life in myasthenia gravis patients from the myasthenia gravis foundation of America registry.
Genetic modifiers of Duchenne and facioscapulohumeral muscular dystrophies.
Quantification and characterization of grouped type I myofibers in human aging.
Subacute demyelinating polyradiculoneuropathy complicating Epstein–Barr virus infection in GATA2 haploinsufficiency.
International clinimetric evaluation of the MG-QOL15, resulting in slight revision and subsequent validation of the MG-QOL15r.
Ocular LEMS or MLOS.
Comparisons of ultrasound-estimated intramuscular fat with fitness and health indicators.
Clinical spectrum of valosin containing protein (VCP)-opathy.
Acute myofascitis as a manifestation of chronic graft-versus-host disease.
Measurement of intramuscular fat by muscle echo intensity.
Changes in α7β1 integrin signaling after eccentric exercise in heat-shocked rat soleus.
Mechanosensitivity may be enhanced in skeletal muscles of spinal cord-injured versus able-bodied men.
Mechanosensitivity may be enhanced in skeletal muscles of spinal cord-injured versus able-bodied men
Does change in acetylcholine receptor antibody level correlate with clinical change in myasthenia gravis?.
The role of chemokines in guillain-barré syndrome.
A randomized, double-blind, placebo-controlled phase II study of eculizumab in patients with refractory generalized myasthenia gravis.
Psychometric evaluation of the myasthenia gravis composite using rasch analysis.
Recommendations for myasthenia gravis clinical trials.
Subacute brachial diplegia associated with west nile virus myelitis.
Re: Practice parameters in myasthenia gravis.
Isolation and transcriptome analysis of adult zebrafish cells enriched for skeletal muscle progenitors.
Practice parameters and focusing research: Plasma exchange for myasthenia gravis.
Intraoperative on-nerve nerve conduction study and conversion factor in the sural nerve.
Dorsal caudal tail and sciatic motor nerve conduction studies in adult mice: Technical aspects and normative data.
3,4-Diaminopyridine is more effective than placebo in a randomized, double-blind, cross-over drug study in LEMS.
Racial differences in myasthenia gravis in Alabama.
Construction of an efficient evaluative instrument for myasthenia gravis: The MG composite.
Statins may aggravate myasthenia gravis.
Less is more, or almost as much: A 15-item quality-of-life instrument for myasthenia gravis.
Electrophysiological differences in seropositive and seronegative Lambert-Eaton myasthenic syndrome.
Exercise-induced cramp, myoglobinuria, and tubular aggregates in phosphoglycerate mutase deficiency.
Electrodiagnostic criteria for carpal tunnel syndrome in axonal polyneuropathy.
Repetitive nerve stimulation of facial muscles in MuSK antibody-positive myasthenia gravis.
Adult polyglucosan body disease: A case report of a manifesting heterozygote.
Electrophysiological diagnostic criteria of Lambert-Eaton myasthenic syndrome.
Myokymia, neuromyotonia, dermatomyositis, and voltage-gated K+ channel antibodies.
Relation between in vivo and in vitro measurements of skeletal muscle oxidative metabolism.
Muscle metabolic economy is inversely related to exercise intensity and type II myofiber distribution.
Distal sensory nerve conduction of the superficial peroneal nerve: new method and its clinical application..
Distal sensory nerve conduction of the superficial peroneal nerve: New method and its clinical application.
Iatrogenic superior gluteal mononeuropathy.
Iatrogenic superior gluteal mononeuropathy..
Stiff-persons' syndrome associated with thymoma and subsequent myasthenia gravis.
Primary respiratory failure as the presenting symptom in Lambert–Eaton myasthenic syndrome.
A benign form of reducing body myopathy.
Multiple sclerosis and hypertrophic demyelinating peripheral neuropathy.
Preparation of cell‐free extracellular matrix from human peripheral nerve.