April McVey

Myasthenia gravis, thymoma, and intestinal pseudo-obstruction: a case report and review.

Clinical findings in MuSK-antibody positive myasthenia gravis: a U.S. experience.

Retrospective chart review of duloxetine and pregabalin in the treatment of painful neuropathy.

Ocular myasthenia gravis in an academic neuro-ophthalmology clinic: clinical features and therapeutic response.

Facial onset sensorimotor neuronopathy syndrome: a case series.

Leg amyotrophic diplegia: prevalence and pattern of weakness at US neuromuscular centers.

Pompe disease: literature review and case series.

A genome-wide association study of myasthenia gravis.

Disease course and therapeutic approach in dermatomyositis: A four-center retrospective study of 100 patients.

Patterns of Weakness, Classification of Motor Neuron Disease, and Clinical Diagnosis of Sporadic Amyotrophic Lateral Sclerosis.

Symptom Management and End-of-Life Care in Amyotrophic Lateral Sclerosis.

Primary Lateral Sclerosis and Early Upper Motor Neuron Disease: Characteristics of a Cross-Sectional Population.

Targeting protein homeostasis in sporadic inclusion body myositis.

Defining SOD1 ALS natural history to guide therapeutic clinical trial design.

Less is More in Diabetic Neuropathy Diagnosis: Comparison of Quantitative Sudomotor Axon Reflex and Skin Biopsy.

Satisfactory Response With Achieving Maintenance Low-Dose Prednisone in Generalized Myasthenia Gravis.