Area of research
Neurology · Physiology
Research interest
Research interests include Peripheral Neuropathies and Disorders, Pain Mechanisms and Treatments, Peripheral Nerve Disorders, and Botulinum Toxin and Related Neurological Disorders.
Clinical Insights Into CASPR1 and CASPR1/Contactin-1 Complex Autoimmune Nodopathies.
Sensitivity of Nerve and Skin Biopsy and Fat Aspirate for Amyloid in Symptomatic Hereditary ATTR Amyloidosis With Peripheral Neuropathy.
GLP-1RA-Associated Diabetic Lumbosacral Radiculoplexus and Common Fibular Neuropathies: A Case-Control Evaluation.
Clinical Manifestations and Treatment Responses in Pediatric Neurofascin 155-IgG4 Autoimmune Nodopathy.
Natural History and Phenotypic Spectrum of Myofibrillar Myopathies and Myopathies Associated With MFM-Related Genes.
Neurologic Clinical, Electrophysiologic, and Pathologic Characteristics of Primary vs Secondary Neurolymphomatosis.
Clinicopathologic Findings in Patients With Paraneoplastic Neuropathies and Antibodies Strongly Associated With Cancer.
Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy
Composite nerve conduction scores and signs for diagnosis and somatic staging of diabetic polyneuropathy: Mid North American ethnic cohort survey.
Clinical, Neurophysiologic, and Pathologic Features in Patients With Early-Onset Postradiation Neuropathy.
Novel approaches to diagnosis and management of hereditary transthyretin amyloidosis
Novel approaches to diagnosis and management of hereditary transthyretin amyloidosis.
Long-term efficacy and safety of inotersen for hereditary transthyretin amyloidosis: NEURO-TTR open-label extension 3-year update
Characteristics of Patients with Hereditary Transthyretin Amyloidosis-Polyneuropathy (ATTRv-PN) in NEURO-TTRansform, an Open-label Phase 3 Study of Eplontersen
Comparison of immune checkpoint inhibitor-related neuropathies among patients with neuroendocrine and non-neuroendocrine tumours.
Risk factors for lumbosacral radiculoplexus neuropathy.
Variable differences of nerve conduction amplitudes versus velocities and distal latencies of healthy subjects assessed in ethnic cohorts.
Design and Rationale of the Global Phase 3 NEURO-TTRansform Study of Antisense Oligonucleotide AKCEA-TTR-LRx (ION-682884-CS3) in Hereditary Transthyretin-Mediated Amyloid Polyneuropathy
Chronic inflammatory demyelinating polyradiculoneuropathy-Diagnostic pitfalls and treatment approach.
Neurofascin-155 Immunoglobulin Subtypes: Clinicopathologic Associations and Neurologic Outcomes.
Small Fiber Neuropathy Incidence, Prevalence, Longitudinal Impairments, and Disability.
Neuromuscular amyloidosis: Unmasking the master of disguise.
Lumbosacral Radiculoplexus Neuropathy: Neurologic Outcomes and Survival in a Population-Based Study.
Expanding the Spectrum of Chronic Immune Sensory Polyradiculopathy: CISP-Plus.
Pure Motor Onset and IgM-Gammopathy Occurrence in Multifocal Acquired Demyelinating Sensory and Motor Neuropathy.
Novel imaging techniques using <sup>18</sup> F-florbetapir PET/MRI can guide fascicular nerve biopsy in amyloid multiple mononeuropathy.
Acute immune sensory polyradiculopathy: a new variant of Guillain-Barré syndrome.
Focal sensory chronic inflammatory demyelinating polyneuropathy (CIDP).
Early data on long‐term efficacy and safety of inotersen in patients with hereditary transthyretin amyloidosis: a 2‐year update from the open‐label extension of the NEURO‐TTR trial
Neuropathy symptom and change: Inotersen treatment of hereditary transthyretin amyloidosis.