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NEJM 386:173-180, Case 1-2022, 2022
Disabling Jaw Clonus in a Patient with Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated with Botulinum Toxin
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Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019
Young Adult with Dysphagia and Severe Weight Loss
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Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017
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Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007
Polymyositis Masquerading as Motor Neuron Disease
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Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
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Amyotrophic lateral Sclerosis Mimic Syndromes, A Population-Based Study
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Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
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Location of the Gene for X-Linked Spinal Muscular Atrophy
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Pathological Laughter & Crying
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Progressive Pontobulbar Palsy With Deafness
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Control of Emotional Expression in Pseudobulbar Palsy
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Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
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Natural History of "Pure" Primary Lateral Sclerosis
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Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
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Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
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Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
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Telemedicine in Neurology
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Hopkins Syndrome
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"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
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Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
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A 42-year-old man with unilateral leg weakness
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Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
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Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
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Powassan Virus-A New Reemerging Tick-Borne Disease
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Mechanisms, Causes, and Effects of Hypercapnia
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Physician-Assisted Death
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Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
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