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Recessive Ataxia With Ocular Apraxia
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Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
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Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023
Neurologic Complications of Babesiosis, United States, 2011-2021
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An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022
Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
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Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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Complex Ataxia
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A 57-Year-Old Woman with Progressive Ataxia and Falls
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Stridor in Multiple System Atrophy
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GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018
An Unusual Fundus Finding in a Teenage Girl
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Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
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Reversible Gait Ataxia
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A 58-year-old man with Progressive Ptosis and Walking Difficulty
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Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
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Extraintestinal Manifestations of Coeliac Disease
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Copper Deficiency
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Diseases of the Nervous System Caused by Nutritional Deficiency, Wernicke-Korsakoff Syndrome (Thiamine B1) Deficiency
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Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lead
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Ataxia, Dementia, and Hypogonadotropism Caused by Disordered Ubiquitination
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
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Multimodal Imaging of Reversible Cerebral Vasoconstriction Syndrome: A Series of 6 Cases
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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Second Consensus Statement on the Diagnosis of Multiple System Atrophy
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Ataxic vs Painful Form of Paraneoplastic Neuropathy
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Mitochondrial DNA Polymerase-y and Human Disease
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Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
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The Neurological Complications of Bariatric Surgery
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Spectrum of Paraneoplastic Neurologic Disorders in Women with Breast and Gynecologic Cancer
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Mitochondrial Respiratory-Chain Diseases
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