Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025
Autoimmune Nodopathies, An Emerging Dignostic Category
Curr Opin Neurol 35:579-585, Martin-Agullar, L.,et al, 2022
Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021
Pernicious Anaemia
BMJ 369:m1319, Mohamed, M.,et al, 2020
Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
Neurol 95:e268-e279, Keddie, S.,et al, 2020
Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
Neurol 92:663-674, Johansen, A.,et al, 2019
Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019
Extraintestinal Manifestations of Coeliac Disease
Nat Rev Gastroenterol Hepatol 12:561-571, Leffler, D.A.,et al, 2015
Pharyngeal-Cervical-Brachial Variant of Guillain-Barr� Syndrome
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Recognizing Guillain-Barr� Syndrome in Preschool Children
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Guillain-Barre Syndrome
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Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
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Chronic Inflammatory Demyelinating Polyneuropathy Presenting with Features of GBS
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A Six-Year-Old Girl with Tick paralysis
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Clinicopath Conf
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Acute Paralytic Poliomyelitis Presenting as Guillain-Barre Syndrome
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Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
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Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
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Frequency of AQP4 and MOG Antibodies in Patients with Optic Neuritis Fulfilling Minimal New Multiple Sclerosis MRI Criteria
Neurol 106:e214753, Deschamps,R.,et al, 2026
Pan-Neurofascin Nodo-Paranodopathy Presenting as Fulminant Guillain-Barre Syndrome
Neurol 105:e213848, Cabral,A.,et al, 2025
Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
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Primary Central Nervous System Vasculitis
NEJM 391:1028-1037, Salvarani,C.,et al, 2024
A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023
Biopsy Negative Giant Cell Arteritis - Revised Diagnostic Criteria
J Stroke Cerebrovasc Dis 31:106660, Finelli, P.F., 2022
Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022
Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022
Neurobrucellosis:The Great Mimicker
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Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature
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The First Examination of Diagnostic Performance of Automated Measurement of the Callosal Angle in 1856 Elderly Patients and Volunteers Indicates that 12.4% of Exams Met the Criteria for Possible Normal Pressure Hydrocephalus
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Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020
Functional Gait Disorders
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Pes Cavus and Neuropathy
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Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018
Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018
FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
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A 57-year-old Man with Subacute Gait Difficulty and Hand Tremor
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Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016
CIDP Diagnostic Pitfalls and Perception of Treatment Benefit
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A Young Woman with Blurred Vision and Distal Paresthesias
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A 20-year-old Woman with Rapidly Progressive Weakness
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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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Criteria for the Diagnosis of Corticobasal Degeneration
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