Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017
A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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A Woman with Intellectual Disability, Amenorrhoea, Seizures, and Balance Problems
JAMA Neurol 73:1494-1495, Hughes, A.J.C.,et al, 2016
Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
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A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008
Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004
Course and Outcome of Acute Cerebellar Ataxia
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Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
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IgG4-Related Leptomeningitis: A Reversible Cause of Rapidly Progressive Cognitive Decline
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Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
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Cognitive Delay in a 7-year-old Girl
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
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Wilson Disease
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
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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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A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021
Congenital Cytomegalovirus Infection
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Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018
Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018
Primary Angiitis of the Central Nervous System
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Reversible Cognitive Decline Diagnosed on Ear Examination
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Chronic Hepatitis C Virus Infection and Neurological and Psychiatric Disorders
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Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
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Frequency, Characteristics, and Risk Factors for Amiodarone Neurotoxicity
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West Nile Virus Neuroinvasive Disease
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Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003
Out of Africa, Trypanosomiasis
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Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997
Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996
Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Risk Factors for Nursing Home Placement in Advanced Parkinson's Disease
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Central Nervous System Involvement in the Eosinophilia-Myalagia Syndrome
Arch Neurol 49:1082-1085, Lynn,J.,et al, 1992
HIV Encephalopathy and Dementia
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Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991
Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991
Ethanol and the Nervous System
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Unrecognized Chronic Lithium Neurotoxic Reactions
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Corticodentatonigral Degeneration with Neuronal Achromasia
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