The Phenotypic Continuum of ATP1A3-Related Disorders
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Alternating Hemiplegia of Childhood:A Study of 10 Pts & Results of Flunarizine Treatment
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024
Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023
Sturge-Weber Syndrome
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CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021
Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021
Neurological Manifestations Among US Government Personnel Reporting Directional Audible and Sensory Phenomena in Havana, Cuba
JAMA 319:1125-1133, 1098, 1079, Swanson, R.L.,et al, 2018
Antibody-Mediated Encephalitis
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Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
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A 13-year-old boy with Chronic Ataxia and Developmental Delay
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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On-Road Driving Impairments in Huntingtons Disease
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Sturge-Weber Syndrome
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Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
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Huntingtons Disease
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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A 23-Year-Old Man With Seizures and Visual Deficit
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Bilirubin Metabolism and Kernicterus
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Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
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Primary Brain Tumors:Review of Etiology Diagnosis and Treatment
Am Fam Physician 49:787-797, Newton,H.B., 1994
Med Trtm of Rasmussen's Syndrome (Chronic Enceph & Epilepsy) :High-Dose Steroids or Immunoglobulins in 19 Pts
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Clinical and Magnetic Resonance Features of the Classic & Akinetic-Rigid Variants of Huntington's Dis
Arch Neurol 50:17-19, Oliva,D.,et al, 1993
Alternating Hemiplegia of Childhood
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A Predictive Model for Delirium in Hospitalized Elderly Medical Patients Based on Admission Characteristics
Ann Int Med 119:474-481, Inouye,S.K.,et al, 1993
Clinicopath Conf
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Coma Assoc with Bursts of Abnor Movements & Cognitive Disturb:Acute Encephalopathy of Obscure Origin
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Chronic Encephalitis (Rasmussen's Syndrome) and Ipsilateral Uveitis
Ann Neurol 32:826-829, Harvey,A.S.,et al, 1992
A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992
A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992
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
A Simple Procedure for General Screening for Functional Disability in Elderly Patients
Ann Int Med 112:699-706, Lachs,M.S.,et al, 1990
Clinical-Pathologic Correlation in Huntington's Disease:A Neuropsychological and Computed Tomography Study
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Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982
Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
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