Cerebromeningeal Haemophagocytic Lymphohistiocytosis
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Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
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Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia
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Isolated Granulomatous Angiitis of the Spinal Cord
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Angelman Syndrome: Clinical Profile
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Erythromelalgia:Review of Clinical Characteristics and Pathophysiology
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Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Conjugal Temporal Arteritis
Neurol 40:1839-1842, Galetta,S.L.,et al, 1990
The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
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Dystonia Gene in Ashkenazi Jewish Population is Located on Chromosome 9q32-34
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The Triumph of Linkage Analysis, Editorial
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Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
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Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
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Primary Progressive Cerebellar Ataxia
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Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
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Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
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Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
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Clinicopath Conf
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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
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Mendelian Etiologies of Stroke
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Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
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Familial Occurrence of Idiopathic Normal-Pressure Hydrocephalus
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Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
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Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
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Familial Association of Giant Cell Arteritis
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Pathogenesis of Pseudotumor Cerebri Syndromes
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Cerebellar Atrophy Demonstrated by Computed Tomography
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Ataxia with Aniridia of Gillespie:A Case Report
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
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Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Neurol 29:880-881, Kuritzky,A.,et al, 1979
Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
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Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
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Clinical Aspects of Spasmodic Dysphonia
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Pseudoxanthoma Elasticum:A Review of Neurological Complications
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Nerve Growth Factor (three parts)
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Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
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Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977
Cause of Weakness in Myasthenia Gravis
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Ocular Motor Abnormalities in Hereditary Cerebellar Ataxia
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Catecholamines & Neurologic Diseases
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Neurotoxicity of Commonly Used Antineoplastic Agents
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Genetic Counseling in Retinitis Pigmentosa
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Clinical Diagnosis of the Dyskinesias
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Lymphomatoid Granulomatosis
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Polyneroupathies of Undetermined Cause
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Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
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Failure of Vision in Childhood
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