Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019
Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019
Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018
Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018
Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
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Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
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Neurological Management of Von Hippel-Lindau Disease
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Intracranial Neoplasms and Paraneoplastic Disorders, Hemangioblastoma of the Cerebellum
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Paraneoplastic Neurological Syndromes
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Central Nervous System Involvement in Whipple Disease
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Mycoplasma Pneumoniae Infection: Neurologic Complications
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The Autosomal Recessive Cerebellar Ataxias
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Central Nervous System Neuronal Surface Antibody Associated Syndromes: Review and Guidelines for Recognition
JNNP 83:638-645, Zuliani,L.,et al, 2012
Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012
Rhombencephalitis A Series of 97 Patients
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Epstein-Barr Virus Infections of the Nervous System
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Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
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Paraneoplastic Syndromes Affecting Brain and Cranial Nerves
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008
Downbeat Nystagmus: Aetiology and Comorbidity in 117 Patients
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Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
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Neuro-Ophthalmologic Manifestations of Paraneoplastic Syndromes
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Superficial Siderosis
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Causative Factors and Epidemiology of Bilateral Vestibulopathy in 255 Patients
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Epilepsy Syndromes in Infancy
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Paraneoplastic Syndromes Involving the Nervous System
NEJM 349:1543-1554, Darnell,R.B. &Posner,J.B., 2003
Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002
Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002
Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
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Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001
Neurology of Ciguatera
JNNP 70:4-8, Pearn,J., 2001
Brainstem Gliomas in Adults: Prognostic Factors and Classification
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Paraneoplastic Syndromes
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Molecular Basis of the Neurodegenerative Disorders
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Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
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Lateral Medullary Infarction
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Calcium Channels in Neurological Disease
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Paraneoplastic Cerebellar Degeneration
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Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
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The Inherited Ataxias and the New Genetics
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Clinicopathological Study of 35 Cases of Multiple System Atrophy
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Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
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