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Ophthalmoplegic Migraine:Reversible Enhancement and Thickening of the Cisternal Segment of the Oculomotor Nerve on Contrast-Enhanced MR Images
AJNR 19:1887-1891, Mark,A.S.,et al, 1998
Cardiac Involvement in Genetically Confirmed Facioscapulohumeral Muscular Dystrophy
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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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Pregnant,Vomiting,and Going Blind
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Paroxysmal Tonic Upgaze:a Reappraisal of Outcome
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Follow-up of Nine Patients with Hurler Syndrome After Bone Marrow Transplantation
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Mucolipidosis Type IV; Characteristic MRI Findings
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Mydriatic Pupil as the Presenting Sign of Common Carotid Artery Dissection
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Occult Giant Cell Arteritis:Ocular Manifestations
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Migrainous Visual Accompaniments are not Rare in Late Life:The Framingham Study
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Pupil Involvement in Patients with Diabetes-Associated Oculomotor Nerve Palsy
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Managing Oculomotor Nerve Palsy
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Ischemic Optic Neuropathy Associated with Internal Carotid Artery Dissection
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Spontaneous Dural Carotid Cavernous Sinus Fistula Pres Isolat Ophthalmoplegia:Eval with MR Angiogr
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Axonal Transection in the Lesions of Multiple Sclerosis
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More on Reflex Sympathetic Dystrophy Syndrome Following Air-Bag Inflation
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Clinicopath Conf
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Proton Spectroscopy in Myotonic Dystrophy, Correlations with CTG Repeats
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Posterior Cerebral Artery Syndromes
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Anesthetic and Surgical Complictions in 219 Cases of Myotonic Dystrophy
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Ocular Findings in Ramsay Hunt Syndrome
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Complete Ophthalmoplegia After Zoster Ophthalmicus
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Cocaine and Pupillary-Sparing Oculomotor Nerve Paresis
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Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
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Pupil-Involving Third-Nerve Palsy and Carotid Stenosis:Rapid Recovery Following Endarterectomy
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Evaluation of Neurologic Function in Gulf War Veterans:A Blinded Case-Control Study
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Successful Treatment of Persistent Migraine Aura with Divalproex Sodium
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997
The Muscular Dystrophies-Clarity or Chaos
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Ocular Myasthenia Gravis:Response to Long Term Immunosuppressive Treatment
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Adult Botulism
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Neuro-Ophthalmic Presentation of Non-Hodgkins Lymphoma
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Paramedian Pontine Infarction
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Clinicopath Conf
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Peripheral Neuropathy Associated with Sicca Complex
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Neuro-Ophthalmic Manifestations of Lyme Disease
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Obstetric Aspects in Women with FSH Muscular Dystrophy, Limb-Girdle Musc Dyst, & Cogen Myopathies
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Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
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X-Linked Emery-Dreifuss Muscular Dystrophy Can Be Diagnosed from Skin Biopsy or Blood Sample
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Bilateral Trochlear Nerve Palsy and Downbeat Nystagmus in a Patient with Cephalic Tetanus
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Serum Autoantibodies in Childhood Opsoclonus-Myoclonus Syndrome:Analysis of Antigenic Targets in Neural Tissues
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Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
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Giant Cell Arteritis With Unusual Flow-Related Neuroophthalmologic Manifestations
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Stroke Mechanisms and Clinical Presentation in Large Subcortical Infarctions
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Arterial Injuries in Transsphenoidal Surgery for Pituitary Adenoma:The Role of Angiography and Endovascular Treatment
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Bilirubin Metabolism and Kernicterus
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Intermittent Diplopia and Strabismus Caused by Ocular Neuromyotonia
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