A Middle-aged Woman with Severe Scoliosis and Encephalopathy
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Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Molybdenum Cofactor Deficiency
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
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Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Aicardi-Gouti�res Syndrome
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Prader-Willi and Angelman Syndromes
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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Cerebrovascular Complications of Fabry's Disease
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The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
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Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
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Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
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Clinical Spectrum of CADASIL:A Study of 7 Families
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
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Hereditary Hemorrhagic Telangiectasia
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Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
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Causal Heterogeneity in Isolated Lissencephaly
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Angelman Syndrome: Clinical Profile
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Anderson-Fabray Disease, A Commonly Missed Diagnosis
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Neurological Manifestations in Xeroderma Pigmentosum
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Familial Porencephaly
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Von Recklinghausen Neurofibromatosis
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Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
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The Lissencephaly, (Agyria) Syndrome in Siblings
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Maternal Epilepsy & Abnormalities of the Fetus & Newborn
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Neonatal Seizures
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
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Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
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Spinal Muscular Atrophy
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Genetics of Cluster Headache Takes a Leap
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A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
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Ehlers-Danlos Syndromes
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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A 10-year-old boy with Bilateral Vision Loss
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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