A Surgical Approach To The Treatment Of Fetal Hydrocephalus
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Placement Of Ventriculo-Amniotic Shunt For Hydrocephalus In A Fetus
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An unusual cause of stroke and hypoxia
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A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
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Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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Clinical Manifestations and Diagnosis of Bicuspid Aortic Valve in Adults
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Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
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Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
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Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Extension of the Clinical Spectrum of Danon Disease
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Familial Dopa-Responsive Cervical Dystonia
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Familial Cervical Artery Dissections: Clinical, Morphologic, and Genetic Studies
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Dopamine-Responsive Dystonia
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Heritability of Carotid Artery Atherosclerotic Lesions
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Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
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Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
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Jaw Drop in Kennedy's Disease
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Cardiac Dysfunction in Neuromuscular Diseases
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Recommendations for the Management of Patients with Unruptured Intracranial Aneurysms
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Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
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Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
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X-Linked Vacuolated Myopathy:Membrane Attack Complex Depos on Muscle Fiber Membr with Calcium Accumul on Sarcolemma
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Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
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Recurrent Spontaneous Arterial Dissections-Risk in Familial Vs Nonfamilial Disease
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Intelligence and the X Chromosome
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X-Linked Malformation of Neuronal Migration
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A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
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Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
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Familial Aorto-Cervicocephalic Arterial Dissections and Congenitally Bicuspid Aortic Valve
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Hereditary Hemorrhagic Telangiectasia
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Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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A Clinical Study of Noonan Syndrome
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Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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The Phenotype of the X-Linked Dystonia-Parkinsonism Syndrome, An Assessment of 42 Cases in the Philippines
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Familial Association of Intracranial Aneurysms and Cervical Artery Dissections
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Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
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X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
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Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
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