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Cerebral Amyloid Angiopathy
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An unusual cause of stroke and hypoxia
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
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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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Bicuspid Aortic Valve - A Silent Danger: Analysis of 50 Cases of Infective Endocarditis
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Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
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Mendelian Etiologies of Stroke
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Abnormal Metabolism of y-Trace Alkaline Microprotein
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Familial Vascular Malformation or Chance Occurrence
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A 51-Year-Old Woman with Abnormal Corups Callosum Signal
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Ears of the Lynx Magnetic Resonance Imaging Sign
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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A Teenager with Persistent Headache
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Ehlers-Danlos Syndromes
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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A Neonate with Micrognathia and Hypotonia
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Red Papules on the Tongue of a Patient with Hemiparesis
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Intracranial Neoplasms and Paraneoplastic Disorders, Meningioma
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Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
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Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
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Screening Patients with a Family History of Subarachnoid Haemorrhage for Intracranial Aneurysms: Screening Uptake, Patient Characteristics and Outcome
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Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Familial Versus Sporadic Cavernous Malformations: Differences in Developmental Venous Anomaly Association and Lesion Phenotype
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