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Pseudoxanthoma Elasticum:A Review of Neurological Complications
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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"Disappearing Infarct" Is Late-Onset MELAS
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Ehlers-Danlos Syndromes
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
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MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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A Young Man with Progressive Vision and Hearing Loss
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The Autosomal Recessive Cerebellar Ataxias
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CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
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Restricted Diffusion in Vanishing White Matter
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Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Screening for Intracranial Aneurysms in ADPKD: A More Accurate Risk Assignment Model Is Needed
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Nearly Completely Reversible Brain Abnormalities in a Patient With Incontinentia Pigmenti
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Autosomal Dominant Moyamoya Disease Maps to Chromosome 17q25.3
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Metabolic Disease and Stroke: MELAS
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Heritability of Carotid Artery Atherosclerotic Lesions
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Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
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Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
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Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
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Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
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Stroke in Williams Syndrome
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Cerebrovascular Complications of Fabry's Disease
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Hereditary Hemorrhagic Telangiectasia
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Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
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On the Inheritance of Intracranial Aneurysms
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Familial Intracranial Aneurysms, A Review
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Nystagmus of Pelizaeus-Merzbacher Disease
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Cerebral Haemorrhage and Berry Aneurysm:Evidence from a Family for a Pattern of Autosomal Dominant Inheritance
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Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
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Epilepsy Octet, Epidemiology, Classification, Natural History, and Genetics of Epilepsy
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Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
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Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
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Cerebral Amyloid Angiopathy, A Critical Review
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Mendelian Etiologies of Stroke
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Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
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Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
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Acid Maltase Deficiency
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Primary Position Vertical Nystagmus & Cerebellar Ataxia
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Dominant Inheritance of Intracranial Berry Aneurysm
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