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Central Nervous System Lesions in von Hippel-Lindau Syndrome
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Cerebral Cavernous Malformations:Incidence and Familial Occurrence
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Vascular Malformations of the Central Nervous System
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations
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Complex Ataxia
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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Cranial Cavernous Malformations
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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 Neonate with Micrognathia and Hypotonia
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Degenerative Diseases of the Nervous System, Olivopontocerebellar Atrophy
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Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
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Familial Dopa-Responsive Cervical Dystonia
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Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
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Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
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Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
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Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
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Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent
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Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
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Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
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Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
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Hereditary Hemorrhagic Telangiectasia
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Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
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Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
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The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993
Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
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Brain Tumors
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Magnetic Resonance Imaging in a Family with Hereditary Cerebral Arteriovenous Malformations
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Friedreich Ataxia
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Familial Cavernous Malformations of the Central Nervous System & Retina
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Mendelian Etiologies of Stroke
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Familial Association of Intracranial Aneurysms & Multiple Congenital Anomalies
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Familial Arteriovenous Malformation of the Brain
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Familial Arteriovenous Malformation
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Familial Vascular Malformation or Chance Occurrence
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Familial Cavernous Angiomas
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