Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Two Sets of Identical Twins with Cervical Artery Dissection Concordant for Temporal Artery Pathology
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Heritability of Carotid Artery Atherosclerotic Lesions
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Hereditary Hemorrhagic Telangiectasia
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Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
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Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
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Pseudoxanthoma Elasticum:A Review of Neurological Complications
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Pediatric Leigh Syndrome
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Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017
MRI Findings of Biotin-Responsive Basal Ganglia Disease Before and After Treatment
Neurol 86:e71-e72, Saeedan, M.B. & Dogar, M.A., 2016
Clinical Manifestations and Diagnosis of Bicuspid Aortic Valve in Adults
UpToDate Nov, Braverman, D.C., 2014
Sturge-Weber Syndrome
MedLink Neurology, July, Comi, A.M., 2013
Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Update on Blepharospasm: Report from the BEBRF International Workshop
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MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
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Parkinsons Disease and Genetics
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Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
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Familial Infantile Bilateral Striatal Necrosis
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Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
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Complete Genomic Screen in Parkinson Disease
JAMA 286:2239-2244, Scott,W.K.,et al, 2001
Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
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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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Hereditary Form of Parkinsonism-Dementia
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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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Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
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Clinical Significance of Fetal Choroid Plexus Cysts
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Preclinical Detection of Parkinson's Disease
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A Large Kindred with Autosomal Dominant Parkinson's Disease
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Acute Profound Dystonia in Infants with Glutaric Acidemia
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Leigh Disease (Subacute Necrotizing Encephalomyelopathy) :CT & MR in Five Cases
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Livedo Reticularis, Porcelain-White Scars, and Cerebral Thromboses
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Clinicopath Conf
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Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
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Cervicomedullary Compression in Young Patients with Achondroplasia:Value of Neurologic & Respiratory Eval
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Autosomal Dominant Osteosclerosis Associated with Familial Spinal Canal Stenosis
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Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
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Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
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Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
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Livedo Reticularis & Cerebrovascular Lesions (Sneddon's Syndrome) , Clin, Radiolog & Path Features in Eight Cases
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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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Familial Lumbar Spinal Stenosis with Acute Disc Herniation, Case Reports of Four Brothers
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Familial Cavernous Angiomas
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Clinical Neurogenetics
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