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Differential
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arcuate scotoma, differential diagnosis of
multiple sclerosis
multiple sclerosis, diagnosis of
tangent screen examination
visual field defect
Showing articles 2150 to 2200 of 2804 << Previous Next >>

Transmission and Age-At-Onset Patterns in Familial Alzheimer's Disease:Evidence for Heterogeneity
Neurol 40:395-403, Farrer,L.A.,et al, 1990

Carotid Plaque Morphology and Risk for Stroke
Stroke 21:148-151, Gomez,C.G., 1990

Positron Emission Tomography in Neuropsychiatric Lupus Erythematosus
Neurol 40:304-308, Stoppe,G.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

The Triumph of Linkage Analysis, Editorial
Ann Neurol 27:111-113, Rosenberg,R.N., 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Acute Mental Status Changes in Children with Systemic Cancer
Pediatrics 85:353-360, DiMario,F.J.&Packer,R.J., 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

A Large Kindred with Autosomal Dominant Parkinson's Disease
Ann Neurol 27:276-282, Golbe,L.I.,et al, 1990

A Brain Transplant that Works
Lancet 335:445-446, , 1990

Alcohol Consumption and Carotid Atherosclerosis in the Lausanne Stroke Registry
Stroke 21:715-720, Bogousslavsky,J.,et al, 1990

Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation
NEJM 322:28-32, 541990., Krivit,W.,et al, 1990

Positron Emission Tomography in Shy-Drager Syndrome
Ann Neurol 28:101-103, Bhatt,M.H.,et al, 1990

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990

Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
JNNP 53:644-648, Boughey,A.M.,et al, 1990

Linkage of DNA Markers at Xq28 to Adrenoleukodystrophy & Adrenomyeloneuropathy Present in the Same Family
Arch Neurol 47:665-669, Willems,P.J.,et al, 1990

Prospective Comparison of a Cohort with Asympt Carotid Bruit & A Population-Based Cohort Without Carotid Bruit
Stroke 21:984-988, Wiebers,D.O.,et al, 1990

Carotid Artery Disease Assessed by Color Doppler Flow Imaging:Correlation with Standard Doppler Sonography & Angiography
AJR 154:1061-1068, Steinke,W.,et al, 1990

Transcranial Doppler Ultrasound Findings in Middle Cerebral Artery Occlusion
Stroke 21:532-537, Kaps,J.,et al, 1990

Assessment:Transcranial Doppler
Neurol 40:680-681, 696-7001990., Caplan,L.R.,et al, 1990

Dissection of the Cervical Internal Carotid Artery. The Role of Doppler/Duplex Studies & Conservative Management
JNNP 53:379-383, Eljamel,M.S.M.,et al, 1990

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Role of Carotid Stenosis in Ischemic Stroke
Stroke 21:1131-1134, Zhu,C.Z.&Norris,J.W., 1990

Cerebrovascular Complications of the Use of the"Crack"Form of Alkaloidal Cocaine
NEJM 323:699-704, Levine,S.R.,et al, 1990

Genetic Testing for Huntington's Disease
BMJ 300:1089-1090, Harper,P.,et al, 1990

Abnormalities of Striatal Projection Neurons and n-Methyl-d-Aspartate Receptors in Presymptomatic Huntington's Disease
NEJM 322:1293-1298, Albin,R.L.,et al, 1990

PET Study in Progressive Supranuclear Palsy, Hypometabolic Pattern
Arch Neurol 47:747-752, Blin,J.,et al, 1990

Wilson's Disease, Development of Neurological Disease after Beginning Penicillamine Therapy
Arch Neurol 47:595-596, Glass,J.D.,et al, 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

Cranial MR in Phenylketonuria
J Comput Assist Tomogr 14:458-460, Shaw,D.W.W.,et al, 1990

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
NEJM 322:1652-1669, Arn,P.H.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990

Transplantation of Human Fetal Dopamine Cells for Parkinson's Disease
Arch Neurol 47:505-512, Freed,C.R.,et al, 1990

Tangier Disease in a Black Patient:An Unusual Clinical Presentation
Am J Med 89:105-108, Lo,W.D.,et al, 1990

National Cancer Institute Workshop Statement
Advances in Clinical Imaging Using Positron Emission Tomography, Arch Int Med 150:735-739, 729990., , 1990

Cerebral Metabolic Asymmetries & Assoc Neuro-psych Patterns in Early Dementia of the Alzheimer Type
Arch Neurol 47:753-760, Haxby,J.V., 1990

Intracranial Aneurysms:Evaluation by MR Angiography
AJR 155:159-165, Ross,J.S.,et al, 1990

Infantile Spasms:I. PET Identified Focal Cortical Dysgenesis in Cryptogenic Cases for Surgical Treatment
Ann Neurol 27:406-413, Shields,W.D.,et al, 1990

Epilepsy Octet, Epidemiology, Classification, Natural History, and Genetics of Epilepsy
Lancet 336:93-96, Shorvon,S.D., 1990

Slowly Progressive Aphasia:Three Cases with Language, Memory, CT and PET Data
JNNP 53:987-993, Kempler,D.,et al, 1990



Showing articles 2150 to 2200 of 2804 << Previous Next >>