Infantile Panthalamic Infarct with a Striking Sonographic Finding:The"Bright Thalamus"
Neuroradiology 35:92-96, Wang,H.S.&Huang,S.C., 1992
A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992
Outlook for the Child with a Cephalocele
Pediatrics 90:914-919, Brown,M.S.,et al, 1992
Giant Axonal Neuropathy:Progressive Clinical and Radiologic CNS Involvement
Neurol 42:2220-2221, Richen,P.&Tandan,R., 1992
Parkinson's Disease in Twins Studied with 18 F-Dopa and Positron Emission tomography
Neurol 42:1894-1900, Burn,D.J.,et al, 1992
Survival of Implanted Fetal Dopamine Cells & Neuro Improvement 12 to 46 Months after Transpl for Parkinson's
NEJM 327:1549-1555, 15891992., Freed,C.R.,et al, 1992
Bilateral Fetal Mesencephalic Grafting in Two Patients with Parkinsonism Induced by MPTP
NEJM 327:1556-1563, 15891992., Widner,H.,et al, 1992
Cerebral Glucose Metabolism in Parkinson's Disease with and without Dementia
Arch Neurol 49:1262-1268, Peppard,R.F.,et al, 1992
Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia
NEJM 327:1069-1074, Bilous,R.W.,et al, 1992
Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992
A Comparison of Two-Dimen Echocard vs Carotid Duplex Scanning in Older Pts with Cerebral Ischemia
Arch Int Med 152:2089-2093, Voyce,S.J.,et al, 1992
Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992
Familial Alzheimer's Disease:Second Gene Locus Located, Markers for Familial Disease May be Available
BMJ 305:1108-1109, Mullan,M., 1992
Hemifacial Spasm:Evaluation of Magnetic Resonance Imaging & Magnetic Resonance Tomographic Angiography
Ann Neurol 32:502-506, Adler,C.H.,et al, 1992
Cerebral Artery Aneurysms in Children Infected with Human Immunodeficiency Virus
J Pediatr 121:927-930, Husson,R.N.,et al, 1992
The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992
Familial Multiple Sclerosis:MRI Findings in Clinically Affected and Unaffected Siblings
JNNP 55:883-886, Teinari,P.J.,et al, 1992
Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
Lancet 340:987-991, Tienari,P.J.,et al, 1992
Magnetic Resonance:A Noninvasive Approach to Metabolism, Circulation, and Morphology in Human Brain Death
Ann Neurol 32:507-511, Aichner,F.,et al, 1992
Central Nervous System Lesions in von Hippel-Lindau Syndrome
JNNP 55:898-901, Neumann,H.P.H.,et al, 1992
Distrib & Correlates of Sonographically Detected Carotid Art Dis in Cardiovasc Health Study
Stroke 23:1752-1760, O'Leary,D.H.,et al, 1992
Detection of Intracranial Emboli in Patients with Symptomatic Extracranial Carotid Artery Disease
Stroke 23:1652-1654, Siebler,M.,et al, 1992
Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
Ann Neurol 31:555-561, Gutmann,D.H.&Collins,F.S., 1992
Crossed Cerebellar Diaschisis and Crossed Cerebellar Atrophy:MR Findings & Clin Symptoms in 26 Pts
AJR 158:1155-1159, Tien,R.D.&Ashdown,B.C., 1992
Prevalence of Extracranial Carotid Artery Disease Detectable by Echo-Doppler in an Elderly Population
Stroke 23:818-822, Pujia,A.,et al, 1992
Autoantibody Against Oxidised LDL and Progression of Carotid Atherosclerosis
Lancet 339:883-900, Salonen,J.T.,et al, 1992
Familial Intracranial Aneurysms, A Review
Stroke 23:1024-1030, terBerg,H.W.M.,et al, 1992
Transcranial Doppler Correlation with Cerebral Angiogaphy in Sickle Cell Disease
Stroke 23:1073-1077, Adams,R.J.,et al, 1992
Reproducibility of Noninvasive Ultrasonic Measure of Carotid Atherosclerosis, Asympt Carotid Plaque Study
Stroke 23:1062-1068, Riley,W.A.,et al, 1992
Prediction of Symptomatic Vasospasm after Subarachnoid Hemorrhage by Transcran Doppler & Cerebral Blood Flow Changes
Stroke 23:674-679, Grosset,D.G.,et al, 1992
Demonstration of Subclavian Steal by MR Angiography
J Comput Assist Tomogr 16:756-759, Turjman,F.,et al, 1992
Moyamoya Disease:Diagnosis with Three-Dimensional Time-of-Flight MR Angiography
Radiology 184:773-778, Yamada,I.,et al, 1992
Dissection of Cranial Arteries in the Neck:Correlation of MRI and Arteriography
Neuroradiology 34:273-278, Sue,D.E.,et al, 1992
Spontaneous Vertebal Artery Dissection Initially Mimicking Myocardial Infarction
Stroke 23:1021-1023, Linden,D.,et al, 1992
Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992
A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992
Effect of Cocaine Use On the Fetus
NEJM 327:399-407, Volpe,J.J., 1992
Presymptomatic Testing for Huntington's Disease in the United Kingdom
BMJ 304:1593-1596, Tyler,A.,et al, 1992
New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992
Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992
Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992
Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
NEJM 327:57, Cossu,P.,et al, 1992
Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992
Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
Ann Neurol 31:663-668, Ryan,S.G.,et al, 1992
Hypertensive Encephalopathy:Findings on CT, MR Imaging, and SPECT Imaging in 14 Cases
AJR 159:379-383, Schwartz,R.B.,et al, 1992
Detecting Susceptibility to Malignant Hyperthermia
BMJ 304:791-792, Ellis,F.R., 1992
The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992
Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992
Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992
Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992