Transient CNS Deficits:A Common, Benign Syndrome in Young Adults
Neurol 38:831-836, Levy,D.E., 1988
Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988
The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988
Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988
The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988
Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987
Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987
Multiple Sclerosis Disease Activity Correlates with Gadolinium-Enhanced Magnetic Resonance Imaging
Ann Neurol 21:300-306, Conzalez-Scarano,F.,et al, 1987
Basilar Artery Stenosis:Middle & Distal Segments
Neurol 37:1742-1746, Pessin,M.S.,et al, 1987
The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987
First-Trimester Prenatal Diagnosis for Huntington's Disease with DNA Probes
et al Lancet 1:1284-1285, Hayden,M.R., 1987
Alzheimer's Disease
Down's Syndrome, & Chromosome 21, Editorial, Lancet 1:1011-1012., , 1987
Computed Tomography of Intracranial Chondroma with Emphasis on Delayed Contrast Enhancement
J Comput Assist Tomogr 11:820-823, Tanohata,K.,et al, 1987
Minimal Thyroid Ophthalmopathy
Neurol 37:1803-1808, Spector,R.H.&Carlisle,J.A., 1987
Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987
Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy
Lancet 2:1294-1296, Forrest,S.M.,et al, 1987
Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986
Clinicopath Conf (Juvenile) Periarteritis Nodosa (Kawasaki Syndrome)
with Involvement of Subcutaneous ( & Cerebral) Arteries, Case 43-1986, NEJM 315:1143-1154, , 1986
Bilateral Congenital Restriction of Upward Eye Movement
Arch Neurol 43:95-96, Tychsen,L.,et al, 1986
CT Enhancement after Prolonged High-Dose Contrast Infusion in the Early Stage of Cerebral Infarction
Stroke 17:424-430, Ito,U.,et al, 1986
Clinicopath. Conference
Malignant Lymphoma, Diffuse Small Cleaved-Cell Type, of Spinal Epidural Space ( & Orbit) , Case 47-1, 86, NEJM1-1409,1986., 1986
Huntington's Disease, Pathogenesis & Management
NEJM 315:1267-1276, Martin,J.B.&Gusella,J.F., 1986
Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986
The Clinical Features & Natural History of the Steele-Richardson-Olszewski Syndrome (Prog Supranuclear Palsy)
Neurol 36:1005-1006, Maher,E.R.,et al, 1986
Vidarabine Versus Acyclovir Therapy in Herpes Simplex Encephalitis
NEJM 314:144-149, Whitley,R.J.,et al, 1986
Dorsal Midbrain Syndrome in Multiple Sclerosis with Magnetic Resonance Imaging Correlation
Can J Neurol Sci 13:62-65, Costantino,A.,et al, 1986
Clinical Decisions in Neuro-Ophthalmology
CV Mosby:154-156, Burde,R.M.,et al, 1985
Takayasu Arteritis, A Study of 32 North American Patients
Medicine 64:89-99, Hall,S.,et al, 1985
Ocular Palsy Preceding Chronic Relapsing Polyneuropathy by Several Weeks
Ann Neurol 17:49-50, Donaghy,M.,et al, 1985
Genetic Prediction & Family Structure in Huntington's Chorea
BMJ 290:1929-1931, Harper,P.S.,et al, 1985
Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs
Lancet 1:655-658, Bakker,E.,et al, 1985
Central Nervous System Toxicity with High-Dose Ara-C
Neurol 35:1475-1479, Hwang,T.,et al, 1985
Relapsing Ophthalmoparesis-Sensory Neuropathy Syndrome
Neurol 35:595-596, Kaplan,J.G.,et al, 1985
A DNA Polymorphism for Huntington's Disease Marks the Future
Arch Neurol 42:20-24, Wexler,N.S.,et al, 1985
Presentation & Management of Parasellar & Suprasellar Metastatic Mass Lesions
JNNP 48:44-49, Kattah,J.C.,et al, 1985
Clin. Path. Conference
External Ophthalmoplegia with Mitochondrial Myopathy, Case Record 3-1985, NEJM 312:171-177985., , 1985
Somatization Disorder, One of Medicine's Blind Spots
JAMA 254:3075-3079, Quill,T.E., 1985
Monocular Elevation Paresis Caused by an Ipsilateral Lesion
Neurol 34:1264-1267, Ford,C.S.,et al, 1984
Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984
Genetic Testing in Huntington's Disease
Ann Neurol 16:511-513, Koller,W.C.,et al, 1984
Vidarabine Encephalopathy
JNNP 47:1351-1354, Cullis,P.A.,et al, 1984
Progressive Multifocal Leukoencephalopathy in a Renal Transplant Recipient
Am J Med 77:333-337, Saxton,C.R.,et al, 1984
Acyclovir Versus Vidarabine in Herpes Simplex Encephalitis
Lancet 2:707-711, Skoldenberg,B.,et al, 1984
Clin Path. Conference
Necrotizing Encephalomyelopath, Secondary to Irradiation & Intrathecal Methotrexate, Case Record 36-, 983, 311:653-662,1984., 1984
Molecular Genetics, Recombinant DNA Techniques, & Genetic Neurological Disease
Ann Neurol 15:511-520, Rosenberg,R.N., 1984
Multifocal CT Enhancement in MS
Neurol 34:341-346, Ebers,G.C.,et al, 1984
Treatment of Herpes Virus Infections
NEJM 309:963-970, 1034-10391983., Hirsch,M.S.,et al, 1983
Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
Ann Neurol 13:273-278, Jackson,J.A.,et al, 1983
Isolated Ocular Myopathy & Celiac Disease in Childhood
Neurol 33:792, Sandyk,R.,et al, 1983
Recombinant DNA & Neurologic Disease:The Coming of a New Age
Neurol 33:622-625, Rosenberg,R.N., 1983