Monozygotic Twins with Parkinson's Disease
Ann Neurol 19:402-405, Koller,W.,et al, 1986
Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
Arch Neurol 43:677-680, Mito,T.,et al, 1986
Efficacy of Primidone in Essential Tremor
Neurol 36:121-124, Koller,W.C.&Royse,V.L., 1986
Alzheimer's Disease
NEJM 314:964-973, Katzman,R., 1986
Narcolepsy & Immunity
BMJ 292:359-360, Parkes,J.D.,et al, 1986
Thyrotoxic Periodic Paralysis
Am J Med 80:146-149, Ferreiro,J.E.,et al, 1986
Autosomal Dominant Osteosclerosis Associated with Familial Spinal Canal Stenosis
Neurol 36:687-692, Yasuda,Y.,et al, 1986
Adynamia Episodica & Paralysis Periodica Paramyotonica
Neurol 36:682-686, Ricker,K.,et al, 1986
Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986
Successful Treatment with Tocainide of Recessive Generalized Congenital Myotonia
Ann Neurol 19:501-504, Streib,E.W., 1986
Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
Neurol 36:511-517, Mulder,D.W.,et al, 1986
Gerstmann-Straussler-Scheinker Disease:Autopsy Study of a Familial Case
Ann Neurol 20:540-543, Vinters,H.V.,et al, 1986
Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
Am J Med 81:931-934, Lesser,B.A.,et al, 1986
Transketolase Abnormality in Tolazamide-Induced Wernicke's Encephalopathy
Neurol 36:1508-1510, Mukherjee,A.B.,et al, 1986
Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man
NEJM 315:744-747, DiMagno,E.P.,et al, 1986
Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986
Familial Long Thoracic Nerve Palsy:A Manifestation of Brachial Plexus Neuropathy
Neurol 36:1251-1253, Phillips,L.H., 1986
Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986
Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
Arch Neurol 43:943-946, Wells,C.R.&Jankovic,J., 1986
Preventive Screening for Fragile X Syndrome
Editorial, Lancet 2:1191-11921986., , 1986
Progressive Myoclonus Epilepsies:Specific Causes & Diagnosis
NEJM 315:296-305, Berkovic,S.F.,et al, 1986
Tangier Disease (Hypo-a-Lipoproteinemia)
Textbook of Child Neurology, 3rd Ed. , Phila, Lea & Febiger, Ch 1, p 86, Menkes,J.H., 1985
Bilateral Carpal Tunnel Syndrome Caused by Graves'Disease
Arch Int Med 145:345-346, Beard,L.,et al, 1985
Measurement of Autoantibodies Against Human Eye Muscle Plasma Membranes in Graves'Ophthalmopathy
BMJ 290:191-192, Faryna,M.,et al, 1985
Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985
Neurological Findings in Patients with the Fragile-X Syndrome
JNNP 48:150-153, Finelli,P.F.,et al, 1985
Intracranial Calcification in Nephrogenic Diabetes Insipidus
JAMA 254:3349-3350, Kanzaki,S.,et al, 1985
Handedness & Essential Tremor
Arch Neurol 42:1082-1083, Biary,N.&Koller,W., 1985
Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985
Association of High Cyanide & Low Sulphur Intake in Cassava-Induced Spastic Paraparesis
Lancet 2:1211-1213, Cliff,J.,et al, 1985
Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985
Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
Ann Neurol 17:297-300, Aikawa,H.,et al, 1985
Cerebral Haemorrhagic Infarction in Young Patients with Hereditary Protein C Deficiency
BMJ 290:350-352, Wintzen,A.R.,et al, 1985
Long-Acting Propranolol in Essential Tremor
Neurol 35:108-110, Koller,W.C., 1985
Metachromatic Leukodystrophy Manifesting as a Schizophrenic Disorder:Computed Tomographic Correlation
Ann Neurol 18:94-95, Finelli,P.F., 1985
Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Arch Neurol 42:1008-1010, Katz,D.A.,et al, 1985
Risk Factors for Stroke, Editorial
Stroke 16:359-360, Wolf,P.A., 1985
Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985
Dystonia & Calcification of the Basal Ganglia
Neurol 35:533-537, Larsen,T.A.,et al, 1985
Gilles de la Tourette's Syndrome, A Review of Clinical, Research & Future Directions for Investigation
Arch Neurol 42:393-397, Caine,E.D., 1985
Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
NEJM 312:874-879, Petito,C.K.,et al, 1985
MR Imaging in Fahr Disease
J Comput Assist Tomogr 9:790-792, Scotti,G.,et al, 1985
Adult GM1-Gangliosidosis:Clinical Patterns & Rectal Biopsy
Neurol 35:875-880, Nakano,T.,et al, 1985
Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985
Pyramidal Tract Deficits & Polyneuropathy in Hyperthyroidism
Am J Med 78:1041-1044, Fisher,M.,et al, 1985
The Cherry-Red Spot in Tay-Sachs & Other Storage Diseases
Ann Neurol 17:356-360, Kivlin,J.D.,et al, 1985
Association Between Essential Tremor & Parkinson's Disease
Ann Neurol 17:329-333, Gereghty,J.J.,et al, 1985
Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985
Febrile Convulsions in a National Cohort Followed up from Birth, I-Prevalence & Recurrence in the First Five Years of Life
BMJ 290:1307-1310, Verity,C.M.,et al, 1985
Portal-Systemic Myelopathy after Portacaval Shunt Surgery
Arch Int Med 145:1921-1922, Lebovics,E.,et al, 1985