Sleep Abnormalities in Progressive Supranuclear Palsy
Ann Neurol 25:577-581, Aldrich,M.S.,et al, 1989
Bilateral Opercular Polymicrogyria
Ann Neurol 25:90-92, Becker,P.S.,et al, 1989
Neonatal Myasthenia Gravis:A New Clinical & Immunologic Appraisal on 30 Cases
Neurol 38:138-142, Morel,E.,et al, 1988
McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988
An Antineuronal Autoantibody in Paraneoplastic Opsoclonus
Ann Neurol 23:528-531, Budde-Steffen,C.,et al, 1988
Regional Pain is Rarely Hysterical
Arch Neurol 45:915-918, Merskey,H., 1988
Progressive Language Impairment without Dementia:A Case with Isolated Category Specific Semantic Defect
JNNP 51:1201-1207, Basso,A.,et al, 1988
Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988
Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988
Seronegative Myasthenia Gravis
Neurol 38:514-517, Soliven,B.C.,et al, 1988
Maternal-Fetal Transmission of Myasthenia Gravis with Acetylcholine-Receptor Antibody
NEJM 318:996, Melber,D., 1988
Autoantibody Activity in Lambert-Eaton Myasthenic Syndrome
Editorial, Lancet 1:9201988., , 1988
Posterior Cortical Atrophy
Arch Neurol 45:789-793, Benson,D.F.,et al, 1988
Hysterical Conversion Reactions Mimicking Neurological Disease
Am J Dis Child 142:1203-1206, Bangash,I.H.,et al, 1988
Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988
MR of Neuronal Migration Anomalies
AJR 150:179-187, Barkovich,A.J.,et al, 1988
Treatment of Patients with Neuropathy and Anti-MAG IgM M-Proteins
Ann Neurol 24:93-97, Nobile-Orazio,E.,et al, 1988
Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988
Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988
Brief Communication: Psychogenic Sensory Loss
J Nerv Ment Dis 176:686-687, Rolak,L.A., 1988
Association Between Lupus Psychosis & Anti-Ribosomal P Protein Antibodies
NEJM 317:265-271, 3091987., Bonfa,E.,et al, 1987
Neurological Clues from Environmental Neurotoxins
BMJ 295:346-347, Martyn,C.N., 1987
Pituitary Growth Hormone from Human Cadavers:Neurologic Disease in Ten Recipients
Neurol 37:1211-1213, Rappaport,E.B.&Graham,D.J., 1987
MR Imaging of Heterotopic Gray Matter
J Comput Assist Tomogr 11:878-879, Hayden,S.A.,et al, 1987
Prions & Neurodegenerative Diseases
NEJM 317:1571-1581, 15971987., Prusiner,S.B., 1987
The Diagnosis of Myasthenia Gravis
Editorial, Lancet 1:658-6601986., , 1986
Myasthenia Gravis without Acetylcholine-Receptor Antibody:A Distinct Disease Entity
Lancet 1:116-118, Mossman,S.,et al, 1986
Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
NEJM 315:997-1003, Lugaresi,E.,et al, 1986
Hypomelanosis of Ito, Wood's Light & Magnetic Resonance Imaging as Diagnostic Measures
Arch Neurol 43:848-850, Ardinger,H.H.&Bell,W.E., 1986
The Pathophysiology of Penicillamine-Induced Myasthenia Gravis
Ann Neurol 20:740-744, Kuncl,R.W.,et al, 1986
Clinicopath Conf
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Neuropeptides in Neurological Disease
Ann Neurol 20:547-565, Beal,M.F.&Martin,J.B., 1986
Acid Maltase Deficiency
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Phosphorylase Deficiency
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Treatment of Peripheral Neuropathies
JNNP 48:1193-1207, Hallett,M.,et al, 1985
Developmental Dyslexia:Four Consecutive Patients with Cortical Anomalies
Ann Neurol 18:222-233, Galaburda,A.M.,et al, 1985
Cerebral Lateralization, Biological Mechanisms, Associations, & Pathology:I
Arch Neurol 42:428-459, 4271985., Geschwind,N.&Galaburda,A.M., 1985
Syndrome of Palatal Myoclonus & Progressive Ataxia:Two Cases with Magnetic Resonance Imaging
Neurol 35:1212-1214, Sperling,M.R.&Herrman,C., 1985
Persistent Vegetative State, Extension of the Syndrome to Include Chronic Disorders
Arch Neurol 42:1045-1047, Walshe,T.M.&Leonard,C., 1985
McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985
Familial Multisystem Atrophy with Possible Thalamic Dementia
Neurol 34:1213-1217, Katz,D.A.,et al, 1984
A New Form of Sea-blue Histiocytosis Associated with Progressive Anterior Horn Cell & Axonal Degeneration
Ann Neurol 16:184-192, Ashwal,S.,et al, 1984
Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983
Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983
Slowly Progressive Aphasia Without Generalized Dementia
Ann Neurol 11:592-598, Mesulam,M.M., 1982
Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982
Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982
Examination of Dental Pulp to Diagnose Infantile Neuroaxonal Dystrophy
Arch Neurol 39:422-423, Carlo,J.,et al, 1982
The Laboratory Diagnosis of Mild Myasthenia Gravis
Ann Neurol 12:238-242, Kelly,J.J.,et al, 1982
Functional Activities Of Autoantibodies To Acetylcholine Receptors & The Clinical Severity of Myasthenia Gravis
NEJM 307:769-775, Drachman,D.B.,et al, 1982