Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992
Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992
Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992
Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992
Intramedullary Spinal Cord Tumors:Significance of Associated Hemorrhage at MR Imaging
Radiology 182:793-796, Nemoto,Y.,et al, 1992
Spontaneous Remission of a Third-Nerve Palsy in Meningeal Lymphoma
Ann Neurol 32:100-102, Galetta,S.L.,et al, 1992
Malignant Tumors in the Pituitary Gland
Arch Neurol 49:555-558, Juneau,P.,et al, 1992
Metastases to the Pituitary-Hypothalamic Axis, An MR Study of 7 Symptomatic Patients
Neuroradiology 34:131-134, Schubiger,O.&Haller,D., 1992
CNS Mycosis Fungoides:CT and MR Findings
J Comput Assist Tomogr 16:529-533, Tein,R.D.,et al, 1992
Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992
Empty Sella Resulting from the Spontaneous Resolution of a Pituitary Macroadenoma
Arch Int Med 152:1920-1923, Robinson,D.B.&Michael,R.D., 1992
Clinicopath Conf
Metastatic Malignant Melanoma, "Encephalitic"Form, in Leptomeninges and Cerebral Cortex, Case 28-199, , NE27:107-116,1992., 1992
Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992
Transesophageal Echocardiography in the Examination of Stroke
Ann Int Med 117:922-932, DeRook,F.A.,et al, 1992
Immunologic Aspects of Neurological and Neuromuscular Diseases
JAMA 268:2918-2922, Zweiman,B.&Levinson,A.I., 1992
Suicide and Patients with Neurologic Diseases, Methodologic Problems
Arch Neurol 49:1296-1303, Stenager,E.N.&Stenager,E., 1992
Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia
NEJM 327:1069-1074, Bilous,R.W.,et al, 1992
Amphotericin B-Associated Leukoencephalopathy
Neurol 42:2005-2010, Walker,R.W.&Rosenblum,M.K., 1992
Familial Rectal Pain:A Type of Reflex Epilepsy?
Ann Neurol 32:824-826, Schubert,R.&Cracco,J.B., 1992
Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992
Delayed Radiation Necrosis of the CNS in Patients Irradiated for Pituitary Tumours
JNNP 55:949-955, Grattan-Smith,P.J.,et al, 1992
Three-and Four-Year Cognitive Outcome in Children with Noncortical Brain Tumors & Whole-Brain RT
Ann Neurol 32:551-554, Radcliffe,J.,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
Linear Accelerator Radiosurgery for Arteriovenous Malformations
J Neurosurg 77:832-841, Friedman,W.A.&Bova,F.J., 1992
Multiple Sclerosis in 54 Twinships:Concordance Rate is Independent of Zygosity
French Res. Gr. of MS, Ann Neurol 32:724-727, 7222., , 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
Cerebrospinal Fluid in Diseases of the Nervous System
W. B. Saunder Co, 2nd Ed, Phila, p. 185, 271, Fishman,R.A., 1992
Familial Cluster Headache:Occurrence in Three Generations
Neurol 42:1399-1400, Spierings,E.L.H.&Vincent,A.J.P.E., 1992
Migraine:Theories of Pathogenesis
Lancet 339:1202-1207, Blau,J.N., 1992
Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992
Occult Epidural Chloroma Complicated by Acute Paraplegia Following Lumbar Puncture
Ann Neurol 31:110-112, Wong,M.C.,et al, 1992
FDG-PET in Pediatric Posterior Fossa Brain Tumors
J Comput Assist Tomogr 16:62-68, Hoffman,J.M.,et al, 1992
Quadriplegia after Chiropractic Manip in Infant with Congen Torticollis by a Spinal Cord Astrocy
J Pediatr 120:266-269, Shafrir,Y.&Kaufman,B.A., 1992
Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992
Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992
De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992
Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992
Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992
Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992
Trends in the Association of Lambert-Eaton Myasthenic Syndrome with Carcinoma
Neurol 42:848-850, Gutmann,L.,et al, 1992
Suspected Low-Grade Glioma:Is Deferring Treatment Safe
Ann Neurol 31:431-436, 4371992., Recht,L.D.,et al, 1992
Low-Grade Gliomas:When to Treat, Editorial
Ann Neurol 31:437-438, Shapiro,W.R., 1992
Spinal Cord Compression from Epidural Metastases
NEJM 327:614-619, Byrne,T.N., 1992
Comparison of Cisternal and Lumbar CSF Examination in Leptomeningeal Metastasis
Neurol 42:1239-1241, Rogers,L.R.,et al, 1992
Twelve Cases of Pituitary Apoplexy
Arch Int Med 152:1893-1899, Vidal,E.,et al, 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