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Addison's disease
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treatment of neurologic disorder
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wide based gait
Showing articles 650 to 700 of 1020 << Previous Next >>

Headache Caused by a Single Lesion of Multiple Sclerosis in the Periaqueductal Gray Area
Headache 33:452-455, Haas,D.C.,et al, 1993

Bacterial Spinal Epidural Abscess, Review of 43 Cases and Literature Survey
Medicine 71:369-385, Darouiche,R.O.,et al, 1992

Amyloidoma of the CNS. I. Clinical and Pathologic Study
Neurol 42:2019-2023, Cohen,M.,et al, 1992

Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
Lancet 340:987-991, Tienari,P.J.,et al, 1992

The Molecular Pathogenesis of Alzheimer's Disease:Clinical Prospects
Lancet 340:1512-1515, Murphy,M., 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Bovine Gangliosides and Acute Motor Polyneuropathy
BMJ 305:1330-1331, Figueras,A.,et al, 1992

"Chronic Sensory Demyelinating Neuropathy":CIDP Presenting as a Pure Sensory Neuropathy
JNNP 55:677-680, Oh,S.J.,et al, 1992

Subacute Idiopathic Demyelinating Polyradiculoneuropathy
Arch Neurol 49:612-616, Hughes,R.,et al, 1992

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

Plasma-Cell Dyscrasia with Polyneuropathy, The Spectrum of POEMS Syndrome
NEJM 327:1919-1923, Miralles,G.D.,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

Cerebral Venous Thrombosis
Neurol Clin 10:87-111, Ameri,A.&Bousser,M-G., 1992

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

A Correlative Triad of Gadolinium-DTPA MRI, EDSS, & CSF-MBP in Relapsing MS Treated with High-Dose Intravenous Methylprednisolone
Neurol 42:63-67, Barkhof,F.,et al, 1992

Subacute Necrotizing Myelopathy:MR Imaging in Four Pathologically Proved Cases
AJR 158:163-169, 1701992., Mirich,D.R.,et al, 1992

Myeloma and Benign Intracranial Hypertension
BMJ 304:685, Wasan,H.,et al, 1992

Clinicopath Conf
Multiple Myeloma, Presenting as Plasmacytoma of Bone Extending into Sphenoid Sinus, Case 21-1992, NE, M 31417-1424,1992., 1992

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Human Herpesvirus-6:Clinical Implications of a Recently Discovered, Ubiquitous Agent
J Pediatr 121:173-181, Leach,C.T.,et al, 1992

Pure Sensory Guillain-Barre Syndrome
JNNP 55:411-415, Miralles,F.,et al, 1992

The Guillain-Barre Syndrome
NEJM 326:1130-1136, Ropper,A.H., 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Neurolymphomatosis:A Clinicopathologic Syndrome Re-emerges
Neurol 42:1136-1141, Diaz-Arrastia,R.,et al, 1992

Tuberculous Meningitis with Acellular Cerebrospinal Fluid in AIDS Patients
AIDS 6:1165-1167, Laguna,F.,et al, 1992

Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
Brain 115:979-989, Harding,A.E.,et al, 1992

Cerebral Infarction Associated with Protein C Deficiency
Stroke 23:108-111, Matsushita,K.,et al, 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Fatal Familial Insomnia:A Second Kindred with Mutation of Prion Protein Gene at Codon 178
Neurol 42:669-670, 1992, Medori,R.,et al, 1992

Prion Disease
NEJM 326:486-487, Johnson,R.T., 1992

Nervous System Lyme Borreliosis-Revisited
Arch Neurol 49:102-107, Finkel,M.J.&Halperin,J.J., 1992

Protein Redistribution Diet Remains Effective in Patients with Fluctuating Parkinsonism
Arch Neurol 49:149-151, Karstaedt,P.J.&Pincus,J.H., 1992

Plasma Exchange in Polyneuropathy Associated with Monoclonal Gammopathy of Undetermined Significance
NEJM 325:1482-1486, Dyck,P.J.,et al, 1991

Myasthenia Gravis in Mothers and Their Newborns
Clin Obstet Gynecol 34:82-99, Plauche,W.C., 1991

The Spongiform Encephalopathies, Editorial
JNNP 54:761-763, Will,R.G., 1991

BA4 Amyloid Protein Deposition in Brain After Head Trauma
Lancet 338:1422-1423, Roberts,G.W.,et al, 1991

Hashimoto's Encephalopathy:A Steroid-Responsive Disorder Associated with High Anti-Thyroid Antibody Titers-Report of 5 Cases
Neurol 41:228-233, Shaw,P.J.,et al, 1991

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Diagnosis and Management of Hormone-Secreting Pituitary Adenomas
NEJM 324:822-831, Klibanski,A.&Zervas,N.T., 1991

Cesarean Section Before Onset of Labor & Motor Function in Infants with Meningomyelocele Diag Antenatally
NEJM 324:662-666, 6901991., Luthy,D.S.,et al, 1991

Sensitivity of Ultrasound in Detecting Spina Bifida
Letter, NEJM 324:769-7721991., , 1991

Diagnosis and Management of Neural-Tube Defects Today
NEJM 324:690-691, Hobbins,J.C., 1991

Cranial Neuropathy Associated with Primary Amyloidosis
Ann Neurol 29:451-454, Traynor,A.E.,et al, 1991

Clinicopath Conf
Tertiary Neurosyphilis, Case 32-1991, NEJM 325:414-422991., , 1991

Cerebrospinal Fluid Protein and Opening Pressure in Idiopathic Intracr Hyperten (Pseudotumor Cerebri)
Neurol 41:1040-1042, Johnston,P.K.,et al, 1991

Inherited Protein C Deficiency and Nonhemorrhagic Arterial Stroke in Young Adults
Neurol 41:1371-1373, Camerlingo,M.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991



Showing articles 650 to 700 of 1020 << Previous Next >>