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Differential
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aphonia
apraxia
apraxia of eyelid closure
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, neck
CAT scan
CAT scan, abnormal
cerebral cortical atrophy
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, multiple
cerebrovascular accident, prognosis in
cerebrovascular accident, recurrent
children
clubfoot as related to neurologic disease
congenital bilateral perisylvian syndrome
congenital malformation
cytoarchitectonics, cerebral cortex
developmental abnormality of brain
developmental retardation
drooling
dysarthria
dyskinesia, buccal lingual facial
dysphagia
electroencephalogram
electroencephalogram, abnormalities of
encephalitis
encephalitis, viral
eye closure
face, inexpressive
facial weakness
facial weakness, bilateral
familial
frontal lobe, pathologic signs of
gag reflex, depressed
herpes simplex encephalitis
heterotopia
insular cortex
intellectual deficit
language disorders in children
malformation, CNS, congenital
mental retardation
MRI
MRI, abnormal
mutism
neuronal migration disorder
neuropathology
nonverbal
opened mouth
operculum syndrome
operculum syndrome, bilateral
pachygyria
palate, paralysis
polymicrogyria
prognosis
pseudobulbar palsy
pseudobulbar palsy, acute
pyramidal tract dysfunction
release phenomena
seizure
seizure, recurrent
speech disorder
symmetric brain lesions
temporal lobe, lesion
temporal lobe, lesion, bilateral
tongue, impaired movements of
tongue, weakness
trismus
Showing articles 100 to 150 of 196 << Previous Next >>

Spontaneous Spinal Epidural Hematoma Another Neurologic Complication of Cocaine
Arch Neurol 53:819-821, Samkoff,L.M.,et al, 1996

Cerebral Dural Arteriovenous Fistulas:Clin & Angiographic Correl with a Revised Class of Venous Drainage
Radiology 194:671-680, Cognard,C.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Spinal Dural Arteriovenous Fistula:The Pathology of Venous Hypertensive Myelopathy
Neurol 45:1309-1313, Hurst,R.W.,et al, 1995

Imaging of the Spinal Cord
JNNP 58:403-416, Stevens,J.M., 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Spinal Dural Arteriovenous Fistulas:Evaluation with MR Angiography
AJNR 16:2029-2043, Bowen,B.C.,et al, 1995

Painful Oculomotor Palsy Caused by Posterior-Draining Dural Carotid Cavernous Fistulas
Arch Ophthalmol 113:1045-1049, Acierno,M.D.,et al, 1995

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

Vascular Neoplasms and Malformations, Ischemia, and Hemorrhage Affecting the Spinal Cord:MR Imaging Findings
AJR 162:685-692, Friedman,D.P.,et al, 1994

Spinal Dural Arteriovenous Fistula:Demonstration Using Phase Contrast MRA
J Comput Assist Tomogr 18:811-814, Provenzale,J.M.,et al, 1994

Brief Report:Relief of Spinal Cord Compression from Vertebral Hemangioma by Intralesional Injection of Absolute Ethanol
NEJM 331:508-511, Heiss,J.D.,et al, 1994

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Intramedullary Cavernous Angiomas of the Spinal Cord:Clinical, Path, & Surgical Manag
Neurosurgery 31:219-230, Ogilvy,C.S.,et al, 1992

Clinicopath Conf
Spinal Dural Arteriovenous Fistula, Case 12-1992, NEJM 326:816-824992., , 1992

Suspected Dural Arteriovenous Fistual:Results with Screening MR Angiography in Seven Patients
Radiology 183:265-271, Chen,J.C.,et al, 1992

Multiple Occult Vascular Malformations of the Brain and Spinal Cord:MRI Diagnosis
Neuroradiology 34:110-111, Bourgouin,P.M.,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

MR Imaging of the Spinal Cord:Current Status and Futue Advances
AJR 159:149-159, Sze,G., 1992

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

Spinal Cord Vascular Disease, Geldmacher D. S. & Nager, B. J. , In Neurology in Clinical Practice
Ed Butterworth-Heinemann, Boston, 2:986991., Bradley,W.C.,et al, 1991

Venous Infarction of the Spinal Cord Resulting from Dural Arteriovenous Fistula:MR Imaging Findings
Larsson, E-M, AJNR 12:739-743991., , 1991

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Dural Arteriovenous Fistulas:Evaluation with MR Imaging
Radiology 175:193-199, DeMarco,J.K.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

MR Imaging of Dural AV Fistuals at the Cavernous Sinus
J Comput Assist Tomogr 14:397-401, Komiyama,M.,et al, 1990

Neuropsychological Changes in Olivopontocerebellar Atrophy
Arch Neurol 47:997-1001, Berent,S.,et al, 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
Neurol 40:1241-1245, Chida,K.,et al, 1990

Cavernous Hemangioma of the Spinal Cord:Report of 2 Unusual Cases
Neurol 40:1791-1793, Lopate,G.,et al, 1990

Computed Tomographic Features of Nonthyroid Extraocular Muscle Enlargement
Ophthalmol 96:1038-1047, Patrinely,J.R.,et al, 1989

Intramedullary Cavernous Angioma with Trigeminal Neuralgia:A Case Report and Reivew of the Literature
Neurosurgery 25:97-101, Saito,N.,et al, 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Spinocerebellar Degeneration:Qualitative & Quantitative MR Analysis of Atrophy
J Comput Assist Tomogr 12:298-303, Nabatame,H.,et al, 1988

Sleep Apnea in Olivopontocerebellar Degeneration:Treatment with Trazodone
Ann Neurol 23:399-401, Salazar-Grueso,E.F.,et al, 1988

Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,et al, 1988

Familial Cavernous Malformations of the Central Nervous System & Retina
Ann Neurol 21:578-583, Dobyns,W.B.,et al, 1987



Showing articles 100 to 150 of 196 << Previous Next >>