Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acanthocytosis
acne vulgaris
aneurysm, pulmonary
arcuate scotoma, differential diagnosis of
arthralgia
arthritis
aspirin
ataxia, cerebellar
Bassen-Kornzweig syndrome
Behcet's syndrome
blindness
brain atrophy
brainstem, lesion of
buphthalmos
calcarine artery
calcification, gyral
calcification, intracranial
cardiac arrest and resuscitation
CAT scan, abnormal
cataracts
cerebral infarction
cerebral venous infarction
cerebral venous thrombosis
cerebrovascular accident
chiasmal syndromes
children
Cockayne's syndrome
complications
consanguinity
cornea, abnormal
deafmute
deafness
developmental retardation
diagnostic criteria
differential diagnosis
dwarfism
electroencephalogram, abnormalities of
emotional lability
erythema nodosum
facial nevus
fluorescein angiography
Friedreich's ataxia
fundus, abnormality of
gadolinium
gargoylism
gastrointestinal bleeding
gastrointestinal disease, neurologic complications
gene
gene mutation
genetic neurologic disorders
genital ulcerations
glaucoma
glaucoma, low tension
glaucoma, visual field defects in
GNAQ gene
gyrus, abnormal
Hallgren's syndrome
headache
heart block
hemangioma
hemangioma, facial
hemangioma, leptomeningeal
hemiparesis
heralding manifestation
heterochromia iridis
Hurler's syndrome
hydrocephalus
hypopyon
intellectual deficit
iridocyclitis
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
memory, impairment of
meningeal enhancement
meningoencephalitis
mental retardation
mental status, abnormal
MRI
MRI, abnormal
MRI, contrast enhanced
mucopolysaccharidoses
myocardial infarction
myopia
neuritis
neurocutaneous disease
neurologic complications of, systemic disease
neurologic disease, diagnoses of
nystagmus
obesity
occipital lobe, infarction
occipital lobe, infarction, bilateral
occipital lobe, lesion of
ocular myopathy
optic atrophy
optic disc
optic neuritis
optic neuropathy
optic neuropathy, ischemic
oral ulcerations
pain, periorbital
papilledema
photophobia
polydactyly
port wine nevus
precipitating factors
prognosis
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
quadrantanopsia, homonymous
retinal artery occlusion
retinal detachment
retinal vasculitis
retinitis pigmentosa
retinopathy
review article
schizophrenia
scotoma
seizure
seizure, children
seizure, focal
seizure, intractable
seizure, neonatal
shock, hypovolemic
skin, lesions in neurologic disorders
Spielmeyer Vogt syndrome
spontaneous remission
strokelike episodes
Sturge-Weber syndrome
systemic illness
thrombophlebitis
transient neurologic deficit
treatment of neurologic disorder
Usher's syndrome
uveitis
vasculitides
vasculopathy
venous thrombosis, non-cerebral
vertebral artery occlusion
vision, blurred
visual field defect
visual field defect, altitudinal
visual fields, constricted
visual loss
workup
Showing articles 3050 to 3100 of 4581 << Previous Next >>

Required Vision Testing for Older Drivers
NEJM 326:1784-1785, Nelson,D.E.,et al, 1992

Startle Disease, or Hyperrekplexia:Clonazepam and Assign of Gene (STHE) to Chromosoma 5q by Linkage Analysis
Ann Neurol 31:663-668, Ryan,S.G.,et al, 1992

Hypertensive Encephalopathy:Findings on CT, MR Imaging, and SPECT Imaging in 14 Cases
AJR 159:379-383, Schwartz,R.B.,et al, 1992

Detecting Susceptibility to Malignant Hyperthermia
BMJ 304:791-792, Ellis,F.R., 1992

Central-Nervous-System Dysfunction after Warm of Hypothermic Cardiopulmonary Bypass
Lancet 339:1383-1384, Wong,B.I.,et al, 1992

Optic Neuropathy and Central Nervous System Disease Associated with Primary Sjogren's Syndrome
Am J Med 92:686-692, Tesar,J.T.,et al, 1992

The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
Ann Neurol 32:207-214, Rowland,L.P., 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Atenolol Compared with Nifedipine:Effect on Cognitive Function and Mood in Elderly Hypertensive Patients
Ann Int Med 116:615-623, Skinner,M.H.,et al, 1992

Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992

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

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Risk Factors for the Neurologic Complications Associated with Aortic Aneurysms
Arch Neurol 49:284-285, Lynch,D.R.,et al, 1992

Carbamazepine-Induced Cardiac Dysfunction, Characterization of Two Distinct Clinical Syndromes
Arch Int Med 152:186-191, Kasarskis,E.J.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 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

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

Lyme Disease Associated with Fibromyalgia
Ann Int Med 117:281-285, Dinerman,H.&Steere,A.C., 1992

Memory Impairment & Depression in Pts with Lym Encephalopathy:Comparison with Fibromyalgia & Nonpsychotic Depressed Pts
Neurol 42:1263-1267, Kaplan,R.F.,et al, 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Phenotypic Expression of the Myotonic Dystrophy Gene in Monozygotic Twins
Neurol 42:1815-1817, Dubel,J.R.,et al, 1992

Psychiatric Disturbances in Metachromatic Leukodystrophy
Arch Neurol 49:401-406, Hyde,T.M.,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

Recent Progress Toward Understanding the Molecular Biology of Von Recklinghausen Neurofibromatosis
Ann Neurol 31:555-561, Gutmann,D.H.&Collins,F.S., 1992

Diagnosis of von Hippel-Lindau in a Pt with Blindness from Bilateral Optic Nerve Hemangioblastomas
AJR 159:403-405, Ginzburg,B.M.,et al, 1992

Paramedian Thalamopeduncular Infarction:Clinical Syndromes and Magnetic REsonance Imaging
Ann Neurol 32:162-171, Tatemichi,T.K.,et al, 1992

Cardiac Arrest Due to Partial Epileptic Seizues
Neurol 42:824-829, Liedholdm,L.J.&Gudjonsson,O., 1992

Risk of Cardiac Events in Atypical Transient Ischaemic Attack or Minor Stroke
Lancet 340:630-633, Koudstaal,P.J.,et al, 1992

Relationship of Cardiac Disease to Stroke Occurrence, Recurrence, and Mortality
Stroke 23:1250-1256, Broderick,J.P.,et al, 1992

Thromboendartectomy of the Symptomatic Occluded Internal Carotid Artery
J Neurosurg 76:752-758, McCormick,P.W.,et al, 1992

Familial Intracranial Aneurysms, A Review
Stroke 23:1024-1030, terBerg,H.W.M.,et al, 1992

Memory Disturbances Following Anterior Communicating Artery Rupture
Ann Neurol 31:473-480, Irle,E.,et al, 1992

Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women
Stroke 23:903-907, Schwitter,J.,et al, 1992

Evoked Potentials in Cerebrotendinous Xanthomatosis and Effect Induced by Chenodeoxycholic Acid
Arch Neurol 49:469-475, Mondelli,M.,et al, 1992

Evaluation and Management of the Patient with Syncope
JAMA 268:2553-2560, Kapoor,W.N., 1992

Clinicopath Conf
Tethered-Cord Syndrome, Occult Myelomeningocele, with Dermal Sinus, Case 47-1992, NEJM 327:1581-1588, 1992, 1992

Delayed Diagnosis of Juvenile Myoclonic Epilepsy
JNNP 55:497-499, Grunewald,R.A.,et al, 1992

Bilateral Thalamic Glioma-Review of Eight Cases with Personality Change and Mental Deterioration
AJNR 13:1225-1230, Partlow,G.D.,et al, 1992

Intraosseous Meningioma:CT and MR Appearance
J Comput Assist Tomogr 16:1000-1001, Lee,H.,et al, 1992

The Ocular Manifestations of Multiple Sclerosis 1, Abnormalities of the Afferent Visual System
JNNP 55:747-752, McDonald,W.I.&Barnes,D., 1992

The Ocular Manifestations of Multiple Sclerosis, 2, Abnormalities of Eye Movements
JNNP 55:863-868, Barnes,D.&McDonald,W.I., 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Central Nervous System Involvement in the Eosinophilia-Myalagia Syndrome
Arch Neurol 49:1082-1085, Lynn,J.,et al, 1992

A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992



Showing articles 3050 to 3100 of 4581 << Previous Next >>