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Differential
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agraphia
akinesia
akinesia of eyelid function
alexia
alpha-fetoprotein
Alzheimer's disease, visual variant
aminoacidurias
ANA
anomic aphasia
anterior cerebral artery
anterior cerebral artery territory infarction
anterior cerebral artery, occlusion, language disorder with
aphasia
aphasia, children
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apraxia
apraxia of eye movements
apraxia of eyelid closure
apraxia of eyelid opening
apraxia, constructional
apraxia, speech
arthritis
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
attention deficit disorder with hyperactivity
autism
automobile accidents
Benedict's solution test
bifid uvula
blepharospasm
brain biopsy
bruxism
calcification, intracranial
carcinoembryonic antigen
carcinoma
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, neck
carphology
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral arteries, territory of
cerebral cortical atrophy
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrovascular accident
cerebrovascular accident, bilateral
Charcot's sign
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cleft palate
Clinical Pathologic Conference(C.P.C.)
cogwheel rigidty
confusion
cortical-basal ganglionic degeneration
degenerative diseases of CNS
dementia
dementia, childhood
dementia, frontotemporal
dementia, presenile
diabetes mellitus
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
drooling
dysarthria
dysphagia
dysplasia of C.N.S.
dystonia
ecchymoses
electroencephalogram
encephalitis
encephalitis, viral
executive dysfunction
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
familial
ferric chloride test
fever
frontal lobe, pathologic signs of
gag reflex, depressed
gait disorder
gait, apraxic
gaze palsy
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
growth retardation
handwriting
hearing problems in children
hemianopia, homonymous
hemiparesis
hypertension
hypotonia
immunodeficiency
immunosuppression
immunosuppressive agents
in situ hybridization
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intelligence quotient
jaw jerk, abnormal
karyotyping
klippel feil syndrome
language disorder in adults
language disorders in children
L-dopa
leukemia
lid
lid abnormalities
lobar atrophy
lymphoma
maple syrup urine disease
masked facies
memory, impairment of
mental retardation
microaneurysm, retinal
micrographia
midline defect in children
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, serial
multiple system atrophy
mutism
myelodysplasia
myoclonus
myoclonus, stimulus sensitive
nasal speech
neglect
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic examination, focal
neuropathology
neuropathology, brain
neuropathy
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
palatopharyngeal incompetence
Parkinson disease
Parkinsonism syndrome
pathology
personality change
phenylketonuria
Pick bodies
Pick's disease
pneumonia
polymerase chain reaction
posterior cortical atrophy
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
ptosis
pure akinesia
radiation hypersensitivity
release phenomena
respirations in CNS disease
retropulsion
Rett's syndrome
review article
rigidity
rocking
scoliosis
seizure
seizure, advice to parents and teachers regarding
seizure, psychosocial aspects of
seizure, treatment of
semantic dementia
simultanagnosia
single photon emission computed tomography
skin, lesions in neurologic disorders
somnolence
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
spinal muscular atrophy
steroid therapy, CNS treatment and complications with
stuttering
systemic lupus erythematosus
tachycardia
tauopathy
telangiectases
temporal lobe, atrophy
thrombocytopenia
urinary incontinence
urine test for metabolic disorders
visual field defect
visuospatial disturbance
walking, difficulty with
wheelchair
white matter disease
word-finding difficulty
Showing articles 300 to 350 of 608 << Previous Next >>

Natural History & Survival of 14 Pts with Corticobasal Degeneration Confirmed as Postmortem Exam
JNNP 64:184-189, Wenning,G.K.,et al, 1998

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Ataxia and Slurred Speech after Artesunate Treatment for Falciparum Malaria
NEJM 336:1328, Miller,L.G.&Panosian,C.B., 1997

Clinicopath Conf
Botulism, Case 22-1997, NEJM 337:184-190997., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Apraxia of Lid Opening
Neurol 48:1491-1503, Boghen,D., 1997

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Broadened Friedreich's Ataxia Phenotype after Gene Cloning, Minimal GAA Expan Causes Late Spastic Ataxia
Neurol 49:1617-1620, Ragno,M.,et al, 1997

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Isolated Pontine Infarctions with Prominent Ipsilateral Midfacial Sensory Signs
Stroke 28:649-651, Masjuan,J.,et al, 1997

Clinicopath Conf
Nonbact Thrombotic Endocarditis, Aortic Valve, with Cerebral, Renal & Splenic Emboli & Multiple Infa, cts, CA se 28-1997,NEJM 337:770-777,1997., 1997

Anterior Opercular Syndrome, Caused by Herpes Simplex Encephalitis
Neurol 49:494-497, McGrath,M.N.,et al, 1997

Paramedian Pontine Infarction
Stroke 28:809-815, Kataoka,S.,et al, 1997

Medial Medullary Stroke:Report of Seven Patients and Review of the Literature
Neurol 48:882-890, Bassetti,C.,et al, 1997

Corticobasal Degeneration:Neuropathologic and Clinical Heterogeneity
Neurol 48:959-969, Schneider,J.A.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Localization of Lesion in Denial of Hemiplegia After Acute Stroke
Stroke 28:67-71, Ellis,S.&Small,M., 1997

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
Mov Dis 12:342-353, Singer,C.,et al, 1997

Cerebellar Induced Aphasia: Case Report of Cerebellar Induced Prefrontal Aphasic Language Phenomena Supported by SPECT Findings
J Neurol Sciences 144:34-43, Mari�n,P.,et al, 1996

Gait Disorders in Older Adults
J Am Geriatr Soc 44:434-452, Alexander,N.B., 1996

Isolated Infarcts of the Pons
Neurol 46:165-175, Bassetti,C.,et al, 1996

Cyclosporine-Associated Mutism in Liver Transplant Patients
Neurol 46:252-254, Valldeoriola,F.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Clinicopath Conf
Demyelinating Disease, Case 8-1996, NEJM 334:715-720996., , 1996

Neuroimaging Findings in Patients on Immunosuppressive Therapy:Experience with Tacrolimus Toxicity
AJR 166:683-688, Appignani,B.A.,et al, 1996

Motor Changes in Presymptomatic Huntington Disease Gene Carriers
Arch Neurol 53:487-492, Siemers,E.,et al, 1996

Neurologic Presentation of Wilson Disease without Kayser-Fleischer Rings
Neurol 46:1040-1043, Demirkiran,M.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Transient Encephalopathy after Paclitaxel (Taxol) Infusion
Neurol 46:1596-1599, Perry,J.R.&Warner,E., 1996

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

Clinicopath Conf
Intravascular Lymphomatosis Involving Brain & Other Organs, Case 30-1996, NEJM 335:952-9596., , 1996

Dysarthria and Lacunar Stroke:Pathophysiologic Aspects
Neurol 47:1135-1141, Urban,P.P.,et al, 1996

Clinicopath Conf
Q Fever, Acute (with Cerebellar and Meningeal Involvement) , Case 38-1996, NEJM 335:1829-1834., , 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Brainstem Tumors in Patients with Neurofibromatosis Type 1:A Distinct Clinical Entity
Neurol 45:1897-1902, Molloy,P.T.,et al, 1995

Functional Dysphonia
BMJ 311:1039-1040, Wilson,J.A.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

The Landau-Kleffner Syndrome
Arch Dis Child 72:386-387, Appleton,R.E., 1995

Thalamic Hemorrhage:A Prospective Study of 100 Patients
Stroke 26:964-970, Kumral,E.,et al, 1995

Clinical and Topographical Range of Callosal Infarction:A Clinical and Radiological Correlation Study
JNNP 59:238-242, Giroud,M.&Duman,R., 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Neuropsychological Detection and Characterization of Preclinical Alzheimer's Disease
Neurol 45:957-962, Jacobs,D.M.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995



Showing articles 300 to 350 of 608 << Previous Next >>