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Differential
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achilles tendon, enlarged
acute ataxia of childhood
acute cerebellar ataxia
agitation
akinetic mute
alcohol intolerance
alcoholism
alternating rapid movement
alternating rapid movement, impaired
ammonia
ANA
anasarca
anemia
angiography, cerebral
ankle edema
anorexia
anti Yo antibody
aphasia
aphonia
areflexia
ascites
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune encephalopathy
automobile accidents
B 12 deficiency
Babinski sign
bacterial infection
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
belligerent
biologic markers
blepharospasm
bradykinesia
brain biopsy
brainstem, atrophy
brainstem, lesion of
CAG repeats
carbon monoxide poisoning
carcinoma
carcinoma of breast
cardiomyopathy
CAT scan
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, perfusion
CAT scan, venography
cataracts
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar cognitive affective syndrome
cerebellar degeneration
cerebellar lesion
cerebellitis
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, location of
cerebrovascular accident, multiple
cerebrovascular accident, silent
ceruloplasmin, serum
choking
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
cognition, slowed
coma
complications
confusion
cortical infarction
cough
cranial nerve palsies
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
crying, pathologic
cystatin C mutation
deep gray nuclei
delay in diagnosis
delirium
delusion
dementia
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, thalamic
dementia, transmissible
depression
dexterity, impaired
diabetes mellitus
diarrhea
diet
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
disorientation
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
DPPX
DPPX, antibodies, encephalitis
drooling
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dysgraphia
dysmetria
dysphagia
dystonia
dystonia, face
dystonia, focal
ear, pain in
echolalia
edema, pedal
EDTA(ehtylenediamine tetraacetic acid)
ejection fraction, abnormal
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, progressive
Epstein-Barr virus
Erdheim-Chester disease
esophageal varices
euphoria
executive dysfunction
eye movement, disorders of
facial expression abnormality
falling
false negative
familial
fatigue
fever
fine motor function, impaired
finger nose finger test
finger numbness
fistula, arterio-venous, dural
foam cells
food-borne infection
Friedreich's ataxia
frontal lobe, atrophy
gait disorder
gammaglobulin therapy, intravenous
gastric partitioning
gaze palsy, horizontal
gene
gene mutation
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
grandiosity
hallucination
hand weakness
hands, fisted
handwriting
head nodding
headache
heel swelling
heel-knee-shin test
hemidystonia
hemorrhage, thalamic
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
hiccoughs
hiccoughs, intractable
histiocytosis
hoarseness
hyperammonemic encephalopathy
hyperesthesia
hyperhomocysteinemia
hyperosmolality
hyperreflexia
hypersomnia
hypoalbuminemia
hypometric saccades
hypotonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunohistochemistry
impulsivity
inattention
incarceration
incontinence, fecal
incoordination
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Kayser-Fleischer ring
lactic dehydrogenase(LDH)
lateropulsion
laughing, pathologic
leg swelling
leukoencephalopathy
leukopenia
level of consciousness, decreased
listeria monocytogenes
listeriosis, CNS
liver disease
liver function enzymes
lobar atrophy
logopenia
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
manganese intoxication
mania
masked facies
medulla oblongata, lesion of
memory, defect of recent
memory, impairment of
meningitis-encephalitis PCR panel
mental status, abnormal
methylmalonic acid, serum
methylmalonic acidemia
micrographia
microhemorrhage, intracerebral
midbrain, atrophy
middle cerebellar peduncle, lesion
misdiagnosis
molecular genetics
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, negative
MRI, punctate pattern
MRI, ring sign
MRI, T1 weighted high signal foci
MRI, venography
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle biopsy
mutism
myelinolysis, extrapontine
myelomalacia
myoclonic jerks
myoclonus
myoclonus, stimulus sensitive
nausea and vomiting
neck pain
neoplastic angioendotheliosis
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neuronopathy
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, sensory
next-generation sequencing
nutritional deficiency
nystagmus
olivary degeneration, hypertrophic
ophthalmoplegia, progressive external
optic atrophy
osmotic demyelination syndrome
otitis, neurologic complications with
palatal myoclonus
paraneoplastic cerebellar degeneration
paranoia
paraphasias
paresthesias
paresthesias, hands
Parkinson disease
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
pathologic reflex
penicillamine
pernicious anemia
personality change
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
pons, lesion of
positional head-hanging test
post infectious cerebellar ataxia
postinfectious
postural abnormality
pregnancy, neurologic complications in
prion disease
prion protein gene
prisoner
prognosis
progressive ataxia and palatal tremor
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychotic behavior
ptosis
ptosis, bilateral
pull test
pursuit eye movements, abnormal
RAPID CT perfusion maps
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
rehabilitation for neurologic disorders
release phenomena
remote effect of cancer on the nervous system
renal stones
retropulsion
reversible neurologic disorder
review article
rigidity
Romberg's sign
saccadic eye movements, abnormal
seizure
sleep pathology and physiology
slit lamp examination
slurred speech
spasticity
speech disorder
speech disorder, non aphasic
speech, loss of
speech, pressured
speech, slowed
spinocerebellar ataxia
spinocerebellar ataxia type 7
splenomegaly
spongy degeneration of brain
spontaneous remission
square wave jerks
staggering
startle myoclonus
startle reaction
suicide
swallow evaluation
symmetric brain lesions
systemic illness
tandem gait, ataxic
tangential
tau protein
tauopathy
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
titubation
tongue, numbness of
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trientine dihydrochloride
trinucleotide repeats
upgaze, paralysis of
urinary incontinence
venous hypertension
venous ischemia
vertigo
vestibulopathy
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weight loss
welder
wheelchair
white matter disease
wide based gait
work loss
workup
writing
zinc
Showing articles 600 to 650 of 777 << Previous Next >>

Clinicopath Conf
Cerebral Mucormycosis, Case 52-1990, NEJM 323:1823-1833990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Antemortem Diagnosis of Diffuse Lewy Body Disease
Neurol 40:1523-1528, Crystal,H.A.,et al, 1990

Dysphagia, Speech Disorders and Centrotemporal Spikes-Waves
Arch Francaises De Pediatrie 47:115-117, Boulloche,J.,et al, 1990

Anterior Cerebral Artery Territory Infarction in the Lausanne Stroke Registry
Arch Neurol 47:144-150, Bogousslavsky,J.&Regli,F., 1990

Caudate Infarcts
Arch Neurol 47:133-143, Caplan,L.R.,et al, 1990

Clinical Features of Proven Basilar Artery Occlusion
Stroke 21:1135-1142, Ferbert,A.,et al, 1990

Narcolspey
NEJM 323:389-394, Aldrich,M.S., 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Extensive Brain Calcif & Prog Dysarthris & Dysphagia Assoc with Chronic Hypoparathyroidism
Arch Neurol 47:1038-1039, Cheek,J.C.,et al, 1990

Acquired Childhood Aphasia
Arch Neurol 47:1324-1328, Loonen,M.C.B.&vanDongen,H.R., 1990

Slowly Progressive Aphasia:Three Cases with Language, Memory, CT and PET Data
JNNP 53:987-993, Kempler,D.,et al, 1990

Paramedian Thalamic and Midbrain Infarcts Associated with Palilalia
JNNP 53:797-799, Yasuda,Y.,et al, 1990

Progressive Aphasia without Dementia:Further Documentation
Ann Neurol 25:411-413, Sapin,L.R.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Anterior Operculum Syndrome
Neurol 39:1169-1172, Mao,C.C.,et al, 1989

Guillain-Barre Syndrome Presenting as High-Altitude Cerebral Edema
NEJM 321:545, Shlim,D.R.&Cohen,M.T., 1989

Multiple Forms of Epileptic Attacks Secondary to a Small Chronic Subdural Haematoma
BMJ 299:439-441, Jones,S.C.,et al, 1989

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Lesions of the Head & Neck in Patients with AIDS:CT and MR Findings
AJNR 9:693-698, Olsen,W.L.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Delayed Speech in Children
BMJ 297:1281-1282, Hall,D., 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Lyme Disease:Acute Focal Meningoencephalitis in a Child
Pediatrics 82:931-934, Feder,H.M.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Diagnosis & Treatment of Aphasia, Part I & Part II
JAMA 259:1043-1047, 1205-12101988., Albert,M.L.&Helm-Estabrooks,N., 1988

Dystonia in Parkinson's Disease:Clinical & Pharmacological Features
Ann Neurol 23:73-78, Poewe,W.H.,et al, 1988

A Double-Blind Trial of Clonazepam in the Treatment of Parkinsonian Dysarthria
Neurol 38:255-258, Biary,N.,et al, 1988

Pharmacotherapy for Aphasia
Neurol 38:877-879, Albert,M.L.,et al, 1988

Aspiration Following Stroke:Clinical Correlates and Outcome
Neurol 38:1359-1362, Horner,J.,et al, 1988

Transient CNS Deficits:A Common, Benign Syndrome in Young Adults
Neurol 38:831-836, Levy,D.E., 1988

Unclear Speech:Recognition & Significance of Unintelligible Speech in Preschool Children
Pediatrics 82:447-452, Coplan,J.&Gleason,J.R., 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Spontaneous Internal Carotid Artery Dissection Presenting as Hypoglossal Nerve Palsy
Stroke 19:1151-1155, Lieschke,G.J.,et al, 1988

The Clinical Spectrum of Alcoholic Pellagra Encephalopathy, A Retrospective Analysis of 22 Cases Studied Pathologically
Brain 111:829-842, Serdaru,M.,et al, 1988

Progressive Language Impairment without Dementia:A Case with Isolated Category Specific Semantic Defect
JNNP 51:1201-1207, Basso,A.,et al, 1988

Mirror-Writing & Reversed Repetition of Digits in a Right-Handed Patient with Left Basal Ganglia Haematoma
JNNP 50:786-788, Chia,L.&Kinsbourne,M., 1987

Acquired Aphasia in Childhood:Clinical & CT Investigations
Neurol 37:1165-1172, Cranberg,L.D.,et al, 1987

Comparison of Formal Language Therapy with Supportive Counseling for Aphasia due to Actue Vascular Accident
Arch Neurol 44:646-649, Hartman,J.&Landau,W.M., 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Miliary Metastasis to the Brain:Clinical & Radiologic Features
Neurol 37:1817-1818, Floeter,M.K.,et al, 1987

Forms of Dystonia in Patients with Parkinson's Disease
Neurol 37:1009-1011, Kidron,D.&Melamed,E., 1987

Swallowing & Speech Production in Parkinson's Disease
Ann Neurol 19:238-287, Robbins,J.,et al, 1986

Giant Axonal Neuropathy:Central Abnormalities Demonstrated by Evoked Potentials
Ann Neurol 19:394-396, Majnemer,A.,et al, 1986

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986



Showing articles 600 to 650 of 777 << Previous Next >>