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Differential
(Click to cross reference)
abscess, intracerebral
abulia
acetazolamide
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
activities of daily living
activities of daily living scale
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adverse drug reaction
affect, flat
agitation
agitation, childhood, acute
akinetic mute
alien hand syndrome
altered states of consciousness
alternating hemiplegia
Alzheimer's disease
ammonia
amyloid plaques
antibiotics, neurologic complications with
anticholinergic drugs
anticholinergic drugs, side effects of
anticholinergic poisoning
antineutrophil cytoplasmic autoantibodies
aphasia
asterixis
ataxia
ataxia, cerebellar
attention span
azidodeoxythymidine
behavioral disorder
Behcet's syndrome
blepharospasm
blood brain barrier
brain atrophy
brain biopsy
brainstem
brainstem, neoplasms of
bruxism
burning feet
burning feet, differential diagnosis of
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, false negative
central nervous system, infection of
central pontine myelinolysis
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral edema
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, protein of
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
children
chorea
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
coccidioidomycosis
coma
compulsivity
concentration, impaired
confusion
confusional state, acute
congenital heart disease
congenital heart disease, CNS complications with
corpus callosum
corpus callosum, lesion of
cyproheptidine
cytomegalic inclusion disease
cytomegalovirus infection
deafness, bilateral progressive vs.unilateral acute
degenerative diseases of CNS
delirium
delusion
dementia
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
depression
diagnostic criteria
dialysis
diplopia
disorientation
drop attacks
drowsiness
dura, thickened
dysarthria
dysequilibrium syndrome
dysphagia
dyspraxia
dystonia
echolalia
electroencephalogram
electroencephalogram, abnormalities of
empyema, subdural
encephalomalacia
encephalopathy
encephalopathy, metabolic
epilepsia partialis continua
executive dysfunction
eye movement, disorders of
falling
familial
fatigue
fever
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, lesion of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
fungal infection, CNS
gait disorder
gait, apraxic
gait, spastic
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
genital ulcerations
glabellar sign
granuloma, pulmonary
granulomatosis with polyangiitis
grasp reflex
grasping
grimacing
hallucination
hallucination, visual
headache
headache, intermittent
headache, vascular
hemianopia, homonymous
hemiballismus
hemiparesis
hemiparesis, transient
hepatic encephalopathy
hepatic encephalopathy, acute
herpes virus
Horner's syndrome
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, normal pressure
hyperkalemia
hypoglycorrhachia
hypophonia
illusions
imbalance
immunosuppression
impulsivity
inattention
inclusion bodies
incontinence, fecal
initiative, lack of
insomnia
intellectual deficit
intellectual deterioration
intracranial pressure, increased
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaundice
laughing, pathologic
leukoencephalopathy
level of consciousness, decreased
lipids
lobar atrophy
logopenia
loss of sympathy
lymphoma involving CNS
lymphoma, primary of CNS
memory, defect of recent
memory, impairment of
meningeal biopsy
meningeal enhancement
meningismus
meningitis
meningitis, fungal
meningitis, granulomatous
meningitis, lymphomatous
meningitis, syphilitic
meningitis, TB
mental status, abnormal
micrographia
migraine
migraine, prophylaxis
misdiagnosis
mongolism
Montreal cognitive assessment
mood change
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, high signal intensity of basal ganglia
MRI, spinal cord
multinucleated giant cell
multiple sclerosis, treatment of
multiple system atrophy
muscle cramp
mutism
myelopathy, vacuolar
myoclonic jerks
myoclonus
nausea and vomiting
neglect
neoplasm, posterior fossa
neoplasm, primary of CNS
nerve conduction studies
neurologic complications
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuropathology
neuropathology, brain
nystagmus
nystagmus, positional
obsessive-compulsive disorder
ocular motility, disorders of
old age, neurology of
opisthotonus
oral ulcerations
pachymeningitis, cranial
palmomental response
papilledema
paraparesis
paraphasias
Parkinsonism syndrome
pathologic reflex
penicillin
perseveration
personality change
petechiae
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
polyneuropathy
polyneuropathy, uremic
portal caval shunt
posterior fossa, signs of
prion disease
progressive neurologic disorder
progressive supranuclear palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, acute
pyramidal tract dysfunction
quadriparesis
release phenomena
renal transplantation
restless leg syndrome
reticulum cell sarcoma
review article
Reye's syndrome
rigidity
rooting reflex
scleritis
sedimentation rate, elevated
seizure
self-grasping
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
slurred speech
snout reflex
stare
startle myoclonus
startle reaction
steroid therapy, CNS treatment and complications with
stooped posture
stuporous
subdural hematoma
suck reflex
systemic illness
tangential
tau protein
tauopathy
temporal lobe, atrophy
tentorium cerebelli
tetany
tongue, ulcer
tonic foot response
toxoplasmosis, acquired
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
Trousseau's sign
tuberculin skin test, positive
upgaze
upgaze, paralysis of
uremia
uremic encephalopathy
uremic twitching
urinary incontinence
very long chain fatty acids
viral infection, CNS
visual impairment
walking, difficulty with
weakness
Wernicke's encephalopathy
wheelchair
white matter disease
word-finding difficulty
wrist drop
writing
Showing articles 0 to 50 of 653 Next >>

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Hepatic Stupor and Coma (Hepatic, or Portal-Systemic Encephalopathy)
Adams & Victors Principles of Neurology Chp 40, pg 1142, Ropper, A.H.,et al, 2014

Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
NEJM 360:171-181, Case 1-2009, 2009

Clinicopath Conf, Neuro-Behcets Disease
NEJM 360:2341-2351, Case 17-2009, 2009

Clinicopath Conf., Pick's Disease, Case 11-2000
NEJM 342:1110-1117, , 2000

Central Anticholinergic Syndrome on Therapeutic Doses of Cyproheptadine
Pediatrics 103:158-160, Watemberg,N.M.,et al, 1999

Clinicopath Conf,Wegener's Granulomatosis with Pachymeningeal Granulomatous Inflammation, Case 9-1999
NEJM 340:945-953, , 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Evaluation of Five Primitive Reflexes in 240 Young Adults
Neurol 51:322, Brown,D.L.,et al, 1998

Clinicopath Conf
Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) , with Amyloid (KURU) Plaques, Case 17-1993, N, JM 328:66,1993., 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Clinicopath Conf
Pick's Diseae, Case 6-1992, NEJM 326:397-405992., , 1992

Two Alien Hand Syndromes
Neurol 42:19-24, Feinberg,T.E.,et al, 1992

Neurological Findings in Alzheimer's Disease and Normal Aging
Arch Neurol 47:625-627, Glasko,D.,et al, 1990

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Significance of Cortical Disinhibition Signs
Neurol 32:169-173, Tweedy,J.,et al, 1982

Self-Grasping:A Focal Neurological Sign
Ann Neurol 12:575-577, Ropper,A.H., 1982

A Syndrome of Early Recognition of Occult Hydrocephalus & Cerebral Atrophy
Quart J Med 183:365, Botez,M.I.,et al, 1977

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Case Records of MGH-NEJM 285:621
1971., , 1971

Neuro CPC of MGH
Multiple Cerebral Abscesses & Infarcts, NEJM 266:610-61762., , 1962

Neuro CPC of MGH
Reticulum Cell Sarcoma of Brain & Meninges, NEJM 265:1205-121061., , 1961

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Manganese Accumulation in the Brain
NEJM 389:1320, Sherman,S.V., 2023

Age-Related Changes in Neurologic Examination and Sensory Nerve Amplitude in the General Population, Aging of the Peripheral Nervous System
Neurol 101:e1351-e1358, Taams,N.E.,et al, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

Extracranial Etiology of Acute Onset Ataxia and Weakness
Neurol 99:898-899, Nordli,D.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

A 48-Year-Old Man Presenting With Diplopia
Neurol 96:399-405, Pehere,N.K.,& Gofer,K., 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 68-Year-Old Man with Proximal Weakness and Seizures
Neurol 97:e423-e428, Chen, T., 2021

Clinical and Genetic Features in Patients with Reflex Bathing Epilepsy
Neurol 97:e577-e586, Accogli, A.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020



Showing articles 0 to 50 of 653 Next >>