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Differential
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abdominal reflex, absent
abducens nerve paralysis
abulia
achilles tendon, enlarged
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
acromicria
Addison's disease
adrenoleukodystrophy
adrenomyeloneuropathy
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
Africa
alcohol injection
alcohol intolerance
alcohol, neurologic complications with
alcoholism
Alexanders disease
Alexanders disease, adult onset
algorithm
alternating rapid movement
ammonia
amniocentesis
amyloid plaques
amyloidoma
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anemia
angiography, spinal
ankle reflex, absent
aphasia
aqueduct of Sylvius, stenosis
aqueductal stenosis
arm weakness
Arnold Chiari malformation
arthralgia
arthritis
astrocytoma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, sensory
ataxia, truncal
ataxic gait
atherosclerosis, generalized
atypical
auditory evoked brainstem potentials
autoantibodies
autoimmune disease
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
axonal spheroid
azidodeoxythymidine
B 12 deficiency
B12
Babinski sign
basal ganglia
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar impression
behavioral disorder
Behcet's syndrome
benign essential tremor
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
bladder dysfunction
brachial plexus neuropathy
brain atrophy
brain biopsy
brain biopsy, negative
brain biopsy, stereotaxic
brainstem
brainstem, dysfunction
brainstem, glioma
brainstem, glioma in children
brainstem, glioma, adult
brainstem, ischemia
brainstem, lesion of
brainstem, neoplasms of
bulbar palsy
burning feet
burning paresthesia
CAG repeats
calcification, intracranial
camptocormia
cane
cannabinoids
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, spine
cataracts
caudate nucleus, atrophy
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral cortex
cerebral palsy
cerebral palsy, associated problems with
cerebral venous thrombosis
cerebroretinal microangiopathy with calcifications and cysts
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, recurrent
cerebrovascular disease
cervical myelopathy
cervical spondylosis
children
choking
cholestanol
chorea
chorea, causes of
chorea, familial
choreoathetosis
chromosomal abnormality
chronic progressive external ophthalmoplegia
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
cobalamin C deficiency
cognition
cold hands sign
coma
complications
concentration, impaired
confusion
congenital infection, CNS
consanguinity
constipation
controversies in neurology
corpus callosum, atrophy of
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
crossed adductor reflex
crying, pathologic
deafmute
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
deep gray nuclei
degenerative cervical myelopathy
degenerative diseases of CNS
delusion
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
depression
dermatitis
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
diarrhea
diarrhea, bloody
diet
differential diagnosis
diplegia, spastic cerebral
diplopia
disability, neurological
disorientation
distal muscle weakness
dysarthria
dysarthria-clumsy hand syndrome
dyskinesia
dysphagia
dysphonia
dyspnea
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, focal
dystonia, painful
dystrophic calcification
ears of the Lynx MR sign
efficacy
electrical sensation
electroencephalogram, abnormalities of
electromyogram
electron microscopy
ELISA
emergency room
emotional lability
encephalitis
encephalitis lethargica
encephalitis, viral
encephalomalacia
encephalopathy
endemic area
endovascular therapy
enzyme, muscle disease
epidemiology of neurology
epileptic encephalopathy
equinovarus
evoked potentials
exome sequencing
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, recurrent
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatigue
fatty acid, elevated plasma content
fever
fine motor function, impaired
finger nose finger test
finger tapping
fistula, arterio-venous
fistula, arterio-venous, dural
fistula, arterio-venous, dural, spinal
fluctuate
fluorescent treponema antibody absorption(FTA-ABS)
foot deformity
foot drop
Friedreich's ataxia
frontal lobe, pathologic signs of
fundus, abnormality of
gadolinium
gait disorder
gait, apraxic
gait, spastic
gaze palsy
gender
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
genital ulcerations
geographic location
Gerstmann-Straussler-Scheinker disease
GFAP gene
girdle sensation
glioblastoma multiforme(astrocytoma Gr.III)
glioma
glioma, low-grade
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
GLUT1 deficiency syndrome
glutamic acid decarboxylase, antibody
granulomatosis with polyangiitis
granulomatous disease
grasp reflex
growth retardation
Guillain Barre syndrome
Hallervorden Spatz disease
hallucination
hammertoes
hand weakness
handwriting
head nodding
head tilt
headache
headache, intermittent
hearing loss
heel-knee-shin test
hemangioma
hemangioma, vertebral
hemianopia
hemiparesis
hepatic failure
hepatitis
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
hepatosplenomegaly
herniated disc
herniated disc, cervical
high arched feet
Hispanics
hoarseness
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
human T-lymphotropic virus type II(HTLV-II)
Huntington's chorea
Huntington's disease, children
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperammonemic encephalopathy
hyperhomocysteinemia
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypersomnia
hypertension
hyperthyroidism
hypothyroidism
hypotonia
imbalance
immunosuppression
immunotherapy
impotence
inborn errors of metabolism
inclusion bodies
incontinence, fecal
incoordination
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
iodine deficiency
iron, brain
irritability
Jamaica ginger paralysis
jaw jerk, abnormal
Jewish
lactic acidemia
laminectomy
laminectomy, cervical
laughing, pathologic
leg spasms
leg spasms, painful
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
leuko-araiosis
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
Lhermitte's sign
life expectancy
liver disease
locked-in syndrome
lymphoma
lymphoma involving CNS
lymphomatoid granulomatosis
Madonna facies
Maghreb
malformation, vascular
mania
marche a petits pas
marihuana
medulla oblongata, lesion of
Melkersson's syndrome
memory, impairment of
meningeal gliomatosis
meningitis, CSF cell count-normal
meningomyelitis
mental retardation
mental status, abnormal
metabolic disorder, primary
methylmalonic acidemia
microangiopathy, brain
microcephaly
Mills syndrome
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mononeuritis multiplex
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, brachial plexus
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, paramagnetic effect
MRI, spinal cord
MRI, spine
MRI, T1 weighted high signal foci
MRS
multinucleated giant cell
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple system atrophy
muscle cramp
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myelopathy, hepatic
myelopathy, vacuolar
myoclonus
myoclonus, epilepsy
myopathy
myopathy, vacuolar
myositis
myositis, ocular
myxedema, neurologic manifestations of
nabiximols
Native Americans
neck pain
neck stiffness
neck weakness
neoplasm, primary of CNS
neoplasm, primary of CNS-classification
neoplasm, primary of CNS-treatment of
nerve biopsy
nerve conduction studies
neuroendocrinology
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropathy, sensory
neurosyphilis
neurotoxin
next-generation sequencing
numb clumsy hands syndrome
numbness, extremity
nystagmus
nystagmus, dissociated
nystagmus, rotary
nystagmus, vertical
obesity
ochronosis
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic neuritis
optic neuropathy
optical coherence tomography
oral ulcerations
orthostatic hypotension
osteoarthrosis
osteoporosis
pain
pain, abdominal
pain, central
pain, foot
pain, leg
pancytopenia
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paraplegin
paraspinal muscle
paresthesias
paresthesias, hands
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, asymmetric onset
Parkinson disease, L-dopa nonresponsive
Parkinson disease, postencephalitic
Parkinson disease, tremor, absence of
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
past pointing
penicillin
pernicious anemia
personality change
pleocytosis of cerebrospinal fluid
poison, organophosphate
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
pons, lesion of
pontine glioma
portal caval shunt
posterior column disease
postural abnormality
practice guidelines
precipitating factors
primary lateral sclerosis
prisoners of war, neurologic complications in
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pursuit eye movements, abnormal
pyramidal
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriparesis, progressive
quadriplegia
radiation therapy, CNS treatment and complications with
Rankin score
rash
Raynaud's phenomenon
regional enteritis
release phenomena
renal stones
respiratory dyskinesias
reticulum cell sarcoma
retinitis pigmentosa
Rett's syndrome
reversible neurologic disorder
review article
rigidity
risk factors
risk-benefit assessment
Rosenthal fibers
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
saccadic eye movements, abnormal
safety
Saudi Arabia
scissors gait
sclerae, hyperpigmented
scleritis
scleroderma
scleroderma, neurologic involvement with
scoliosis
scoliosis, neurologic association with
scotoma
screening
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, children
sensorineural hearing loss
sensory level
sensory loss
sensory loss, cutaneous
serologic testing
serologic testing of cerebrospinal fluid
short stature
shunt procedure, ventricular
sinusitis
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep apnea
slow virus infection of CNS
snout reflex
solitary scerlosis
somatosensory evoked potentials
somnolence
spartin
spastic ataxia
spastic diplegia
spastic dysphonia
spastic paraplegia, type 11
spasticity
spasticity, treatment of
spastin
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal cord, vascular disorders Affecting
spinal cord, vascular malformation of
spinal xanthomatosis
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 7
splenomegaly
spondylolysis
status epilepticus
stereotyped behavior
steroid therapy, CNS treatment and complications with
stiff legs
stiff man syndrome
strabismus
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
substantia nigra
symmetric brain lesions
syphilis, diagnosis and treatment
syphilis, meningomyelitis
syphilis, neurologic complications with
syringomyelia
systemic illness
tachycardia
tectal glioma
tendon, enlarged
thrombocytopenia
thyroiditis
tinnitus
titubation
toe walking
tone, muscle, increased
tongue, enlarged
tongue, impaired movements of
tongue, ulcer
tonic foot response
tonsillar herniation of cerebellum
toxins, nervous system
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, jaw
tremor, leg
tremor, postural
tremor, treatment of
tremor, voice
trinucleotide repeats
ulcerative colitis
ulcers, fingertip
undiagnosed
upgaze, paralysis of
urea-cycle enzymopathies
urinary frequency
urinary incontinence
urinary urgency
urine, dark
vegetarianism
vertigo
vibratory sensation, abnormal
viral infection
viral infection, CNS
viral isolation
virus, slow
visual acuity, decreased
visual evoked response
visual loss
vitamin deficiency
walking frame
walking, difficulty with
war
weakness
weakness, progressive
weakness, proximal
weight loss
Western immunoblot test
wheelchair
white matter disease
wide based gait
word-finding difficulty
writers cramp
writing
xanthoma, tendon
Showing articles 50 to 100 of 2247 << Previous Next >>

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

Spinal Cord Syphilis Associated with Human Immunodeficiency Virus Infection:A Treatable Myelopathy
Am J Med 91:101-103, Berger,J.R., 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Chiari I Malformations:Clinical and Radiologic Reappraisal
Radiology 183:347-353, Elster,A.D.&Chen,M.Y.M., 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

Essential Tremor:Clinical Correlates in 350 Patients
Neurol 41:234-238, Lou,J.&Jankovic,J., 1991

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

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
Ann Neurol 25:419-420, Iwasaki,Y.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

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

Hyperthyroidism Presenting as Pyramidal Tract Disease
BMJ 297:1395-1396, Shaw,P.J.,et al, 1988

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

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

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

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Portal-Systemic Myelopathy after Portacaval Shunt Surgery
Arch Int Med 145:1921-1922, Lebovics,E.,et al, 1985

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

Post-encephalitic Parkinsonism:Current Experience
JNNP 44:670-676, Rail,D.,et al, 1981

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Spastic Gait & Acquired Aqueductal Stenosis in an Adult
Arch Neurol 37:116, Watson,C.P., 1980

Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980

Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979

Jamaica Ginger Paralysis
Arch Neurol 35:530, Morgan,J.P.,et al, 1978

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

Lymphomatoid Granulomatosis
Human Pathology 3:457, Liebow,A.,et al, 1972

Brain Stem Tumors of Childhood & Adolescence
Am J Dis Child 119:465-472, Panitch,H.S.,et al, 1970

A 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Glial Fibrillary Acidic Protein Autoimmunity
Neurol 98:e653-e668, Gravier-Dumonceau, A.,et al, 2022

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Longitudinally Extensive Spinal Cord Lesions in a Middle-Aged Man
Neurol 98:419-424, Xi, N. & Zhou, Y., 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

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

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021



Showing articles 50 to 100 of 2247 << Previous Next >>