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Differential
(Click to cross reference)
abdominal distention
abdominal reflex, absent
abducens nerve paralysis
abscess, intracerebral
abulia
aceruloplasminemia
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome myelopathy
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acquired immunodeficiency syndrome-related complex
acrocyanosis
acute disseminated encephalomyelitis
acute disseminated encephalomyelitis, multiphasic
acute respiratory distress syndrome
addiction, heroin
Addison's disease
adrenomyeloneuropathy
adult polyglucosan body disease
adverse drug reaction
agenesis of corpus callosum
aggression
agitation
Aicardi-Goutieres syndrome
alcohol intolerance
algorithm
altered states of consciousness
alternating rapid movement
Alzheimer's disease
amenorrhea
amniocentesis
amphotericin B
amyloid plaques
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ANA
anemia
anemia, megaloblastic
aneurysm, vertebral basilar system
angiitis, granulomatous of CNS
ankle clonous
ankle reflex, absent
anomic aphasia
anorexia
antecedent illness
anterior horn cell disease
anterior tibial muscle weakness
anti GQ1b IgG antibody
anticholinergic drugs
anticoagulant, complications of
anticoagulant, treatment
antiviral agents
aphasia
arachnodactyly
areflexia
Argyll Robertson pupil
arm swing, reduced
Arnold Chiari malformation
aspiration
astrocytoma
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atherosclerosis, generalized
atherosclerosis, premature
atrioventricular block
attention deficit disorder with hyperactivity
attention span
atypical
auditory evoked brainstem potentials
autism
autoantibodies
autoimmune disease
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
azidodeoxythymidine
B 12 deficiency
B12
Babinski sign
Babinski sign in new born
bacterial infection
bacterial infection, CNS
ballismus, bilateral
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bedridden
behavior modification
behavioral disorder
Behcet's syndrome
Bell's phenomenon
Bickerstaff's brainstem encephalitis
bladder dysfunction
blepharospasm
blindness
blinking
bone marrow biopsy
bradykinesia
brain atrophy
brain biopsy
brain biopsy, false negative
brain biopsy, stereotaxic
brainstem
brainstem, glioma
brainstem, glioma in children
brainstem, glioma, adult
brainstem, infarction of
brainstem, ischemia
brainstem, lesion of
brainstem, neoplasms of
brucellosis
brucellosis, nervous system involvement with
Brudzinski's sign
bruxism
bulbar palsy
bulbar palsy, progressive
burning feet
burning paresthesia
CAG repeats
calcification, intracranial
calculations
camptocormia
cane
carbamazepine
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, metrizamide
CAT scan, myelogram with
cataracts
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar hemangioma
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral folate deficiency syndrome
cerebral infarction
cerebral palsy
cerebral peduncle
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure increased
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, vascular territory involved
cerebrovascular disease
ceruloplasmin, serum
cervical spondylosis
Chaddock's sign
Charcot-Marie-Tooth
cherry red spot
cherry red spot-myoclonus syndrome
chilbran skin lesions
children
choking
cholestanol
chorea, causes of
chorea, familial
choreoathetosis
chorioretinitis
choroid plexus
choroid plexus, tumor of
chromosomal abnormality
chromosome 2
chromosome 6
chromosome 9
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
claudication, intermittent of cauda equina
cleft lip
cleft palate
Clinical Pathologic Conference(C.P.C.)
clivus
clonus
clonus, finger
clubfoot as related to neurologic disease
cobalamin C deficiency
coccidioidomycosis
cognition
Collier's sign
coma
complications
comprehension, impaired
compression fracture
concentration, impaired
confusion
congenital bilateral perisylvian syndrome
congenital malformation
congenital malformation, non CNS
consanguinity
constipation
controversies in neurology
convergence, impaired
conversion reaction
copper
copper deficiency
corneomandibular reflex
coronavirus
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cortical-basal ganglionic degeneration
COVID-19
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
C-reactive protein, elevated
critical care unit
cry, abnormal
crying, pathologic
cryptococcal meningitis
cyst, epidermoid of CNS
cysticercosis
cytomegalic inclusion disease
D-dimer
deafness
decompressive spinal cord surgery
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
Dejerine's sign
Dejerine-Sottas syndrome
delay in diagnosis
dementia
dementia, childhood
dementia, familial
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
dental procedure, neurologic complications with
dentate nuclei
dentate nuclei, lesion of
denture cream
depression
developmental abnormality of brain
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diaphragmatic paralysis
diaphragmatic paralysis, causes of
diarrhea
diet
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
digiti quinti sign
diplopia
disability, neurological
disorientation
distal muscle atrophy
distal muscle weakness
dizziness
dopa responsive dystonia
Dravet syndrome
drooling
dropped head syndrome
drowsiness
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dysmetria
dysmorphic
dysphagia
dysphonia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, children
dystonia, focal
dystonia, treatment of
ear, abnormal
ears of the Lynx MR sign
electrical sensation
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
emergencies, neurologic
emergencies, neurosurgical
emotional lability
Emperor's clothes syndrome
empyema, epidural-spinal
encephalitis
encephalitis lethargica
encephalitis, brainstem
encephalitis, viral
encephalopathy
encephalopathy, acute
encephalopathy, Hashimoto's
encephalopathy, progressive
enzyme, defect
enzyme, muscle disease
eosinophilia
ependymal
ependymoma
epidemiology of neurology
epileptic encephalopathy
episodic disorders
episodic neurologic deficits
evoked potentials
executive dysfunction
exome sequencing
eye movement, disorders of
face, numbness of
facial anomalies
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatal familial insomnia
fatigue
feeding disorder
ferritin, elevated
ferritinemia
fetal alcohol syndrome
fever
fine motor function, impaired
finger nose finger test
fingers, abnormal
Fisher's syndrome
flaccid paralysis
folic acid
folic acid deficiency
foot deformity
foot drop
fragile-X syndrome
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gadolinium
gag reflex, depressed
gait disorder
gait, apraxic
gait, spastic
gammaglobulin therapy, intravenous
gangliosidosis GM2
gastric partitioning
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
giant axonal neuropathy
girdle sensation
glabellar sign
glioblastoma multiforme(astrocytoma Gr.III)
glioma
glioma, low-grade
gliomatosis cerebri
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamate dehydrogenase deficiency
glutamic acid decarboxylase, antibody
Google
granular osmiphilic material
grasp reflex
grasping
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, variant forms of
Hallervorden Spatz disease
hammertoes
hand weakness
hands, fisted
handwriting
head lag
head tilt
headache
headache, positional
headache, recurrent
headache, severe
hearing loss
heel-knee-shin test
hematoma, epidural-spinal
hemiparesis
hemiplegia
hemiplegia, progressive
hemosiderosis of CNS, superficial
hepatomegaly
hepatosplenomegaly
herniated disc
herniated disc, cervical
heterotopia
hexosaminidase-A
high arched feet
hip flexor weakness
Hispanics
history of neurology
Hodgkin's disease
Hoffmann's sign
homocysteine, serum
homocystinuria
horse bite
human immunodeficiency virus type 1
hydrocephalus
hydrocephalus, communicating
hydrocephalus, congenital
hydrocephalus, exvacuo
hypercalcemia
hypercapnia
hypereosinophilic syndrome(HES)
hyperhidrosis
hyperhomocysteinemia
hyperparathyroidism
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypersegmented polys
hypertelorism
hypertension
hyperthermia
hyperthyroidism
hypertonia
hypoglycorrhachia
hypoglycorrhachia, causes of
hypomyelination
hypophonia
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypotonia
hypotonia, infants
imbalance
imbalance, postural
immunosuppression
impotence
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic intranuclear
incontinence, fecal
incoordination
initiative, lack of
insomnia
intellectual deficit
intellectual deterioration
interferon alpha
internal capsule
internet
internuclear ophthalmoplegia
interobserver agreement
intrauterine
intrinsic hand muscles, wasting of
introverted
intubation
iron, brain
iron, serum, low
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw jerk, abnormal
Jewish
karyotyping
Kernig's sign
ketoacidosis
Krabbe's disease
lactic acidemia
lacunar infarction
laminectomy, cervical
laminectomy, lumbar
language disorder in adults
Lasegues sign
lathyrism
laughing, pathologic
L-dopa
left-right orientation
leg spasms, painful
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
leptospirosis
lethargy
leukemia
leukemia, neurologic findings assoc.with
leuko-araiosis
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
Lhermitte's sign
life expectancy
lipid storage disorder of CNS
liver biopsy
liver disease
lobar atrophy
locked-in syndrome
logopenia
loss of sympathy
low back pain
lymphadenopathy
lymphadenopathy, hilar
lymphoma
lymphoma involving CNS
lysosomal storage disease
magnetic stimulation
magnetic stimulation, brain
malformation, CNS, congenital
malformation, vascular
manganese intoxication
meconium staining
mediastinum, lymph-node biopsy
mediastinum, mass of
memory, defect of recent
memory, impairment of
meningeal biopsy
meningeal enhancement
meningeal gliomatosis
meningitis
meningitis, actinomycotic
meningitis, aseptic
meningitis, bacterial
meningitis, blastomyces
meningitis, brucellosis
meningitis, candida
meningitis, carcinomatous
meningitis, chronic
meningitis, chronic benign lymphocytic
meningitis, cladosporium
meningitis, coenurosis
meningitis, CSF cell count-normal
meningitis, cysticercosis
meningitis, echinococcal
meningitis, eosinophilic
meningitis, fungal
meningitis, helminthic
meningitis, histoplasma
meningitis, leptospira
meningitis, lymphomatous
meningitis, Mollaret's
meningitis, neutrophilic
meningitis, nocardia
meningitis, paracoccidioides
meningitis, pneumococcal
meningitis, post myelography
meningitis, recurrent
meningitis, syphilitic
meningitis, TB
meningitis, toxoplasma
meningoencephalitis
meningoencephalitis, toxoplasma
mental retardation
mental retardation, familial
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, late-infantile
methyl benzene
methylmalonic acid, serum
methylmalonic acidemia
microcephaly
micrognathia
micropthalmia
midbrain, lesion of
middle cerebellar peduncle, lesion
Mills syndrome
mimics
miosis
misdiagnosis
mitochondrial disease
molecular genetics
Montreal cognitive assessment
mortality
motor dysfunction
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, contrast enhanced, high dose
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, gradient-echo
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, hypointense signal foci on
MRI, linear enhancement
MRI, negative
MRI, nodular enhancement
MRI, paramagnetic effect
MRI, ring sign
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, susceptibility weighted
MRS
multinucleated giant cell
multiple sclerosis
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle spasm
muscle weakness
mutism
mycoplasma
mycoplasma pneumoniae
myelitis
myelitis, longitudinal
myelitis, post infectious
myelitis, transverse
myelogram
myelogram, cervical
myelomalacia
myeloneuropathy
myelopathy
myelopathy hand
myelopathy, chronic progressive
myelopathy, vacuolar
myeloradiculopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
nausea and vomiting
neck pain
neck stiffness
neck weakness
neglect
neoplasm, primary intracerebral
neoplasm, primary of CNS
neoplasm, primary of CNS-classification
neoplasm, primary of CNS-metastasizing to subarachnoid space
neoplasm, primary of CNS-treatment of
nerve biopsy
nerve conduction studies
nerve root hypertrophy
neuroendocrinology
neurofibrillary degeneration
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuronal ceroid-lipofuscinosis
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, peripheral
neuropathy, sensory
neuropsychiatry
neuroradiology
neurotoxin
next-generation sequencing
night sweats
nitrous oxide
nonverbal
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
nystagmus, rotary
nystagmus, upbeating on upgaze
nystagmus, vertical
ocular dysmetria
ocular flutter
ocular motility, disorders of
oculogyric crisis
old age, neurology of
operculum syndrome, bilateral
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
opisthotonus
opsoclonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
optic nerve, lesion of
optic neuropathy
oral contraceptives
orthostatic hypotension
oscillopsia
osteomyelitis
osteomyelitis, spinal
pain
pain, back
pain, foot
pain, interscapular
pain, severe
palmomental response
palpebromandibular synkinesia
pancytopenia
papilledema
paralysis
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, flaccid
paraparesis, spastic
paraplegia
paraplegia, in flexion
paraplegia, progressive
parathormone
parathyroid adenoma
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, asymmetric onset
Parkinson disease, hemiparesis in
Parkinson disease, L-dopa nonresponsive
Parkinson disease, postencephalitic
Parkinson disease, tremor, absence of
Parkinson disease, unilateral
Parkinson disease, young onset
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal neurologic disorder
PAS positive
PAS positive material in the brain
past pointing
pathologic reflex
patient information and support
pediatric neurology
perivascular enhancement
pernicious anemia
perseveration
Persistent postural-perceptual dizziness
personality change
pes cavus
pharyngeal sensation
photic sneeze reflex
Pick bodies
Pick's disease
pinealoma
pituitary stalk
pituitary stalk, lesion of
plantar reflex
pleocytosis of cerebrospinal fluid
polyglucosan body
polyglucosan body disease
polymicrogyria
polyneuropathy
polyneuropathy, familial
pons, infarction of
pons, lesion of
pontine glioma
position sensation, abnormal
posterior column disease
posterior inferior cerebellar artery syndrome
posterior leukoencephalopathy syndrome
postictal neurologic deficits
postural abnormality
precipitating factors
precocious puberty
premature infant
prenatal
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prion disease
prognosis
progressive encephalomyelitis with rigidity syndrome
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pupil
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
pure dysarthria
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
radiculopathy
rash
Raynaud's phenomenon
rectal biopsy
recurrent
reflex, cutaneous
release phenomena
renal failure
renal stones
repetition, impaired
respirator
respiratory dyskinesias
respiratory failure
respiratory tract infection
retinal degeneration
retinal detachment
retinal exudates
retinitis pigmentosa
retinopathy
retropulsion
reversible neurologic disorder
review article
rigidity
risk factors
Romberg's sign
rooting reflex
rubella encephalitis, progressive
saccadic eye movements, abnormal
saddle anesthesia
sarcoidosis
sarcoidosis, CNS
scalp tenderness
schizophrenia
scleroderma
scleroderma, neurologic involvement with
SCN1A gene
scoliosis
scotoma
screening
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, focal
seizure, hysterical
seizure, intractable
seizure, neonatal
seizure, tonic-clonic
selective serotonin reuptake inhibitors
senile plaques
sensory level
sensory loss
sensory loss, cutaneous
serologic testing
serotonin norepinephrine reuptake inhibitors
severe acute respiratory syndrome
single photon emission computed tomography
skin, lesions in neurologic disorders
skin, temperature difference
skull x-ray, abnormal
sleep pathology and physiology
slow virus infection of CNS
slurred speech
sneeze
snout reflex
sodium channel dysfunction
somatosensory evoked potentials
somnolence
spastic ataxia
spastic diplegia
spastic paraplegia, type 11
spastic paraplegia, type 7
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal stenosis
spinal stenosis, familial
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 7
spinocerebellar degeneration
spongy degeneration of brain
spontaneous remission
startle myoclonus
startle reaction
status epilepticus
steroid therapy, CNS treatment and complications with
stooped posture
strabismus
striatonigral degeneration
striatonigral degeneration, infantile
striopallidodentate calcifications, familial idiopathic
subarachnoid hemorrhage
subdural effusion
substantia nigra
suck reflex
superior cerebellar artery infarction
superior sagittal sinus thrombosis
swallowing
symmetric brain lesions
syncope
syringomyelia
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
tandem gait, ataxic
tangential
tau protein
tauopathy
Tay-Sachs disease
tectal glioma
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular enlargement
thalamus, lesion of
thalamus, lesion of-bilateral
thyrotoxicosis
tinnitus
titubation
toe walking
tone, muscle, increased
tongue, fasciculations of
tongue, impaired movements of
tonic foot response
toxoplasmosis, acquired
toxoplasmosis, CNS
transient neurologic deficit
transilumination of skull
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
tripping
unconsciousness
undiagnosed
upgaze
upgaze, paralysis of
urinary frequency
urinary incontinence
urinary retention
urinary urgency
uveitis
vaccination, neurologic complications with
valsalva maneuver
vegetarianism
ventricular enlargement
vertigo
vertigo, episodic
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual acuity, decreased
visual evoked response
visual fields, constricted
visual loss
vitamin deficiency
vitamin E
vitamin E deficiency
Vogt-Koyanagi-Harada syndrome
walking frame
walking, delayed
walking, difficulty with
Wallerian degeneration
watershed infarcts
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
white matter disease, periventricular
wide based gait
workup
x-linked mental retardation
x-ray, spine
x-ray, thoracic spine
zinc
zoonoses
Showing articles 0 to 50 of 1808 Next >>

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

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

A Young Health Woman with Difficult-to-Wean Acute Ventilator Dependence
Neurol 94:e1340-e1343, Chandrashekhar, S.,et al, 2020

Neurologic Features in Severe SARS-CoV-2 Infection
NEJM 382:2268-2270, e110, , 2020

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

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

Finger Clonus
Neurol 86:e118-e119, Moccia,M.,et al, 2016

A Young Man with Acute Encephalopathy Loss of Vision, and Upper Motor Neuron Signs
Neurol 86:e173-e176, Elkhider, H.,et al, 2016

A 34-Year-Old Man with Headache, Diploplia, and Hemiparesis
Neurol 86:e28, Lincoln, M.R.,et al, 2016

Idiopathic Thoracic Spontaneous Spinal Epidural Hematoma
Case Reports Surg doi:10.1155/2016/5430708, Aycan, A.,et al, 2016

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

A 73-year-old Man with Diplopia and Ataxia
Neurol 85:e96-e100, Gupta, H.V.,et al, 2015

Multiple-System Atrophy
NEJM 372:249-263, Fanciulli, A. & Wenning, G.K., 2015

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Clinical Case Conference: A 41-Year-Old Woman with Progressive Weakness and Sensory Loss
Ann Neurol 75:9-19, Stephen, C.D.,et al, 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
Adams & Victors Principles of Neurology Chp 41, pg 1172, Ropper, A.H.,et al, 2014

A Young Woman with Rapid Mental Deterioration and Leukoencephalopathy
Neurol 83:e182-e186, Biotti, D.,et al, 2014

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1107, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

A Horse Bite to Remember
Lancet 376:1194, Brouwer,M.C.,et al, 2010

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Clinicopath Conf, Neurosarcoidosis
NEJM 360:802-809, Case 6-2009, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Clinicopath Conf., Gliomatosis Cerebri
Neurol 69:600-606, Fleming,J.O.,et al, 2007

Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
Neuropathology 27:434-441, Iwasaki,Y.,et al, 2007

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Glabellar and Palmomental Reflexes in Parkinsonian Disorders
Neurol 63:1096-1098, Brodsky,H.,et al, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003



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