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Differential
(Click to cross reference)
abdominal cramps
abdominal reflex, absent
acute disseminated encephalomyelitis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
ageusia
akinetic mute
alcohol
Alexanders disease
Alexanders disease, adult onset
aminoacidopathies
aminoacidurias
amnestic syndrome
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
anatomy of
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angina pectoris
anhidrosis
anosmia
anti MAG antibodies
antispasticity drugs
aphasia
arteriopathy
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
autonomic dysfunction
Babinski sign
baclofen
basal ganglia, infarction
basal ganglia, lesion of
behavioral disorder
benign essential tremor
beta adrenergic blocker
bladder dysfunction
blink reflex
bone marrow transplantation
brain biopsy
brainstem
brainstem, infarction of
brainstem, lesion of
burning paresthesia
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
CAT scan, demyelinating disease
CAT scan, serial
catecholamine
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, immunoglobulins of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
Charcot-Marie-Tooth
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congenital malformation
congestive heart failure
corneal dystrophy
cortical blindness
cortical blindness, transient
crying, pathologic
cyst, porencephalic
cystinuria
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, cerebrovascular disease causing
dementia, presenile
dementia, subcortical
dementia, thalamic
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
dilantin
diplopia
disability, neurological
dopamine
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysphagia
dystonia
dystonia musculorum deformens
echocardiogram
echolalia
electrical sensation
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
ELISA
emotional lability
encephalitis
encephalitis, viral
encephalomalacia
encephalopathy
encephalopathy, metabolic
enzyme, defect
evoked potentials
exercise intolerance
eye, pain in
Fabry's disease
facial nerve palsy
facial weakness
facial weakness, bilateral
Fahr disease
familial
fatigue
fever
flexor spasm
gadolinium
gait disorder
gamma amino butyric acid
gamma amino butyric acid-mimetic drug
gamma knife therapy
gangliosidosis GM2
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
glioma
glutaric acidemia
granular osmiphilic material
haloperidol
head injury
head nodding
headache
hearing loss
hearing loss, bilateral
heavy metal intoxication
hemianopia
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatolenticular degeneration(Wilson's disease)
hiccoughs
HLA
holoprosencephaly
homovanillic acid
hormone replacement
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
incoordination
intellectual deficit
intellectual deterioration
interferon
interferon beta 1-a
interferon beta 1-b
intrathecal antispasticity drugs
iron, brain
Japan
Krabbe's disease
lactic acidemia
lacunar infarction
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
Lhermitte's sign
lipid storage disorder of CNS
liver disease
Lorenzo's oil
low birth weight
magnetic susceptibility
malformation, CNS, congenital
maple syrup urine disease
MELAS syndrome
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metronidazole
microhemorrhage, intracerebral
migraine
misdiagnosis
mitochondrial disease
monoamines
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, volumetry
multiple sclerosis
multiple sclerosis, asymptomatic
multiple sclerosis, chronic progressive
multiple sclerosis, clinical patterns
multiple sclerosis, conjugal
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, etiology of
multiple sclerosis, familial
multiple sclerosis, linoleic acid in
multiple sclerosis, misdiagnosis
multiple sclerosis, parental transmission
multiple sclerosis, pathogenesis
multiple sclerosis, prognosis
multiple sclerosis, risk factors for
multiple sclerosis, spinal form
multiple sclerosis, treatment of
muscle biopsy
myelin basic protein gene
myelinolysis, extrapontine
myelitis
myelitis, longitudinal
myelitis, transverse
myelomalacia
myelopathy
myelopathy, chronic progressive
myocardial infarction
myoclonus
mysoline
nausea and vomiting
neurochemistry
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuropathology
neuropathy
neuropathy, peripheral
neurotransmitter
norepinephrine
Notch3 gene
nystagmus
obsessive-compulsive disorder
occipital lobe, infarction
occipital lobe, lesion of
old age, neurology of
optic atrophy
optic atrophy, bilateral
optic atrophy, hereditary
optic nerve, hypoplasia of
optic neuritis
optic neuritis, bilateral
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
palatal myoclonus
palilalia
paraparesis
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paratrigeminal syndrome
paresthesias
Parkinson disease
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
periventricular leukomalacia
phenylketonuria
phenylketonuria, adult onset
pimozide
pleocytosis of cerebrospinal fluid
poison, neurologic problems with
polymerase chain reaction
pons, lesion of
posterior cerebral artery territory infarction
posterior leukoencephalopathy syndrome
premature infant
prevention of neurologic disorders
primary lateral sclerosis
prognosis
propranolol
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiation therapy, stereotactic
ragged-red fibers
Red flags
regional enteritis
renal stones
retrovirus
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
risk factors
Rosenthal fibers
Sandhoff's disease
Schilder's disease
scotoma
scotoma, central
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
smell
spasticity
spasticity, treatment of
speech disorder
speech, loss of
spinal cord
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spontaneous remission
steroid therapy, CNS treatment and complications with
stimulation, deep brain
symmetric brain lesions
systemic lupus erythematosus
tardive dyskinesia
taste
Tay-Sachs disease
temporal lobe, lesion, bilateral
thalamic tumors
thalamic tumors, bilateral
thalamotomy
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
thyrotoxicosis
tic
tinnitus
tongue, impaired movements of
top of the basilar syndrome
torticollis
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, jaw
tremor, leg
tremor, rubral
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
twins
ulcerative colitis
uremia
urinary frequency
urinary incontinence
urinary urgency
vasculitides
vasculopathy
vasospasm, cerebral
vertigo
vertigo, episodic
very long chain fatty acids
viral infection
viral infection, CNS
vision loss, sequential
visual acuity, decreased
visual evoked response
visual loss
visual loss, progressive
visual loss, sudden
visual loss, transient
walking, difficulty with
water channel antibodies
weakness
Wernicke's encephalopathy
white matter disease
workup
Showing articles 2050 to 2100 of 5493 << Previous Next >>

Clinical Pathological Conference, Scleroderma, Spastic Paraparesis & Chronic Myelogenous Leukemia
Prov. VAH, Dec. 12, 77., Finelli,P.F., 1850

Diabetes Insipidus As A First Manifestation In Multiple Sclerosis
, Thouvenot, E.,et al,

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

Disseminated Brain Infarcts Associated with Uterine Myoma
Stroke 57:e61-e62, Elbischger,J.,et al, 2026

Peripheral Neuropathy, A Review
JAMA 335:255-266, Mauermann,M.L. & Staff,N.P., 2026

Clinicopathologic Conference, Lyme Neuroborreliosis and Coinfection with Babesia Microti
NEJM 394:383-391, Case 3-2026, 2026

Treatment for Brain Metastases with Stereotactic Radiation vs Hippocampal-Avoidance Whole Brain Radiation, A Randomzid Clinical Trial
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Secondary Prevention after Ischemic Stroke
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A 69-Year Old Man With Rapid Cognitive Decline and Abnormal Movements
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Neurosyphilis with Abnormal in the Bilateral Pons and Multifocal Cranial Nerve Enhancement
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Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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A 55-Year-Old Man with Rapidly Progressive Weakness and Numbness
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Cerebral Syphilitic Vasculitis Presenting with Recurrent Stroke
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Niemann-Pick Type C Disease
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Bilateral Posterior Limb Internal Capsule T2 Hyperintensity and Severe Cerebellar Atrophy in 2 Lifelong Friends
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Ribbon-Like Sign in Convexity Subarachnoid Hemorrhage
Ann Neurol 99:881-882, Liu,S-X.,et al, 2026

A 41-Year-Old Man Presenting with Right Foot Tingling
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A 52-Year Old Man with Acute-Onset Blindness
Neurol 106:e214827, Brown,A.M.,et al, 2026

A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
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Validation of the Boston Criteria Version 2.0 for Cerebral Amyloid Angiopathy in Patients Presenting with Intracerebral Hemorrhage
Neurol 104:e213460, Downes,M.H.,et al, 2025

Clinicopathologic Conference, Diffuse Meningeal Melanomatosis
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Recurrent Ischemic Strokes Due to Os Odontoideum
Ann Neurol 98:1315-1317, Wang,J.,et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
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A 56-Year-Old Woman with Right-Sided Weakness and Recurrent MRI Lesions
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Multivessel Cerebral Occlusion in Noonan Syndrome
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A 24-Year-Old Man With Persistent Spontaneous Dizziness
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Neuropathologic Changes in People with Essential Tremor With Dementia
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Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
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A Woman with Subacute Progression of Distal Upper Extremity Weakness
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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Melas Syndrome
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Anti-NMDAR Encephalitis Triggered by EBV and HSV-1
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Rocky Mountain Spotted Fever Encephalitis and "Starry Sky" Pattern on MRI, A Case Report
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Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
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A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
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Bilaterally Symmetrical Globus Pallidus Infarction
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A 32 Year-Old Woman with Recurrent Intracerebral Hemorrhages
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A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
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Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

Submaxiomal Angioplasty for Severe Intracranial Atherosclerotic Stenosis":Benefit of Revascularization at Last
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"Innumerable" lesion burden on brain MRI - a diagnostic approach
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Vertebrobasilart Dolichoectasia Presenting with Multiple Cranial Nerve Involvement
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
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Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
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A 9-Year-Old Girl with CNS Immune Dysregulation
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Infantile Epileptic Spasms Syndrome (West Syndrome)
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AAV9-Mediated Gene Therapy for Infantile-Onset Pompes Disease
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Collaboration on the Optimal Timing of Anticoagulation after Ischaemic Stroke and Atrial Fibrillation:A Systematic Review and Prospective Individual Participant Data Meta-Analysis of Randomised Controlled Trials (CATALYST)
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Showing articles 2050 to 2100 of 5493 << Previous Next >>