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Differential
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abscess, intracerebral

abscess, intracranial

abscess, vertebral

accomodation, abnormal

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acute disseminated encephalomyelitis

adolescent medicine

advances in neurology

adverse drug reaction

agnosia, tactile

alcohol intolerance

alcohol intoxication

alternating rapid movement

alternating rapid movement, impaired

amaurosis fugax

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anemia, hemolytic

anemia, megaloblastic

anesthesia, general

aneurysm, abdominal aortic

aneurysm, intracranial, screening for

angiography, cerebral

angiotensin-converting enzyme, inhibitors

ankle reflex, absent

ankle, swelling of

anterior horn cell disease

anterior tibial muscle weakness

anti citrullinated antibody

antibiotic prophylaxis

anticoagulant, treatment in CVD

anticonvulsants

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiviral agents

apraxia, constructional

arrhythmia, cardiac

arterial dissection

arterial dissection, carotid

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, pulmonary

arthrogryposis multiplex

ascending paralysis

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atrial fibrillation

atrial paralysis

atrioventricular block

attention deficit disorder with hyperactivity

autoimmune disease

automobile accidents

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

B 12 deficiency

bacterial infection

Balint's syndrome

basal ganglia, calcification of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavioral disorder

Bergmann's gliosis

biopterin deficiency

blinking, reduced

bone density, increased

bone marrow suppression

bone marrow transplantation

border zone infarct

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

brachial neuritis

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

burning paresthesia

calcification, intracranial

calf hypertrophy

caloric testing

cardiovascular disease

carotid artery atherosclerosis

carotid artery disease

carotid artery occlusion, intracranial

carotid artery stenosis

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, abscess, cerebral

CAT scan, chest

CAT scan, emission, abnormal

CAT scan, myelogram with

CAT scan, ring sign

celiac disease, adult

central cord syndrome

central core disease

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hypoplasia

cerebellar lesion

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral embolism, carotid origin

cerebral infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, young adult

ceruloplasmin, serum

cervical myelopathy

cervical spine abnormality

cervical spondylosis

Charcot-Marie-Tooth

cheiralgia paresthetica

chest x-ray, abnormal

cholesterol, HDL

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

cognition, slowed

cogwheel rigidty

coin lesion on chest X-ray

cold hands sign

collagen vascular disease

collateral circulation

compression fracture

compression neuropathy

conduction block

congenital deformities

congenital heart disease

congenital malformation

congestive heart failure

contractures, joint

contraindications

controversies in neurology

convergence, impaired

cornea, abnormal

Cornelia de Lange syndrome

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, thinning

cortical dysplasia, focal

cortical hand knob

cortical hand knob infarct

cortical infarction

cortical infarction, small

cortical topography

cortical vein thrombosis

cortical wrist drop

costoclavicular syndrome

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

Craniosynostosis

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

Creutzfeldt-Jakob disease, genetic

cryopyrin-associated periodic syndrome

cyclophosphamide

cyst, perineural

Dawson's fingers

deep gray nuclei

dementia, familial

dementia, frontotemporal

dementia, rapidly progressive

demyelinating disease

denervation of muscle

dental procedure, neurologic complications with

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diamond on quadriceps

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digits, abnormal

digits, shortened

diplegia, brachial

disability rating scale, neurological

disability, neurological

disc space infection

disc space narrowing

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

diurnal variation

dopa responsive dystonia

dural sinus thrombosis

dysdiadochokinesia

dysostosis multiplex

dysplasia of C.N.S.

dystonia, children

dystonia, focal

dystonia, treatment of

dystrophic calcification

electrical sensation

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, activation procedures

embolism, paradoxical

embolism, septic

Emery-Dreifuss muscular dystrophy

emotional lability

empyema, epidural-spinal

encephalomyelitis

encephalopathy, progressive

endocarditis, neurologic manifestations with

endocarditis, prophylaxis

endocarditis, subacute bacterial

endocarditis, treatment of

endovascular therapy

entrapment neuropathy

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic neurologic deficits

epistaxis, recurrent

erythema migrans

esophageal reflux

esophageal varices

evoked potentials

exome sequencing

eye movement, disorders of

eyebrows, abnormal

face, numbness of

facial appearance, abnormal

facial nerve palsy

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

feeding disorder

fetal movements, reduced

fibrinolytic agents, contraindications

fine motor function, impaired

finger nose finger test

finger numbness

finger swelling

finger weakness

fingernails, abnormal

fingernails, white

fingers, abnormal

fistula, arterio-venous

fistula, arterio-venous, pulmonary

folic acid deficiency

fracture, long bone

Friedreich's ataxia

frontotemporal dementia, behavioral variant

gait, festinating

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastroenteritis

gastrointestinal bleeding

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

girdle sensation

glutamic acid decarboxylase, antibody

Gowers maneuver

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Hallgren's syndrome

handcuff neuropathy

headache, positional

headache, progressive

heart block, complete

heavy metal intoxication

heel-knee-shin test

hematocrit, neurologic complications with elevation of

hematuria, gross

hematuria, microscopic

hemianopia, homonymous

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herniated disc, central

herniated disc, cervical

high arched feet

histochemistry of muscle

Horner's syndrome

human immunodeficiency virus type 1

human immunodeficiency virus type 1, false positive

human immunodeficiency virus type 2

Hurler's syndrome

hyperamylasemia

hyperhidrosis, palmar

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hypertensive crisis

hypertensive encephalopathy

hypoglycorrhachia

hypomyelination

hypoproteinemia

hypoprothrombinemia

hypothalamus, damage to

hypothalamus, lesion of

hypotonia, infants

imbalance, postural

immune reconstitution inflammatory syndrome

immunoelectrophoresis, serum

immunohistochemistry

immunosuppression

immunosuppressive agents

imperforate anus

implantable cardioverter defibrillator

inclusion body myositis

infection, recurrent

influenza A virus

influenza B virus

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia, unilateral

interstitial pulmonary fibrosis

intestinal biopsy

intracerebral hemorrhage

intracerebral hemorrhage, young adult

intracranial hypertension, benign

intracranial pressure, increased

intrinsic hand muscles

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaw contractures

jaw jerk, abnormal

joint hypermobility

juvenile distal and segmental muscular atrophy

Kayser-Fleischer ring

Kearns-Sayre syndrome

kinesia paradoxica

Krabbe's disease

kyphoscoliosis, neurologic causes of

labyrinth, disorder of

labyrinthitis, acute

lactic dehydrogenase(LDH)

Laurence-Moon-Bardet-Biedl syndrome

leg weakness, bilateral

lens, dislocation of

leukoencephalopathy, differential diagnosis

Lewy body disease, diffuse

Lhermitte's sign

life expectancy

life support, withdrawal of

limb-girdle weakness

liver function enzymes

liver transplantation

low birth weight

lymphadenopathy

lymphocytic interstitial pneumonitis

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malabsorption syndrome

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, screening for

malformation, Vein of Galen

malignant hyperpyrexia

malignant hypertension

marche a petits pas

Marfan syndrome

marfanoid skeletal abnormalities

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, chronic

meningitis, CSF cell count-normal

meningoencephalitis

mental retardation

mental status, abnormal

methylmalonic acid, serum

microangiopathy, brain

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

mitochondrial disease

mitral valve prolapse

molecular genetics

monoclonal gammopathy

mononeuropathy multiplex

monoparesis, focal

motor neuron disease

movement disorder

movement disorder, extrapyramidal

moyamoya, adult

MRI, angiography

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, punctate pattern

MRI, spinal cord

MRI, T1 weighted fat suppression

MRI, venography

mucopolysaccharidoses

multiple myeloma

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle spasm, paraspinal

muscle strength, testing

muscle tenderness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, congenital, Ullrich

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, familial incidence of

myasthenic syndrome

mycotic aneurysm

myeloma, osteosclerotic

myeloneuropathy

myelopathy, chronic progressive

myocardial biopsy

myocardial infarction

myoclonic jerks

myopathy, distal

myopathy, distal, vacuolar

myopathy, quadriceps

myopathy, vacuolar

myositis ossificans, progressive

myositis, acute of childhood

myositis, ocular

myositis, post infectious

myotonia dystrophica

nausea and vomiting

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve hypertrophy

neural tube defect

neuritis, heavy metals causing

neurocutaneous disease

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuronal migration disorder

neuronopathy, sensory

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

neuropathy, vasculitic, systemic

numb clumsy hands syndrome

numbness, extremity

nystagmus, direction fixed

nystagmus, rotary

nystagmus, spontaneous

occupational neurologic disorders

occupational neuropathies

ocular myopathy

oculodentodigital dysplasia

old age, neurology of

opportunistic infection

opportunistic infection, CNS

optic atrophy, bilateral

optic neuropathy

orbit, lesions of

osteolytic lesion, causes of

osteomyelitis, spinal

pacemaker, cardiac-transvenous

pain, abdominal

Pallister-Hall syndrome

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraproteinemia

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinsonism syndrome

paroxysmal nonkinesigenic dyskinesia

patient information and support

pectus excavatum

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

personality change

photosensitivity, skin

physical therapy

pigmentary retinopathy

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pleural effusion

polycythemia, secondary

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy, familial

pons, lesion of

portal caval shunt

position sensation, abnormal

positive sharp waves

posterior column disease

posterior cortical atrophy

posterior fossa

posterior fossa, lesion of

postural abnormality

precentral gyrus

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary intracranial hypotension

prisoners of war, neurologic complications in

progressive multifocal leucoencephalopathy

progressive neurologic disorder

prolactin, elevated

proprioception, abnormal

proximal muscle atrophy

pseudohypertrophy

pseudomedian nerve palsy

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoretinitis pigmentosa

pseudoulnar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, unilateral

pulmonary infiltrates

pupil, ectopic-congenital

pure motor stroke

pursuit eye movements, abnormal

pyramidal tract dysfunction

radial nerve, palsy of

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Raynaud's phenomenon

real-time quaking-induced conversion

recruitment, reduced

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

remote effect of cancer on the nervous system

renal failure, acute

renal tubular acidosis

repetitive nerve stimulation

respiratory failure

respiratory tract infection

reticulum cell sarcoma

retinal detachment

retinitis pigmentosa

Rett's syndrome

rhabdomyosarcoma

rheumatoid arthritis

rheumatoid arthritis factor(R.A.factor)

rheumatoid arthritis, neurologic complications of

riboflavin transporter deficiency

rigid spine syndrome

rippling muscle disease

Rolandic artery

root lesion, nerve

saccadic eye movements, abnormal

sarcoglycanopathy

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sedimentation rate, elevated

seizure, children

seizure, precipitating factors

seizure, stimulus sensitive

seizure, treatment of

sensorimotor stroke

sensorineural hearing loss

sensory loss, asymmetric

sensory loss, cortical

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing, quantitative

serologic testing

serologic testing, false negative

shoulder, numbness

shoulder, pain in

simultanagnosia

single photon emission computed tomography

Sjogren's syndrome

skin, discoloration

skin, hyperextensible

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

small vessel disease

sodium valproate

spastic diplegia

speech disorder

speech disorder, childhood

Spielmeyer Vogt syndrome

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, lesion of

spinal cord, vascular malformation of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 7

spirochete infection

splenium of corpus callosum

splinter hemorrhages

spontaneous muscle activity

spontaneous remission

sports medicine, neurology of

square wave jerks

startle myoclonus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stiff man syndrome

stooped posture

strokelike episodes

subarachnoid hemorrhage

subcortical U fibers

superior sagittal sinus thrombosis

swallow evaluation

sweating, abnormality of

symmetric brain lesions

sympathetic block

systemic illness

tandem gait, ataxic

Tangier's disease

teeth, abnormal

telangiectases, retinal

thalamus, lesion of-bilateral

thoracic outlet syndromes

thrombocytopenia

tongue, fasciculations of

tongue, swelling

toxic encephalopathy

toxic oil syndrome

toxoplasmosis, CNS

transient ischemic attack

travel, foreign

treatment of neurologic disorder

tremor, intention

tremor, postural

tremor, resting

trigeminal nerve, lesion of

trigeminal neuropathy

trinucleotide repeats

type 1 muscle fiber

tyrosine hydroxylase deficiency

ulcers, fingertip

ulnar nerve, compression of

ulnar neuropathy

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

Usher's syndrome

vertebral erosion

vibratory sensation

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual loss, progressive

visuospatial disturbance

vitamin deficiency

voice, abnormality of

Walker-Warburg syndrome

walking, delayed

walking, difficulty with

weakness, congenital

weakness, generalized

weakness, progressive

weakness, proximal

white matter disease

wide based gait

winging of scapula

word-finding difficulty

WORLD spelling test

x-linked mental retardation

x-ray, cervical spine

Showing articles 100 to 150 of 13433 << Previous Next >>

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Clinicopath. Conference
Acquired Immunodeficiency Syndrome, Rhabdomyosarcoma, with Extensive Metastases, Case 9-1986, NEJM 3, 4:620,1986., 1986

Vertigo and Dizziness
In Diseases of the Nervous System, Asbury, A. K. , et al, W B Saunders, p. 561, Brandt,T., 1986

Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
Am J Med 77:86-92, Press,O.L.W.,et al, 1984

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Polyneuropathy, Skin Hyperpigmentation, Edema, & Hypertrichosis in Localized Osteosclerotic Myeloma
Neurol 27:675, Iwashita,H.,et al, 1977

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Neuro Complica of Coeliac Disease & Trop Sprue, Neurology of GI Disease
1974, Major Problems in Neurology V-3, W. B. Saunders Co, Ltd., Pallis,C.A.&Lewis,P.D., 1974

Neurologic Manifest. of Infective Endocarditis:A Review
Stroke 4:958, Greenlee,J.E.,et al, 1973

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Neurological Disorders Associated with Adult Celiac Disease
Brain 89:683, Cooke,W.T.,et al, 1966

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
Stroke 57:148-156, Mania-Paris,L.,et al, 2026

CT Perfusion Abnormality in Hypoglycemic Focal Neurological Deficits
Stroke 57:e6-e7, Mikito,S.,et al, 2026

A 41-Year-Old Man with Steroid-Responsive Hemiparesis
Neurol 106:e214088, Obaidi,Z.A.,et al, 2026

Reversible Leukoencephalopathy and Parkinsonism Due to CNS Involvement in Cryoglobulinemia
Neurol 106:e214622, German,A.,et al, 2026

Progressive Quadriparesis and Falls in a 66-Year-Old Man With Longstanding Human Immunodeficiency Virus
Neurol 106:e214621, Ong,B.A. & Carlson,A.K., 2026

Medical Management and Revascularization for Asymptomatic Carotid Stenosis
NEJM 394:219-231 296, Hrott,T.G.,et al, 2026

Clinicopathologic Conference, Disseminated Infection with Hypervirulent Klebsiella Pneumoniae
NEJM 394:282-294, Case 202026, 2026

Uncommon Faces of Disk Herniation: Atypical Imaging Presentations and Mimics
AJNR 47:244-251, Galante,M-J.,et al, 2026

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

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

Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
AJNR 47:513-520, Bruen,R.,et al, 2026

Mucormycosis
NEJM 394:684-698, Kontoyiannia,D.P. & Walsh, T.J., 2026

Neurosyphilis with Abnormal in the Bilateral Pons and Multifocal Cranial Nerve Enhancement
Ann Neurol 99:283-284, Zhang,Y.,et al, 2026

Miliary Perivascular Space Enhancement in Sepsis-Associated Posterior Reversible Encephalopathy Syndrome
Neurol 106:e214654, Hutchinson,V.A.,et al, 2026

Unilateral Primary Angiitis of the Central Nervous System: A Rare and Under-Recognized Entity
AJNR 47:589-595, Rai,P.,et al, 2026

Brain CT for Diagnosis of Intracranial Disease in Ambulatory Patients with Cancer:Assessment of the Diagnostic Value of Scanning without Contrast Prior to With Contrast
AJNR 47:694-698, Wang,E.,et al, 2026

Zorevunersen in Children and Adolescents with Dravet Syndrome
NEJM 394:969-982, Laux,L.,et al, 2026

Niemann-Pick Type C Disease
www.UpToDate.com, Nov, Schiffmann, R., 2026

Association of Changes in Activity Patterns with Brain Atrophy and Disability Progression in People with Multiple Sclerosis
Neurol 106:e214678, e214742, Fitzgerald,K.C.,et al, 2026

Using Susceptibility-Based Imaging in Highly Active Late-Onset Multiple Sclerosis
Neurol 106:e214794, Sosa,S.M.,et al, 2026

A 49-Year-Old Man with Meningoencephalitis and Persistent Altered Mental Status
Neurol 106:e214777, Hariswar,P.T.,et al, 2026

Polymyalgia Rheumatica
NEJM 394:1097-1109, Dejaco,C.,et al, 2026

Multiple Giant Perivascular Spaces in Hypomelanosis of Ito
Ann Neurol 99:825-826, Chammas,D.E.,etal, 2026

Iatrogenic Cerebral Amyloid Angiopathy after Cardiac Surgery, Two Case Reports
Neurol 106:e214819, Brunet de Courssou,J-B.,et al, 2026

Clinical Manifestations of Primary CNS T-Cell Lymphoma, Retrospective Study of Histopathologic, Molecular, and Neuroimaging Fetures
Neurol 106:e24744, Muller,K.J.,et al, 2026

Showing articles 100 to 150 of 13433 << Previous Next >>