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Differential
(Click to cross reference)

abscess, intracerebral

acanthocytosis

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

advances in neurology

adverse drug reaction

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

Alzheimer's disease

Alzheimer's disease, diagnosis of

Alzheimer's disease, familial

Alzheimer's disease, pathogenesis

Alzheimer's disease, preclinical

Alzheimer's disease, risk factors in

Alzheimer's disease, treatment of

Alzheimer's disease, visual variant

anterior horn cell disease

antibiotic prophylaxis

anticholinesterase

anxiety

aortic valve, bicuspid

aortic valve, insufficiency

aortic valve, lesion of

aortic valve, stenosis

aphasia

aphasia, children

aphasia, progressive

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-sensory

apolipoprotein E

APP gene

apraxia

apraxia, constructional

arterial dissection, aorta

arteriopathy

arteriovenous malformation

arteriovenous malformation, pulmonary

ataxia telangiectasia

attention deficit disorder with hyperactivity

auditory and vestibular pathways

auditory evoked brainstem potentials

autism

autistic behavior

automatic implantable cardioverter-defibrillator

automobile accidents

autonomic dysfunction

Babinski sign

basal ganglia, calcification of

basal ganglia, infarction

basal ganglia, lesion of

behavioral disorder

Benedict's solution test

bicaudate index

bifid uvula

biologic markers

biotinidase deficiency

bladder dysfunction

bone marrow transplantation

brachial plexus

brachial plexus neuropathy

calcification, intracranial

calcification, muscle

calcium oxalate crystals

CAT scan, emission, abnormal

cataracts

caudate nucleus

caudate nucleus, atrophy

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, subcortical

cerebral palsy

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebral palsy, work up

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, cryptogenic

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonarterial territory

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease

cesarean section

Charcot-Marie-Tooth

cherry red spot

chest x-ray, abnormal

chromosomal abnormality

cisterna magna, enlarged

cisternogram, radionuclide

cleft palate

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

clubfoot as related to neurologic disease

compression neuropathy

compression neuropathy, recurrent

conduction block

confidentiality

congenital heart disease

congenital myasthenic syndromes

congestive heart failure

contraindications

controversies in neurology

corpus callosum, atrophy of

corpus callosum, lesion of

creatine phosphokinase(CPK)elevated

cryptorchidism

cyanosis

deafness

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, cerebrovascular disease causing

dementia, childhood

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, subcortical

demyelinating disease

denervation of muscle

depression

dermatoglyphics

descending paralysis

developmental abnormality of brain

developmental evaluation

developmental retardation

diabetes mellitus

diagnostic criteria

diarrhea

differential diagnosis

dilated aortic root

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

disability rating scale, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dysarthria-clumsy hand syndrome

echocardiogram, contrast

echocardiogram, transesophageal

echocardiogram, transthoracic

echolalia

edema, pedal

ejection fraction

ejection fraction, abnormal

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

electromyogram

electron microscopy

embolism

embolism, paradoxical

emergencies, neurologic

Emery-Dreifuss muscular dystrophy

encephalopathy

endocarditis

endocarditis, acute bacterial

endocarditis, infectious

endocarditis, prophylaxis

enophthalmous

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

executive dysfunction

exome sequencing

eye movement, disorders of

Fabry's disease

face, elongated

face, numbness of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

fibrinolytic agents, contraindications

fibroma, ungual

fine motor function, impaired

fistula, arterio-venous, pulmonary

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

fundus, abnormality of

gastrointestinal bleeding

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucose tolerance test, abnormal

granular osmiphilic material

hearing problems in children

hemianopia, homonymous

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hemorrhoids

hepatic failure

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

hydrocephalus

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hypertrophic cardiomyopathy

hyponatremia

hypopigmentation of skin

inborn errors of metabolism

inflexibility, mental

informed consent

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intrauterine infection

intrinsic hand muscles, wasting of

Jewish

joint hypermobility

karyotyping

karyotyping, cerebrospinal fluid

klippel feil syndrome

language disorder in adults

language disorders in children

L-dopa

L-dopa, drug interactions with and side effects of

lead poisoning

learning disability

learning disability, in children

leg weakness, bilateral

leucine-rich repeat kinase 2 gene

leukocyte enzyme abnormality

lid closure, weakness of

lipid storage disorder of CNS

locus ceruleus, lesion of

Lorenzo's oil

lymphangiomyomatosis

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular, cerebral

malignant hyperpyrexia

mania

manic-depressive

maple syrup urine disease

McLeod syndrome

median neuropathy

MELAS syndrome

memory, impairment of

meningioma

meningioma, familial

meningioma, multiple

meningitis, carcinomatous

mental retardation

mental retardation, familial

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

metachromatic leukodystrophy, juvenile

microangiopathy, brain

microcephaly

micrognathia

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

midline defect in children

migraine

migratory lesion pattern

mild cognitive impairment

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

molecular genetics

mongolism

mononeuropathy

mononeuropathy multiplex

mononeuropathy, children

mortality

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, negative

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle spasm

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

mutism

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, familial incidence of

myelin protein zero gene

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplasm, primary of CNS-familial occurrence

nephrocalcinosis

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

neurofibromatosis 2, presymptomatic

neurogenic bladder

neurogenic vs.myopathic atrophy

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular junction

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neurosis

newborn, evaluation of

next-generation sequencing

night blindness

nigrostriatal pathway

occipital lobe, infarction

ophthalmoplegia

optic atrophy

orthostatic hypotension

ovarian insufficiency

oxalosis, primary

pacemaker, cardiac-transvenous

pain

pain, foot

pain, increased response

pain, wrist

palatopharyngeal incompetence

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

paresthesias

paresthesias, feet

paresthesias, lower extremity

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, familial

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

patient information and support

photosensitivity, skin

PICU

Pittsburgh Compound B

platelet inhibiting drugs

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy

positional head-hanging test

posterior cerebral artery territory infarction

posterior cortical atrophy

practice guidelines

preclinical

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

proteinuria

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pupil, dilated and fixed, bilateral

pyramidal

pyramidal tract dysfunction

reading disorder, acquired

reversible neurologic disorder

review article

RFLPs

rhabdomyolysis

rhabdomyosarcoma of heart

rigidity

risk factors

risk-benefit assessment

saccadic eye movements, abnormal

Sandhoff's disease

scoliosis

scoliosis, neurologic association with

screening

seizure

seizure, advice to parents and teachers regarding

seizure, familial

seizure, psychosocial aspects of

seizure, treatment of

self-mutilation

senile plaques

sensorineural hearing loss

sensory loss

sensory loss, truncal

sensory nerve action potentials

shoulder-girdle wasting

simian crease

simultanagnosia

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

slit lamp examination

small vessel disease

SMN1 gene

somatosensory evoked potentials

Southern immunoblot test

spastic ataxia

spasticity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

spina bifida

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar degeneration

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

spontaneous muscle activity

spontaneous remission

stimulation, deep brain

subthalamic nucleus deep brain stimulation

sudden death

suprascapular neuropathy

sural nerve

sweating, abnormality of

temporal lobe, lesion

temporal lobe, lesion, bilateral

term infant

testicular enlargement

thrombocytopenia

tinnitus

titubation

tomaculous neuropathy

tongue, fasciculations of

transient ischemic attack

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

tremor, thalamic stimulation for suppression of

trinucleotide repeats

tuberous sclerosis, screening for

ultrasonography, nerve

uremia

urinary incontinence

urine test for metabolic disorders

valvulopathy

varicose veins

vasculopathy

very long chain fatty acids

vestibulopathy

vibratory sensation, abnormal

visual field defect

visual impairment

visuospatial disturbance

vitamin E deficiency

voice, abnormality of

Von Hippel Lindau

Von Hippel Lindau, carrier

Von Hippel Lindau, screening protocol for

walking frame

walking, difficulty with

weakness

weakness, fatiguable

weakness, generalized

weakness, progressive

web sites

weight loss

wheelchair

whistle, inability to

white matter disease

whole genome sequencing

wide based gait

winging of scapula

Wolff-Parkinson-White syndrome

Wood's light

word-finding difficulty

workup

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

Showing articles 100 to 150 of 2129 << Previous Next >>

Neurological Findings in Patients with the Fragile-X Syndrome
JNNP 48:150-153, Finelli,P.F.,et al, 1985

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Familial Stroke Syndrome Associated with Mitral Valve Prolapse
Ann Neurol 7:130-134, Rice,G.P.A.,et al, 1980

Heterozygous Expression Of X-Linked Mental Retardation & X-chromosome Marker fra (X) (q27)
NEJM 303:662-664, Turner,G.,et al, 1980

Cytogentic Diagnosis Of Meningeal Carcinomatosis
NEJM 303:1479, Kristoffersson,U.,et al, 1980

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Neurol 29:880-881, Kuritzky,A.,et al, 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

Use of L-Dopa in the Detection of Presymptomatic Huntington's Chorea
NEJM 286:1332, Klawans,H.,et al, 1972

Presymptomatic Detection of Huntington's Chorea
BMJ 540, 1972 Sept., , 1972

Pediatric Neurology
Psych Annals 2:1, , 1972

Ethical & Social Issues in Screening for Genetic Disease-Screening for Genetic Disease-A Group Report
NEJM 286:1129, 1972, 286:1155972., , 1972

Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both
NEJM 274:384, Renuart,A., 1966

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

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

MELAS Presenting as Bilateral Symmetric Occipital and Temporal Cortices Lesions, A Case Report and Literature Review
Neurologist 30:75-79, Liu,Q.,et al, 2025

A 2-Year-Old Girl with Acute Encephalopathy After Febrile Systemic Illness
Neurol 105:e213970, Westendfortp,W.F.,et al, 2025

A 63-Year-Old Female Patient Presenting with Orthostatic Hypotension and Ataxia
Neurol 105:e213993, Shen,F.,et al, 2025

A 9-Year-Old Girl with CNS Immune Dysregulation
Neurol 105:e213999, Marefi,A.,et al, 2025

Infantile Epileptic Spasms Syndrome (West Syndrome)
Stat Pearls PMID:30725936, Smith,M.S.,et al, 2025

Adult-Onset Coats Plus, A Case of Leukoencephalopathy with Calcifications, a Tumefactive Brain Lesion, and a Presumed Autoimmune Disease
Neurol 105:e214124, Gerrao,C.,et al, 2025

Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
Neurol 105:e214099, Mizutani,H.,et al, 2025

Clinicopathologic Conference, Chagas Disease
NEJM 393:1216-1225, Case 27-2025, 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,et al, 2025

A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
Neurol 105:e214297, Chen,Z., et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
Neurol 104: e213682, Hayakawa,I.,et al, 2025

AAV9-Mediated Gene Therapy for Infantile-Onset Pompes Disease
NEJM 392:2438-2446, 2477, Ma,X.,et al, 2025

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

Reversible Cerebral Perfusion Abnormalities in Deep Cerebral Venous Thrombosis
Neurol 103:e210127, Wang,W. & Han,X., 2024

Tenecteplase for Stroke - Opening the Window?
NEJM 390:760-761, Leifer,D.,, 2024

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Showing articles 100 to 150 of 2129 << Previous Next >>