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abdominal reflex, absent

abducens nerve paralysis

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

Addison's disease

adrenoleukodystrophy

adrenomyeloneuropathy

adult polyglucosan body disease

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

alcohol injection

alcohol intolerance

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alternating rapid movement

amyloid plaques

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

angiography, spinal

ankle reflex, absent

aqueduct of Sylvius, stenosis

aqueductal stenosis

Arnold Chiari malformation

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, generalized

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal spheroid

azidodeoxythymidine

B 12 deficiency

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

behavioral disorder

Behcet's syndrome

benign essential tremor

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

bladder dysfunction

brachial plexus neuropathy

brain biopsy, negative

brain biopsy, stereotaxic

brainstem, dysfunction

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

burning paresthesia

calcification, intracranial

carotid angiogram

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, spine

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, 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

chorea, causes of

chorea, familial

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

cold hands sign

concentration, impaired

congenital infection, CNS

controversies in neurology

corpus callosum, atrophy of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

crossed adductor reflex

crying, pathologic

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

deep gray nuclei

degenerative cervical myelopathy

degenerative diseases of CNS

delay in diagnosis

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diagnostic criteria

diarrhea, bloody

differential diagnosis

diplegia, spastic cerebral

disability, neurological

distal muscle weakness

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

dystonia, focal

dystonia, painful

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electroencephalogram, abnormalities of

electron microscopy

emotional lability

encephalitis lethargica

encephalitis, viral

encephalomalacia

endovascular therapy

enzyme, muscle disease

epidemiology of neurology

epileptic encephalopathy

evoked potentials

exome sequencing

facial nerve palsy

facial nerve palsy, bilateral

facial nerve palsy, recurrent

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

fatty acid, elevated plasma content

fine motor function, impaired

finger nose finger test

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

fluorescent treponema antibody absorption(FTA-ABS)

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe, pathologic signs of

fundus, abnormality of

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

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

growth retardation

Guillain Barre syndrome

Hallervorden Spatz disease

headache, intermittent

heel-knee-shin test

hemangioma, vertebral

hepatic failure

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

herniated disc, cervical

high arched feet

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, non-communicating(obstructive)

hyperammonemic encephalopathy

hyperhomocysteinemia

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

immunosuppression

inborn errors of metabolism

inclusion bodies

incontinence, fecal

intellectual deficit

intellectual deterioration

intrinsic hand muscles, wasting of

iodine deficiency

Jamaica ginger paralysis

jaw jerk, abnormal

lactic acidemia

laminectomy, cervical

laughing, pathologic

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

life expectancy

locked-in syndrome

lymphoma involving CNS

lymphomatoid granulomatosis

malformation, vascular

marche a petits pas

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

mitochondrial disease

molecular genetics

mononeuritis multiplex

motor neuron disease

movement disorder

movement disorder, extrapyramidal

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, T1 weighted high signal foci

multinucleated giant cell

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle stiffness

muscle weakness

muscle weakness, proximal

myasthenia gravis

myeloneuropathy

myelopathy, chronic progressive

myelopathy, hepatic

myelopathy, vacuolar

myoclonus, epilepsy

myopathy, vacuolar

myositis, ocular

myxedema, neurologic manifestations of

Native Americans

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-treatment of

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, brain

neuropathy, peripheral

neuropathy, sensory

next-generation sequencing

numb clumsy hands syndrome

numbness, extremity

nystagmus, dissociated

nystagmus, rotary

nystagmus, vertical

oculogyric crisis

ophthalmoplegia

ophthalmoplegia, progressive external

optic neuropathy

optical coherence tomography

oral ulcerations

orthostatic hypotension

pain, abdominal

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, spastic

paraparesis, spastic, tropical

paraspinal muscle

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

pernicious anemia

personality change

pleocytosis of cerebrospinal fluid

poison, organophosphate

polyglucosan body

polyglucosan body disease

polymerase chain reaction

pons, lesion of

portal caval shunt

posterior column disease

postural abnormality

practice guidelines

precipitating factors

primary lateral sclerosis

prisoners of war, neurologic complications in

progressive neurologic disorder

proprioception, abnormal

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

radiation therapy, CNS treatment and complications with

Raynaud's phenomenon

regional enteritis

release phenomena

respiratory dyskinesias

reticulum cell sarcoma

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

risk-benefit assessment

Rosenthal fibers

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

sclerae, hyperpigmented

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

sensorineural hearing loss

sensory loss, cutaneous

serologic testing

serologic testing of cerebrospinal fluid

shunt procedure, ventricular

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

slow virus infection of CNS

solitary scerlosis

somatosensory evoked potentials

spastic diplegia

spastic dysphonia

spastic paraplegia, type 11

spastic paraplegia, type 7

spasticity, treatment of

speech disorder

speech disorder, childhood

speech, loss of

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

status epilepticus

stereotyped behavior

steroid therapy, CNS treatment and complications with

stiff man syndrome

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

substantia nigra

superior cerebellar peduncle

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

systemic illness

teeth, abnormal

teeth, number of in infants

tendon, enlarged

thrombocytopenia

tone, muscle, increased

tongue, enlarged

tongue, impaired movements of

tonic foot response

tonsillar herniation of cerebellum

toxins, nervous system

transient ischemic attack

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, postural

tremor, treatment of

trinucleotide repeats

ulcerative colitis

ulcers, fingertip

upgaze, paralysis of

urea-cycle enzymopathies

urinary frequency

urinary incontinence

urinary urgency

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral isolation

visual acuity, decreased

visual evoked response

vitamin deficiency

walking, difficulty with

weakness, progressive

weakness, proximal

Western immunoblot test

white matter disease

wide based gait

word-finding difficulty

xanthoma, tendon

Showing articles 200 to 250 of 2301 << Previous Next >>

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

Balance, Falls, and Hearing Loss: Is It Time for a Paradigm Shift?
JAMA Otolaryngol Head Neck Surg doi:10.1001/JAMAoto.2020.0415, Lubetzky, A.V., 2020

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Diagnosis and Treatment of Parkinson Disease
JAMA 323:548-560, Armstrong, M.J. & Okun, M.S., 2020

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

Spinal Dural Arteriovernous Fistula Presented with Rapidly Progressive Myelopathy, Longitudinally Extensive Spinal Cord Lesion, Pleocytosis with Polymorphonuclear Predominance, and Decreased Cerebrospinal fluid Glucose Levels:A Case Report
Rinsho Shinkeigaku 60:699-705, Kitazaki,Y.,et al, 2020

An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
Cureus DOI:10.7759/cureus,8608, Gupta,A. & Dhingra,A., 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Clinical Features of Syphilitic Myelitis with Longitudinally Extensive Myelopathy on Spinal Magnetic Resonance Imaging
World J Clin Cases 7:1282-1290, Yuang,J-L.,et al, 2019

Acute Paraplegia in a Healthy Child
BMJ 367:L6257, Haque, A.K.M.,et al, 2019

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

Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
NEJM 381:47-54, Mandel-Brehm, C.,et al, 2019

Suicide and Suicide Attempts after Subthalamic Nucleus Stimulation in Parkinson Disease
Neurol 93:e97-e105, Giannini, G.,et al, 2019

Vestibular Migraine
BMJ 366:L4213, Li, V.,et al, 2019

Cervical Synovial Cyst Leading to Spinal Cord Compression
Neurol 93:e318-e319, Urits, I.,et al, 2019

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

A 78-year-old Man with a Gait Disorder
Neurol 93:223-227, Saucedo, M.,et al, 2019

Peripheral Neuropathy Associated with Silver Toxicity
Neurol 92:481-483, Naddaf, E.,et al, 2019

A 54-year-old man with Dyspnea and Muscle Weakness
Neurol 92:e1136-e1140, Chertcoff, A.,et al, 2019

Serum NFL discriminates Parkinson Disease from Atypical Parkinsonisms
Neurol 92:e1479-e1486, Marques, T.M.,et al, 2019

Placebo-Controlled, Randomized, Double-Blind Study of IncobotulinumtoxinA for Sialorrhea
Neurol 92:e1982-e1991, Jost, W.H.,et al, 2019

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Stridor in Multiple System Atrophy
Neurol 93:630-639, Cortelli, P.,et al, 2019

A 55-Year-Old Woman Presenting with Ataxia and Numbness 1 Year After Ileum Resection
Neurol 93:675-679, Cassano, V.,et al, 2019

A Case of Progressive Myelopathy in a Middle-Aged Woman
JAMA Neurol 76:1253-1254, Muccilli, A.,et al, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Hand Posture as Localizing Sign in Adult Focal Epileptic Seizures
Ann Neurol 86:793-800, Ferando, I.,et al, 2019

Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
JAMA Neurol 76:1397-1398, Gupta, S.,et al, 2019

Prolonged Microgravity Affects Human Brain Structure and Function
AJNR 40:1878-1885, Roberts,D.R.,et al, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

When to Start Levodopa Therapy for Parkinsons Disease
NEJM 380:389-390, Bressman, S. & Saunders-Pullman, R., 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

MR Imaging of the Brain in Neurologic Wilson Disease
AJNR 40:178-183, Yu, X.-E.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Showing articles 200 to 250 of 2301 << Previous Next >>