Neudle.com: atrophy hand

Differential
(Click to cross reference)

abdominal muscle paralysis

abductor pollicis brevis

abscess, vertebral

acanthocytosis

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acromicria

Addison's disease

adult polyglucosan body disease

advances in neurology

aggression

alcohol intoxication

alcohol, neurologic complications with

alcoholic polyneuropathy

alcoholism

algorithm

alien hand syndrome

alternating rapid movement

alveolar hypoventilation

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anatomy of

anemia

anemia, megaloblastic

anesthesia, general

Angelman syndrome

angiography, neurologic complications with

anisocoria

ankle reflex, absent

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti citrullinated antibody

anti mGluR1 encephalitis

anti Tr antibodies

anti Yo antibody

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants, untoward effects of

antithyroid antibodies

antiviral agents

aphasia

aphasia, progressive, primary

aphonia

applause sign

apraxia

apraxia of eye movements

apraxia, constructional

arterial dissection, carotid

arthralgia

arthrogryposis multiplex

ataxia telangiectasia

atlanto axial dislocation, congenital

atrioventricular block

atrophy, muscle

attention deficit disorder with hyperactivity

attention span

atypical

autoantibodies

autoimmune cerebellar ataxia

autoimmune disease

autonomic dysfunction

autoregulation, cerebral

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

behavior, combative

behavioral disorder

Bence Jones protein

benign essential tremor

biologic markers

BiPAP

bitemporal visual field defect

bone marrow suppression

bone marrow transplantation

border zone infarct

botulinum toxin

botulinum toxin, complications of

brachial neuritis

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

brainstem, neoplasms of

breast feeding

bruit

bruit, supraclavicular

bulbar palsy

bulbar palsy, progressive

calcification, intracranial

calf atrophy

calf hypertrophy

camptocormia

campylobacter infection

carcinoma

carcinoma of lung

carcinoma of ovary

cardiac catheterization, neurologic complications

cardiomegaly

cardiomyopathy

cardiovascular disease

caries

carotid artery atherosclerosis

carotid artery disease

carotid artery stenosis

carpal tunnel syndrome

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

cavernous sinus, syndrome

central core disease

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebellum

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, small, deep

cerebral ischemia

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, incidence of

cerebrovascular accident, location of

cerebrovascular accident, mimics

cheiralgia paresthetica

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

choroid plexus, abnormality of

chromosomal abnormality

chronic progressive external ophthalmoplegia

Chvostek sign

cimetidine

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

collagen vascular disease

coma

compartment syndrome

compartment syndrome, medial brachial fascial

complications

compression neuropathy

conduction block

confusion

confusional state, acute

congenital infection, CNS

congenital myopathy

congestive heart failure

corneal reflex, abnormal

corneal reflex, absent

corona radiata

corpus callosotomy

corpus callosum

corpus callosum, atrophy of

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, neoplasm of

corpus callosum, thinning

cortical hand knob

cortical hand knob infarct

cortical infarction

cortical infarction, small

cortical muscular atrophy

cortical topography

cortical wrist drop

cortical-basal ganglionic degeneration

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, weak

crying, pathologic

cryptococcal meningitis

cryptococcoma, cerebral

cryptorchidism

cultured skin fibroblasts

cytomegalovirus infection

cytomegalovirus infection, congenital

deafness

degenerative diseases of CNS

denervation of muscle

denervation potentials

dentate nuclei, lesion of

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

diarrhea

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diplegia, brachial

diplopia

disability, neurological

disc space infection

disc space narrowing

discitis

disconnection syndrome

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dizziness

dopa responsive dystonia

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze

drooling

drug abuse

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dystonia, post traumatic

dystonia, treatment of

dystrophic calcification

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electron microscopy

electrophoretic pattern, CSF

Emery-Dreifuss muscular dystrophy

emotional lability

empyema, epidural-spinal

encephalitis

encephalitis, autoimmune

encephalitis, episodic

encephalitis, human immunodeficiency virus type 1

encephalocele

encephalopathy

encephalopathy, progressive

enterovirus

enterovirus infection of CNS

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

ependymitis

epidemiology of neurology

episodic neurologic deficits

exercise-induced vascular symptoms

exome sequencing

exophthalmus

extremity, cold

eye movement, disorders of

eye, pain in

eyes, sunken

face, numbness of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

fetal movements, reduced

fetus

fever

fibrillations

fine motor function, impaired

finger flexor weakness

finger nose finger test

finger swelling

finger tapping

finger weakness

fingernails, abnormal

fracture, long bones, nerve injury with

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal lobe, behavior with disease of

frontal lobe, infarction

frontal lobe, lesion of

fungal infection, CNS

gammaglobulin therapy, intravenous

ganglion

Gantzer's muscle

gastrocnemius muscle weakness

gastroenteritis

gastrointestinal perforation

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genital hypoplasia

Gerstmann-Straussler-Scheinker disease

globus pallidus, lesion of

glycogen debranching enzyme deficiency

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

guanethidine

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, prognosis of

gumma

Guyon's canal

gynecomastia

Hallervorden Spatz disease

hallucination

hallucination, auditory

Hand-Schuller-Christian disease

heart block, complete

heart murmur

heavy metal intoxication

heel-knee-shin test

hemangioma

hemidiaphragm, paralysis of

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc

herniated disc, thoracic

herpes zoster

high arched feet

high arched palate

histamine-2 receptor blockers

histochemistry

histochemistry of muscle

Horner's syndrome

hospice

human immunodeficiency virus type 1

hyperhidrosis, palmar

hyperpigmentation of skin

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypopigmentation of skin

hyporeflexia

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypothalamus, lesion of

hypothyroidism

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

immunosuppressive agents

immunotherapy

impulsivity

inability to sit up

inability to stand on tiptoes

inattention

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

incoordination

infant, evaluation of

infantile tremor syndrome

intellectual deterioration

intelligence quotient

interosseous muscles

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles

intrinsic hand muscles, wasting of

introverted

iron, brain

islet cell tumor

Jakob-Creutzfeldt disease

jaundice

jaw jerk, abnormal

Jewish

juvenile distal and segmental muscular atrophy

Klinefelter's syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

laminectomy

laminectomy, lumbar

lateral cutaneous nerve of forearm

learning disability, in children

leg atrophy

leg numbness

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leprosy

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukopenia

level of consciousness, decreased

levitation

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

lipid storage disorder of CNS

liver disease

liver function enzymes

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lysosomal storage disease

Madonna facies

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

mania

Man-In-The-Barrel syndrome

marche a petits pas

Martin-Gruber anastamosis

masked facies

mastoid opacification

mechlorethamine

median nerve

median nerve, lesion of

median neuropathy

medical-legal aspects of neurology

medulla oblongata, neoplasm of

Mees lines

memory, defect of recent

memory, impairment of

meningeal enhancement

meninges

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, children

meningitis, factors influencing mortality in

meningitis, late neurologic sequelae in

meningitis, lymphomatous

meningitis, neurologic aspects and complications of

mental retardation

mental status, abnormal

merosin

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methotrexate

methylmalonic acid, serum

methylmalonic acidemia

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

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy

mononeuropathy, motor

motor neuron disease, juvenile form

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, high signal foci on

MRI, mass effect on

MRI, muscle

MRI, negative

MRI, peripheral nerve

MRI, skull bone changes

MRI, spinal cord

MRI, spine

MRI, T1 weighted fat suppression

MRS

mucopolysaccharidoses

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple sclerosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

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, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myelomalacia

myeloneuropathy

myelopathy

myelopathy, chronic progressive

myocardial biopsy

myocardial infarction

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myxedema, neurologic manifestations of

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, pituitary

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve grafting

nerve hypertrophy

nerve injury

nerve repair, end to end

nerve root enhancement

nerve root hypertrophy

neuritis

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory and motor

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, bicycle

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuroprotective agents

next-generation sequencing

numbness, generalized

nystagmus

nystagmus, rotary

obesity

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

orthopnea

orthostatic hypotension

osteomyelitis

osteomyelitis, spinal

osteoporosis

ovarian dysgenesis

pacemaker, cardiac-transvenous

paralysis, asymmetric

paraspinal muscle weakness

parietal lobe, lesion of

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

past pointing

pelvic mass

penguin silhouette sign

penicillamine

penis, small

percussion induced muscle contraction

pericardial effusion

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral blood smear, abnormal

periventricular leukomalacia

photosensitivity, skin

physical therapy

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

POEMS syndrome

POLR3B

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, familial

pons, atrophy

pons, lesion of

position sensation, abnormal

positional head-hanging test

positive sharp waves

posterior column disease

posterior fossa

posterior fossa, lesion of

posterior interosseous neuropathy

postoperative neurologic complications

postural abnormality

Prader-Labhart-Willi syndrome

precentral gyrus

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

primary aldosteronism

prisoners of war, neurologic complications in

prognosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

prolactin, elevated

pronator syndrome

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

pseudomedian nerve palsy

pseudomyotonia

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoulnar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

purple glove syndrome

purple hands

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

radial nerve, palsy of

radial pulse, unilateral decrease of

radiculopathy

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

reading disorder, acquired

recruitment

recruitment, reduced

recurrent

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

release phenomena

remote effect of cancer on the nervous system

renal failure

repetitive nerve stimulation

respirator

respiratory failure

respiratory tract infection

reverse split hand sign

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rippling muscle disease

rubella encephalitis, progressive

rubella virus

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis

sarcoidosis, CNS

scalenus anticus syndrome

sciatica

scissors gait

scleroderma

scleroderma, neurologic involvement with

scoliosis

scoliosis, neurologic association with

screening

sea-blue histiocytes

sedimentation rate

sedimentation rate, elevated

sensorineural hearing loss

sensory level

sensory loss

sensory loss, cortical

sensory loss, glove-stocking

sensory loss, patchy

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing, quantitative

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

short stature

shoulder, numbness

shoulder, pain in

shoulder, swelling of

shoulder-hand syndrome

shoveling

sinemet

single photon emission computed tomography

sinuses, diseases of

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

skull bone, erosion

sleep

sleep pathology and physiology

slit lamp examination

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spina bifida

spinal cord

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinocerebellar ataxia

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

spitting

splenium of corpus callosum

splenomegaly

spontaneous muscle activity

sports medicine, neurology of

staggering

standing difficulty

status epilepticus

stem cell transplantation

steppage gait

stereotyped behavior

steroid

steroid therapy, CNS treatment and complications with

stillbirth

stooped posture

storage disease of CNS

strabismus

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

stuttering

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subarachnoid hemorrhage

subclavian artery stenosis

sweating, abnormality of

swimming

symmetric brain lesions

sympathetic block

syphilis, neurologic complications with

teeth, number of in infants

temper tantrums

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of-bilateral

thallium poisoning

thermography

thoracic outlet syndromes

tongue, fasciculations of

tongue, protrusion of

torticollis, post traumatic

toxoplasmosis, CNS

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor, post traumatic

trigeminal nerve, abnormality of

trinucleotide repeats

tripping

Trousseau's sign

tuberculoma of CNS

tyrosine hydroxylase deficiency

ulcers, fingertip

ulnar nerve

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

urine test in toxic screen

urine, dark

vascular endothelial growth factor

vasculopathy

vegetarianism

ventricular enlargement

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision, blurred

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual loss

visual symptoms

visuospatial disturbance

voice, abnormality of

Volkmann's ischemia

walking frame

walking, delayed

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

web sites

weight loss

Werdnig-Hoffman disease

word-finding difficulty

workup

wrist drop

writing

X-linked bulbospinal neuronopathy

yelling

zinc

Showing articles 300 to 350 of 2843 << Previous Next >>

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022

Transocular Sonography in Acute Arterial Occlusions of the Eye in Elderly Patients
PlusOne doi.org/10.1371/journal.pone.0247072, Czihal, M.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

A 79-Year-Old Woman with Subacute Bilateral Visual Loss
Neurol 97:e1159-e1165, Rossi, S.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Nitromethane-Induced Acute Reversible Encephalopathy
Neurol 97:e1361-e1362, Palumbo, G.,et al, 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

A Middle-Aged Man with a History of Muscle Pain Presenting with Progressive Leukoencephalopathy and Subsequent Coma
Neurol 97:910-915, Jakobsson, A.S.,et al, 2021

The First Examination of Diagnostic Performance of Automated Measurement of the Callosal Angle in 1856 Elderly Patients and Volunteers Indicates that 12.4% of Exams Met the Criteria for Possible Normal Pressure Hydrocephalus
AJNR 42:1942-1948, Morzage, M.,et al, 2021

A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
Neurol 97:958-963, Davalos, L.,et al, 2021

A 49-Year-OLD Woman with Progressive Numbness and Gait Instability
Neurol 97:342-347, Zahid, A.,et al, 2021

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

A 6-Year-Old Boy with Muscle Twitching
Neurol 96:e301-e304, Lewis, H.S.,et al, 2021

Clinicopathologic Conference, Mycobacterium Tuberculosis Meningitis
NEJM 384:166-176, Case 1-2021, 2021

Acute Flaccid Myelitis: Cause, Diagnosis, and Management
Lancet 394:334-397, Murphy, O.C.,et al, 2021

Cranial Nerve Disorders Associated with Immune Checkpoint Inhibitors
Neurol 96:e866-e875, Vogrig, A.,et al, 2021

Clinicopathologic Conference, Lympohplasmic Lymphoma of the CNS (Bing-Neel Syndrome)
NEJM 384:745-753, Case 6-2021, 2021

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

Natural History of "Pure" Primary Lateral Sclerosis
Neurol 96:e2231-e2238, Hassan, A.,et al, 2021

Clenched Fists as an Unusual Presentation of Focal Neuromyotonia
Neurol 97:e429-e430, Dhanapalaratnam, R.,et al, 2021

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

Teaching Video NeuroImages: Jaw Clonus in Amyotrophic Lateral Sclerosis
Neurol 96:e2563, Goel, A.,et al, 2021

Recurrent Perimesencephalic Nonaneurysmal Subarachoid Hemmorrhage Within a Short Period of Time:A Case Report
World J Clin Cases 16:3356-3364, Li,J.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

A Case of Primary Leptomeningeal Lymphoma Presenting with Hydrocephalus Characterized by Disproportionately Large Fourth Vehicle
NMCCRJ 8:399-404, Nohira, S.,et al, 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

"Motor Band Sign" in Susceptibility-Weighted Imaging in Motor Neuron Disease
Ann India Acad Neurol 23:821-822, Prabhu,A.N., 2020

Bilateral Middle Cerebellar Peduncle Lesions:Neuroimaging Features and Differential Diagnoses
Brain Behav 10:e01778, Jiang,J.,et al, 2020

Immunoglobulin G4-Related Orbital Disease with Bilateral Optic Perineuritis and Maxillary Nerves Involvement:A Case Report
Ophthalmol Ther 9:1089-1099, Hung,C-H., 2020

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
J Clin Med 9:1-12, Rizzo, G.,et al, 2020

Looking Beyond the Usual
Delhi J Ophthal doi:7869/djo.555, Shakrawal, J.,et al, 2020

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

Analysis of 70 patients with hydrocephalus due to cobalamin C deficiency
Neurol 95:e3129-e3137, He, R.,et al, 2020

Imaging Review of Paraneoplastic Neurologic Syndromes
AJNR 41:2176-2187, Madhavan, A.A.,et al, 2020

Burning Pain in the Legs
NEJM 383:e18, Sacks, C.A., 2020

Showing articles 300 to 350 of 2843 << Previous Next >>