Neudle.com: muscle atrophy focal

Differential
(Click to cross reference)

abdominal contractions

abdominal protrusion

abductor pollicis brevis

abscess, intracerebral

abscess, intracerebral, multiple

abscess, intracerebral, treatment of

abscess, lung

abscess, vertebral

acanthocytosis

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

Adies pupil

advances in neurology

aggression

alcohol intoxication

alcohol, neurologic complications with

alcoholic polyneuropathy

alcoholism

algorithm

alien hand syndrome

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

Alzheimer's disease

amaurosis fugax

amphiphysin antibodies

amyloid

amyloid angiopathy, cerebral

amyloidosis

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, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anatomy of

anemia

anemia, megaloblastic

aneurysm

aneurysm, anterior communicating

aneurysm, intracranial

angiitis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, neurologic complications with

anisocoria

ankle reflex, absent

ankylosing spondylitis

anoctaminopathy

anorexia

anterior horn cell disease

anterior interosseous neuropathy

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

antibiotics

anticoagulant, complications of

anticoagulant, treatment

antiviral agents

aphasia

aphasia, progressive, primary

aphonia

applause sign

apraxia

apraxia of eye movements

apraxia, constructional

apraxia, speech

aqueduct of Sylvius, obstruction

arterial dissection, carotid

arterial dissection, vertebral

arthralgia

arthrogryposis multiplex

ascending paralysis

aspirin

asthma

asthma, poliomyelitis-like syndrome with

autonomic dysfunction

autonomic neuropathy

B 12 deficiency

Babinski sign

Babinski sign in new born

bacterial infection

BAL

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

behavioral disorder

Bence Jones protein

benign essential tremor

biologic markers

BiPAP

bitemporal visual field defect

bone marrow suppression

botulinum toxin, complications of

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial neuritis, prognosis of

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

bradykinesia

brain atrophy

brain biopsy

brain biopsy, false negative

brain biopsy, negative

brainstem, infarction of

brainstem, lesion of

Brueghel's syndrome

bruit

bruit, supraclavicular

bulbar palsy

bulbar palsy, progressive

calcification, intracranial

cardiac catheterization, neurologic complications

cardiomegaly

cardiomyopathy

cardiovascular disease

caribbean

carotid artery atherosclerosis

carotid artery disease

carotid artery occlusion, neck

carotid artery stenosis

carpal tunnel syndrome

CAT scan, abscess, cerebral

CAT scan, contrast enhanced

CAT scan, disappearing lesion on

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, serial

CAT scan, spine

CD4 counts

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, clinical diagnosis

cerebrovascular accident, etiology

cerebrovascular accident, incidence of

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, topographic pattern

cerebrovascular accident, vascular territory involved

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cheiralgia paresthetica

chelation therapy

chemotherapy, CNS treatment and complications with

chromosomal abnormality

chromosome 17

Chvostek sign

cisterna magna

cisternogram, radionuclide

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

clonazepam

clubfoot as related to neurologic disease

coccidioidomycosis

cognition

cold temperature

collapsin response mediator protein 5 IgG

coma

comorbidities

compartment syndrome

compartment syndrome, medial brachial fascial

complications

compression neuropathy

conduction block

confusion

confusional state, acute

congestive heart failure

conjugate gaze, forced

conjunctivitis

contactin associated protein like 2 antibodies

conversion reaction

corneal reflex, abnormal

corneal reflex, absent

corona radiata

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, neoplasm of

cortical hand knob

cortical hand knob infarct

cortical hemorrhage

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

Creutzfeldt-Jakob disease, genetic

cyst, cortical parenchyma

cyst, perineural

cyst, ventricular

cysticercosis

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cystinosis

cytomegalic inclusion disease

degenerative diseases of CNS

dementia, frontal lobe type

dementia, frontotemporal

dementia, rapidly progressive

demyelinating disease

denervation of muscle

denervation potentials

developmental milestones

developmental milestones, loss of

dexterity, impaired

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

diabetic mononeuropathy

diagnostic criteria

diarrhea

differential diagnosis

difficulty climbing stairs

diffuse idiopathic skeletal hyperostosis

disability rating scale, neurological

disability, neurological

disc space infection

disc space narrowing

discitis

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

downward gaze

dropped head syndrome

drug abuse

drug abuse, neurologic complications of

dural sinus thrombosis

dying

dysarthria

dysferlinopathy

dyskinesia, buccal lingual facial

dystonia, post traumatic

dystrophic calcification

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electrocorticogram

electroencephalogram, abnormalities of

electromyogram

electromyogram, decremental response

electron microscopy

embolism

emotional lability

empyema, epidural-spinal

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, episodic

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, Rasmussen's

encephalitis, viral

encephalomyelitis

encephalopathy

encephalopathy, acute

endemic area

entrapment neuropathy

enzyme, defect

enzyme, muscle disease

eosinophilia

epidemiology of neurology

epilepsia partialis continua

episodic neurologic deficits

exercise-induced vascular symptoms

exophthalmus

extremity, cold

eye movement, disorders of

face, numbness of

facial nerve palsy

facial weakness

facial weakness, bilateral

fine motor function, impaired

finger flexor weakness

finger weakness

fingernails, abnormal

fourth ventricle, cyst

fracture, long bones, nerve injury with

frontal behavioral spatial syndrome

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontal lobe, space occupying lesion of

gammaglobulin therapy, intravenous

gaze palsy, horizontal

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

genu of corpus callosum

girdle sensation

glabellar sign

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen debranching enzyme deficiency

glycogen storage disease

granuloma, pulmonary

granulomatous disease

grasp reflex

groin pain

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guyon's canal

gynecomastia

hallucination, auditory

Hand-Schuller-Christian disease

headache

headache, severe

hearing loss

heavy metal intoxication

helminthic infection of CNS

hematoma, intracerebral

hemianopia, homonymous

hemiatrophy, cerebral

hemidystonia

hemiparesis

hemiparesis, transient

hemiplegia

hemiplegia, progressive

heralding manifestation

herniated disc

herniated disc, thoracic

herpes simplex encephalitis

herpes simplex encephalitis, diagnosis of

high arched feet

highly active antiretroviral therapy

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, transient

hyperhidrosis, palmar

hypertension, cerebrovascular disease with

hyperthyroidism

hypoglycemia

hypoglycorrhachia

hypokalemic periodic paralysis

hypotension, systemic

hypothalamus

hypothalamus, disturbance of

hypotonia

hypotonia, infants

hypoxia

iatrogenic neurologic disorders

immunology and the nervous system

immunosuppressive agents

immunotherapy

inability to stand on tiptoes

inborn errors of metabolism

incidence

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

internuclear ophthalmoplegia

interosseous muscles

intracerebral hemorrhage

intracerebral hemorrhage, causes of

intracerebral hemorrhage, differential diagnosis of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, multiple

intracranial hypertension, benign

intracranial pressure, increased

intranasal medication

intrinsic hand muscles

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

Japan

jaundice

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

juxtacortical hemorrhage

ketogenic diet

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

lacunar infarction, differential diagnosis of

lacunar infarction, hemorrhagic

laminectomy

laminectomy, lumbar

language disorder in adults

leg weakness, bilateral

leg weakness, unilateral

leucine rich glioma inactivated 1 antibodies

leukemia

leukoencephalitis, acute necrotizing hemorrhagic

leukoencephalopathy

leukopenia

level of consciousness, decreased

levitation

Lewy body disease, diffuse

Lhermitte's sign

life expectancy

life support, withdrawal of

limbic encephalitis

linear lesion

liver disease

liver function enzymes

lobar atrophy

locked-in syndrome

low back pain

lumbar puncture, complications of

lumbosacral plexopathy

lumbosacral plexus, neuritis

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignancy, occult

Man-In-The-Barrel syndrome

Martin-Gruber anastamosis

masked facies

mastoiditis

median nerve

median nerve, lesion of

median neuropathy

Mees lines

memory, defect of recent

memory, impairment of

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, fungal

meningitis, leptospira

meningitis, syphilitic

meningitis, TB

meningoencephalitis

mental status, abnormal

methotrexate

methylmalonic acid, serum

Mexican

Mexico

microangiopathy, brain

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

monoclonal gammopathy

monomelic amyotrophy

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

mononeuropathy, motor

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, disappearing lesion on

MRI, functional

MRI, lumbosacral plexus

MRI, muscle

MRI, negative

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, spine

MRI, susceptibility weighted

MRI, T1 weighted fat suppression

MRS

multinucleated giant cell

multiple myeloma

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle spasm

muscle spasm, paraspinal

muscle stiffness

muscle swelling

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenia gravis, paraneoplastic

myelopathy, chronic progressive

myoclonus, stimulus sensitive

myopathy, carcinomatous

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, inclusion body, hereditary

myopathy, quadriceps

myopathy, radiation-induced

myopathy, thyroid disease causing

myxedema, neurologic manifestations of

neoplasm, intracranial

neoplasm, intracranial, differential diagnosis of

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

nephritis

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve repair, end to end

nerve root hypertrophy

neuritis

neuritis, causes of

neuritis, heavy metals causing

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic disease, tempo

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuromuscular junction

neuronal cell surface antigen

neuronal intranuclear inclusion disease

neuronopathy

neuronopathy, sensory

neuronopathy, sensory and motor

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, bicycle

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, paraneoplastic

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuroprotective agents

occupational neurologic disorders

occupational neuropathies

ocular bobbing

ocular motility, disorders of

onconeural antibodies

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection, CNS

opsoclonus-myoclonus syndrome

optic atrophy

optic neuropathy

osteomyelitis

osteomyelitis, spinal

otitis, neurologic complications with

owl's eye sign of spinal cord

paralysis, asymmetric

paralysis, recurrent

paraneoplastic cerebellar degeneration

parasitic infection, CNS

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

pericardial effusion

peripheral blood smear

peripheral blood smear, abnormal

peripheral nerve, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

poliomyelitis

poliomyelitis, neonatal

poliomyelitis-like illness

polyclonal gammopathy

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

polyradiculoneuropathy

pons, infarction of

pons, lesion of

porphyria

position sensation, abnormal

positive sharp waves

posterior fossa

posterior fossa, lesion of

posterior inferior cerebellar artery syndrome

posterior interosseous neuropathy

posterior longitudinal ligament, ossification of

postoperative neurologic complications

postpartum

precentral gyrus

precipitating factors

pregnancy, neurologic complications in

premature infant

primary aldosteronism

primary lateral sclerosis

primary thrombocythemia

prion disease

prisoners of war, neurologic complications in

prognosis

progranulin

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

pronator syndrome

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

pseudomedian nerve palsy

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoulnar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pupil, abnormality in neurologic disorders

pupil, tonic

pure motor hemiplegia

pure motor stroke

pure sensory stroke

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriplegia, transient

quality of life

radial nerve

radial nerve, palsy of

radial pulse, unilateral decrease of

radiation therapy, CNS treatment and complications with

radiculopathy

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

Raynaud's phenomenon

real-time quaking-induced conversion

reflex sympathetic dystrophy

release phenomena

remote effect of cancer on the nervous system

repetitive nerve stimulation

respirator

respiratory failure

respiratory tract infection

retinopathy

retrocollis

retrovirus

reverse split hand sign

reversible neurologic disorder

review article

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis

scalenus anticus syndrome

schizophrenia

sciatic neuropathy

scleroderma

scleroderma, neurologic involvement with

sclerosis, bone

scotoma

scotomata, scintillating

screening

sedimentation rate

sedimentation rate, elevated

seizure, surgical treatment of

seizure, treatment of

sensorimotor stroke

sensorineural hearing loss

sensory loss

sensory loss, cortical

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing, quantitative

sequencing difficulty

shunt procedure, ventricular

Sjogren's syndrome, neurologic manifestations of

skew deviation

skin, lesions in neurologic disorders

sleep

sleep pathology and physiology

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, enlargement

spinal cord, infarction of

spinal cord, injury of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal stenosis

spinal stenosis, cervical canal

spinocerebellar ataxia type 3/Machado Joseph disease

spirochete infection

spitting

splenium of corpus callosum

splenomegaly

spondylosis

spontaneous muscle activity

sports medicine, neurology of

steroid therapy, CNS treatment and complications with

stiff man syndrome

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subclavian artery stenosis

subdural effusion

subdural hematoma

subdural hematoma, interhemispheric

suck reflex

sulfone

superior sagittal sinus

superior sagittal sinus thrombosis

suprascapular nerve

suprascapular neuropathy

supraspinatus muscle

swallow evaluation

sweating, abnormality of

swimming

symmetric brain lesions

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

temporal lobe, atrophy

temporalis muscle wasting

tetany

thoracic outlet syndromes

thromboangiitis obliterans cerebri

tomaculous neuropathy

tongue, atrophy

tongue, fasciculations of

torticollis, post traumatic

toxoplasmosis, CNS

transient ischemic attack

transient neurologic deficit

transilumination of skull

trauma

travel, foreign

treatment of neurologic disorder

tremor

tremor, intention

tremor, post traumatic

trigeminal nerve, abnormality of

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

urine test in toxic screen

visual evoked response

visual impairment

visual loss

visual loss, transient

visual symptoms

visuospatial disturbance

Volkmann's ischemia

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weight loss

weightlifting

Werdnig-Hoffman disease

word-finding difficulty

Showing articles 250 to 300 of 5377 << Previous Next >>

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

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Nusinersen in Adult Patients with Spinal Muscular Atrophy
Neurol 95:e413-e416, Moshe-Lilie, O.,et al, 2020

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

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

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

Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
J Clin Neurol 16:714-716, Pancheri, E.,et al, 2020

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

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

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

A 65-year-old man with Asymmetric Weakness and Parethesias
Neurol 93:856-861, Harada, Y.,et al, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

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

Subacute Progressive Sensorimotor Symptoms
BMJ 365:doi:10.1136/bmj.l1923, Francis, A.,et al, 2019

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

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

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

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 379:2452-2461, Case 39-2018, 2018

A 22-year-old Man Presenting with Headache and Right Leg Jerks
Neurol 91:891-895, Schupper, A.J.,et al, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
Ann Neurol 81:147-151, Lee, M.,et al, 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

A Woman in Her 60s with Chronic Meningitis from Aspergillus
JAMA Neurol 74:348-352, Pichler, M.R.,et al, 2017

Mechanisms, Causes, and Effects of Hypercapnia
UptoDate Dec, Feller-Kopman, D.J. & Schwartzstein, R.M., 2016

Showing articles 250 to 300 of 5377 << Previous Next >>