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Differential
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abdominal distention

abdominal muscle paralysis

acanthocytosis

acid maltase deficiency

acid maltase deficiency, adult

aciduria

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acute coronary syndrome

addiction, heroin

advances in neurology

adverse drug reaction

agitation

alcohol

alcohol, neurologic complications with

alcoholic withdrawal states, DT's, convulsions, etc.

alveolar hypoventilation

aminoacidurias

amyloidosis

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

aneurysm, intracranial, delayed cerebral ischemia with

angina pectoris

angiography, neurologic complications with

angiotensin-converting enzyme

animal exposure

anoctaminopathy

anosmia

anterior horn cell disease

anterior tibial muscle weakness

anti signal recognition particle antibody

anticholinergic drugs

anticholinergic drugs, side effects of

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants

anticonvulsants, hypersensitivity syndrome

anticonvulsants, untoward effects of

aspartate aminotransferase

atherosclerosis, generalized

atrioventricular block

autonomic dysfunction

axonal degeneration

azidodeoxythymidine

bacteremia

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

baldness

basal ganglia, calcification of

basal ganglia, degeneration

brain natriuretic peptide

calcification, intracranial

calcification, muscle

carbon monoxide poisoning

carcinoma

carcinoma of esophagus

carcinoma of pancreas

cardiac arrest

cardiac arrest and resuscitation

cardiac enzymes

cardiac output

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

cardiac tumor

cardiomegaly

cardiomyopathy

cardiopulmonary bypass

cardiovascular disease

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, contrast enhanced

CAT scan, emission, abnormal

CAT scan, gray matter enhancement

caudate nucleus, atrophy

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar infarction

cerebellar lesion

cerebral edema

cerebral edema, cytotoxic

cerebral embolism

cerebral embolism, cardiac origin

cerebral ischemia

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular disease, cardiovascular disease with

channelopathy

chemosis

chemotherapy, CNS treatment and complications with

chest pain

chest x-ray, abnormal

chromosomal abnormality

chromosome 19

chronic fatigue syndrome

Chvostek sign

Clinical Pathologic Conference(C.P.C.)

clorazepate dipotassium

clozapine

clubfoot as related to neurologic disease

cocaine

coenzyme Q10

coenzyme Q10 deficiency

compartment syndrome, gluteal

complications

compression neuropathy

conduction block

confusion

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

Congo red stain

conjunctival injection

coronary artery bypass

coronavirus

cough

COVID-19

cranial nerve palsies

creatine kinase

creatine phosphokinase BB isoenzyme elevation

creatine phosphokinase isoenzyme elevation

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

cryptococcal meningitis

cultured skin fibroblasts

delayed muscle relaxation

delirium

dentate nuclei

dermatomyositis

dermatomyositis, childhood

descending paralysis

desmin

developmental disability

developmental retardation

diabetes mellitus

diagnostic criteria

dialysis

diamond on quadriceps

diaphragmatic paralysis

diarrhea

differential diagnosis

difficulty climbing stairs

dilantin

dilantin, hypersensitivity to

disability, neurological

dislocated hip, congenital

disorientation

disseminated intravascular coagulation(DIC)

distal muscle atrophy

distal muscle weakness

DNA probes

dopamine antagonist

doxycycline

dropped head syndrome

drug abuse

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dystonia, drug induced

dystroglycanopathies

dystrophic calcification

echocardiogram, transesophageal

eclampsia

eclampsia, postpartum

edema, facial

edema, periorbital

ehrlichiosis

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, video monitoring with

electromyogram

electromyogram, decremental response

electron microscopy

embolism

embolism, atheromatous

embolism, cholesterol

embolism, paradoxical

emergencies, neurologic

emergency room

Emery-Dreifuss muscular dystrophy

encephalitis

encephalitis, brainstem

encephalitis, paraneoplastic

encephalomyopathy

encephalopathy

encephalopathy, acute

endocarditis

endocarditis, acute bacterial

endocarditis, infectious

endocarditis, marantic

endocarditis, neurologic manifestations with

enolase

enteritis

entrapment neuropathy

enzyme treatment

enzyme, defect

enzyme, muscle disease

enzyme, serum

eosinophilia

eosinophilia-myalgia syndrome

eosinophilic fasciitis

epidemiology of neurology

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial swelling

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

femoral artery catheterization

fine motor function, impaired

gammaglobulin therapy, intravenous

gastrointestinal bleeding

gastrointestinal disease, neurologic complications

gastrointestinal motility

gastrointestinal perforation

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

glycogen storage disease

hallucination, visual

head injury, defibrination following

head injury, management of

heart block, complete

heart murmur

heliotrope rash

hematuria, microscopic

hemidiaphragm, paralysis of

hemiparesis

hemorrhagic diathesis

heralding manifestation

hereditary myopathy with early respiratory failure

herpes simplex encephalitis

herpes virus

heterophile antibody test

high arched palate

hip flexor weakness

histochemistry

histochemistry of muscle

HMGcoA reductase inhibitors

hoarseness

Horner's syndrome

H-reflex testing

human diploid cell rabies vaccine

human immunodeficiency virus type 1

hyperpigmentation of skin

hypersensitivity reaction

hypoparathyroidism, idiopathic

hyporeflexia

hypotension, systemic

iatrogenic neurologic disorders

idiopathic inflammatory myopathy

imbalance

immune checkpoint inhibitors

immune-related adverse events

immunoelectrophoresis, serum

immunosuppressive agents

inability to sit up

inclusion bodies

inclusion body myositis

infection

infectious mononucleosis

infectious mononucleosis, neurologic findings with

influenza A virus

influenza B virus

infusion-associated reaction

insect sting

intellectual deficit

interferonopathy

interstitial pulmonary fibrosis

intestinal pseudoobstruction

intracranial pressure, increased

intrinsic hand muscles, wasting of

ipecac

ipilimumab

Isaacs syndrome

ischemic exercise test

Kearns-Sayre syndrome

ketamine

ketoconazole

Kugelberg-Welander syndrome

kyphosis

lactic acidemia

lactic dehydrogenase(LDH)

learning disability

learning disability, in children

leg swelling

leg weakness, bilateral

leg weakness, unilateral

Legionella pneumophilia

leukoencephalopathy, toxic

leukopenia

levamisole

level of consciousness, decreased

lid closure, weakness of

liver function enzymes

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malabsorption

malabsorption syndrome

malignant hyperpyrexia

malignant papulosis

manic-depressive

marathon running

masseter muscle weakness

McArdle's disease

McLeod syndrome

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, CSF findings in

meningitis, fungal

meningitis, leptospira

meningitis, predisposing factors in

meningitis, spinal fluid smear and culture of

meningitis, TB

meningoencephalitis

meningoencephalitis, amoebic

meningoencephalitis, mumps

meningoencephalopathy

mental retardation

mental status, abnormal

middle cerebral artery, occlusion of

mimics

miosis

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve vegetation

MNGIE syndrome

mogadon

molecular genetics

mononeuritis multiplex

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, cardiac

MRI, contrast enhanced

MRI, muscle

MRI, negative

multiple sclerosis

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle phosphorylase deficiency

muscle relaxant

muscle spasm

muscle stiffness

muscle strength, testing

muscle swelling

muscle swelling, focal

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscle-eye-brain disease

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, Duchenne, neonatal screening

muscular dystrophy, Duchenne, presymptomatic detection

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

muscular dystrophy, neurogenic hypothesis of

muscular dystrophy, pattern of muscle involvement

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, non motor symptoms

myocardial biopsy

myocardial infarction

myocardial infarction, acute

myopathy, centronuclear

myopathy, critically ill

myopathy, desmin

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, genetic

myopathy, hereditary

myopathy, hypocalcemic

myopathy, hypokalemic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, autoimmune

myopathy, necrotizing, immune-mediated

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, steroid responsive

myopathy, thyroid disease causing

myositis, acute of childhood

myositis, bacterial

myositis, focal

myositis, post infectious

myxedema, neurologic manifestations of

nausea and vomiting

neck weakness

nemaline rod myopathy

nemaline rod myopathy, adult onset

neonatal screening, genetic neurologic disorders

neoplasm, intracranial

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve conduction studies, motor

neuroleptic malignant syndrome

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic symptoms

neurological intensive care

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuromyotonia

neuromyotonia and axonal neuropathy

neuron specific enolase

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, acute

neuropathy, cryoglobulinemic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, vasculitic, systemic

neurosis

neurosis, treatment of

neurosyphilis

neurotoxin

next-generation sequencing

occupational neurologic disorders

ocular motility, disorders of

ocular myopathy

oculopharyngeal muscular dystrophy

olanzapine

old age, neurology of

opened mouth

ophthalmoplegia

ophthalmoplegia, progressive external

ophthalmoplegic migraine

opportunistic infection

opsoclonus

orange peel appearance of skin

orthopnea

overlap syndrome

oxazepam

pacemaker, cardiac-transvenous

paralysis, asymmetric

paramyotonia congenita

paraparesis

paraspinal muscle

paraspinal muscle weakness

Parkinson disease, drug induced

Parkinsonism syndrome

percussion induced muscle contraction

peripheral blood smear

peripheral blood smear, abnormal

personality change

phosphorylase b kinase deficiency

pleocytosis of cerebrospinal fluid

pleural effusion

pneumonia

poison, neurologic problems with

poliomyelitis

polyclonal gammopathy

polymerase chain reaction

polymicrogyria

polymyositis

polymyositis, eosinophilic

polyneuropathy

polyneuropathy, critically ill

polyneuropathy, critically ill, children

Pompe's disease of glycogen storage

portacatheter

positive sharp waves

post polio syndrome

posterior leukoencephalopathy syndrome

posterior leukoencephalopathy syndrome, location

postural abnormality

potassium channel antibodies

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proteinuria

protozoan infection

proximal muscle atrophy

proximal myotonic myopathy

pruritus

pseudohypertrophy

pseudomyotonia

pseudostatus epilepticus

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

pulmonary hypertension

pulmonary infiltrates

pupil

pupil, abnormality in neurologic disorders

remote effect of cancer on the nervous system

renal failure

renal failure, acute

repetitive nerve stimulation

respirator

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

retina, abnormal

retinal lesion

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rippling muscle disease

risk factors

risk-benefit assessment

risperidone

Sabin-Feldman dye test

safety

salivation, excessive

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure

seizure, differential diagnosis of

seizure, hysterical

seizure, nonepileptic

selective serotonin reuptake inhibitors

self-mutilation

sensorineural hearing loss

sensory nerve action potentials

serum alanine aminotransferase

serum glutamic oxaloacetic transaminase

serum glutamic pyruvic transaminase

serum lipase, elevated

severe acute respiratory syndrome

sex reassignment surgery

shoulder-girdle wasting

simvastatin

single photon emission computed tomography

Sjogren's syndrome

skin, biopsy

skin, lesions in neurologic disorders

skin, thickened

sleep apnea

slit lamp examination

small vessel disease

sodium channel dysfunction

somnolence

sore throat

speech disorder, childhood

speech, delayed development of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, intermediate form

spinocerebellar degeneration

spirochete infection

splenomegaly

sports medicine, neurology of

standing difficulty

staphylococcus aureus

statin therapy

statin therapy, discontinuation

statin therapy, dose

status asthmaticus

status epilepticus

status epilepticus, nonconvulsive

status epilepticus, psychogenic

steppage gait

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, metastatic carcinoma deposits causing

sudden death

suicide

survival motor neuron gene

sweating

symptomatic

syncope

syphilis, neurologic complications with

systemic illness

systemic lupus erythematosus

tachycardia

tachypnea

telangiectases, periungual

temporalis muscle hypertrophy

temporalis muscle swelling

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

toilet seat neuropathy

tone, muscle, increased

tongue, biting

tongue, enlarged

tongue, fasciculations of

tongue, weakness

torticollis

toxoplasma complement fixation test

toxoplasma gondii

toxoplasmosis, acquired

toxoplasmosis, CNS

toxoplasmosis, muscle

transgender

transient ischemic attack

treatment of neurologic disorder

trinucleotide repeats

urine test in toxic screen

walking, difficulty with

weakness, generalized

weakness, progressive

weakness, proximal

weakness, severe

weaning from respirator, failure to

whistle, inability to

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

yersinia enterocolitica

Showing articles 250 to 292 of 292 << Previous

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Upadacitinib - An Up-and-Comer for Treatment of Giant-Cell Arteritis
NEJM 392:2062-2064, Koster,M.J. & Warrington,K.J., 2025

Cancer Frequency in MuSK Myasthenia Gravis and Histological Evidence of Paraneoplastic Etiology
Ann Neurol 96:1020-1025, Falso,S.,et al, 2024

Paraneoplastic Calmodulin Kinase-Like Vesicle-Associated Protein (CAMKV) Autoimmune Encephalitis
Ann Neurol 96:21-33, Gilligan,M.,et al, 2024

Polymyalgia Rheumatica
Lancet 402:1459-1472, Espigol-Frigole,G.,et al, 2023

Lenvatinib Therapy for Advanced Thyroid Cancer: Real-Life Data on Safety, Efficacy, and Some Rare Side Effects
JENDSO 6:1-7, Hamidi, S.,et al, 2022

Atypical Posterior Reversible Encephalopathy Syndrome Associated with Lenvatinib Therapy in a Patient with Metastatic Thyroid-Cancer
Cancer Reports doi:10.1002/cnr2.1605, Abhishek, M.,et al, 2022

Progressive Vertebrobasilar Vasculopathy and Stroke Secondary to Giant Cell Arteritis
Stroke 53:e435-e438, Mahjoub, Y.,et al, 2022

Polymyalgia Rheumatica and Giant Cell Arteritis
JAMA 324:993-994, Buttgereit, F.,et al, 2020

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

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

Tocilizumab Treatment for New Onset Refractory Status Epilepticus
Ann Neurol 84:940-945, Jun, J.,et al, 2018

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

Trial of Tocilizumab in Giant-Cell Arteritis
NEJM 377:317-328,385, Stone, J.H.,et al, 2017

Rituximab as Treatment for anti-MuSK myasthenia gravis
Neurol 89:1069-1077, Hehir, M.K.,et al, 2017

Tocilizumab for Induction and Maintenance of Remission in Giant Cell Arteritis: A Phase 2, Randomised, Double-Blind, Placebo-Controlled Trial
Lancet 387:1921-1927,1882, Villiger, P.M.,et al, 2016

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

Long-lasting Treatment Effect of Rituximab in MuSK Myasthenia
Neurol 78:189-193, Diaz-Manera,J.,et al, 2012

T2* and FSE MRI Distinguishes Four Subtypes of Neurodegeneration With Brain Iron Accumulation
Neurol 70:1614-1619, McNeill,A.,et al, 2008

Pallidal Stimulation Improves Pantothenate Kinase-Associated Neurodegeneration
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Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
Lancet 365:410-412, Nichols, W.C., et al, 2005

Are MuSK Antibodies the Primary Cause of Myasthenic Symptoms?
Neurol 62:1945-1950,1920, Selcen,D.,et al, 2004

Diagnostic Approach in Patients with Symmetric Imaging Lesions of the Deep Gray Nuclei
The Neurologist 9:250-261, Finelli,P.F.&DiMario,Jr,F.J., 2003

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
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Magnetic Resonance Imaging of Brain Iron in Health and Disease
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Reverse Shapiro's Syndrome:Hirayama
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Hallervorden-Spatz Disease with Bilat Invol of Globus Pallidus & Substantia Nigra:MR Demonstra
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Follow-up MR STudies in Hallervorden-Spatz Disease
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Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
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Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
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MR Imaging of a Group I Case of Hallervorden-Spatz Disease
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Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985

MR Imaging of Hallervorden-Spatz Disease
J Comput Assist Tomogr 9:491-493, Littrup,P.J.,et al, 1985

Hallervorden-Spatz Disease:Cysteine Accumulation & Cysteine Dioxygenase Deficiency in the Globus Palladus
Ann Neurol 18:482-489, Perry,T.L.,et al, 1985

Computed tomography in Hallervorden-Spatz disease
Neurol 30:1128-1130, Dooling,E.C.,et al, 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Pyruvate-Kinase-Deficiency-Caused Hemolytic Anemia
Neurol 29:510-513, Rutgers,M.J.,et al, 1979

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
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Neuro CPC of MGH
Metachromatic Leukodystrophy, NEJM 267:1198-12041962., , 1962

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