Neudle.com: extensor posturing

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Differential
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abdominal distention

abdominal muscle paralysis

abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

abscess, intracerebral

aceruloplasminemia

acetylcholine receptor antibody

achilles tendon, enlarged

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome myelopathy

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acute disseminated encephalomyelitis

acute disseminated encephalomyelitis, multiphasic

acute respiratory distress syndrome

acyl CoA dehydrogenase deficiency

addiction, heroin

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adult polyglucosan body disease

adverse drug reaction

affect, inappropriate

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alcohol intolerance

altered states of consciousness

alternating rapid movement

Alzheimer's disease

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

anemia, megaloblastic

aneurysm, vertebral basilar system

angiitis, granulomatous of CNS

ankle reflex, absent

antecedent illness

anterior horn cell disease

anterior tibial muscle weakness

anti GQ1b IgG antibody

anti Hu antibody

antibodies to voltage-gated calcium channels

anticholinergic drugs

anticoagulant, complications of

anticoagulant, treatment

anticoagulant, treatment in CVD

antiviral agents

Argyll Robertson pupil

arm swing, reduced

Arnold Chiari malformation

arrhythmia, cardiac

asterixis, causes of

asterixis, unilateral

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atherosclerosis, generalized

atherosclerosis, premature

atrioventricular block

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

azidodeoxythymidine

B 12 deficiency

Babinski sign in new born

bacterial infection

bacterial infection, CNS

ballismus, bilateral

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

behavior modification

behavioral disorder

behavioral disorder, acute

Behcet's syndrome

Bell's phenomenon

benign essential tremor

bent spine syndrome

Bickerstaff's brainstem encephalitis

bladder dysfunction

bone marrow biopsy

bone marrow infarction

bone marrow necrosis

bone marrow transplantation

Borrelia burgdorferi infection

botulinum toxin

botulinum toxin, complications of

botulism immune globulin

botulism, infant

brain biopsy, false negative

brain biopsy, stereotaxic

brainstem, atrophy

brainstem, glioma

brainstem, glioma in children

brainstem, glioma, adult

brainstem, hemorrhage, primary

brainstem, infarction of

brainstem, ischemia

brainstem, lesion of

brainstem, neoplasms of

brucellosis, nervous system involvement with

Brudzinski's sign

Brueghel's syndrome

bulbar palsy, childhood

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

campylobacter infection

carcinoma of lung

cardiac arrest and resuscitation

cardiovascular disease

carnitine deficiency

carnitine deficiency myopathy

carotid angiogram

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, dense artery sign

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, myelogram with

cauda equina, enhancement

central core disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar infarction

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral edema, origin and treatment

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, mechanical extraction

cerebral folate deficiency syndrome

cerebral infarction

cerebral peduncle

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, amonia

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, flow cytometry

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, glutamine

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, prognosis in

cerebrovascular accident, vascular territory involved

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, predisposed factor in

ceruloplasmin, serum

cervical spondylosis

Chaddock's sign

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chilbran skin lesions

chorea, causes of

chorea, familial

chorea, Sydenham's

choreoathetosis

choroid plexus, tumor of

chromosomal abnormality

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

chronic progressive external ophthalmoplegia

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

coccidioidomycosis

collagen vascular disease

comprehension, impaired

compression fracture

concentration, impaired

conduction block

congenital bilateral perisylvian syndrome

congenital heart disease

congenital malformation

congenital malformation, non CNS

congenital myopathy

congestive heart failure

contractures, joint

controversies in neurology

convergence, impaired

conversion reaction

copper deficiency

corneomandibular reflex

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, thinning

cortical blindness

cortical-basal ganglionic degeneration

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine kinase

creatine phosphokinase MB isoenzyme elevation

creatine phosphokinase(CPK)elevated

critical care unit

crying, pathologic

cryptococcal meningitis

cultured skin fibroblasts

cyclic vomiting

cyst, epidermoid of CNS

cystatin C mutation

decerebrate posture

decerebrate Posture, unilateral

decompressive spinal cord surgery

decorticate posture

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine's sign

Dejerine-Sottas syndrome

delay in diagnosis

dementia, childhood

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

denervation of muscle

denervation potentials

dense basilar artery sign

dense middle cerebral artery sign

dental procedure, neurologic complications with

dentate nuclei, lesion of

dermatomyositis

descending paralysis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diaphragmatic paralysis

diaphragmatic paralysis, causes of

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

digiti quinti sign

diplegia, brachial

disability, neurological

distal muscle atrophy

distal muscle weakness

doll's head maneuver

dopa responsive dystonia

Dravet syndrome

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug induced neurologic disorders

drug withdrawal

dysdiadochokinesia

dysferlinopathy

dyskinesia, buccal lingual facial

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, drug induced

dystonia, focal

dystonia, post traumatic

dystonia, treatment of

dystrophic calcification

ears of the Lynx MR sign

electrical sensation

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

embolism, paradoxical

embolism, vertebral-basilar artery

emergencies, neurologic

emergencies, neurosurgical

Emery-Dreifuss muscular dystrophy

emotional lability

Emperor's clothes syndrome

empyema, epidural-spinal

encephalitis lethargica

encephalitis, brainstem

encephalitis, viral

encephalomyelitis

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

endocarditis, subacute bacterial

endovascular therapy

enzyme, muscle disease

epidemiology of neurology

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

Erdheim-Chester disease

evoked potentials

executive dysfunction

exercise intolerance

exercise-induced neurologic dysfunction

exercise-related muscle strength increase

exome sequencing

extensor digitorum brevis

eye movement, disorders of

face, elongated

face, numbness of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failure to thrive

FARS2 deficiency

fatal familial insomnia

feeding disorder

ferritin, elevated

fetal alcohol syndrome

fine motor function, impaired

finger nose finger test

fingers, abnormal

Fisher's syndrome

flaccid paralysis

folic acid deficiency

foot drop, bilateral

fragile-X syndrome

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal balding

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

gastric dilatation, acute

gastric partitioning

gastrocnemius muscle weakness

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

giant axonal neuropathy

girdle sensation

glioblastoma multiforme(astrocytoma Gr.III)

glioma, low-grade

gliomatosis cerebri

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

glutamic acid decarboxylase, antibody

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

granular osmiphilic material

Guillain Barre syndrome

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, pharyngeal-cervical-brachial variant

Guillain Barre syndrome, variant forms of

Hallervorden Spatz disease

hallucination, olfactory

headache, positional

headache, recurrent

headache, severe

heat intolerance

heel-knee-shin test

hematoma, epidural-spinal

hemifacial spasm

hemiplegia, progressive

hemoglobin abnormality, neurologic complications of

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic encephalopathy, acute

hepatic failure

hepatic failure, acute

hepatitis B virus

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

herniated disc, cervical

herpes simplex virus

hexosaminidase-A

high arched feet

high arched palate

highly active antiretroviral therapy

hip flexor weakness

histochemistry of muscle

history of neurology

HMGcoA reductase inhibitors

Hodgkin's disease

Hoffmann's sign

homocysteine, serum

H-reflex testing

human immunodeficiency virus type 1

Huntington's chorea

hydroxychloroquine

hyperammonemic encephalopathy

hyperbilirubinemia

hypereosinophilic syndrome(HES)

hyperhomocysteinemia

hyperintense vessel sign

hyperparathyroidism

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypersegmented polys

hyperthyroidism

hypoglycorrhachia

hypoglycorrhachia, causes of

hypomyelination

hyponatremia with cerebral disorders

hyponatremic encephalopathy

hypotension, systemic

hypothalamus, disturbance of

hypothermia, causes of

hypotonia, infants

iatrogenic neurologic disorders

ileus, paralytic

imbalance, postural

immune checkpoint inhibitors

immune-related adverse events

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intranuclear

inclusion body myositis

incontinence, fecal

infant, evaluation of

infectious mononucleosis

infectious mononucleosis, neurologic findings with

initiative, lack of

intellectual deficit

intellectual deterioration

interferon alpha

internal capsule

internuclear ophthalmoplegia

interobserver agreement

interstitial pulmonary fibrosis

intestinal biopsy

intestinal pseudoobstruction

intracranial pressure, increased

intracranial pressure, increased, treatment of

intrinsic hand muscles, wasting of

iron, serum, low

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw jerk, abnormal

Krabbe's disease

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

laminectomy, cervical

laminectomy, lumbar

language disorder in adults

laughing, pathologic

left-right orientation

leg spasms, painful

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life expectancy

limb-girdle weakness

limbic encephalitis

lipid lowering agent

lipid storage disorder of CNS

lipid storage myopathy

liver function enzymes

liver transplantation

locked-in syndrome

loss of sympathy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

magnetic stimulation

magnetic stimulation, brain

malformation, CNS, congenital

malformation, vascular

manganese intoxication

masseter muscle wasting

meconium staining

mediastinum, lymph-node biopsy

mediastinum, mass of

mediastinum, widening

medical-legal aspects of neurology

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningeal gliomatosis

meningitis, actinomycotic

meningitis, aseptic

meningitis, bacterial

meningitis, blastomyces

meningitis, brucellosis

meningitis, candida

meningitis, carcinomatous

meningitis, chronic

meningitis, chronic benign lymphocytic

meningitis, cladosporium

meningitis, coenurosis

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, echinococcal

meningitis, eosinophilic

meningitis, fungal

meningitis, helminthic

meningitis, histoplasma

meningitis, leptospira

meningitis, lymphomatous

meningitis, Mollaret's

meningitis, neutrophilic

meningitis, nocardia

meningitis, paracoccidioides

meningitis, pneumococcal

meningitis, post myelography

meningitis, recurrent

meningitis, syphilitic

meningitis, toxoplasma

meningoencephalitis

meningoencephalitis, toxoplasma

mental retardation

mental retardation, familial

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, late-infantile

methylmalonic acid, serum

methylmalonic acidemia

microhemorrhage, intracerebral

midbrain, lesion of

middle cerebellar peduncle, lesion

mitochondrial disease

mitral valve lesion

mixed connective tissue disease

molecular genetics

monoclonal antibodies

monoclonal gammopathy

monomelic myositis

Montreal cognitive assessment

motor dysfunction

motor neuron disease

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR, hyperintense vessels

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, linear enhancement

MRI, nodular enhancement

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multicore myopathy

multinucleated giant cell

multiple sclerosis

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle stiffness

muscle strength, testing

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, facioscapulohumeral

muscular dystrophy, LAMA2

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, drug induced

myasthenia gravis, limb-girdle

myasthenia gravis, paraneoplastic

myasthenia gravis, presenting manifestations

myasthenic syndrome

mycoplasma pneumoniae

myelitis, longitudinal

myelitis, post infectious

myelitis, transverse

myelogram, cervical

myeloneuropathy

myelopathy hand

myelopathy, chronic progressive

myelopathy, vacuolar

myeloradiculopathy

myoclonic jerks

myoclonus, epilepsy

myokymia, facial

myopathy, acute

myopathy, axial

myopathy, centronuclear

myopathy, critically ill

myopathy, distal

myopathy, distal Laing

myopathy, distal, vacuolar

myopathy, drug-induced

myopathy, focal

myopathy, genetic

myopathy, inflammatory

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, necrotizing, immune-mediated

myopathy, proximal

myopathy, radiation-induced

myopathy, steroid induced

myopathy, toxic

myopathy, vacuolar

myositis, bacterial

myositis, eosinophilic

myositis, focal

myositis, fungal

myositis, granulomatous

myositis, ocular

myositis, parasitic

myotonia dystrophica

myotonia dystrophica, classification

myxedema, neurologic manifestations of

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, metastatic to CNS

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplasm, primary of CNS-classification

neoplasm, primary of CNS-intraventricular

neoplasm, primary of CNS-metastasizing to subarachnoid space

neoplasm, primary of CNS-treatment of

nerve conduction studies

nerve root enhancement

nerve root hypertrophy

neuroendocrinology

neurofibrillary degeneration

neurogenic bladder

neurologic complications of, chronic pulmonary disease

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neurological intensive care

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

neuropsychiatry

next-generation sequencing

night blindness

nutritional deficiency

nystagmus, gaze-evoked

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, vertical

ocular dysmetria

ocular motility, disorders of

ocular myopathy

oculogyric crisis

oculopharyngeal muscular dystrophy

old age, neurology of

operculum syndrome, bilateral

ophthalmoplegia

ophthalmoplegia, plus syndrome

ophthalmoplegia, progressive external

ophthalmoplegia, total

optic chiasm, enlarged

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

oral contraceptives

organ transplantation

oropharyngeal weakness

orthostatic hypotension

osteomyelitis, spinal

pain, abdominal

pain, interscapular

palmomental response

palpebromandibular synkinesia

paraneoplastic ganglionopathy

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, familial spastic, variants

paraparesis, flaccid

paraparesis, spastic

paraplegia, in flexion

paraplegia, progressive

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, hemiparesis in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, postencephalitic

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic disorder

PAS positive material in the brain

patent foramen ovale

pathologic reflex

patient information and support

pediatric neurology

Penumbra System

perivascular enhancement

pernicious anemia

peroneal nerve palsy

peroneal nerve, lesion of

peroxisomal disease

Persistent postural-perceptual dizziness

persistent vegetative state

personality change

pharyngeal sensation

photic sneeze reflex

pituitary stalk

pituitary stalk, lesion of

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

poison, organophosphate

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, familial

pons, infarction of

pons, lesion of

pontine hemorrhage

position sensation, abnormal

positive sharp waves

posterior column disease

posterior inferior cerebellar artery syndrome

posterior leukoencephalopathy syndrome

postictal neurologic deficits

postoperative neurologic complications

postural abnormality

precipitating factors

precocious puberty

prenatal diagnosis by amniocentesis

primary lateral sclerosis

progressive encephalomyelitis with rigidity syndrome

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

proximal muscle atrophy

proximal myotonic myopathy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

ptosis, bilateral

ptosis, unilateral

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

pure dysarthria

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis, progressive

radiation therapy, CNS treatment and complications with

ragged-red fibers

Raynaud's phenomenon

reflex, brainstem

reflex, cutaneous

release phenomena

remote effect of cancer on the nervous system

repetition, impaired

repetitive nerve stimulation

respiratory dyskinesias

respiratory failure

respiratory tract infection

retinal degeneration

retinal detachment

retinal exudates

retinitis pigmentosa

reversible neurologic disorder

rheumatic heart disease

rheumatoid arthritis

rigid spine syndrome

rubella encephalitis, progressive

saccadic eye movements, abnormal

saddle anesthesia

sarcoidosis, CNS

scalp tenderness

Schilder's disease

scleroderma, neurologic involvement with

sea-blue histiocytes

sedimentation rate, elevated

seizure, children

seizure, familial

seizure, febrile

seizure, hysterical

seizure, intractable

seizure, neonatal

seizure, tonic-clonic

selective serotonin reuptake inhibitors

sensory loss, cutaneous

sensory symptoms

serologic testing

serologic testing of cerebrospinal fluid

serotonin norepinephrine reuptake inhibitors

severe acute respiratory syndrome

shunt procedure, ventricular

sickle cell disease

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome

skin, lesions in neurologic disorders

skin, temperature difference

skull x-ray, abnormal

sleep pathology and physiology

slow virus infection of CNS

sodium channel dysfunction

somatosensory evoked potentials

spastic diplegia

spastic dysphonia

spastic paraplegia, type 11

spastic paraplegia, type 7

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal reflexes

spinal stenosis

spinal stenosis, familial

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 7

spinocerebellar degeneration

spongy degeneration of brain

spontaneous movements

spontaneous remission

standing difficulty

startle myoclonus

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

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

subarachnoid hemorrhage

substantia nigra

superior cerebellar artery infarction

superior sagittal sinus thrombosis

symmetric brain lesions

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

Tay-Sachs disease

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

tensilon test, false positive

testicular atrophy

testicular enlargement

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

thrombus, mural

tone, muscle, increased

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, impaired movements of

tongue, weakness

tonic cerebellar fits

tonic foot response

torticollis, post traumatic

toxoplasmosis, acquired

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trinucleotide repeats

unconsciousness

upgaze, paralysis of

urinary frequency

urinary incontinence

urinary retention

urinary urgency

vaccination, neurologic complications with

valsalva maneuver

ventricular enlargement

vertebral infarction

vertigo, episodic

very long chain fatty acids

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

visual evoked response

visual fields, constricted

vitamin deficiency

vitamin E deficiency

Vogt-Koyanagi-Harada syndrome

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

Wallerian degeneration

watershed infarcts

weakness, acute

weakness, episodic

weakness, fluctuating

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

Western immunoblot test

white matter disease

white matter disease, periventricular

wide based gait

winging of scapula

x-linked mental retardation

x-ray, thoracic spine

Showing articles 200 to 233 of 233 << Previous

Extensor Digitorum Brevis-a Predictor of Neuropathy in the Leg
BMJ 284:238, Kirkpatrick,C.T., 1982

Depression-Induced Neurologic Dysfunction
NEJM 305:642, Brumback,R.A.,et al, 1981

Post-encephalitic Parkinsonism:Current Experience
JNNP 44:670-676, Rail,D.,et al, 1981

Guidelines for the Determination of Death
JAMA 246:2184-2186, , 1981

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Clinical Criteria for Diagnosis of Machado-Joseph Disease:Report of a Non-Azorean Portuguese Family
Neurol 30:319-322, Lima,L.,et al, 1980

Three Primitive Reflexes in Normal Adults
Neurol 30:184-188, Jacobs,L.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Jaw Reflex in Friedreich Ataxia
Neurol 29:1049-1050, Salisachs,P., 1979

Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations
Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979

Familial Inverted Choreoathetosis
Neurol 29:1627-1631, Fisher,M.,et al, 1979

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Elevated Manganese Levels Associated with Dementia & Extrapyramidal Signs
Neurol 27:213, Banta,R.G.,et al, 1977

Cervical Myelographic Changes in Hypertrophic Interstitial Polyneuropathy
Ann Neurol 2:83, Hammerschlag,S.B.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Interpretation of Plantar Reflexes:Biasing Effect of Other Signs and Symptoms
JNNP 40:787-789, vanGijn,J.&Bonke,B., 1977

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

Neurologic Soft Signs in Schizophrenia & Character Disorders
Arch Gen Psych 33:845-853, Quitkin,R.,et al, 1976

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Case Records of MGH
NEJM 29l:l4l, 1974; 29l:263, 1974 Subscute Sclerosing Panencephalitis., , 1974

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis
Am J Med 52:128, Hermans,P.,et al, 1972

Persistent Vegetative State After Brain Damage (A Syndrome in Search of a Name)
Lancet 734, 1972 April., , 1972

Case Records of MGH-NEJM 287:506
1972 Lacunar Infarcts & Pontine Hemorrhage., , 1972

The planter Reflex of the Newborn
NEJM 285:502, Hogan,G.,et al, 1971

Brain Stem Tumors of Childhood & Adolescence
Am J Dis Child 119:465-472, Panitch,H.S.,et al, 1970

Early Descriptions of Common Neurologic Signs
Mayo Clinic Proc 43:807, Gutrecht,J., 1968

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

Neuro CPC of MGH
Cerebral Embolism & Infarction, NEJM 267:1084-109162., , 1962

Neurological & Psychiatric Signs Associated with SLE
JAMA l60:455, Clark,E.,et al, 1956

Clinical Pathological Conference, Scleroderma, Spastic Paraparesis & Chronic Myelogenous Leukemia
Prov. VAH, Dec. 12, 77., Finelli,P.F., 1850

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

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