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abdominal distention

abdominal reflex, absent

abducens nerve paralysis

abducens nerve paralysis, bilateral

abducens nerve paralysis, children

absence in petit mal epilepsy

accomodation, abnormal

acquired immunodeficiency syndrome

acral sensory symptoms

ACTH, ectopic syndrome of

acute ataxia of childhood

acute intermittant porphyria

acyl CoA dehydrogenase deficiency

Addison's disease

adverse drug reaction

alcohol intolerance

alcohol, neurologic complications with

alcoholic polyneuropathy

alkylating agents

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

amphiphysin antibodies

amyloid angiopathy, cerebral

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis-like syndrome

anal wink response

ANA-negative systemic lupus erythematosus

anemia, megaloblastic

anesthesia, general

aneurysm, intracranial

angiography, cerebral

angiography, neurologic complications with

animal exposure

ankle reflex, absent

ankle, swelling of

antecedent illness

anterior horn cell disease

anterior spinal artery

anterior spinal artery infarction

anterior tibial muscle weakness

anti citrullinated antibody

anti GQ1b IgG antibody

anti MAG antibodies

antibiotics, neurologic complications with

antibodies to voltage-gated calcium channels

anticoagulant, treatment

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, dosage

anticonvulsants, mechanism of action of

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiganglioside antibodies

antiviral agents

apraxia of eye movements

arm swing, reduced

arrhythmia, cardiac

ascending paralysis

ataxia telangiectasia

ataxia, acute onset

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atrial fibrillation

auditory evoked brainstem potentials

autoimmune disease

automatic behavior

automobile accidents

autonomic cardiovascular reflexes

autonomic dysfunction

axonal degeneration

axonal spheroid

azidodeoxythymidine

B 12 deficiency

B cell lymphoma

bacterial infection

Balint's syndrome

barbiturate anesthesia

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

Bassen-Kornzweig syndrome

behavioral disorder

Bell's phenomenon

benign epilepsy of childhood

benign essential tremor

bicaudate index

Bickerstaff's brainstem encephalitis

bicycle injuries

bladder dysfunction

blood brain barrier

blood dyscrasias, neurologic findings with

bone marrow biopsy

bone marrow suppression

bone marrow transplantation

botulinum toxin

botulism antitoxin

botulism immune globulin

botulism, infant

brain scan, abnormal

brainstem, lesion of

Brown-Vialetto-Van Laere syndrome

bulbar palsy, acute

burning paresthesia

burst suppression pattern, electroencephalogram

calf hypertrophy

campylobacter infection

carcinoma of bladder

carcinoma of breast

carcinoma of lung

carcinoma of pancreas

carcinoma of stomach

cardiac arrest and resuscitation

cardiac transplantation

cardiovascular disease

carnitine deficiency myopathy

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, chest

CAT scan, complication with

CAT scan, emission, abnormal

CAT scan, metrizamide

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus

caudate nucleus, atrophy

caudate nucleus, lesion of

cavernous sinus

cavernous sinus syndrome, bilateral

cavernous sinus, syndrome

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellum, disease of

cerebral cortex

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, seizure with

cerebrovascular disease

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

Chinese paralytic syndrome

chorea, familial

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

chronic graft versus host disease

chronic idiopathic anhidrosis

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

coma, medically induced

conduction block

confusional state, acute

congenital heart disease

congenital myasthenic syndromes

congenital myopathy

congestive heart failure

contractures, joint

contrast agents, neurotoxicity of

controversies in neurology

conus medullaris, lesion of

convergence, impaired

conversion reaction

cornea, abnormal

cornea, opacity of

corneal reflex, abnormal

corpus callosum, lesion of

cortical blindness

corticofugal inhibition

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

critical care unit

critical illness

cyclophosphamide

cystic fibrosis, neurologic complications with

cystoisospora belli

cytomegalovirus infection

deep gray nuclei

deep tendon reflexes

degenerative diseases of CNS

Dejerine-Sottas syndrome

delay in diagnosis

dementia, transmissible

denervation of muscle

denervation potentials

descending paralysis

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes mellitus

diabetes mellitus, chemical

diagnostic criteria

diaphragmatic paralysis

dichotic hearing

dideoxycytidine

differential diagnosis

difficulty climbing stairs

dilantin, factors influencing metabolism of

dilantin, toxicity

diplegia, brachial

disability, neurological

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

down-beat nystagmus

drug induced neurologic disorders

drug induced neurologic disorders in children

drug interactions

drug withdrawal

dysdiadochokinesia

dyskinesia, buccal lingual facial

dystonia, children

edema, periorbital

electrical sensation

electrocardiogram, abnormal

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, indications

electroencephalogram, monitoring, continuous

electroencephalogram, periodic complexes

electroencephalogram, spike activity

electroencephalogram, urgent

electroencephalogram, video monitoring with

electromyogram, decremental response

electromyogram, incremental response

electron microscopy

electrophoretic pattern, serum

emergencies, neurologic

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, Powassan

encephalitis, unknown etiology

encephalitis, viral

encephalomyelitis

encephalomyelitis, paraneoplastic

encephalopathy, progressive

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

eosinophilic granulomatosis with polyangiitis

epidemiology of neurology

epilepsia partialis continua

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

erectile dysfunction

evoked potentials

exercise intolerance

exercise-related muscle strength increase

exome sequencing

extraocular muscle lesion

eye movement, disorders of

face, elongated

face, numbness of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial sweating, unilateral

facial weakness

facial weakness, bilateral

failed medical management

failure to thrive

febrile infection-related epilepsy syndrome

feeding disorder

fine motor function, impaired

fingernails, abnormal

Fisher's syndrome

Fisher's syndrome, atypical

flaccid paralysis

flu-like illness

fluorescent treponema antibody absorption(FTA-ABS)

fluoroquinolones

flushing, unilateral

fontanel, bulging

food-borne infection

foot drop, bilateral

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal lobe status

fundus, abnormality of

F-wave response

gamma amino butyric acid

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gasserian ganglia

gastroenteritis

gastrointestinal disease, neurologic complications

gastrointestinal motility

gaze palsy, horizontal

gaze palsy, supranuclear

gaze palsy, vertical

general paresis of the insane

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

geographic location

Gerstmann-Straussler-Scheinker disease

girdle sensation

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glucose tolerance test, abnormal

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

gluten-free diet

Gowers maneuver

granuloma, eosinophilic

granulomatous disease

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, ataxic form

Guillain Barre syndrome, axonal form

Guillain Barre syndrome, complications

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, etiology of

Guillain Barre syndrome, infantile and childhood form

Guillain Barre syndrome, neuropathology of inflammatory lesion of

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, pharyngeal-cervical-brachial variant

Guillain Barre syndrome, prognosis of

Guillain Barre syndrome, sensory

Guillain Barre syndrome, variant forms of

hallucination, auditory

hallucination, visual

head circumference

headache, elderly

headache, paroxysmal

headache, positional

heat intolerance

heavy metal intoxication

heel-knee-shin test

hemidiaphragm, paralysis of

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herpes simplex virus

herpes virus infection

herpes, genital

high arched feet

high arched palate

hip flexor weakness

hippocampus, hyperintense

histamine-2 receptor blockers

histochemistry of muscle

Hodgkin's disease

Hodgkin's disease, neurologic involvement with

Horner's syndrome

hospital length of stay

hot cross bun sign

H-reflex testing

human diploid cell rabies vaccine

human immunodeficiency virus type 1

hydrocephalus, communicating

hyperalimentation

hyperamylasemia

hyperemisis gravidarum

hyperhomocysteinemia

hyperparathyroidism

hyperperfusion syndrome

hyperphosphatasia

hyperpyrexia, CNS disorder causing

hyperthyroidism

hypocholesterolemia

hypoglycemic coma

hypoglycorrhachia

hypokalemic alkalosis

hypokalemic paralysis

hypokalemic periodic paralysis

hypoosmolality of serum

hypoparathyroidism

hypoparathyroidism, idiopathic

hypophosphatemia

hypopigmentation of skin

hypotension, systemic

hypotonia, causes of

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

ideomotor apraxia

ileus, paralytic

immune checkpoint inhibitors

immunoelectrophoresis, serum

immunofluorescence

immunofluorescent"band"test

immunosuppression

immunosuppressive agents

inability to sit up

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inattention, auditory

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infant, evaluation of

infantile neuronal degeneration

infantile spasm

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intestinal obstruction

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, lobar

intracranial hypertension, benign

intracranial pressure, increased

intraneural hemorrhage

intrathecal chemotherapy

intrinsic hand muscles, wasting of

Isaacs syndrome

Jakob-Creutzfeldt disease

joint hypermobility

juvenile myoclonus epilepsy

Korsakoff's psychosis

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

laryngeal spasm

leg weakness, bilateral

leg weakness, unilateral

Lennox-Gastaut syndrome

leukemia, neurologic findings assoc.with

leukoencephalopathy

level of consciousness, decreased

Lewy body disease, diffuse

Lhermitte's sign

lid closure, weakness of

light-near dissociation, causes of

limbic encephalitis

liver function enzymes

long bone lesion

Lowe's syndrome

lumbar puncture, complications of

lumbosacral radiculopathy

lung transplantation

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lymphoma, primary of CNS

malabsorption syndrome

malformation, CNS, congenital

malignancy, occult

malignant hyperpyrexia

McLeod syndrome

median neuropathy

mediastinum, mass of

medication withdrawal

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal biopsy, false negative

meningeal enhancement

meningitis, aseptic

meningitis, basilar

meningitis, carcinomatous

meningitis, elderly

meningitis, leukemic

meningitis, lupus

meningitis, lymphomatous

meningitis, neutrophilic

meningitis, recurrent

meningitis, syphilitic

meningoencephalitis

meningoencephalopathy

mental retardation

mental status, abnormal

mesial temporal sclerosis

metabolic acidosis

methylhydrazine derivatives

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, intractable

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

monoamine oxidase inhibitors

monoclonal gammopathy

mononeuritis multiplex

mononeuritis multiplex, causes of

mononeuropathy multiplex

mononeuropathy, children

motor dysfunction

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, hyperkinetic

MRI, abnormal, seizure causing

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal foci on

MRI, optic nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, sulcal hyperintensity

multicore myopathy

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple organ failure

multiple sclerosis

multiple sclerosis, acute

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle relaxant

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, LAMA2

myasthenia gravis

myasthenia gravis, congenital

myasthenia gravis, etiology of

myasthenia gravis, neuromuscular junction in

myasthenia gravis, treatment of

myasthenic syndrome

myasthenic syndrome, treatment of

mycoplasma pneumoniae

myelitis, longitudinal

myelogram, cervical

myelogram, complications of

myelogram, metrizamide

myeloma, osteosclerotic

myelopathy, carcinomatous

myoclonic jerks

myoclonus, epilepsy

myoclonus, segmental

myokymia, facial

myopathy, acute

myopathy, centronuclear

myopathy, critically ill

myopathy, drug-induced

myopathy, hereditary

myopathy, metabolic

myopathy, mitochondrial

myopathy, necrotizing

myopathy, steroid induced

myopathy, toxic

myotonic discharges

nausea and vomiting

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, metastatic to Dura

neoplasm, primary intracerebral

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve growth factor

nerve hypertrophy

nerve root enhancement

nerve root hypertrophy

neuralgia, treatment of

neuritis, heavy metals causing

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, burden

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic examination, abnormal

neurologic signs

neurologic symptoms

neurological intensive care

neurolymphomatosis

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal intranuclear inclusion disease

neuronal migration disorder

neuronopathy, sensory

neuroophthalmology

neuropathology, brain

neuropathy, acute

neuropathy, asymptomatic

neuropathy, ataxic

neuropathy, chronic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, small-fiber

neuropathy, small-fiber, painful sensory

neuropathy, toxic

neuropsychiatry

next-generation sequencing

nitrogen mustard

NMDA antagonists

nonsteroidal anti-inflammatory drug

numbness, ascending

numbness, extremity

numbness, generalized

nutritional deficiency

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, monocular

nystagmus, vertical

occipital lobe, lesion of

occupational neurologic disorders

oculovestibular reflex

old age, neurology of

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, neonatal

ophthalmoplegia, postinfectious

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

optic nerve, enhancement

optic nerve, hypoplasia of

optic neuritis, bilateral

optic neuropathy

oral contraceptives

organ transplantation

oropharyngeal weakness

orthostatic hypotension

overlap syndrome

pain, abdominal

pain, absence or indifference to

pain, threshold

pain, total body

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paraneoplastic ganglionopathy

paraparesis, flaccid

paraplegia, acute

paraproteinemia

parenteral alimentation

paresthesias, feet

paresthesias, generalized

paresthesias, hands

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, asymmetric onset

Parkinson disease, axial symptoms

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, L-dopa nonresponsive

Parkinson disease, rapid progression

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal exertion-induced dyskinesia

paroxysmal hemiplegia

paroxysmal neurologic deficits

pathologic reflex

penguin silhouette sign

periarteritis nodosa

pericardial effusion

pericardial friction rub

periodic paralysis

periodic paralysis, thyrotoxic

perioral numbness

peripheral blood smear

peripheral blood smear, abnormal

pernicious anemia

petit mal status

photosensitivity, skin

plasma cell dyscrasia

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

poliomyelitis-like illness

polycystic kidneys

polymerase chain reaction

polymerase chain reaction, false negative

polyneuritis, acute sensory

polyneuropathy, acute sensory

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, childhood

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyneuropathy, familial

polyneuropathy, lymphomatous

polyneuropathy, subacute idiopathic demyelinating

polyneuropathy, uremic

polyradiculoneuropathy

pons, lesion of

position sensation

position sensation, abnormal

positional head-hanging test

positive sharp waves

posterior column disease

postictal encephalopathy

postoperative neurologic complications

postural abnormality

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, neurologic complications in

prevention of neurologic disorders

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

prolactin, elevated

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false positive

protozoan infection

pseudoathetosis

pseudobulbar palsy

pseudointernuclear ophthalmoplegia

pseudostatus epilepticus

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, acute

psychosis, cause of

psychosocial aspects

psychotic behavior

ptosis, acute onset

ptosis, bilateral

ptosis, unilateral

pulmonary embolism

pulmonary infiltrates

pulmonary nodules

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, dilated, unilateral

pupil, light reflex, abnormal

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriceps atrophy

quadriparesis, progressive

quadriplegia, transient

quality of life

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

reflex, brainstem

reflex, cutaneous

remote effect of cancer on the nervous system

renal failure, acute

renal transplantation

renal tubular acidosis

repetitive nerve stimulation

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory paralysis, pharmacologic

respiratory tract infection

reticular activating system

reticulum cell sarcoma

retina, abnormal

retinal hemorrhages

retinitis pigmentosa

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

riboflavin transporter deficiency

rigidity, axial

Riley-Day syndrome

root lesion, nerve

saccadic eye movements, abnormal

saddle anesthesia

salivation, excessive

sclerosis, bone

scoliosis, neurologic association with

sedimentation rate, elevated

segmental demyelination

seizure, adult onset

seizure, age of onset

seizure, centrencephalic

seizure, children

seizure, classification of

seizure, complications following

seizure, diagnosis of

seizure, differential diagnosis of

seizure, drug resistance

seizure, drug-induced

seizure, elderly

seizure, equivalents

seizure, etiology of

seizure, familial

seizure, febrile

seizure, febrile, risk of epilepsy following

seizure, headache with

seizure, hysterical

seizure, injury following

seizure, intractable

seizure, intractable, treatment of

seizure, minor motor

seizure, nonconvulsive

seizure, nonepileptic

seizure, occipital lobe

seizure, paradoxical

seizure, petit mal

seizure, photosensitive

seizure, prognosis in adults

seizure, prognosis in childhood

seizure, psychomotor-frontal lobe

seizure, psychomotor-temporal lobe

seizure, psychosocial aspects of

seizure, reading induced

seizure, recurrent

seizure, risk factors for

seizure, self-induced

seizure, sexual manifestations with

seizure, stimulus sensitive

seizure, surgical treatment of

seizure, tonic-clonic

seizure, treatment of

seizure, treatment of, first

seizure, treatment of, monotherapy

seizure, withdrawal

seizure, workup of

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss, asymmetric

sensory loss, band distribution

sensory loss, patchy

sensory loss, truncal

sensory nerve action potentials

sensory polyneuropathy

sequencing difficulty

serologic testing

serum alanine aminotransferase

serum lipase, elevated

severe acute respiratory syndrome

shunt procedure, ventricular

Shy-Drager syndrome

simultanagnosia

single photon emission computed tomography

single-fiber electromyography

Sjogren's syndrome

skin, darkening of

skin, lesions in neurologic disorders

skull x-ray, abnormal

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

small vessel vasculitis

sodium valproate

sodium valproate, intravenous

sodium valproate, toxicity

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, loss of

spinal cord, enlargement

spinal cord, infarction of

spinal cord, lesion of

spinal cord, pathologic exam of

spinal headache

spinal muscular atrophy

spinal muscular atrophy, classification

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spinopontine atrophy, dominant

spirochete infection

spongy degeneration of brain

spontaneous remission

standing difficulty

status asthmaticus

status epilepticus

status epilepticus, intractable

status epilepticus, nonconvulsive

status epilepticus, psychogenic

status epilepticus, recurrent

stem cell transplantation

steroid therapy, CNS treatment and complications with

stimulant drugs

striatum, lesion of

subdural hematoma

sulcal effacement

superior oblique palsy

suspended sensory loss

sweating, abnormality of

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, meningomyelitis

syphilis, neurologic complications with

syphilis, ocular

systemic illness

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporal lobe, status

temporal lobectomy

tensilon test, false positive

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

third nerve palsy

thrombocytopenia

thrombotic thrombocytopenia purpura

thyroid function tests

tick-borne encephalitis

tomaculous neuropathy

tongue, fasciculations of

tongue, impaired movements of

tongue, numbness of

tongue, weakness

toxic encephalopathy

toxins, nervous system

transcobalamin II, abnormal

transcobalamin II, hereditary absence of

transient neurologic deficit

transverse smile

treatment of neurologic disorder

treatment, empirical

tremor, cerebellar

tremor, postural

tremor, resting

trigeminal neuralgia, treatment of

trigeminal neuropathy

trinucleotide repeats

tyrosine hydroxylase deficiency

ulcerative colitis

ulnar neuropathy

ultrasonography, nerve

unconsciousness

upgaze, paralysis of

urinary incontinence

urinary retention

urine osmolality, elevated

urine test for metabolic disorders

urine test in toxic screen

vaccination, neurologic complications with

vascular endothelial growth factor

vectors of infection

Venereal Disease Research Laboratory test

vibratory sensation

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

viral isolation

vision, blurred

visual acuity, decreased

visual evoked response

visual impairment

visual symptoms

vitamin deficiency

vitamin E deficiency

vitamin supplementation

vocal cord paralysis

voice, abnormality of

Waldenstrom's macroglobulinemia

walking, difficulty with

Watson-Schwartz reaction

weakness, acute

weakness, episodic

weakness, fatiguable

weakness, generalized

weakness, infant

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weakness, severe

weaning from respirator, failure to

Wernicke's encephalopathy

West Nile fever

white matter disease

wide based gait

winging of scapula

xeroderma pigmentosa

X-linked bulbospinal neuronopathy

x-linked mental retardation

Showing articles 150 to 200 of 343 << Previous Next >>

Nonconvulsive Status Epilepticus in Thrombotic Thrombocytopenic Purpura
Neurol 47:1079-1081, Blum,A.S.&Drislane,F.W., 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Acute Lumbosacral Polyradiculopathy Due to Cytomegalovirus in Advanced HIV Disease:CSF Findings in 17 Patients
JNNP 61:456-460, Miller,R.F.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

Permanent Hemiparesis Due to Partial Status Epilepticus
Neurol 45:187-188, Borchert,L.D.&Labar,D.R., 1995

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

Reading-Induced Absence Seizures
Neurol 45:1623-1624, Singh,B.,et al, 1995

Complex Partial Status Epilepticus Accompanied by Serious Morbidity and Mortality
Neurol 45:1499-1504, Krumholz,A.,et al, 1995

Site of Autonomic Dysfunction in a Patient with Ross'Syndrome and Postganglionic Horner's Syndrome
Neurol 45:2094-2096, Wolfe,G.I.,et al, 1995

Lamotrigine for the Treatment of Epilepsy in Childhood
J Pediatr 127:991-997, Besag,F.M.C.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Polyarteritis Nodosa-Induced Quadriplegia
Ann Int MEd 122:731-732, Smith,D.L.,et al, 1995

Acute Lumbosacral Polyradiculopathy in Acquired Immunodeficiency Syndrome:Experience in 23 Patients
Ann Neurol 35:53-58, So,Y.T.&Olney,R.K., 1994

Rapidly Evolving Myopathy with Myosin-Deficient Muscle Fibers
Ann Neurol 35:273-279, 2571994., Al-Lozi,M.T.,et al, 1994

Ceftazidime-Related Nonconvulsive Status Epilepticus
Arch Int Med 154:586-589, Klion,A.D.,et al, 1994

Clinicopath Conf
Chronic Idiopathic Anhidrosis, Case 29-1994, NEJM 331:259-265994., , 1994

Baclofen-induced Generalized Nonconvulsive Status Epilepticus
Ann Neurol 36:113-114, Zak,R.,et al, 1994

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

Acute Sensory Neuronopathy:Report of a Child with Remarkable Clinical Recovery
Neurol 44:762-764, Fernandez,J.M.,et al, 1994

Complex Partial Status Epilepticus:A Recurrent Problem
JNNP 57:835-837, Cockerell,O.C.,et al, 1994

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

Ifosfamide-Induced Nonconvulsive Status Epilepticus
Arch Neurol 50:1104-1105, Wengs,W.J.,et al, 1993

The Neurologic Syndrome of Vitamin E Deficiency:A Significant Cause of Ataxia
Neurol 43:2167-2169, Kayden,H.J., 1993

2', 3'-Dideoxycytidine (ddC) Toxic Neuropathy:A Study of 52 Patients
Neurol 43:358-362, Berger,A.R.,et al, 1993

Clinicopath Conf
Axonal Polyneuritis Assoc with IgA Lambda Multiple Myeloma, Case 21-1993, NEJM 328:1550-1558993., , 1993

Accelerated Neuropathy of Renal Failure
Arch Neurol 50:536-539, Ropper,A.H., 1993

Polyneuropathy Complicating Bone marrow and Solid Organ Transplantation
Neurol 43:1513-1518, Amato,A.A.,et al, 1993

Life Threatening Focal Status Epilepticus Due to occult Cortical Dysplasia
Arch Neurol 50:695-700, Desbiens,R.,et al, 1993

Ciprofloxacin-Induced Complex Partial Status Epilepticus Manifesting as an Acute Confusional State
Neurol 43:1619-1621, Isaacson,S.H.,et al, 1993

Juvenile Myoclonic Epilepsy
Arch Neurol 50:594-598, Grunewald,R.A.&Panayiotopoulos,C.P., 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

Complex Partial Status Epilepticus in a Patient with Dural Metastases
Neurol 43:2389-2392, Steg,R.E.,et al, 1993

Acute Myopathy and Neuropathy in Status Asthmaticus:Case Report and Literature Review
Muscle & Nerve 16:84-90993., Lacomis,D.,et al, 1993

Serum anti-GQ1b IgG antibody is Associated with Ophthalmoplegia in Miller Fisher Syndrome and Guillain-Barre Syndrome: Clinical and Immunohistochemical Studies
Neurol 43:1911-1917, Chiba, A.,et al, 1993

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

The Guillain-Barre Syndrome
NEJM 326:1130-1136, Ropper,A.H., 1992

Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992

Ceftazidime Encephalopathy:Absence Status and Toxic Hallucinations
JNNP 55:333-334, Jackson,G.D.&Berkovic,S.F., 1992

Aspartame Exacerbates EEG Spike-Wave Discharge in Children with Generalized Absence Epilepsy:A Double-Blind Study
Neurol 42:1000-1003, Camfield,P.R.,et al, 1992

Effect of Add-on Amantadine Therapy for Refractory Absence epilepsy
J Pediatr 121:819-821, Shahar,E.M.&Brand,N., 1992

Typical Absence Seizures in Adults:Clinical, EEG, Video-EEG Findings & Diagnostic/Syndr Consider
JNNP 55:1002-1008, Panayiotopoulos,C.P.,et al, 1992

Prolonged Absence Status epilepticus Assoc with Carbamazepine, Increased ICP & Trans MRI Abnor
Neurol 42:2198-2201, Callahan,D.J.&Noetzel,M.J., 1992

Delayed Diagnosis of Juvenile Myoclonic Epilepsy
JNNP 55:497-499, Grunewald,R.A.,et al, 1992

Nonconvulsive Generalized Status Epilepticus and AIDS
Ann Int Med 116:171-172, Wong,M.C., 1992

Clinical and EEG Features of Status Epilepticus in Comatose Patients
Neurol 42:100-104, Lowenstein,D.H.&Aminoff,M.J., 1992

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