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abdominal muscle paralysis

abductor pollicis brevis

abscess, vertebral

acetylcholine receptor antibody

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

Addison's disease

adult polyglucosan body disease

advances in neurology

alcohol intoxication

alcohol, neurologic complications with

alcoholic polyneuropathy

alien hand syndrome

alternating rapid movement

alveolar hypoventilation

amyloid plaques

amyotrophic chorea-acanthocytosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, complications with

amyotrophic lateral sclerosis, diagnosis of

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anemia, megaloblastic

anesthesia, general

aneurysm, intracranial

Angelman syndrome

angiography, neurologic complications with

ankle reflex, absent

anterior horn cell disease

anterior interosseous neuropathy

anterior tibial muscle weakness

anti citrullinated antibody

anti mGluR1 encephalitis

anti Tr antibodies

anti Yo antibody

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants, untoward effects of

antineurofascin antibodies

antithyroid antibodies

antiviral agents

aphasia, progressive, primary

apraxia of eye movements

apraxia, constructional

arm swing, reduced

arrhythmia, cardiac

arterial dissection

arterial dissection, carotid

arthrogryposis multiplex

arylsulfatase A

arylsulfatase B

ascending paralysis

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

atlanto axial dislocation, congenital

atrioventricular block

atrophy, muscle

attention deficit disorder with hyperactivity

autoimmune cerebellar ataxia

autoimmune disease

autonomic dysfunction

autoregulation, cerebral

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

axonal degeneration

B 12 deficiency

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

behavior, combative

behavioral disorder

Bence Jones protein

benign essential tremor

biologic markers

bitemporal visual field defect

bladder dysfunction

blind spot, enlarged

blinking, reduced

bone marrow suppression

bone marrow transplantation

border zone infarct

botulinum toxin

botulinum toxin, complications of

brachial neuritis

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

brainstem, atrophy

brainstem, lesion of

brainstem, neoplasms of

bruit, supraclavicular

bulbar palsy, progressive

burning paresthesia

calcification, intracranial

calf hypertrophy

campylobacter infection

carcinoma of lung

carcinoma of ovary

cardiac catheterization, neurologic complications

cardiovascular disease

carotid artery atherosclerosis

carotid artery disease

carotid artery stenosis

carpal tunnel syndrome

carpo-pedal spasm

Castleman's disease

CAT scan, abdomen

CAT scan, abnormal

CAT scan, contrast enhanced

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, pelvis

cavernous sinus, syndrome

central core disease

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, small, deep

cerebral ischemia

cerebral peduncle

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, enzymes in

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, complications with

cerebrovascular accident, incidence of

cerebrovascular accident, location of

cerebrovascular accident, mimics

cervical collar

cervical myelopathy

Charcot-Marie-Tooth

cheiralgia paresthetica

chelation therapy

chemotherapy, CNS treatment and complications with

cherry red spot

cherry red spot-myoclonus syndrome

chest x-ray, abnormal

chewing, impaired

cholesterol, HDL

choreoathetosis

choroid plexus, abnormality of

chromosomal abnormality

chronic progressive external ophthalmoplegia

claudication, extremity

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

Cockayne's syndrome

cogwheel rigidty

cold hands sign

cold temperature

collagen vascular disease

compartment syndrome

compartment syndrome, medial brachial fascial

complex regional pain syndrome

compression neuropathy

conduction block

confusional state, acute

congenital infection, CNS

congenital myopathy

congestive heart failure

contactin associated protein like 1 antibodies

contactin associated protein like 1 auto antibodies.(CNTN1)

contractures, joint

conversion reaction

cornea, opacity of

corneal reflex, abnormal

corneal reflex, absent

corpus callosotomy

corpus callosum

corpus callosum, atrophy of

corpus callosum, infarction of

corpus callosum, lesion of

corpus callosum, neoplasm of

corpus callosum, thinning

cortical hand knob

cortical hand knob infarct

cortical infarction

cortical infarction, small

cortical muscular atrophy

cortical topography

cortical wrist drop

cortical-basal ganglionic degeneration

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

crying, pathologic

cryptococcal meningitis

cryptococcoma, cerebral

cultured skin fibroblasts

Cushing's syndrome

cyclophosphamide

cyst, parenchymal

cyst, perineural

cyst, subcortical

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

dementia, presenile

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dermatomyositis

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic mononeuropathy

diagnostic criteria

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diplegia, brachial

disability, neurological

disc space infection

disc space narrowing

disconnection syndrome

disease modifying agents

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dorsal column stimulator

down-beat nystagmus

down-beat nystagmus, primary position of gaze

drug induced neurologic disorders

dysdiadochokinesia

dysferlinopathy

dyskinesia, buccal lingual facial

dystonia, children

dystonia, focal

dystonia, post traumatic

dystonia, treatment of

dystrophic calcification

eating disorder

electrical sensation

electrical stimulation, spinal nerves

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electromyogram, decremental response

electron microscopy

electrophoretic pattern, CSF

Emery-Dreifuss muscular dystrophy

emotional lability

empyema, epidural-spinal

encephalitis, autoimmune

encephalitis, episodic

encephalitis, human immunodeficiency virus type 1

encephalopathy, progressive

enterovirus infection of CNS

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

erectile dysfunction

erythromelalgia

evoked potentials

exercise intolerance

exercise-induced vascular symptoms

exome sequencing

extremity, cold

eye movement, disorders of

face, numbness of

facial appearance, abnormal

facial weakness

facial weakness, bilateral

facioscapulohumeral syndrome

failed medical management

failure to thrive

fatal familial insomnia

fatigable chewing

feeding disorder

fetal movements, reduced

fine motor function, impaired

finger flexor weakness

finger nose finger test

finger swelling

finger weakness

fingernails, abnormal

fingerprint bodies

flaccid paralysis

foot drop, bilateral

fornix, lesion of

fracture, long bone

fracture, long bones, nerve injury with

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal lobe, behavior with disease of

frontal lobe, infarction

frontal lobe, lesion of

fungal infection, CNS

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

Gantzer's muscle

gastrocnemius muscle weakness

gastroenteritis

gastrointestinal perforation

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genital hypoplasia

Gerstmann-Straussler-Scheinker disease

giant cell arteritis

girdle sensation

globus pallidus

globus pallidus, lesion of

glycogen debranching enzyme deficiency

glycogen storage disease

GM1 ganglioside antibodies

Gowers maneuver

granular osmiphilic material

granulomatous disease

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, prognosis of

Hallervorden Spatz disease

hallucination, auditory

handcuff neuropathy

handlebar palsy

Hand-Schuller-Christian disease

heart block, complete

heavy metal intoxication

heel-knee-shin test

hemidiaphragm, paralysis of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

hereditary myopathy with early respiratory failure

herniated disc, thoracic

high arched feet

high arched palate

histamine-2 receptor blockers

histochemistry of muscle

Horner's syndrome

human immunodeficiency virus type 1

hyperadrenalism

hyperamylasemia

hyperhidrosis, palmar

hyperhomocysteinemia

hyperinsulinism

hyperparathyroidism

hyperpigmentation of skin

hypersegmented polys

hyperthyroidism

hypogonadism, hypogonadotropic

hypokalemic periodic paralysis

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypotension, systemic

hypothalamus, disturbance of

hypothalamus, lesion of

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

IgG4-related disease

imbalance, postural

immunologic disease

immunosuppressive agents

inability to sit up

inability to stand on tiptoes

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inclusion body myositis

infant, evaluation of

infantile tremor syndrome

injection neuropathy

intellectual deficit

intellectual deterioration

intelligence quotient

interosseous muscles

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles

intrinsic hand muscles, wasting of

islet cell tumor

Jakob-Creutzfeldt disease

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

Klinefelter's syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

laminectomy, lumbar

lateral cutaneous nerve of forearm

laughing, pathologic

learning disability

learning disability, in children

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

lid closure, weakness of

life expectancy

life support, withdrawal of

lipid storage disorder of CNS

liver function enzymes

lumbrical muscles

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma involving CNS

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

Man-In-The-Barrel syndrome

marche a petits pas

Martin-Gruber anastamosis

mastoid opacification

mechlorethamine

median nerve, lesion of

median neuropathy

medical-legal aspects of neurology

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, children

meningitis, factors influencing mortality in

meningitis, late neurologic sequelae in

meningitis, lymphomatous

meningitis, neurologic aspects and complications of

mental retardation

mental status, abnormal

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylmalonic acid, serum

methylmalonic acidemia

microangiopathy, brain

microglial nodules

midbrain, atrophy

midbrain, lesion of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

mitochondrial disease

mitral valve prolapse

molecular genetics

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

monomelic amyotrophy

mononeuritis multiplex

mononeuropathy, motor

monoparesis, focal

motor dysfunction

motor neuron disease

motor neuron disease, juvenile form

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, high signal foci on

MRI, lumbosacral plexus

MRI, mass effect on

MRI, peripheral nerve

MRI, skull bone changes

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted fat suppression

mucopolysaccharidoses

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple sclerosis

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle spasm, paraspinal

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, causes of

muscle weakness, insidious onset of

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, congenital, Fukuyama type

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myelitis, longitudinal

myelitis, transverse

myeloneuropathy

myelopathy, chronic progressive

myelopathy, tract-specific

myocardial biopsy

myocardial infarction

myoclonic jerks

myoclonus, epilepsy

myopathy, amyloid

myopathy, autoimmune

myopathy, centronuclear

myopathy, desmin

myopathy, distal

myopathy, distal, vacuolar

myopathy, distal, Welander's

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, inflammatory

myopathy, mitochondrial

myopathy, myofibrillar

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, vacuolar

myotonia dystrophica

myxedema, neurologic manifestations of

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

neoplasm, pituitary

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nephrotic syndrome

nerve conduction studies

nerve conduction studies, motor

nerve conduction studies, sensory

nerve hypertrophy

nerve repair, end to end

nerve root enhancement

nerve root hypertrophy

neuritis, heavy metals causing

neuroendocrinology

neurofibrillary degeneration

neurofibromatosis 1

neurogenic bladder

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic evaluation

neurologic examination, focal

neurologic signs

neurologic symptoms

neurolymphomatosis

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronal intranuclear inclusion disease

neuronopathy, sensory and motor

neuroophthalmology

neuropathology, brain

neuropathy, autoimmune

neuropathy, bicycle

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, iatrogenic

neuropathy, medication induced

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory

neuropathy, toxic

neuroprotective agents

next-generation sequencing

Niemann-Pick disease

night blindness

nitrogen mustard

node of Ranvier

nodopathy, autoimmune

numbness, ascending

numbness, extremity

numbness, generalized

nystagmus, rotary

occupational neurologic disorders

occupational neuropathies

ocular motility, disorders of

old age, neurology of

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

orthostatic hypotension

osteomyelitis, spinal

ovarian dysgenesis

overlap syndrome

owl's eye sign of spinal cord

pacemaker, cardiac-transvenous

pain, abdominal

pain, interscapular

pain, management of chronic

pain, neuropathic

palliative care

paracentral lobule

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paraparesis, flaccid

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

paresthesias, feet

paresthesias, hands

parietal lobe, lesion of

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, L-dopa nonresponsive

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive material in the brain

patient information and support

penguin silhouette sign

percussion induced muscle contraction

pericardial effusion

periodic paralysis

periodic paralysis, thyrotoxic

peripheral blood smear

peripheral blood smear, abnormal

periventricular leukomalacia

pernicious anemia

Perrault syndrome

personality change

pheochromocytoma

photosensitivity, skin

physical therapy

pigmentary retinopathy

pituitary stalk

pituitary, lesion of

pleocytosis of cerebrospinal fluid

pleural effusion

pneumoencephalogram(PEG)

poliomyelitis-like illness

polyclonal gammopathy

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyneuropathy, familial

pons, lesion of

Poretti-Boltshauser syndrome

position sensation, abnormal

positional head-hanging test

positive sharp waves

post traumatic pain syndrome

posterior column disease

posterior fossa

posterior fossa, lesion of

posterior interosseous neuropathy

postoperative neurologic complications

postural abnormality

Prader-Labhart-Willi syndrome

precentral gyrus

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

primary aldosteronism

prisoners of war, neurologic complications in

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive spinal muscular atrophy

progressive supranuclear palsy

prolactin, elevated

pronator syndrome

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

pseudohypertrophy

pseudomedian nerve palsy

pseudoperipheral palsy

pseudoradial nerve palsy

pseudoulnar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

ptosis, unilateral

puberty, delayed

pure motor stroke

purple glove syndrome

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriceps atrophy

quadriceps weakness

quality of life

radial nerve, palsy of

radial pulse, unilateral decrease of

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

Raynaud's phenomenon

reading disorder, acquired

recruitment, reduced

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

release phenomena

REM sleep behavior disorder

remote effect of cancer on the nervous system

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retinal degeneration

retinitis pigmentosa

retrobulbar neuritis

Rett's syndrome

reverse split hand sign

reversible neurologic disorder

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rigid spine syndrome

rigidity, axial

rippling muscle disease

Rolandic artery

root lesion, nerve

rubella encephalitis

rubella encephalitis, progressive

saccadic eye movements, abnormal

salivation, excessive

sarcoidosis, CNS

scalenus anticus syndrome

scleroderma, neurologic involvement with

scoliosis, neurologic association with

sea-blue histiocytes

sedimentation rate

sedimentation rate, elevated

seizure, children

seizure, neonatal

sensorimotor stroke

sensorineural hearing loss

sensory loss, cortical

sensory loss, glove-stocking

sensory loss, patchy

sensory loss, pseudoradicular

sensory loss, truncal

sensory symptoms

sensory testing, quantitative

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

shoulder, numbness

shoulder, pain in

shoulder, swelling of

shoulder-hand syndrome

single photon emission computed tomography

sinuses, diseases of

skin, darkening of

skin, discoloration

skin, lesions in neurologic disorders

skin, temperature difference

skull bone, erosion

sleep pathology and physiology

slit lamp examination

small vessel disease

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

spinal cord, cervical

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, ischemic lesion of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinocerebellar ataxia

spinocerebellar ataxia type 12

spinocerebellar ataxia type 3/Machado Joseph disease

splenium of corpus callosum

spontaneous muscle activity

sports medicine, neurology of

standing difficulty

status epilepticus

stem cell transplantation

stereotyped behavior

steroid therapy, CNS treatment and complications with

stooped posture

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

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

subarachnoid hemorrhage

subclavian artery stenosis

substantia nigra

swallow evaluation

sweating, abnormality of

symmetric brain lesions

sympathetic block

syphilis, neurologic complications with

syphilis, ocular

systemic illness

tandem gait, ataxic

Tangier's disease

teeth, abnormal

teeth, number of in infants

temper tantrums

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of

thalamus, lesion of-bilateral

thallium poisoning

thoracic outlet syndromes

thrombocytopenia

Tolosa Hunt syndrome

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, swelling

tongue, weakness

tonic foot response

torticollis, post traumatic

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

tremor, post traumatic

tremor, postural

tremor, resting

tremor, treatment of

tremor, writing

trigeminal nerve, abnormality of

trinucleotide repeats

Trousseau's sign

tuberculoma of CNS

tyrosine hydroxylase deficiency

ulcers, fingertip

ulnar nerve, compression of

ulnar nerve, deep palmar branch of

ulnar neuropathy

ultrasonography

unconsciousness

unconsciousness, episodic

unconsciousness, transient

upgaze, paralysis of

urinary incontinence

urine test in toxic screen

vascular endothelial growth factor

ventricular enlargement

vertebral erosion

vertigo, positional

vibratory sensation, abnormal

violent behavior

viral infection

viral infection, CNS

Virchow-Robin spaces, dilated

vision, blurred

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual symptoms

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

voice, abnormality of

Volkmann's ischemia

walking, delayed

walking, difficulty with

weakness, congenital

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

white matter disease

wide based gait

winging of scapula

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 2850 to 2900 of 2948 << Previous Next >>

Brain Stem Arteriovenous Malformations
Arch Ophthalmol 86:255, Lessel,S.,et al, 1971

The Natural History of SLE by Prospective Analysis
Medicine 50:85, Estes,D.,et al, 1971

Spinabifida & Hydrocephalus
BMJ 4:796, Cook,R., 1971

Infantile Spinal Muscular Atrophy
Arch Neurol 25:276, Wilkins,R.,et al, 1971

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Hemifacial Atrophy
Brit J Oral Surg 9:102, Vickery,I.M., 1971

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

Dominant Juvenile Optic Atrophy
Arch Ophthalmol 85:133, Caldwell,J.,et al, 1971

Neurological Involvement in SLE
Singapore Med J 12:18, Tay,C.H.,et al, 1971

Pituitary Apoplexy in Five Patients with Pituitary Tumors
BMJ 2:267, Epstein,S.,et al, 1971

Down-Beat Nystagmus
Neuroophthal System of Ophthal Vol. XII, St. Louis, C. V. Mosby Co, 1971, p. 878., Duke-Elder,S.&Scott,G.L., 1971

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Occupational Nerve Lesions
In Handbook of Clinical Neurology 7:326-343, 1970, Edited by Vinken & Bruyn Chp. 12., Spaans,F., 1970

Multiple Cranial Nerve Signs From Supratentorial Tumors
J Neurosurg 33:178, Needham,C.,et al, 1970

Aqueductal Stenosis & Hydrocephalus After Mumps Encephalitis
NEJM 283:l505, Timmons,G.,et al, 1970

Acquired Sixth-Nerve Paresis in Children
Arch Ophthal 83:574-579, Robertson,D.M.,et al, 1970

The Nervous System in Sickle Cell Disease
Afr J Med Sci 1:33, Adelove,A.,et al, 1970

Diagnosis & Differentiation of Various Types of Hydrocephalus in Adults by Angiography
B J Radiol 43:383, Boller,F.,et al, 1970

Clinical Spectrum of Ocular Bobbing
JNNP 33:771, Susac,J.O.,et al, 1970

Olivopontocerebellar Atrophies:A Review
Medicine 49:227, Konigsmark,B., 1970

Internuclear Ophthalmoplegia, Typical & Atypical
Arch Ophthal 84:583, Cogan,D.G., 1970

Fetal & Newborn Virus Infections
J Pediatr 77:315, Overall,J.,et al, 1970

Abnormal Head Size, In Neurology In Pediatrics
(Ed) , 1970 Year Book Med. Publishers, p. 61., Bray,P.F., 1970

Hydrocephalus Due to Ectasia of the Basilar Artery
J Neurol Sci 8:465, Ekbom,K.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Further Experience with the Syndrome of"Normal"Pressure Hydrocephalus
J Neurosurg 31:279, Ojemann,R.G.,et al, 1969

Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
Am J Ophthalmol 67:561, Johnson,R.V.,et al, 1969

Experimental Virus-Induced Hydrocephalus
J Neurosurg 3l:l, Margolis,G.,et al, 1969

Encephalitis with Myoclonus in Whipple's Disease
JNNP 32:338, Stoupel,N.,et al, 1969

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Cerebrospinal Fluid Pulsations in Occult Hydrocephalus due to Ectasia of Basilar Artery
Acta Neurochir 20:l, Ekbom,K.,et al, 1969

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Olfactory Groove Tumor, In Clin. Neuro-ophthalmol
(Ed) , 3rd edition, The Williams & Wilkins Co, Baltimore, 1969, p. 2175-2177., Walsh,F.B., 1969

Parietal Lobe Syndromes
In Handbk of Clinical Neurology, Vinken & Bruyn, Ed, North-Holland Publ Co, Amsterdam, V2, Ch21, p., 84wesbury,E.C.O., 1969

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

Degen. & Exog. Lesions of the Pallidum & Striatum
In:Vinker P. J. , Bruyn G. W. eds. Handbook of Clin Neurol Vol 6, Amsterdam:N. Holland Publ 1968:652, ellinger,D., 1968

Degen. & Exog. Lesions of the Pallidum & Striatum
In:Vinker P. J. , Bruyn G. W. eds. Handbook of Clin Neurol Vol. 6 Amsterdam:N. Holland Publ 1968:672, ellinger,D., 1968

Nine Neuropathies
Med Ann of the Dist of Columbia 37:89, Stevens,H., 1968

The Mechanism of Normal Pressure Hydrocephalus
J Neurol Sci 7:48l, Geschwind,N., 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Whipple's Disease Presenting with Ocular Inflammation & Minimal Intestinal Symptoms
John's Hopkin's Med Jour 123:175, Knox,D.L.,et al, 1968

Increased Intracanial Pressure & Pulmonary Edema, Pt. I
J Neurosurg 28:112, Ducker,T.B., 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Function of the Basal Ganglia
Handbook of Clinical Neurology 6:90-115, Ward,A., 1968

Neuropathological Findings in Three Cases of Persistent Dyskinesia following Phenothiazine Medication
J Neurol Sci 7:263, Hunter,R.,et al, 1968

Diphenylhydantoin Intoxication & Cerebrospinal Fluid Protein
Neurol 18:1009-1011, Rawson,M.D., 1968

Myopathy of the Quadriceps Muscles
J Neurol Sci 7:201, VanWijngaarden,G.K.,et al, 1968

The Oculopharyngeal Syndrome
JAMA 203:1003, Murphy,S.F.,et al, 1968

Sensory Symptoms, In Multiple Sclerosis
Livingston Ltd.:100-106, McAlpine,D.,et al, 1968

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