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Differential
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abducens nerve paralysis

abducens nerve paralysis, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adult polyglucosan body disease

advances in neurology

alien hand syndrome

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

angiography, neurologic complications with

anterior horn cell disease

anterior spinal artery infarction

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants, untoward effects of

antiviral agents

apraxia of eye movements

arm swing, reduced

arrhythmia, cardiac

arterial dissection

arterial dissection, vertebral

asthma, poliomyelitis-like syndrome with

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

autonomic dysfunction

B 12 deficiency

basement membrane

basement membrane thickening

basophilic stippling of red blood cells

bladder dysfunction

border zone infarct

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial neuritis, prognosis of

brachial plexus

brachial plexus injury

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

brachial plexus, lesion of

bulbar palsy, progressive

burning paresthesia

calf amyotrophy

cardiac catheterization, neurologic complications

carotid artery disease

cashew nut sign

CAT scan, abnormal

CAT scan, emission, abnormal

central nervous system, infection of

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar lesion

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, artery to artery

cerebral embolism, cardiac origin

cerebral infarction

cerebral venous thrombosis

cerebrovascular accident

cerebrovascular accident, etiology

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, vascular territory involved

cervical collar

Charcot-Marie-Tooth

chelation therapy

cholesterol, HDL

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cold temperature

compartment syndrome

compartment syndrome, medial brachial fascial

compression neuropathy

conduction block

corpus callosum, infarction of

corpus callosum, lesion of

cortical hand knob

cortical hand knob infarct

cortical hemorrhage

cortical infarction

cortical infarction, small

cortical muscular atrophy

cortical topography

cortical-basal ganglionic degeneration

cranial neuropathy

cranial neuropathy, multiple

Creutzfeldt-Jakob disease, genetic

crying, pathologic

degenerative diseases of CNS

delay in diagnosis

dementia, frontotemporal

denervation of muscle

denervation potentials

developmental milestones, loss of

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

diplegia, atonic

diplegia, brachial

disability, neurological

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

down-beat nystagmus

drug abuse, neurologic complications of

drug induced neurologic disorders

dural sinus thrombosis

dysdiadochokinesia

dyskinesia, buccal lingual facial

electrical sensation

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, inflammatory disease

emotional lability

entrapment neuropathy

enzyme, muscle disease

epidemiology of neurology

episodic neurologic deficits

erectile dysfunction

extremity, cold

face, numbness of

facial weakness

facial weakness, bilateral

fine motor function, impaired

finger swelling

finger weakness

flaccid paralysis

flail arm syndrome

flu-like illness

foot drop, bilateral

fracture, long bone

Friedreich's ataxia

Friedreich's ataxia, late onset

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

girdle sensation

granular osmiphilic material

heavy metal intoxication

heralding manifestation

highly active antiretroviral therapy

hip flexor weakness

human immunodeficiency virus type 1

hypersegmented polys

iatrogenic neurologic disorders

ideomotor apraxia

inclusion bodies

incontinence, fecal

infraspinatus muscle

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

juvenile distal and segmental muscular atrophy

juxtacortical hemorrhage

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lacunar infarction

laughing, pathologic

Leber's hereditary optic neuropathy

leg weakness, bilateral

leg weakness, unilateral

Leigh's disease

leukoencephalopathy

Lhermitte's sign

life expectancy

life support, withdrawal of

livedo reticularis

lumbosacral plexopathy

lumbosacral plexus, neuritis

Man-In-The-Barrel syndrome

median nerve, lesion of

median neuropathy

memory, impairment of

mental status, abnormal

microangiopathy, brain

midbrain, atrophy

middle cerebral artery territory infarction

middle cerebral artery, emboli to

middle cerebral artery, occlusion of

Minamata disease

mitochondrial disease

mitochondrial encephalomyopathy

mitochondrial recessive ataxic syndrome

molecular genetics

monoclonal gammopathy

monomelic amyotrophy

mononeuropathy chronic inflammatory demyelinating

monoparesis, focal

motor neuron disease

movement disorder

MRI, brachial plexus

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, lumbosacral plexus

MRI, peripheral nerve

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multifocal acquired demyelinating sensory motor neuropathy

multiple myeloma

multiple system atrophy

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, distal weakness

myelin protein zero gene

myelitis, longitudinal

myeloneuropathy

myocardial infarction

myoclonic jerks

myoclonus, cortical

myoclonus, stimulus sensitive

neoplasm, intracranial

neoplasm, primary intracranial

neoplasm, primary of CNS

nerve conduction studies

nerve conduction studies, sensory

nerve enlargement

nerve root hypertrophy

neuritis, heavy metals causing

neuroendocrinology

neurogenic bladder

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

neuroophthalmology

neuropathy, ataxic

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, onion bulb

neuropathy, painful

neuropathy, peripheral

neuropathy, sensory

neuropathy, toxic

neuroprotective agents

night blindness

numbness, extremity

occupational neurologic disorders

occupational neuropathies

ophthalmoplegia

opportunistic infection, CNS

optic neuropathy

optic neuropathy, hereditary

orthostatic hypotension

owl's eye sign of spinal cord

paralysis, acute

paralysis, asymmetric

paraparesis, spastic

paraproteinemia

paresthesias, hands

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease, axial symptoms

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

peripheral blood smear

pernicious anemia

peroxisomal disease

physical therapy

pleocytosis of cerebrospinal fluid

poison, mercury

poliomyelitis-like illness

polyglucosan body

polyglucosan body disease

polyneuropathy, chronic inflammatory demyelinating

polyradiculoneuropathy

position sensation

positive sharp waves

posterior column disease

posterior fossa

posterior fossa, lesion of

precentral gyrus

precipitating factors

pregnancy, neurologic complications in

primary lateral sclerosis

progressive multifocal leucoencephalopathy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

proximal muscle atrophy

pseudoathetosis

pseudobulbar palsy

pseudoperipheral palsy

pseudoulnar palsy

psychological testing

psychomotor retardation

pupil, dilated and fixed, bilateral

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

rapidly progressing neurologic illness

real-time quaking-induced conversion

recruitment, reduced

reflex sympathetic dystrophy

reflex sympathetic dystrophy, children

Refsum's disease

remote effect of cancer on the nervous system

respiratory failure

retinitis pigmentosa

reverse split hand sign

reversible neurologic disorder

rigidity, axial

Rolandic artery

saccadic eye movements, abnormal

scalenus anticus syndrome

sciatic neuropathy

sensorimotor stroke

sensorineural hearing loss

sensory loss, cortical

sensory loss, cutaneous

sensory loss, leg

sensory loss, patchy

sensory loss, pseudoradicular

sensory loss, truncal

sensory nerve action potentials

sensory symptoms

sensory testing, quantitative

sequencing difficulty

shell fish poisoning

shoulder, numbness

shoulder, pain in

shoulder, weakness

shoulder-hand syndrome

skin, discoloration

skin, temperature difference

sleep pathology and physiology

small vessel disease

spinal cord, cervical

spinal cord, compression of

spinal cord, enlargement

spinal cord, infarction of

spinal cord, ischemic lesion of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 6

spinocerebellar degeneration

splenium of corpus callosum

spontaneous muscle activity

sports medicine, neurology of

stellate-ganglion block

stem cell transplantation

strokelike episodes

superior sagittal sinus thrombosis

suprascapular nerve

suprascapular neuropathy

supraspinatus muscle

sweating, abnormality of

sympathetic block

systemic illness

tandem gait, ataxic

Tangier's disease

thallium poisoning

thoracic outlet syndromes

thrombocytopenia

tomaculous neuropathy

tongue, atrophy

treatment of neurologic disorder

trinucleotide repeats

ulnar neuropathy

urinary incontinence

vascular endothelial growth factor

vestibular areflexia

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual fields, constricted

visual impairment

visual symptoms

vitamin deficiency

walking, difficulty with

walking, difficulty with in dark

watershed infarcts

weakness, acute

weakness, focal

weakness, generalized

weakness, progressive

weakness, proximal

West Nile fever

white matter disease

wide based gait

winging of scapula

word-finding difficulty

Showing articles 1650 to 1700 of 2428 << Previous Next >>

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Hippocampal Sclerosis Can be Reliably Detected by Magnetic Resonance Imaging
Neurol 40:1869-1875, Jackson,G.D.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Serial Magnetic Resonance Imaging in Neonatal Hypoxic-Ischemic Encephalopathy
J Pediatr 117:694-700, Byrne,P.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Perineal Reflex Sympathetic Dystrophy Treated with Bilateral Lumbar Sympathectomy
Ann Int Med 113:633-634, Olson,W.L., 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
NEJM 323:1488-1489, Johns,D.R., 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Internuclear Ophthalmoplegia in the Chiari Type II Malformation
Neurol 40:1850-1854, Arnold,A.C.,et al, 1990

Jugular Foramen Neuromas:A Review of 14 Cases
Surg Neurol 34:205-211, Tan,L.C.,et al, 1990

Surgical Treatment of Progressive Visual Loss in Traumatic Optic Neuropathy, Report of Two Cases
J Neurosurg 70:799-801, Guy,J.,et al, 1989

Internuclear Ophthalmoplegia in Tuberculous Meningitis
Tubercle 70:61-64, Teoh,R.,et al, 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Acute Ascending Myelopathy of the Spine
Spine 14:1084-1089, Yablon,I.G.,et al, 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

MR Imaging of Neurocysticercosis
AJR 153:857-866, Teitelbaum,G.P.,et al, 1989

A Radiologic Study of Dynamic Processes in Lacunar Dementia
Stroke 20:1488-1493, Tanaka,Y.,et al, 1989

A New Sign of Neurofibromatosis on Magnetic Resonance Imaging of Children
Arch Neurol 46:1222-1224, Goldstein,S.M.,et al, 1989

The Cerebellum in Sagittal Plane-Anatomic-MR Correlation:1. The Vermis
AJR 153:829-835, Courchesne,E.,et al, 1989

Interhemispheric Transfer in Patients with Incomplete Section of the Corpus Callosum, Verification with MRI
Arch Neurol 46:437-443, Risse,G.L.,et al, 1989

Outcome After Posthemorrhagic Ventriculomegaly in Comparison with Mild Hemorrhage Without Ventriculomegaly
J Pediatr 114:109-114, Shankaran,S.,et al, 1989

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
Neurol 39:440-442, Schaffert,D.A.,et al, 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Cerebellar Degeneration in Neuroleptic Malignant Synd:Neuropath & Review of Lit Concerning Heat-Related Nervous Syst Injury
JNNP 52:387-391, Lee,S.,et al, 1989

Multiple Sclerosis-Like Illness Occurring with Human Immunodeficiency Virus Infection
Neurol 39:324-329, Berger,J.R.,et al, 1989

Neurological Disease Associated with Antiphospholipid Antibodies
Ann Neurol 25:221-227, Briley,D.P.,et al, 1989

The Natural History of Prenatally Diagnosed Cerebral Ventriculomegaly
JAMA 261:1785-1788, Drugan,A.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Neurologic Findings in Men with Isolated Hypogonadotropic Hypogonadism
Neurol 39:223-226, Schwankhau,J.D.,et al, 1989

Syndrome of Cerebellar Ataxia and Hypogonadotrophic Hypogonadism:Evidence for Pituitary Gonadotrophin Deficiency
JNNP 52:407-409, Fox,A.C.K.,et al, 1989

Cerebellar Atrophy Following Acute Intoxication with Phenytoin
Neurol 39:432-433, Masur,H.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

Hypesthetic Ataxic Hemiparesis in a Thalamic Lacune
Stroke 20:819-821, Lee,N.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Cerebrovascular Disease & Antiphospholipis Antibodies in SLE, Lupus-Like Dis, & Primary Antiphospholipid Synd
Am J Med 86:391-399, Asherson,R.A.,et al, 1989

MR Imaging in Progressive Suupranuclear Palsy and Shy-Drager Syndrome
J Comput Assist Tomogr 13:555-560, Savoiardo,M.,et al, 1989

Frontal Lobe Syndrome in a Patient with Bilateral Globus Pallidus Lesions
Arch Neurol 46:1024-1027, Strub,R.L., 1989

Magnetic Resonance Imaging of Spinal Cord Lesions in Multiple Sclerosis
JNNP 52:459-466, Honig,L.S.&Sheremata,W.A., 1989

Quantitation of Cerebral Atrophy in Preclinical and End-Stage Alzheimer's Disease
Ann Neurol 25:450-459, delaMonte,S.M., 1989

Intermittent Obstructive Hydrocephalus in the Arnold-Chiari Malformation
Ann Neurol 26:401-404, Vrabee,T.R.,et al, 1989

Radiation-Induced Dementia in Patients Cured of Brain Metastases
Neurol 39:789-796, DeAngelis,L.M.,et al, 1989

Showing articles 1650 to 1700 of 2428 << Previous Next >>