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abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

adult polyglucosan body disease

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

Alexanders disease

alpha glucosidase

alveolar hypoventilation

Alzheimer's disease

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, juvenile

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis-like syndrome

anesthesia, general

angiography, cerebral, false negative

angiography, cerebral, negative

ankylosing spondylitis

anterior horn cell disease

anterior tibial muscle weakness

antibodies to measles

antiviral agents

arrhythmia, cardiac

arylsulfatase A

ascending paralysis

aspartate aminotransferase

ataxia telangiectasia

ataxia, cerebellar

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autoimmune disease

autonomic dysfunction

autonomic neuropathy

axonal degeneration

B 12 deficiency

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basement membrane

basement membrane thickening

biologic markers

bladder dysfunction

bone marrow biopsy

brainstem, atrophy

brainstem, lesion of

brucellosis, nervous system involvement with

bulbar palsy, progressive

calcification, intracranial

Canavan's disease

cardiac arrest and resuscitation

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, spine

cataracts, congenital

cauda equina, enhancement

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, recurrent

cerebrovascular accident, women

Charcot-Marie-Tooth

chilbran skin lesions

choreoathetosis

Clinical Pathologic Conference(C.P.C.)

congestive heart failure

copper deficiency

corpus callosum

corpus callosum, infarction of

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical infarction

cranial nerve enhancement

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

critical care unit

crying, pathologic

cultured skin fibroblasts

cyst, parenchymal

deafness, bilateral

deafness, sudden

deep gray nuclei

degenerative diseases of CNS

Dejerine-Sottas syndrome

delayed dentition

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

denervation of muscle

denervation potentials

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

difficulty climbing stairs

difficulty going down stairs

diffuse idiopathic skeletal hyperostosis

diplopia, transient

disability, neurological

distal muscle weakness

dural sinus thrombosis

dysdiadochokinesia

dysferlinopathy

dystonia, children

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

emotional lability

encephalitis, focal

encephalopathy, acute

encephalopathy, anoxic

encephalopathy, metabolic

encephalopathy, post anoxic

enzyme treatment

enzyme, muscle disease

episodic neurologic deficits

evoked potentials

exercise intolerance

exome sequencing

extraocular muscle lesion

eye movement, disorders of

facial appearance, abnormal

facial nerve palsy

facial weakness

facial weakness, bilateral

failure to thrive

feeding disorder

flail arm syndrome

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, lesion of

frontal lobe, pathologic signs of

fundus, abnormality of

funduscopic exam

gastric partitioning

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

genu of corpus callosum

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycogen storage disease

GM1 ganglioside antibodies

Guillain Barre syndrome, differential diagnosis of

head circumference

headache, positional

hearing loss, bilateral

hearing loss, sudden, bilateral

hemiparesis, transient

heralding manifestation

high arched feet

high arched palate

highly active antiretroviral therapy

human immunodeficiency virus type 1

Huntington's chorea

hyperhomocysteinemia

hyperpyrexia, CNS disorder causing

hypoglycorrhachia

hypomyelination

hypotension, systemic

hypotonia, infants

hypoxic encephalopathy

iatrogenic neurologic disorders

immunosuppressive agents

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

intellectual deficit

intellectual deterioration

interferon alpha

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

Krabbe's disease

laminar necrosis, cortical

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

Lewy body disease, diffuse

life expectancy

life support, withdrawal of

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

Marinesco-Sjogren syndrome

masseter muscle wasting

memory, defect of recent

memory, impairment of

meningeal biopsy

meningeal enhancement

meningitis, melanomatous

mental retardation

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

microangiopathy, brain

microangiopathy, retina

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal gammopathy

motor neuron disease

movement disorder

MRI, contrast enhanced

MRI, diffusion tensor

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, functional

MRI, high signal foci on

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multiple organ failure

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscular dystrophy

muscular dystrophy, cardiovascular changes with

muscular dystrophy, congenital

muscular dystrophy, limb-girdle

myeloneuropathy

myelopathy, chronic progressive

myoclonic jerks

myopathy, acute

myopathy, critically ill

myopathy, drug-induced

myopathy, steroid induced

myotonia dystrophica

nausea and vomiting

nerve conduction studies

nerve root enhancement

neurogenic bladder

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic evaluation

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuronal degeneration

neuropathology, brain

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory

neuroprotective agents

neurotoxicity, acute

next-generation sequencing

nutritional deficiency

occipital lobe, lesion of

old age, neurology of

ophthalmoplegia

optic nerve, hypoplasia of

optic neuropathy

optic neuropathy, nutritional

pain, abdominal

paralysis, recurrent

paraparesis, spastic

Parkinson disease

patient information and support

pediatric neurology

percussion induced muscle contraction

persistent vegetative state

personality change

pleocytosis of cerebrospinal fluid

polyglucosan body

polyglucosan body disease

polymerase chain reaction

polyneuropathy, critically ill

polyneuropathy, critically ill, children

polyradiculoneuropathy

Pompe's disease of glycogen storage

pons, lesion of

posterior column disease

posterior longitudinal ligament, ossification of

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

primary lateral sclerosis

progressive myoclonic epilepsy

progressive neurologic disorder

proximal muscle atrophy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, abnormality in neurologic disorders

pyramidal tract

pyramidal tract dysfunction

quadriplegia, transient

ragged-red fibers

rapidly progressing neurologic illness

reading disorder, acquired

respiratory failure

retina, abnormal

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

reversible neurologic disorder

Rosenthal fibers

saccadic eye movements, abnormal

Schilder's disease

sedimentation rate, elevated

seizure, children

sensorineural hearing loss

serologic testing

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

slow virus infection of CNS

small vessel disease

speech disorder, childhood

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, cervical canal

splenium of corpus callosum

spongy degeneration of brain

spontaneous remission

standing difficulty

startle reaction

steroid therapy, CNS treatment and complications with

striatum, lesion of

striatum, lesion of, bilateral

strokelike episodes

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

subdural hematoma

superior sagittal sinus thrombosis

survival motor neuron gene

Susac's syndrome

symmetric brain lesions

systemic illness

tandem gait, ataxic

teeth, abnormal

teeth, number of in infants

temporal lobe, atrophy

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, atrophy

tongue, enlarged

tongue, fasciculations of

tongue, weakness

toxic encephalopathy

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, intention

trigeminal neuralgia

trinucleotide repeats

urinary incontinence

urine test for metabolic disorders

viral infection

viral infection, CNS

visual acuity, decreased

visual tracking

visuospatial disturbance

vitamin deficiency

vitamin E deficiency

Waldenstrom's macroglobulinemia

walking, delayed

walking, difficulty with

weakness, acute

weakness, generalized

weakness, progressive

weakness, proximal

weaning from respirator, failure to

white matter disease

white matter disease, periventricular

white matter disease, subcortical

wide based gait

winging of scapula

word-finding difficulty

X-linked neuropathy

Showing articles 700 to 750 of 4861 << Previous Next >>

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

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

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

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,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

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

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

Trochanteric Sciatic Neuropathy
Neurol 39:1539-1541, Crisci,C.,et al, 1989

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

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

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
Neuroradiology 30:500-505, Weisberg,L.A.&Stazio,A., 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis
Ann Neurol 23:418-420, Goodin,D.S.,et al, 1988

A Double-Blind Study of the Effectiveness of Cyclosporine in Amyotrophic Lateral Sclerosis
Arch Neurol 45:381-386, Appel,S.H.,et al, 1988

Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,et al, 1988

Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,et al, 1988

Distal Vacuolar Myopathy with Complete Heart Block
Arch Neurol 45:698-699, Krendel,D.A.,et al, 1988

Neurologic and Cognitive Deficits in Children with Cystinosis
J Pediatr 112:912-914, Trauner,D.A.,et al, 1988

Deep Branch Ulnar Neuropathy Due to Giant Cell Tumor:Report of a Case
Neurol 38:327-329, Rafecas,J.C.,et al, 1988

Magnetic Resonance Imaging of Cerebral Lesions in Pts with the Sjogren Syndrome
Ann Int Med 108:815-823, Alexander,E.L.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988

Use of Composite Scores (Megascores) to Measure Deficit in Amyotrophic Lateral Sclerosis
Neurol 38:405-408, Andres,P.L.,et al, 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Diffuse Lewy Body Disease and Progressive Dementia
Neurol 38:1520-1528, Burkhardt,C.R.,et al, 1988

Compressive Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in Cyclists
JNNP 51:1588-1590, Hankey,G.J.&Gubbay,S.S., 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Diagnosis of Thoracic Outlet Syndrome, Value of Sensory & Motor Conduction Studies & Quantitative EMG
Arch Neurol 44:1161-1163, Smith,T.&Trojabor,W., 1987

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

Progressive Nemaline (Rod) Myopathy Associated with HIV Infection
NEJM 317:1602-1603, Dalakas,M.C.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

MR Findings in Normal-Pressure Hydrocephalus:Significace & Comparison with Other Forms of Dementia
Jr. , et al, J Comput Assist Tomogr 11:923-93187., Jack,C.R., 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Neurological Clues from Environmental Neurotoxins
BMJ 295:346-347, Martyn,C.N., 1987

Showing articles 700 to 750 of 4861 << Previous Next >>