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acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, heralded by neurologic invol

advance directives

advances in neurology

adverse drug reaction

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

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, epidemiology of

amyotrophic lateral sclerosis, etiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

amyotrophic lateral sclerosis, treatment of

amyotrophic lateral sclerosis, work up

amyotrophic lateral sclerosis-like syndrome

animal exposure

anterior horn cell disease

anti citrullinated antibody

antiviral agents

arm swing, reduced

ataxia, progressive

autoimmune disease

automatic behavior

automobile accidents

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Behcet's syndrome

botulinum toxin

brainstem, infarction of

brainstem, lesion of

bulbar palsy, acute

bulbar palsy, progressive

CAT scan, emission

CAT scan, emission, abnormal

central nervous system, infection of

cerebellar atrophy, primary

cerebellar lesion

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cervical collar

cervical spine injury

cervical spine injury, treatment of

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

chondroitin sulfate C

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cold temperature

conduction block

congenital heart disease

cortical-basal ganglionic degeneration

cost effectiveness

cranial neuropathy

crying, pathologic

cyclophosphamide

degenerative diseases of CNS

delay in diagnosis

dementia, frontotemporal

developmental milestones, loss of

developmental retardation

diagnostic criteria

diaphragmatic paralysis

differential diagnosis

disability, neurological

distal muscle atrophy

distal muscle weakness

drug interactions

electroencephalogram, abnormalities of

emotional lability

encephalitis, autoimmune

encephalitis, viral

enterovirus infection of CNS

epidemiology of neurology

episodic disorders

episodic neurologic deficits

episodic unconsciousness

ethics in neurology

exercise intolerance

extremity, cold

facial weakness, bilateral

fine motor function, impaired

flaccid paralysis

flail arm syndrome

gag reflex, depressed

gamma amino butyric acid

gammaglobulin therapy, intravenous

gastrostomy, percutaneous endoscopic

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital ulcerations

GM1 ganglioside antibodies

Guillain Barre syndrome

Hallervorden Spatz disease

heralding manifestation

highly active antiretroviral therapy

history of neurology

human immunodeficiency virus type 1

Huntington's chorea

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunohistochemistry

immunosuppression

immunosuppressive agents

inborn errors of metabolism

intellectual deficit

intellectual deterioration

intermittent positive pressure breathing

intrinsic hand muscles, wasting of

jaw jerk, abnormal

juvenile distal and segmental muscular atrophy

Kugelberg-Welander syndrome

lactic acidemia

laminectomy, cervical

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

life expectancy

life support, withdrawal of

life support, withholding of

life sustaining treatment

locked-in syndrome

lymphadenopathy

lysosomal storage disease

medical-legal aspects of neurology

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, neutrophilic

mental status, abnormal

metabolic disorder, primary

midbrain, atrophy

molecular genetics

monomelic amyotrophy

motor neuron disease

motor neuron disease, misdiagnosis

motor neuron disease, spontaneous recovery

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, disappearing lesion on

MRI, paramagnetic effect

MRI, spinal cord

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple sleep latency test

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Duchenne

myasthenia gravis

myasthenia gravis, treatment of

myelitis, longitudinal

myelopathy, ischemic

myopathy, steroid responsive

myotonia dystrophica

narcotic analgesics

nausea and vomiting

nerve conduction studies

nerve conduction studies, motor

nerve growth factor

neurofibromatosis 1

neurofibromatosis 2

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neurologic testing

neuromuscular disease, electrodiagnosis of

neuronal degeneration

neuroophthalmology

neuropathology, brain

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, peripheral

neuropathy, peripheral, treatment

neuroprotective agents

neurotransmitter

next-generation sequencing

NMDA antagonists

ophthalmoplegia

ophthalmoplegia, total

oral ulcerations

owl's eye sign of spinal cord

pain, management of chronic

palliative care

paralysis, acute

paralysis, acute areflexic

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

Parkinson disease

Parkinson disease, atypical

Parkinson disease, axial symptoms

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

paroxysmal neurologic deficits

patient information and support

penguin silhouette sign

peroxisomal disease

personality change

phrenic nerve pacemaker

physician assisted suicide

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poliomyelitis-like illness

polyneuropathy, chronic inflammatory demyelinating

positive sharp waves

practice guidelines

pregnancy, neurologic complications in

prevention of neurologic disorders

primary lateral sclerosis

progressive neurologic disorder

progressive supranuclear palsy

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract dysfunction

quality of life

radiation therapy, salivary gland

rapidly progressing neurologic illness

recombinant DNA

REM sleep behavior disorder

remote effect of cancer on the nervous system

renal cell carcinoma

respiratory arrest

respiratory failure

respiratory tract infection

retinitis pigmentosa

reverse split hand sign

rheumatoid arthritis

rheumatoid arthritis, neurologic complications of

rigidity, axial

risk-benefit assessment

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

seizure, children

seizure, treatment of

sensory symptoms

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serum alanine aminotransferase

skin, lesions in neurologic disorders

sleep offset paralysis

sleep onset paralysis

sleep paralysis

sleep pathology and physiology

speech disorder

speech disorder, childhood

spinal cord degeneration

spinal cord, cervical

spinal cord, compression of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

sports medicine, neurology of

stem cell transplantation

stimulant drugs

superoxide dismutase

survival motor neuron gene

synucleinopathy

tandem gait, ataxic

thalamus, lesion of

thyrotropin-releasing hormone

tongue, atrophy

tongue, fasciculations of

treatment of neurologic disorder

unconsciousness

unconsciousness, episodic

unconsciousness, transient

urea-cycle enzymopathies

viral infection

viral infection, CNS

vision, blurred

visual impairment

visual symptoms

walking, difficulty with

weakness, generalized

weakness, progressive

Werdnig-Hoffman disease

West Nile fever

Showing articles 950 to 1000 of 10627 << Previous Next >>

Acute Respiratory Failure in Motor Neuron Disease
Arch Neurol 40:30-32, Hill,R.,et al, 1983

Effect on Weakness & Spasticity in Amyotrophic Lateral Sclerosis of Thyrotropin-Releasing Hormone
Lancet 2:73-75, Engel,W.K.,et al, 1983

Familial Porencephaly
Arch Neurol 40:567-569, Berg,R.A.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Progressive Supranuclear Palsy:Clinical Features & Response to Treatment in 16 Patients
Ann Neurol 13:273-278, Jackson,J.A.,et al, 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Neurological Complications of Immunization
Ann Neurol 12:119-128, Fenichel,G.M., 1982

Neurogenic Arthrogryposis in One Identical Twin, Sul
Arch Neurol 39:717-718, Yi,C.,et al, 1982

Treatment of the Guillain-Barre Syndrome by Plasma Exchange
JNNP 45:847-850, Kennard,C.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

A Prospective Study of Lacunar Infarction Using Computerized Tomography
Neurol 32:49-56, Donnan,G.A.,et al, 1982

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Plasmapheresis in the Treatment of Four Cases of Guillain-Barre Syndrome (acute form)
Ital. J Neurol Sci 4:331-3361981., Zerbi,D.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Idiopathic Inflammatory Orbital Pseudotumor in Childhood
Ophthalmology 88:565-574, Mottow-Lippa,L., et al, 1981

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Progressive Bulbar Paralysis Associated With Neurgl Deafness, A Nosological Entity
Arch Neurol 37:214-216, Alberica,R.,et al, 1980

Ocular Myasthenia:Diagnosis & Therapy
In Neuro-Ophthalmology, Vol X ed. by J. Glaser. CV Mosby Co, St. Louis, Daroff,R., 1980

Poliomyelitis Worldwide
Editorial, BMJ 280:1555-15561980., , 1980

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

Midline Granuloma
Topel J. L. in Vinken P. J. & Bruyn, G. N. (Eds) Handbook of Clin Neurol, Vol 39, North-Holland Publ, Co, Amsterda, 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Intubation for Acute Respiratory Failure in Guillain-Barre Syndrome
JAMA 242:1650-1651, Newsum,J.K.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

The Cubital Tunnel Syndrome:Diagnosis & Precise Localization
Ann Neurol 6:56-59, Miller,R.G., 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Tarsal Tunnel Syndrome:Electrophysiological Study
Ann Neurol 5:327-330, Oh,S.J.,et al, 1979

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Showing articles 950 to 1000 of 10627 << Previous Next >>