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advances in neurology

Alzheimer's disease

aminoacidopathies

amyloid angiopathy, cerebral

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, atypical

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

angiostrongylus cantonensis

anterior horn cell disease

aphasia, progressive, primary

ascending paralysis

asthma, poliomyelitis-like syndrome with

ataxia, progressive

behavioral disorder

biologic markers

bulbar palsy, acute

bulbar palsy, progressive

burning paresthesia

calf hypertrophy

CAT scan, abnormal

CAT scan, emission, abnormal

central nervous system, infection of

cerebellar atrophy, primary

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cervical osteophyte

cervical spondylosis

cervical spondylosis, differential diagnosis of

cervical spondylosis, misdiagnosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

congenital heart disease

controversies in neurology

cost effectiveness

creatine phosphokinase(CPK)elevated

crying, pathologic

degenerative diseases of CNS

delay in diagnosis

dementia, age at onset

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

developmental retardation

dexterity, impaired

diagnostic criteria

differential diagnosis

diplegia, atonic

diplegia, brachial

disability, neurological

distal muscle weakness

emotional lability

epidemiology of neurology

episodic neurologic deficits

evidence-based research

evoked potentials

exercise intolerance

facial weakness, bilateral

finger weakness

flaccid paralysis

flail arm syndrome

frontal lobe, atrophy

frontotemporal dementia, behavioral variant

F-wave response

gag reflex, depressed

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guillain Barre syndrome, variant forms of

headache, progressive

health insurance

helminthic infection of CNS

hemiplegia, progressive

heralding manifestation

Huntington's chorea

hypoglycorrhachia

hypotonia, infants

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, ubiquitin

inclusion body myositis

inflexibility, mental

intellectual deficit

internal capsule

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

jaw jerk, abnormal

lactic acidemia

laminectomy, cervical

laughing, pathologic

leg weakness, bilateral

leg weakness, unilateral

Lewy body disease, diffuse

life expectancy

locked-in syndrome

lysosomal storage disease

meningitis, eosinophilic

metabolic disorder, primary

molecular genetics

monomelic amyotrophy

motor neuron disease

movement disorder

MRI, functional

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, susceptibility weighted

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle atrophy, progressive

muscle stiffness

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

myasthenia gravis

myelopathy, ischemic

myopathy, autoimmune

myopathy, quadriceps

neurologic complications of, surgery

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic symptoms

neurologic testing

neuronal degeneration

neuropathy, motor, multifocal

neuroprotective agents

next-generation sequencing

owl's eye sign of spinal cord

pain, increased response

palliative care

paralysis, acute

paralysis, acute areflexic

paralysis, asymmetric

paraparesis, familial spastic

paraparesis, familial spastic, classification

paraparesis, spastic

parasitic infection

parasitic infection, CNS

Parkinson disease

Parkinsonism syndrome

paroxysmal neurologic deficits

patient information and support

peroxisomal disease

personality change

physical therapy

pleocytosis of cerebrospinal fluid

poliomyelitis-like illness

polyglucosan body disease

polymerase chain reaction

practice guidelines

pregnancy, neurologic complications in

primary lateral sclerosis

progressive neurologic disorder

proximal muscle atrophy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

pyramidal tract

pyramidal tract dysfunction

quadriceps atrophy

quadriceps weakness

raw fish ingestion

release phenomena

respiratory failure

saccadic eye movements, abnormal

scoliosis, neurologic association with

shoulder, subluxation

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep pathology and physiology

somatosensory evoked potentials

somatosensory evoked potentials, dermatomal

speech disorder

speech, loss of

spinal cord degeneration

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

stereotyped behavior

sternocleidomastoid muscle

steroid therapy, CNS treatment and complications with

superoxide dismutase

survival motor neuron gene

temporal lobe, atrophy

tongue, atrophy

tongue, fasciculations of

tongue, impaired movements of

travel, foreign

treatment of neurologic disorder

trinucleotide repeats

urea-cycle enzymopathies

urinary incontinence

viral infection

viral infection, CNS

viral isolation

walking, difficulty with

weakness, generalized

weakness, progressive

word-finding difficulty

X-linked bulbospinal neuronopathy

Showing articles 300 to 350 of 4573 << Previous Next >>

Benign Focal Amyotrophy
Arch Neurol 41:678-679, Riggs,J.E.,et al, 1984

Severe Neurological Disease Associated with Hyperparathyroidism
Ann Neurol 15:453-456, Patten,B.M.,et al, 1984

Conjugal Amyotrophic Lateral Sclerosis
Ann Neurol 14:699, Paolino,E.,et al, 1983

Adult Polyglucosan Body Disease:Clinical & Nerve Biopsy Findings in Two Cases
Ann Neurol 13:440-444, Vos,A.L.M.,et al, 1983

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

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

Amyotrophic Lateral Sclerosis & Pet Exposure
NEJM 309:244-245, Schenkman,M.,et al, 1983

Mercury Intoxication Simulating Amyotrophic Lateral Sclerosis
JAMA 250:642-643, Adams,C.R.,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

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

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

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

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

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

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

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

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

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

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

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,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

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

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

Diaphragmatic Paralysis in Motor Neuron Disease
Neurol 28:18, Parhad,I.M.,et al, 1978

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Control of Emotional Expression in Pseudobulbar Palsy
Arch Neurol 34:717, Lieberman,A.,et al, 1977

Cervical Spondylotic Myelopathy with Reversible Fasciculations in the Lower Extremities
Arch Neurol 34:774, Kasdon,D., 1977

Viruslike Particles in Amytrophic Lateral Sclerosis:Electron Microscopical Study of a Case
Ann Neurol 1:290, Pena,C.E., 1977

Lower Motor Neuron Disease with Spinocerebellar Degeneration
Ann Neurol 2:524, Page,R.W.,et al, 1977

Antibody Titers to Coxsackieviruses in Amyotrophic Lateral Sclerosis
NEJM 295:107, Cremer,N.E.,et al, 1976

Postradiation Motor Neuron Syndrome
Arch Neurol 33:786, Sadowsky,C.H.,et al, 1976

Frequency of Nerve Fiber Degeneration of Peripheral Motor & Sensory Neurons in Amyotrophic Lateral Sclerosis
Neurol 25:781, Dyck,P.J.,et al, 1975

Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in a Diabetic
Arch Neurol 32:564, Finelli,P.F., 1975

Showing articles 300 to 350 of 4573 << Previous Next >>