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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acute intermittant porphyria
advances in neurology
algorithm
allodynia
amyloid
amyloidosis
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
anemia
angiostrongylus cantonensis
anterior horn cell disease
anti citrullinated antibody
anti IgLON5
antiviral agents
aphasia
aphasia, progressive, primary
aphonia
apnea
areflexia
arm atrophy
arm weakness
ascending paralysis
ataxia
ataxia, progressive
ataxic gait
autoantibodies
autonomic dysfunction
Babinski sign
basophilic stippling of red blood cells
behavioral disorder
BiPAP
bone marrow biopsy
botulism
brachial amyotrophic diplegia
bulbar palsy
bulbar palsy, acute
bulbar palsy, progressive
burning feet
burning paresthesia
cachexia
CAG repeats
cane
carcinoma
CAT scan, emission, abnormal
CD4 counts
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
cervical osteophyte
cervical spine
cervical spondylosis
cervical spondylosis, differential diagnosis of
cervical spondylosis, misdiagnosis
Chinese paralytic syndrome
chondroitin sulfate C
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
coma, episodic
conduction block
confusion
constipation
conversion reaction
cranial neuropathy
creatine phosphokinase(CPK)elevated
crying, pathologic
cyclophosphamide
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, frontotemporal
dementia, presenile
denervation of muscle
denervation potentials
depression
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diphtheria
diplegia, atonic
diplegia, brachial
disorientation
distal muscle atrophy
distal muscle weakness
drooling
dying
dysarthria
dysphagia
dysphonia
dyspnea
electromyogram
electrophoretic pattern, serum
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
endemic area
eosinophilia
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
evoked potentials
exercise
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
finger weakness
fish poisoning
flaccid paralysis
fluency
foot drop
frontotemporal dementia, behavioral variant
F-wave response
gag reflex, depressed
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
GM1 ganglioside antibodies
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
gynecomastia
hallucination
hand weakness
headache
headache, progressive
heavy metal intoxication
helminthic infection of CNS
heralding manifestation
highly active antiretroviral therapy
hoarseness
hospice
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hyperthyroidism
hypoglycorrhachia
hypophonia
hyporeflexia
imbalance
immunohistochemistry
immunosuppressive agents
immunotherapy
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion body myositis
inflexibility, mental
intellectual deficit
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
laminectomy, cervical
laughing, pathologic
lead and the nervous system
lead poisoning
leg atrophy
leg weakness, bilateral
leg weakness, unilateral
lid closure, weakness of
life expectancy
lobar atrophy
locked-in syndrome
Lyme disease
lymphoma
lymphoma involving CNS
Man-In-The-Barrel syndrome
masseter muscle wasting
meningismus
meningitis, eosinophilic
mimics
misdiagnosis
monoclonal gammopathy
monomelic amyotrophy
mortality
motor neuron disease
motor neuron disease, misdiagnosis
motor neuron disease, spontaneous recovery
MRI
MRI, abnormal
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelogram
myelomalacia
myelopathy
myelopathy, ischemic
myelopathy, chronic progressive
myeloradiculopathy
myoclonus
myopathy
myopathy, autoimmune
myopathy, quadriceps
myopathy, steroid responsive
myositis
nasal speech
nausea and vomiting
neck weakness
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuroendocrinology
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuropathology
neuropathology, peripheral nerves
neuropathy
neuropathy, acute
neuropathy, amyloid
neuropathy, diphtheritic
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, painful
neuropathy, peripheral, treatment
neuropathy, toxic
neuroprotective agents
neurotoxin
next-generation sequencing
osteomalacia
pain
pain, abdominal
pain, increased response
palliative care
paralysis, acute
paralysis, acute areflexic
paralysis, asymmetric
paranoia
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraproteinemia
parasitic infection
parasitic infection, CNS
paraspinal muscle
parathormone
parathyroid adenoma
paresthesias
Parkinsonism syndrome
pathology
patient information and support
personality change
Pick's disease
pleocytosis of cerebrospinal fluid
poison, mercury
poliomyelitis
poliomyelitis-like illness
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyradiculoneuropathy
porphyria
positive sharp waves
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
radial nerve, palsy of
raw fish ingestion
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal cell carcinoma
renal stones
respirator
respiratory failure
respiratory tract infection
retrovirus
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
riluzole
risk factors
screening
seizure
sensory symptoms
shell fish poisoning
single photon emission computed tomography
sleep
sleep pathology and physiology
snail
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spastic ataxia
spasticity
speech disorder
speech, loss of
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spondylosis
stereotyped behavior
sternocleidomastoid muscle
steroid
steroid therapy, CNS treatment and complications with
sushi
syringomyelia
tandem gait, ataxic
tick paralysis
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
toxins, nervous system
trauma
travel history
travel, foreign
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
urinary incontinence
viral infection
viral infection, CNS
viral isolation
vocalizations
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
word-finding difficulty
wrist drop
X-linked bulbospinal neuronopathy
Showing articles 300 to 350 of 4087 << Previous Next >>

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

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

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

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

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

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

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

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

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

Epidermoid Tumors Involving the Fourth Ventricle
Neurosurgery 9:9-13, Rosario,M.,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

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

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

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

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

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

Poliomyelitis-A Persistent Problem
NEJM 288:370, Weinstein,L., 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973



Showing articles 300 to 350 of 4087 << Previous Next >>