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acetazolamide
acid maltase deficiency
advances in neurology
adverse drug reaction
airway obstruction
alopecia
alveolar hypoventilation
Alzheimer's disease
Alzheimer's disease, familial
amniocentesis
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anasarca
anesthesia, general
anterior interosseous neuropathy
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticoagulant, treatment
anticoagulant, treatment in CVD
anticonvulsants
anticonvulsants, untoward effects of
antihistamines
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
aspirin
asymptomatic
ataxia
ataxia, paroxysmal
atelectasis
atrioventricular block
audiogram
auditory evoked brainstem potentials
autoimmune disease
automatic implantable cardioverter-defibrillator
axonopathy, distal
baldness
basal ganglia, calcification of
botulism
brachial neuritis
bradycardia
brainstem, lesion of
cachexia
CAG repeats
calcification, intracranial
calcium antagonist
calcium channel dysfunction
cancer of colon
carbamazepine
carbamazepine, toxicity
carcinoma
carcinoma of ovary
carcinoma of pancreas
carcinoma of uterus
cardiac arrest
cardiac arrest and resuscitation
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomegaly
cardiomyopathy
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
central core disease
central nervous system, infection of
cerebral blood flow
cerebral embolism
cerebral embolism, cardiac origin
cerebral ischemia
cerebrovascular accident
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
cholestasis
chromosomal abnormality
chromosome 19
chromosome 3
chronic progressive external ophthalmoplegia
clubfoot as related to neurologic disease
complications
compression neuropathy
conduction block
confidentiality
congenital birth defects
congenital heart disease
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
corneal dystrophy
corpus callosum
corpus callosum, thinning
coumarin
creatine phosphokinase(CPK)elevated
defibrillator, implanted
degenerative diseases of CNS
dementia, thalamic
dentatorubral-pallidoluysian atrophy
dermatomyositis
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
dilantin
dilantin, toxicity
diplopia
distal muscle weakness
DNA probes
dropped head syndrome
drug induced neurologic disorders
dysphagia
echocardiogram
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
electronystagmography
electronystagmography, abnormal
electrophoretic pattern, serum
electroretinograph
embolism
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
entrapment neuropathy
epidemiology of neurology
erythrocyte
evoked potentials
exercise
exercise electrocardiography
eye closure
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
falling
false negative
familial
familial hemiplegic migraine
Fazio-Londe's disease
floppy infant
fluorescein angiography
fragile-X syndrome
Friedreich's ataxia
frontal balding
F-wave response
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
glucose tolerance test, abnormal
gray matter
Guillain Barre syndrome
Guyon's canal
hand weakness
hearing loss
heart block
heart block, complete
heavy metal intoxication
high arched feet
high arched palate
histochemistry
histochemistry of muscle
H-reflex testing
huntingtin
Huntington's chorea
hydrocephalus
hydrops fetalis
hypercapnia
hyperinsulinism
hyperkalemic periodic paralysis
hyperostosis
hyperparathyroidism
hypersomnia
hypokalemia
hypokalemic periodic paralysis
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
intellectual deficit
intelligence quotient
iris, abnormal
kaliuresis
Kearns-Sayre syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
lid abnormalities
lid closure, weakness of
lid retraction, lower
life expectancy
lordosis
malignancy screen
malignant hyperpyrexia
manic-depressive
median neuropathy
Melkersson's syndrome
mental retardation
metabolic acidosis
mexiletine
microcephaly
micrognathia
migraine
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
modafinil
molecular genetics
mononeuropathy
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, functional
MRI, muscle
MRS
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myasthenic syndrome
myocarditis
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopathy, proximal
myopathy, thyroid disease causing
myositis
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonia, causes of
myotonia, treatment of
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuritis, causes of
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurogenic vs.myopathic atrophy
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular disease, electrodiagnosis of
neuronal migration disorder
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, motor, multifocal
neuropathy, peripheral
newborn, evaluation of
nifedipine
ocular myopathy
oculovestibular reflex
ophthalmoplegia
optic atrophy
orbicularis oculi muscle
orbit, lesions of
ovarian tumor
pacemaker, cardiac-transvenous
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
physical activity
platelet inhibiting drugs
pleural effusion
pneumonia
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
polyneuropathy
porphyria
posterior interosseous neuropathy
postoperative neurologic complications
potassium channel antibodies
potassium channel dysfunction
pregnancy, neurologic complications in
prevention of neurologic disorders
procainamide
prognosis
proptosis
proximal myotonic myopathy
psychological testing
ptosis
ptosis, bilateral
pulmonary function tests
radionuclide angiocardiography
recombinant DNA
respiratory failure
review article
RFLPs
rhabdomyolysis
risk factors
saccadic eye movements
saccadic eye movements, abnormal
safety
sarcoidosis
screening
seizure
sensorineural hearing loss
single photon emission computed tomography
sleep apnea
slit lamp examination
sodium channel dysfunction
somnolence
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 6
spinocerebellar degeneration
stiff man syndrome
sudden death
taurine
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
testicular atrophy
thoracic outlet syndromes
thyrotoxicosis
tocainide
torticollis
transient ischemic attack
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
twins
ulnar neuropathy
ultrasonography
ventricular tachycardia
viral infection, CNS
visual evoked response
weakness
weaning from respirator, failure to
Werdnig-Hoffman disease
wheelchair
white matter disease
white matter disease, periventricular
workup
X-linked bulbospinal neuronopathy
Showing articles 700 to 750 of 882 << Previous Next >>

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

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

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

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

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

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

Ocular Complications of Tangier Disease
Am J Med 83:991-994, Pressley,T.A.,et al, 1987

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

Reflex Sympathetic Dystrophy, A Review
Arch Neurol 44:555-561, Schwartzman,R.J.&McLellan,T.L., 1987

Thermography in Childhood Reflex Sympathetic Dystrophy
J Pediatr 111:551-555, Lightman,H.I.,et al, 1987

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

Explanation & Management of Neurological Disability
BMJ 294:1203-1205, Critchley,E.M.R.&Mitchell,J.D., 1987

Motor Neuron Disease & Paraproteinemia
Neurol 37:335-337, Rudnicki,S.,et al, 1987

Current Status of Thyrotropin-Releasing Hormone Therapy in Amyotrophic Lateral Sclerosis
Comm. on Health Care Issues, Amer Neuro Assoc, Ann Neurol 22:541-54387., , 1987

A Rating Scale for Amyotrophic Lateral Sclerosis:Description & Preliminary Experience
Ann Neurol 22:328-333, Appel,V.,et al, 1987

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Clinincopath Conf
Progressive Muscular Atrophy & Diabetic Neuromuscular Disease, Case 21-1987, NEJM 316:1326-13357., , 1987

Lathyrism:Evidence for Role of the Neuroexcitatory Aminoacid BOAA
Lancet 2:1066-1067, Spencer,P.S.,et al, 1986

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Slow Resolution of Multifocal Weakness & Fasciculation:A Reversible Motor Neuron Syndrome
Neurol 36:1260-1263, Chad,D.A.,et al, 1986

Motor Neuron Disease & Plasma Cell Dyscrasia
Neurol 36:1429-1436, Shy,M.E.,et al, 1986

Alzheimer's Disease, Parkinson's Disease, & Motoneurone Disease:Abiotropic Interaction Between Ageing & Environment
Lancet 2:1067-1068, Calne,D.B.,et al, 1986

From Benign Fasciculations & Cramps to Motor Neuron Disease
Neurol 36:997-998, Shepherd-Fleet,W.&Watson,R.T., 1986

Delayed Postirradiation Lower Motor Neuron Syndrome
Ann Neurol 19:308-309, Gallego,J.,et al, 1986

Primary Amyloidosis with Peripheral Neuropathy & Signs of Motor Neuron Disease
Neurol 36:1125-1127, Abarbanel,J.M.,et al, 1986

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986

A Double-Blind, Placebo-Controlled Trial of TRH in Amyotrophic Lateral Sclerosis
Neurol 36:141-145, Caroscio,J.T.,et al, 1986

Controlled Trial of Thyrotropin Releasing Hormone in Amyotrophic Lateral Sclerosis
Neurol 36:146-151, Brooke,M.H.,et al, 1986

Amyotrophic Lateral Sclerosis:Effects of Administration of Thyrotropin-Releasing Hormone
Neurol 36:152-159, Mitsumoto,H.,et al, 1986

Amyotrophic Lateral Sclerosis, Associated Clinical Disorders & Immunological Evaluations
Arch Neurol 43:234-238, Appel,S.H.,et al, 1986

Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
Neurol 36:511-517, Mulder,D.W.,et al, 1986

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Causalgia as a Complication of Meningococcal Meningitis
BMJ 292:1710, McLelland,J.&Ellis,S.J., 1986

Reflex Sympathetic Dystrophy of the Face, Report of Two Cases & a Review of the Literature
Arch Neurol 43:693-695, Jaeger,B.,et al, 1986

Classification of Peripheral Neuropathy:The Long and the Short of It
Muscle & Nerve 9:711-719986., Sabin,T.J., 1986

Pathological Laughter & Crying
In Frederiks, J. A. M. (Ed) Handbook of Clinical Neurology, Elsevier Science Publ, 45:219, Poeck,K., 1985

Amyotrophic Lateral Sclerosis:Part 1. Clinical Features, Pathology, & Ethical Issues in Management
Ann Neurol 18:271-280, Tandan,R.,et al, 1985

Amytrophic Lateral Sclerosis:Part 2, Etiopathogenesis
Ann Neurol 18:419-431, Tandan,R.,et al, 1985

Isolation of LAV/HTLV-III From a Patient with Amyotrophic Lateral Sclerosis
NEJM 313:324-325, Hoffman,P.M.,et al, 1985

ALS & Pet Exposure
Neurol 35:717-720, Tarras,S.,et al, 1985

Progressive Dementia, Visual Deficits, Amyotrophy, & Microinfarcts
Neurol 35:789-796, Kaplan,J.G.,et al, 1985

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Post-Polio Syndrome
J Med Assoc Ga 74:510-511, Bailey,A.A., 1985

Tangier Disease (Hypo-a-Lipoproteinemia)
Textbook of Child Neurology, 3rd Ed. , Phila, Lea & Febiger, Ch 1, p 86, Menkes,J.H., 1985

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

Amyotrophic Lateral Sclerosis:A Double-Blind Crossover Trial of Thyrotropin-Releasing Hormone
JNNP 47:1332-1334, Imoto,K.,et al, 1984

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984



Showing articles 700 to 750 of 882 << Previous Next >>