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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 300 to 350 of 797 << Previous Next >>

Isolated Ocular Myopathy & Celiac Disease in Childhood
Neurol 33:792, Sandyk,R.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982

External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
J Comput Assist Tomogr 6:1006-1009, Merlis,A.L.,et al, 1982

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Progressive Muscle Disease in a Young Woman With Family History of Duchenne's Muscular Dystrophy
Arch Neurol 39:378-380, Olson,B.J.,et al, 1982

Serial Two-dimensional Echocardiography in Duchenne Muscular Dystrophy
Neurol 32:1101-1105, Goldberg,S.J.,et al, 1982

An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
Ann Neurol 12:395-398, Taylor,D.A.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Hypoparathyroidism & Elevated Muscle Enzymes
Neurol 30:192-195, Shane,E.,et al, 1980

Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
Neurol 30:497-501, Lane,R.J.M.,et al, 1980

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Lymphocyte Capping in Muscular Dystrophy
Neurol 29:1419-1421, Hauser,S.L.,et al, 1979

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Allopurinol Not Effective In Muscular Dystrophy
NEJM 301:785, Bakouche,P.,et al, 1979

5'-Nucleotidase Activity in Duchenne Muscular Dystrophy
NEJM 301:726, Scholte,H.R.,et al, 1979

Carrier Detection in Duchenne Muscular Dystrophy
Neurol 29:1423-1425, Tagliavini,J.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Elevated Skeletal-Muscle Enzymes During Quinidine Therapy
NEJM 300:1218, Weiss,M.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Clinical Symposia, Scoliosis
CIBA, 30:21978., Keim,H.A., 1978

Deformed Erythrocytes in Muscular Dystrophies
Neurol 28:842-844, Grassi,E.,et al, 1978

Alteration in Erythrocyte Membrane Structure in Duchenne Muscular Dystrophy
Ann Neurol 4:253-256, Wakayama,Y.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Prenatal Diagnosis of Duchenne's Muscular Dystrophy
NEJM 297:968, Mahoney,M.J.,et al, 1977

X-linked Muscular Dystrophy
Ann Neurol 2:414, Furukawa,T.,et al, 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Carrier Detection in Duchenne Muscular Dystrophy
NEJM 294:193, Roses,A.D.,et al, 1976

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

Comprehensive Mangagement of Duchenne Muscular Distrophy
Arch Phys Med & Rehab Mar 1971, pp110., Johnson,E.,et al, 1971

"Sick"Motoneurones A Unifying Concept of Muscle Disease
Lancet 321, 1971 Feb., McComas,A.J.,et al, 1971

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

Ocular Myopathy
Arch Neurol 20:1, Magora,A.,et al, 1969

Chronic Progressive External Ophthalmoplegia
Arch Ophthalmol 82:845, Daroff,R., 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969



Showing articles 300 to 350 of 797 << Previous Next >>