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Differential
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amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ANA
areflexia
arrhythmia, cardiac
atrioventricular block
autoantibodies
autoimmune disease
bradycardia
bulbar palsy
calf hypertrophy
camptocormia
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
central core disease
cerebral embolism
cerebrovascular accident
children
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
congestive heart failure
contractures, joint
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
delay in diagnosis
dermatomyositis
developmental retardation
diamond on quadriceps
differential diagnosis
dislocated hip, congenital
distal muscle weakness
dysarthria
dysphagia
dyspraxia
dystrophic calcification
electromyogram
Emery-Dreifuss muscular dystrophy
enzyme, muscle disease
epidemiology of neurology
exercise
facial weakness
falling
familial
fasciculation
fatigue
fibrillations
finger flexor weakness
finger weakness
foot drop
gender
gene
gene mutation
genetic neurologic disorders
genetic testing
Gowers maneuver
hand pain
hand weakness
heart block
heart block, complete
heart murmur
hemiparesis
heralding manifestation
hyperreflexia
hypoparathyroidism
hyporeflexia
hypotonia
hypotonia, infants
immunosuppressive agents
inclusion body myositis
intrinsic hand muscles, wasting of
jaw jerk, abnormal
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
leg weakness, bilateral
life expectancy
limb-girdle weakness
lordosis
malignant hyperpyrexia
mental retardation
Mills syndrome
misdiagnosis
mitral valve prolapse
molecular genetics
motor neuron disease
MRI, abnormal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle stiffness
muscle strength, testing
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, distal, Miyoshi
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenic syndrome
myocarditis
myoglobinuria
myopathy
myopathy, autoimmune
myopathy, distal
myopathy, distal, vacuolar
myopathy, hypocalcemic
myopathy, inclusion body
myopathy, quadriceps
myopathy, vacuolar
myositis
neck weakness
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuropathology
overlap syndrome
pacemaker, cardiac-transvenous
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, hands
polymyositis
positive sharp waves
prognosis
progressive neurologic disorder
proximal muscle atrophy
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
repetitive nerve stimulation
respiratory failure
review article
rhabdomyolysis
rigid spine syndrome
sarcoglycan
sarcoglycanopathy
scoliosis
scoliosis, neurologic association with
sedimentation rate, elevated
steroid
stiff joints
sudden death
toe walking
treatment of neurologic disorder
type 1 muscle fiber
type 2 muscle fiber
urine, dark
weakness
weakness, generalized
weakness, progressive
weakness, proximal
winging of scapula
workup
Showing articles 350 to 361 of 361 << Previous

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

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

Syndromes of Central Motor Disorder
in Vinken, P. J. , Bruyn, G. W. , ed. , Handbook of Clinical Neurology, Vol. 1, North-Holland Publ C, , Amsterdam, 19Rondot, P., 1969

Surgical Anatomy of the Hand
Clinical Symposia,Ciba 21:66-109, Lampe,E.W., 1969

Parkinson's Disease
In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Neurological Disorders Associated with Adult Celiac Disease
Brain 89:683, Cooke,W.T.,et al, 1966

Recognition, Prognosis, & Treatment of the Guillain-Barre Syndrome (Acute Idiopathic Polyneuritis)
Med Clin North Am 47:1371, Eiben,R.,et al, 1963

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease
, Witiw,C.D.&OToole,J.E.,



Showing articles 350 to 361 of 361 << Previous