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Differential
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acetazolamide
acid maltase deficiency
advances in neurology
adverse drug reaction
airway obstruction
anesthesia, general
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
antihistamines
arrhythmia, cardiac
ataxia
ataxia, paroxysmal
calcium antagonist
calcium channel dysfunction
carbamazepine
cardiomyopathy
CAT scan
CAT scan, muscle
central core disease
chewing, impaired
children
chloride channel dysfunction
clubfoot as related to neurologic disease
congenital myopathy
congestive heart failure
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
differential diagnosis
dilantin
drug induced neurologic disorders
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
facial weakness, bilateral
falling
familial
familial hemiplegic migraine
floppy infant
Friedreich's ataxia
gene mutation
genetic neurologic disorders
Guillain Barre syndrome
heart block
high arched feet
hydrocephalus
hyperkalemic periodic paralysis
hypokalemia
hypokalemic periodic paralysis
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
inclusion body myositis
kaliuresis
lordosis
malignant hyperpyrexia
metabolic acidosis
mexiletine
micrognathia
migraine
molecular genetics
MRI
MRI, abnormal
MRI, muscle
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle stiffness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, mitochondrial
myotonia
myotonia congenita
myotonia dystrophica
myotonia, treatment of
neurologic disease, diagnoses of
neurologic evaluation
neuropathy
neuropathy, amyloid
newborn, evaluation of
nifedipine
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
polymyositis
potassium channel antibodies
potassium channel dysfunction
procainamide
prognosis
respiratory failure
review article
rhabdomyolysis
seizure
sodium channel dysfunction
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
temporalis muscle wasting
term infant
tocainide
treatment of neurologic disorder
trinucleotide repeats
tubular aggregates, muscle
workup
Showing articles 150 to 173 of 173 << Previous

Cylindrical Spirals in a Familial Neuromuscular Disorder
Ann Neurol 7:550-556, Bove,K.E.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

Cholestasis & Myotonic Dystrophy
(letter) NEJM 301:329-330979., Theodore,Ch.,et al, 1979

Isaac Syndrome with Laryngeal Involvement:An Unusual Presentation of Myokymia
Neurol 29:1612-1615, Jackson,D.L.,et al, 1979

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Erythrocyte Metabolism in Muscular Dystrophy
Arch Neurol 35:592-595, Danon,M.J.,et al, 1978

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

Hypothyroidism with True Myotonia
JNNP 41:1013-1015, Venables,G.S.,et al, 1978

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

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

Myasthenia Gravis & Myotonic Dystrophy in a 13-year-old Girl
Neurol 27:546, Schoen,R.T., 1977

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

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Important Advances in Clinical Medicine
West J Med 123:128, Mosier,J.M.,et al, 1975

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

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

Preclinical Detection of Dystrophia Myotonica
BMJ 124, 1972 April., , 1972

Electrodiagnosis of Neuromuscular Disease
Bull Univ Maryland School Med 56:33, Kemble,F., 1971

Ophthalmoplegia In Myotonic Dystrophy
Am J Ophthalmol 71:1231-1235, Lessell,S.,et al, 1971

Early Recognition of Heterozygotes for the Gene for Dystrophia Myotonica
JNNP 33:279, Bundey,S.,et al, 1970

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

The Cerebral Defect & Myopathy in Myotonic Dystrophy
Neurol 17:1106, Rosman,N.,et al, 1967



Showing articles 150 to 173 of 173 << Previous