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Differential
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abdominal distention
acid maltase deficiency
advances in neurology
algorithm
amniocentesis
anesthesia, general
antibodies to voltage-gated calcium channels
arrhythmia, cardiac
ataxia
ataxia, paroxysmal
calcium channel dysfunction
calf hypertrophy
cardiac transplantation
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, muscle
central core disease
children
chloride channel dysfunction
clubfoot as related to neurologic disease
complications
congenital myopathy
congestive heart failure
contractures, joint
creatine phosphokinase(CPK)elevated
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
dystrophin
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electrocardiogram, LVH
ELISA
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
erythrocyte
familial
familial hemiplegic migraine
floppy infant
Friedreich's ataxia
gait disorder
gait, waddling
gastric dilatation, acute
gastrointestinal motility
gene
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
Gowers maneuver
Guillain Barre syndrome
hand weakness
heart block
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
inclusion body myositis
intellectual deficit
intestinal pseudoobstruction
left ventricular dilatation
life expectancy
lordosis
lymphocyte capping, diminished
malignant hyperpyrexia
mental retardation
migraine
molecular genetics
mortality
MRI
MRI, muscle
muscle biopsy
muscle pain
muscle weakness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, systemic membrane defect
myoglobinuria
myopathy
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopathy, quadriceps
myotonia congenita
myotonia dystrophica
neurologic disease, diagnoses of
neurologic evaluation
neuropathy
neuropathy, amyloid
newborn, evaluation of
paramyotonia congenita
paroxysmal neurologic deficits
periodic paralysis
physical therapy
polymerase chain reaction
potassium channel antibodies
potassium channel dysfunction
prenatal diagnosis by amniocentesis
prognosis
pseudohypertrophy
psychiatric disorder
quadriceps atrophy
recombinant DNA
respiratory failure
review article
RFLPs
rhabdomyolysis
rippling muscle disease
scoliosis
seizure
sodium channel dysfunction
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
steroid therapy, CNS treatment and complications with
toe walking
treatment of neurologic disorder
weakness
weakness, progressive
web sites
Western immunoblot test
workup
Showing articles 2050 to 2055 of 2055 << Previous

Myasthenic Syndrome in Patients with ALS
et al Neurol 9:627, Mulder,D.W., 1959

Localization of Lesions Causing Horner's Syndrome
Arch Ophthamol 44:710, Jaffe,N., 1950

Causalgia of the Face, Two Cases Successfully Treated by Sympathectomy
BMJ 1:804-805, Bingham,J.A.W., 1947

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

Degenerative Diseases of the Nervous System, Primary Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1112, Ropper, A.H.,et al,

10 Things You Should Know About Cerebral Amyloid Angiopathy
Stroke 57:e69-e742026, Charidimou,A.,



Showing articles 2050 to 2055 of 2055 << Previous