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Differential
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abdominal muscle paralysis
abiotrophy
advances in neurology
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anterior tibial muscle weakness
arrhythmia, cardiac
arthrogryposis multiplex
atrioventricular block
bradycardia
calf atrophy
calf hypertrophy
carcinoma
cardiomegaly
cardiomyopathy
central core disease
Charcot-Marie-Tooth
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
collagen vascular disease
complications
congenital myopathy
creatine phosphokinase(CPK)elevated
dermatomyositis
descending paralysis
distal muscle weakness
dysphagia
dystroglycanopathies
dystrophin
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
epidemiology of neurology
erythrocyte
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
foot drop
gait disorder
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Guillain Barre syndrome
hearing loss
hearing problems in children
heart block
immunohistochemistry
immunologic disease
immunosuppressive agents
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
klippel feil syndrome
Kugelberg-Welander syndrome
lid closure, weakness of
life expectancy
lordosis
lymphocyte capping, diminished
methotrexate
molecular genetics
mononeuropathy
mortality
motor neuron disease
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle diseases, characteristics of
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenic crisis
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, mitochondrial
myopathy, steroid induced
myopathy, thyroid disease causing
myositis
myotonia dystrophica
neck weakness
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neurocardiology
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neuropathy
neuropathy, diabetic
ocular myopathy
oculopharyngeal muscular dystrophy
ophthalmoplegia
poliomyelitis
polymyositis
polyneuropathy
porphyria
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
pseudohypertrophy
ptosis
ptosis, bilateral
quality of life
rash
respirator
respiratory failure
retinal detachment
retinopathy
review article
sarcoidosis
scapulohumeral syndrome
scapuloperoneal syndrome
sensorineural hearing loss
shoulder-girdle wasting
sloped shoulders
spinal muscular atrophy
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
sudden death
systemic illness
telangiectases
telangiectases, retinal
torticollis
transverse smile
treatment of neurologic disorder
vision, failure of in childhood
visual loss
weakness, progressive
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
Showing articles 850 to 873 of 873 << Previous

Neurocutaneous Disease
in Dermatology in General Medicine, Fitzpatrick, et al, eds, McGraw Hill, 1971, pp. 1379-1434., Adams,R., 1971

Rubella, Clinical Manifestations & Management
Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969

Neurogenic Muscular Atrophy of Infancy with Prolonged Survival
Brain 92:9, Munsat,T.,et al, 1969

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:551, Meadows,J.C.,et al, 1969

Parietal Lobe Syndromes
In Handbk of Clinical Neurology, Vinken & Bruyn, Ed, North-Holland Publ Co, Amsterdam, V2, Ch21, p., 84wesbury,E.C.O., 1969

Nine Neuropathies
Med Ann of the Dist of Columbia 37:89, Stevens,H., 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy (II)
Arch Neurol 18:619, Dyck,P.,et al, 1968

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Amyotrphic Lateral Sclerosis
Arch Neurol 16:357, Hirano,A.,et al, 1967

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

The Remote Effects of Cancer on the Nervous System
Proc Roy Soc Med 60:683, Wilkinson,M., 1967

"Myopathic"Changes in Chronically Denervated Muscle
Arch Neurol 16:14-24, Drachman,D.B.,et al, 1967

Motor Neurone Disease as a Manifestation of Neoplasm
Brain 88:479, Brain,L.,et al, 1965

Seronegative Ocular Syphilis & Neurosyphilis, Neuro-Ophthalmology Symposium, U. of Miami
(Ed) , St. Louis:C. V. Mosby Co. , 1965, p. 1, Smith,J.L., 1965

Cervical Myelopathy with Fasciculations in the Lower Extremities
J Neurosurg 20:948, King,R.B.,et al, 1963

Course & Prognosis in Amyotrophic Lateral Sclerosis
Arch Neurol 8:17, Mackay,R., 1963

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Amyotrophic Lateral Sclerosis:Clinical Syndrome Differential Diagnosis
Med Clin North Am 44:1013, Mulder,D.W., 1960

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

Neuro CPC of MGH
Cervical Spondylosis with Protruded Disk, NEJM 261:715-7201959., , 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

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

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



Showing articles 850 to 873 of 873 << Previous