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Differential
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advances in neurology
adverse drug reaction
alveolar hypoventilation
anesthesia, general
arrhythmia, cardiac
aspiration
asymptomatic
atrial fibrillation
atrial flutter
atrioventricular block
automatic implantable cardioverter-defibrillator
baldness
benign congenital hypotonia
bradycardia
cachexia
calf hypertrophy
carcinoma
cardiac transplantation
cardiomegaly
cardiomyopathy
cardiovascular disease
cataracts
cerebral embolism
cerebral embolism, cardiac origin
cerebrovascular accident
children
chromosome 19
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
complications
conduction block
congestive heart failure
contractures, joint
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
defibrillator, implanted
dermatomyositis
diamond on quadriceps
differential diagnosis
disability, neurological
distal muscle weakness
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dystroglycanopathies
dystrophic calcification
dystrophin
dystrophin associated proteins
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electrocardiogram, LVH
electromyogram
electron microscopy
embolism
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy, carrier
enzyme, muscle disease
epidemiology of neurology
exercise
exercise electrocardiography
facial appearance, abnormal
facial weakness
facial weakness, bilateral
falling
familial
fibrillations
Friedreich's ataxia
gastrocnemius muscle weakness
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Gowers maneuver
Guillain Barre syndrome
hammertoes
heart block
heart block, complete
high arched feet
high arched palate
hip pain
Holter monitoring
hypercapnia
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
intellectual deficit
left ventricular dilatation
life expectancy
limb-girdle weakness
mental retardation
misdiagnosis
mitral valve prolapse
molecular genetics
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle hypertrophy
muscle pain
muscle stiffness
muscle strength, testing
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myasthenia gravis
myocardial biopsy
myocarditis
myoglobinuria
myopathy
myopathy, myofibrillar
myopathy, quadriceps
myositis
myotonia
myotonia dystrophica
myotonia dystrophica, type 2
myotonic discharges
neck weakness
neurocardiology
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular disease, electrodiagnosis of
neuropathy
neuropathy, amyloid
old age, neurology of
Oppenheim muscular dystrophy
pacemaker, cardiac-transvenous
pathology
percussion induced muscle contraction
physical activity
polymyositis
pregnancy, neurologic complications in
prevention of neurologic disorders
prognosis
progressive muscular dystrophy
progressive neurologic disorder
pseudohypertrophy
ptosis
pulmonary embolism
quadriceps atrophy
quality of life
radionuclide angiocardiography
respirator
respiratory failure
review article
rhabdomyolysis
rigid spine syndrome
rippling muscle disease
risk factors
sarcoglycan
sarcoglycanopathy
scoliosis
shoulder, pain in
slit lamp examination
steroid
steroid therapy, CNS treatment and complications with
sudden death
symptomatic
systemic illness
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
thrombus, mural
toe walking
transient ischemic attack
treatment of neurologic disorder
trinucleotide repeats
urine, dark
ventricular tachycardia
walking frame
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
wheelchair
winging of scapula
workup
Showing articles 300 to 350 of 988 << Previous Next >>

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

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

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

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

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

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

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

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

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

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

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

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,et al, 1978

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

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

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

Pathology of Malignant Hyperpyrexia
BMJ Editorial 249, 1973, Feb., , 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

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

Diphenylhydantoin for Myotonia Congenita-Correspondence
NEJM 286:893, , 1972

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

Congenital Dystrophia Myotonica
Neurol 22:443, Dyken,P.D., 1972

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

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

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

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

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

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969



Showing articles 300 to 350 of 988 << Previous Next >>