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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 950 to 1000 of 1074 << Previous Next >>

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Selective Use of Two-Dimensional Echocardiography in Stroke Syndromes
Editorial, Ann Int Med 95:112-1141981., , 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Cardiogenic Dementia--A Myth
Lancet 2:743-744, Emerson,T.R.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

Intracardiac Electrophysiologic Techniques in Recurrent Syncope of Unknown Cause
Ann Int Med 95:542-548, DiMarco,J.P.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

The Reflex Sympathetic Dystrophy Syndrome (RSDS)
Am J Med 70:23-30, Kozin,F.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Gross Demonstration of Atrophic Cauda Equina Roots in Motor Neuron Disease, An Improved Method
Arch Neurol 37:394, Meneses,A., 1980

Infantile Neuronal Degeneration Masquerading as Werdnig-Hoffmann Disease
Ann Neurol 8:317-324, Steiman,G.S.,et al, 1980

Fetal Hydantoin Syndrome, Neuroblastoma, & Hemorrhagic Disease in a Neonate
Jr. , et al, JAMA 244:1464-146580., Allen,R.W., 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Abetalipoproteinemia, Report of Two Cases & Review of Therapy
Arch Neurol 37:659-662, Illingworth,D.R.,et al, 1980

Horner Syndrome with Causalgia
Neurol 30:534-535, Bernad,P.G.,et al, 1980

Diagnosis of Infatile Neuroaxonal Dystrophy by Skin Biopsy
Ann Neurol 7:377-379, Wisniewski,K.,et al, 1980

Management of Hypoventilation in Motor Neuron Disease Presenting with Respiratory Insufficiency
Ann Neurol 7:188-191, Sivak,E.D.,et al, 1980

Juvenile Muscular Atrophy Localized to Arms
Arch Neurol 37:297-299, Singh,N.,et al, 1980

Familial Tapetorentinal Degeneration & Epilepsy
Arch Neurol 36:544-546, Cohan,S.L.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Management of Concomitant, Symptomatic Surgical Lesions of the Coronary & Carotid Arteries
Surg Neurol ll:70-72, Rollinson,R.D.,et al, 1979

Amyotrophic Lateral Sclerosis With Ophthalmoplegia; A Cliniocopathologic Study
Arch Neurol 36:615-617, Harvey,D.G.,et al, 1979

Remission of a Syndrome Indistinguishable from Motor Neuron Disease after Resection of Bronchial Carcinoma
BMJ 2:176-177, , 1979

Clinical Pathological Conference
Amyotrophic Lateral Sclerosis, Case Record 46-1979, NEJM 301:1104-1111979., , 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

TIA, Stroke, & Mitral Valve Prolapse
Neurol 29:886-889, Watson,R.T., 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy
Arch Neurol 36:317-318, Russman,B.S.,et al, 1979

Spirometry in Amyotrophic Lateral Sclerosis
Arch Neurol 36:74-80, Fallat,R.J.,et al, 1979

Age & Cerebrospinal-Fluid Protein in Motor-Neuron Disease
NEJM 300:437-438, Guiloff,R.J.,et al, 1979

Double-Blind Study of Modified Neurotoxin in Motor Neuron Disease
Neurol 29:77-81, Tyler,H.R., 1979

Subacute Motor Neuronopathy:A Remote Effect of Lymphoma
Ann Neurol 5:271-287, Schold,S.C.,et al, 1979

Sarcoidosis & Its Ophthalmic Manifestations
Am J Ophthmol 86:648-655, Obenauf,C.D.,et al, 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Distal Chronic Spinal Muscular Atrophy Involving the Hands
JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978

Amyotrophic Lateral Sclerosis
Arch Neurol 35:638-642, Rosen,A.D., 1978

Cellular Immunity In Guamanians with Amyotrophic Lateral Sclerosis & Parkinsonism-Dementia
NEJM 299:680-685, Hoffman,P.M.,et al, 1978

Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions
Ann Neurol 4:245-249, Iwata,M.,et al, 1978

Weakness in Malignancy:Evidence for a Remote Effect of Tumor on Distal Axons
Ann Neurol 4:268-274, Barron,S.A.,et al, 1978

Human Pneumatic Tourniquet Paralysis
Neurol 28:787-793, Bolton,C.F.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978



Showing articles 950 to 1000 of 1074 << Previous Next >>