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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 750 to 800 of 1074 << Previous Next >>

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Differentiation of Convulsive Syncope and Epilepsy with Head-up Tilt Testing
Ann Int Med 115:871-876, Grubb,B.P.,et al, 1991

The Autonomic and Hemodynamic Effects of Oral Theophylline in Patients with Vasodepressor Syncope
Arch Int Med 151:2425-2429, Nelson,S.D.,et al, 1991

Syncope:1991
Am J Med 90:1-5, Linzer,M., 1991

Utility of Upright Tilt-Table Testing in the Evaluation and Management of Syncope of Unknown Origin
Am J Med 90:6-10, Grubb,B.P.,et al, 1991

Diagnostic Evaluation of Syncope
Am J Med 90:91-106, Kapoor,W., 1991

A Prognostic System for Transient Ischemia or Minor Stroke
Ann Int Med 114:552-557, Kerman,W.N.,et al, 1991

Postmortem Studies of the Heart in Three Fatal Cases of the Eosinophilia-Myalgia Syndrome
Ann Int Med 115:102-110, James,T.N.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Perineal Reflex Sympathetic Dystrophy Treated with Bilateral Lumbar Sympathectomy
Ann Int Med 113:633-634, Olson,W.L., 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990

Effects of Pancreatic Transplantation on Diabetic Neuropathy
NEJM 322:1031-1037, Kennedy,W.R.,et al, 1990

Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome
Pediatrics 85:984-990, Glauser,T.A.,et al, 1990

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

Prenatal Prediction of Risk of the Fetal Hydantoin Syndrome
NEJM 322:1567-1572, Buehler,B.A.,et al, 1990

Diabetic Autonomic Neuropathy
BMJ 301:565-566, Bilous,R.W., 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Clinical Study of 227 Patients with Lacunar Infarcts
Stroke 21:842-847, Arboix,A.,et al, 1990

International Trends in Stroke Mortality:1970-1985
Stroke 21:989-992, Bonita,R.,et al, 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Cardiac Evaluation of the Patient with Stroke
Stroke 21:14-23, Sirna,S.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Carotid Plaque Morphology and Risk for Stroke
Stroke 21:148-151, Gomez,C.G., 1990

The Movement Disorder of Reflex Sympathetic Dystrophy
Neurol 40:57-61, Schwartzman,R.J.&Kerrigan,J., 1990

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989



Showing articles 750 to 800 of 1074 << Previous Next >>