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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
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cardiac transplantation
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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
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muscle wasting, diffuse
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muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
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muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
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muscular dystrophy, limb-girdle
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myasthenia gravis
myocardial biopsy
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myotonia dystrophica
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neck weakness
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neurologic disease, diagnoses of
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old age, neurology of
Oppenheim muscular dystrophy
pacemaker, cardiac-transvenous
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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
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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 700 to 750 of 988 << Previous Next >>

Cardiovascular Diseases and Stroke in African-Americans and Other Racial Minorities in the US
Stroke 22:551-568, , 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Invasive Treatment for Coronary Artery Disease in the Elderly
Arch Int Med 151:1085-1088, Gold,S.,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

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,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

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

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

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

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

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

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

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

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

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

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

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

The Diagnostic Sensitivity of Electrophysiologic Testing in patients with Syncope Caused by Transient Bradycardia
NEJM 321:1703-1707, Fujimura,O.,et al, 1989

Prediction of Carotid Stenosis Progression by Lipid & Hematologic Measurements
Neurol 39:1325-1331, Grotta,J.C.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Neuroaxonal Dystrophy Due to Lysosomal a-N-Acetylgalactosaminidase Deficiency
NEJM 320:1735-1740, Schindler,D.,et al, 1989

Tilting Towards a Diagnosis in Recurrent Unexplained Syncope
Lancet 1:658-660, Fitzpatrick,A.&Sutton,R., 1989



Showing articles 700 to 750 of 988 << Previous Next >>