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Differential
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abdominal distention
acid maltase deficiency
advances in neurology
algorithm
amniocentesis
anesthesia, general
antibodies to voltage-gated calcium channels
arrhythmia, cardiac
ataxia
ataxia, paroxysmal
calcium channel dysfunction
calf hypertrophy
cardiac transplantation
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, muscle
central core disease
children
chloride channel dysfunction
clubfoot as related to neurologic disease
complications
congenital myopathy
congestive heart failure
contractures, joint
creatine phosphokinase(CPK)elevated
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
dystrophin
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electrocardiogram, LVH
ELISA
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
erythrocyte
familial
familial hemiplegic migraine
floppy infant
Friedreich's ataxia
gait disorder
gait, waddling
gastric dilatation, acute
gastrointestinal motility
gene
gene therapy
genetic counselling
genetic diagnosis, prenatal
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genetic neurologic disorders
Gowers maneuver
Guillain Barre syndrome
hand weakness
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hypotonia
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
inclusion body myositis
intellectual deficit
intestinal pseudoobstruction
left ventricular dilatation
life expectancy
lordosis
lymphocyte capping, diminished
malignant hyperpyrexia
mental retardation
migraine
molecular genetics
mortality
MRI
MRI, muscle
muscle biopsy
muscle pain
muscle weakness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, systemic membrane defect
myoglobinuria
myopathy
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopathy, quadriceps
myotonia congenita
myotonia dystrophica
neurologic disease, diagnoses of
neurologic evaluation
neuropathy
neuropathy, amyloid
newborn, evaluation of
paramyotonia congenita
paroxysmal neurologic deficits
periodic paralysis
physical therapy
polymerase chain reaction
potassium channel antibodies
potassium channel dysfunction
prenatal diagnosis by amniocentesis
prognosis
pseudohypertrophy
psychiatric disorder
quadriceps atrophy
recombinant DNA
respiratory failure
review article
RFLPs
rhabdomyolysis
rippling muscle disease
scoliosis
seizure
sodium channel dysfunction
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
steroid therapy, CNS treatment and complications with
toe walking
treatment of neurologic disorder
weakness
weakness, progressive
web sites
Western immunoblot test
workup
Showing articles 1900 to 1950 of 2055 << Previous Next >>

Adult Polyglucosan Body Disease:Clinical & Nerve Biopsy Findings in Two Cases
Ann Neurol 13:440-444, Vos,A.L.M.,et al, 1983

Precautions Recommended in Treating Patients with Aids
NEJM 308:156, Masci,J.R.,et al, 1983

Progressive Multifocal Leukoencephalopathy in Acquired Immunodeficiency Syndrome
NEJM 309:492-493, Bedri,J.,et al, 1983

Outbreak of Central-Nervous-System Toxoplasmosis in Western Europe & North America
Lancet 1:781-784, Luft,B.J.,et al, 1983

Fatal CNS Toxoplasmosis in a Homosexual Man
Neurol 33:926-927, Delaney,P.,et al, 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Joseph Disease in a Non-Portuguese Family
Neurol 33:74-80, Sakai,T.,et al, 1983

Conjugal Amyotrophic Lateral Sclerosis
Ann Neurol 14:699, Paolino,E.,et al, 1983

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Monocular Polyopia
Arch Neurol 40:756-757, Hirst,L.W.,et al, 1983

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Central-Nervous-System Toxoplasmosis In Homosexual & Heterosexual Adults
NEJM 307:498-499, Hauser,W.E.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Electro-oculographic Findings in Machado-Joseph Disease
Neurol 32:1272-1276, Dawson,D.M.,et al, 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Neurogenic Arthrogryposis in One Identical Twin, Sul
Arch Neurol 39:717-718, Yi,C.,et al, 1982

Progressive Multifocal Leukoencephalopathy In A Male Homosexual With T-Cell Immune Deficiency
NEJM 307:1436-1438, Miller,J.R.,et al, 1982

Neuroaxonal Dystrophy in Young Adults:A Clinicopathological Study of Two Unrelated Cases
Ann Neurol 11:335-343, Williamson,K.,et al, 1982

Examination of Dental Pulp to Diagnose Infantile Neuroaxonal Dystrophy
Arch Neurol 39:422-423, Carlo,J.,et al, 1982

Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Type I Fiber Atrophy & Internal Nuclei, A Form of Centronuclear Myopathy
Arch Neurol 39:520-524, Peyronnard,J-M.,et al, 1982

Ocular Disorders Associated with a New Severe Acquired Cellular Immunodeficiency Syndrome
Am J Ophthalmol 93:393-402, Holland,G.N.,et al, 1982

Retinal Cotton-Wool Spots in a Patient with Pneumocystis Carinii Infection
NEJM 314:184-185, Kwok,S.,et al, 1982

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

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

Bilateral Vocal Cord Paralysis in a Patient With Familial Hypertrophic Neuropathy
Arch Neurol 38:532, Johnson,J.A.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

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

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

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

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980

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

Cramps, Muscle Pain, & Tubular Aggregates
Arch Neurol 37:715-717, Lazaro,R.P.,et al, 1980

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

Proximal Muscle Weakness in Uremia
Arch Neurol 37:555-558, Lazaro,R.P.,et al, 1980

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

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

Dejerine-Sottas Disease Revisited
Arch Neurol 37:67-68, Stran,R., 1980

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



Showing articles 1900 to 1950 of 2055 << Previous Next >>