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Differential
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abdominal muscle paralysis
abiotrophy
advances in neurology
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anterior tibial muscle weakness
arrhythmia, cardiac
arthrogryposis multiplex
atrioventricular block
bradycardia
calf atrophy
calf hypertrophy
carcinoma
cardiomegaly
cardiomyopathy
central core disease
Charcot-Marie-Tooth
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
collagen vascular disease
complications
congenital myopathy
creatine phosphokinase(CPK)elevated
dermatomyositis
descending paralysis
distal muscle weakness
dysphagia
dystroglycanopathies
dystrophin
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
epidemiology of neurology
erythrocyte
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
foot drop
gait disorder
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Guillain Barre syndrome
hearing loss
hearing problems in children
heart block
immunohistochemistry
immunologic disease
immunosuppressive agents
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
klippel feil syndrome
Kugelberg-Welander syndrome
lid closure, weakness of
life expectancy
lordosis
lymphocyte capping, diminished
methotrexate
molecular genetics
mononeuropathy
mortality
motor neuron disease
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle diseases, characteristics of
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenic crisis
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, mitochondrial
myopathy, steroid induced
myopathy, thyroid disease causing
myositis
myotonia dystrophica
neck weakness
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neurocardiology
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
neurologic disease, diagnoses of
neuropathy
neuropathy, diabetic
ocular myopathy
oculopharyngeal muscular dystrophy
ophthalmoplegia
poliomyelitis
polymyositis
polyneuropathy
porphyria
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
pseudohypertrophy
ptosis
ptosis, bilateral
quality of life
rash
respirator
respiratory failure
retinal detachment
retinopathy
review article
sarcoidosis
scapulohumeral syndrome
scapuloperoneal syndrome
sensorineural hearing loss
shoulder-girdle wasting
sloped shoulders
spinal muscular atrophy
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
sudden death
systemic illness
telangiectases
telangiectases, retinal
torticollis
transverse smile
treatment of neurologic disorder
vision, failure of in childhood
visual loss
weakness, progressive
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
Showing articles 650 to 700 of 788 << Previous Next >>

A Rating Scale for Amyotrophic Lateral Sclerosis:Description & Preliminary Experience
Ann Neurol 22:328-333, Appel,V.,et al, 1987

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Clinincopath Conf
Progressive Muscular Atrophy & Diabetic Neuromuscular Disease, Case 21-1987, NEJM 316:1326-13357., , 1987

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Causalgia as a Complication of Meningococcal Meningitis
BMJ 292:1710, McLelland,J.&Ellis,S.J., 1986

Reflex Sympathetic Dystrophy of the Face, Report of Two Cases & a Review of the Literature
Arch Neurol 43:693-695, Jaeger,B.,et al, 1986

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Motor Neuron Disease & Plasma Cell Dyscrasia
Neurol 36:1429-1436, Shy,M.E.,et al, 1986

A Double-Blind, Placebo-Controlled Trial of TRH in Amyotrophic Lateral Sclerosis
Neurol 36:141-145, Caroscio,J.T.,et al, 1986

Controlled Trial of Thyrotropin Releasing Hormone in Amyotrophic Lateral Sclerosis
Neurol 36:146-151, Brooke,M.H.,et al, 1986

Amyotrophic Lateral Sclerosis:Effects of Administration of Thyrotropin-Releasing Hormone
Neurol 36:152-159, Mitsumoto,H.,et al, 1986

Amyotrophic Lateral Sclerosis, Associated Clinical Disorders & Immunological Evaluations
Arch Neurol 43:234-238, Appel,S.H.,et al, 1986

Familial Adult Motor Neuron Disease:Amyotrophic Lateral Sclerosis
Neurol 36:511-517, Mulder,D.W.,et al, 1986

Post-Polio Syndrome
J Med Assoc Ga 74:510-511, Bailey,A.A., 1985

Amyotrophic Lateral Sclerosis:Part 1. Clinical Features, Pathology, & Ethical Issues in Management
Ann Neurol 18:271-280, Tandan,R.,et al, 1985

Amytrophic Lateral Sclerosis:Part 2, Etiopathogenesis
Ann Neurol 18:419-431, Tandan,R.,et al, 1985

Isolation of LAV/HTLV-III From a Patient with Amyotrophic Lateral Sclerosis
NEJM 313:324-325, Hoffman,P.M.,et al, 1985

ALS & Pet Exposure
Neurol 35:717-720, Tarras,S.,et al, 1985

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Tangier Disease (Hypo-a-Lipoproteinemia)
Textbook of Child Neurology, 3rd Ed. , Phila, Lea & Febiger, Ch 1, p 86, Menkes,J.H., 1985

Pathological Laughter & Crying
In Frederiks, J. A. M. (Ed) Handbook of Clinical Neurology, Elsevier Science Publ, 45:219, Poeck,K., 1985

Amyotrophic Lateral Sclerosis:A Double-Blind Crossover Trial of Thyrotropin-Releasing Hormone
JNNP 47:1332-1334, Imoto,K.,et al, 1984

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984

Inhibition of Terminal Axonal Sprouting by Serum From Patients with Amyotrophic Lateral Sclerosis
NEJM 311:933-939, Gurney,M.E.,et al, 1984

Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
Ann Neurol 16:642-648, Schmitt,H.P.,et al, 1984

The Cerebrohepatorenal (Zellweger) Syndrome
NEJM 310:1141-1146, Moser,A.E.,et al, 1984

Small Bowel Resection with Vitamin E Deficiency & Progressive Spinocerebellar Syndrome
Neurol 34:1046-1052, Bertoni,J.M.,et al, 1984

Iatrogenic Causalgia
Arch Neurol 41:821-824, Horowitz,S.H., 1984

Monomelic Amyotrophy
Arch Neurol 41:388-394, Gourie-Devi,M.,et al, 1984

Benign Focal Amyotrophy
Arch Neurol 41:678-679, Riggs,J.E.,et al, 1984

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

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

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

Acute Respiratory Failure in Motor Neuron Disease
Arch Neurol 40:30-32, Hill,R.,et al, 1983

Effect on Weakness & Spasticity in Amyotrophic Lateral Sclerosis of Thyrotropin-Releasing Hormone
Lancet 2:73-75, Engel,W.K.,et al, 1983

Amyotrophic Lateral Sclerosis & Pet Exposure
NEJM 309:244-245, Schenkman,M.,et al, 1983

Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
Neurol 33:237-240, Djupesland,G.,et al, 1983

Reflex Sympathetic Dystrophy (Causalgia) Treatment with Guanethidine
Arch Neurol 40:430-432, Tabira,T.,et al, 1983

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

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 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

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

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

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



Showing articles 650 to 700 of 788 << Previous Next >>