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Differential
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advances in neurology
allodynia
amyloidosis
anesthesia, general
anterior horn cell disease
areflexia
arm weakness
asymptomatic
autonomic dysfunction
bone scanning
bulging of biceps
burning paresthesia
calf amyotrophy
calf atrophy
calf hypertrophy
cardiomyopathy
children
Clinical Pathologic Conference(C.P.C.)
creatine phosphokinase(CPK)elevated
cyanosis
descending paralysis
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DYSF gene
dysferlin
dysferlinopathy
dyspnea
edema, pedal
electromyogram
electron microscopy
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
foot drop
gait disorder
gait, waddling
gene
gene mutation
gene therapy
genetic neurologic disorders
genetic testing
Gowers maneuver
guanethidine
hemidiaphragm, paralysis of
hereditary myopathy with early respiratory failure
hoarseness
hypercalcemia
hyperhidrosis
inability to sit up
India
Kugelberg-Welander syndrome
leg atrophy
leg weakness, unilateral
lid closure, weakness of
life expectancy
livedo reticularis
misdiagnosis
molecular genetics
monoclonal gammopathy
monomelic amyotrophy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle hypertrophy
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, amyloid
myopathy, hereditary
myopathy, quadriceps
nerve conduction studies
neurologic disease, diagnoses of
neurologic examination
orthopnea
osteoporosis
pain
pain, leg
physical therapy
plasma cell dyscrasia
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
reflex sympathetic dystrophy
reflex sympathetic dystrophy, children
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
scoliosis
shoulder-girdle wasting
skin, temperature difference
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
steppage gait
steroid therapy, CNS treatment and complications with
survival motor neuron gene
sympathetic block
thermography
titinopathy
toe walking
tongue, enlarged
trauma
treatment of neurologic disorder
urine, dark
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
wheelchair
whistle, inability to
winging of scapula
Showing articles 2000 to 2050 of 2351 << Previous Next >>

Cerebral Atrophy & Functional Deficits In Alcoholics Without Clinically Apparent Liver Disease
Neurol 31:377-385, Carlen,P.L.,et al, 1981

Cerebellar Atrophy Demonstrated by Computed Tomography
Neurol 31:405-412, Koller,W.C.,et al, 1981

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

Parainfectious Acute Obstructive Hydrocephalus
Ann Neurol 10:62-63, Yanofsky,C.S.,et al, 1981

Antenatal Treatments Of Hydrocephalus
NEJM 303:1021-1023, Birnholz,J.C.,et al, 1981

Cerebellar Degeneration With Hodgkin's Disease
Arch Neurol 38:253-256, Brazis,P.W.,et al, 1981

Toxic Optic Neuropathy Caused by Benoxaprofen
BMJ 283:193-194, Dodd,M.J.,et al, 1981

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

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

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

Kluver-Bucy Syndrome in Pick disease:Clinical & patho-logic Correlations
Neurol 31:1415-1422, Cummings,J.L.,et al, 1981

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

Epidermoid Tumors Involving the Fourth Ventricle
Neurosurgery 9:9-13, Rosario,M.,et al, 1981

Subcortical Arteriosclerotic Encephalopathy:A Clinical & Radiological Investigation
JNNP 44:294-304, Loizou,L.A.,et al, 1981

Visual involvement in Friedreich's Ataxia & Hereditary Spastic Ataxia
Arch Neurol 38:75-79, Livingstone,I.R.,et al, 1981

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

Lipomembranous Polycystic Osteodysplasia with Progressive Dementia
J Comput Assist Tomogr 5:580-582, Laasonen,E.M.,et al, 1981

Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980

Cerebellar Degeneration Due to Chronic Phenytoin Therapy
Ann Neurol 7:18-23, McLain,L.W.,et al, 1980

Surgically Correctable Lesions Solely Detected by CT Scan in Adult-Onset Chronic Epilepsy
Ann Neurol 7:344-347, Jabbari,B.,et al, 1980

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

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Hazards of Oral Anticoagulants During Pregnancy
JAMA 243:1549-1551, Stevenson,R.E.,et al, 1980

Cerebellar Softening
Ann Neurol 8:133-140, Scotti,G.,et al, 1980

Clinical Aspects of CNS Cysticercosis
Arch Int Med 140:1309-1313, Shanley,J.D.,et al, 1980

Lobar Cerebral Hemorrhages:Acute Clinical Syndromes in 26 Cases
Ann Neurol 8:141-147, Ropper,A.H.,et al, 1980

A pedigree of Amyotrophic Chorea With Acantho-cytosis
Arch Neurol 37:514-517, Kito,S.,et al, 1980

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

Motor Neuropathy Associated with Cimetidine
BMJ 281:974-975, Walls,T.J.,et al, 1980

Masticatory Spasm in Facial Hemiatrophy
Ann Neurol 7:585-587, Kaufman,M.D., 1980

Acetazolamide-Induced Improvement in Hydro-cephalus
Arch Neurol 37:376, Donat,J.F., 1980

Acridine Orange-Nucleic Acid Fluorescence
Arch Neurol 37:641-644, Perl,D.P.,et al, 1980

Acne Fulminans with Inflammatory Myopathy
Neurol 8:67-69, Noseworthy,J.H.,et al, 1980

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

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Pseudotumor Cerebri, Clinical Profile & Visual Outcome in 63 Patients
Mayo Clin Proc 55:541-546, Rush,J.A., 1980

Alcoholic Downbeat Nystagmus
Ann Ophthalmol 1127-1131, October 1980., Costin,J.A.,et al, 1980

Leber's Optic Neuropathy
Editorial, BMJ 280:1097-10981980., , 1980

Dapsone-induced Optic Atrophy & Motor Neuropathy
BMJ 281:1180, Homeida,M.,et al, 1980

Ocular Defects in Children with Cerebral Palsy
BMJ 281:487-488, Black,P.D., 1980

Computed tomography in Hallervorden-Spatz disease
Neurol 30:1128-1130, Dooling,E.C.,et al, 1980

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

Enlarged Cerebral Ventricular System in Infant Achondroplastic Dwarf
Neurol 30:767-769, Mueller,S.M., 1980

Unusual Effects of Metrizamide Lumbar Myelography
Arch Neurol 37:588-589, Kelley,R.E.,et al, 1980

Treatment of Intractable Temporal Lobe-Limbic Epilepsy (Complex Partial Seizures) by Temporal Lobectomy
Ann Neurol 8:455-459, Glaser,G.H., 1980

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

Blindness Following Tentorial Herniation
Ann Neurol 8:186-190, Keane,J.R., 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980



Showing articles 2000 to 2050 of 2351 << Previous Next >>