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Differential
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advances in neurology
ammonia
anesthesia, general
anterior tibial muscle weakness
antiviral agents
areflexia
arrhythmia, cardiac
ataxia
ataxic gait
atrial fibrillation
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
Babinski sign
biopterin deficiency
bradycardia
bradykinesia
calf hypertrophy
cardiomegaly
cardiomyopathy
cardiovascular disease
cerebral embolism
cerebral embolism, carotid origin
cerebral palsy
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 14
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
consanguinity
contractures, joint
corpus callosum, lesion of
cough
creatine phosphokinase(CPK)elevated
developmental disability
developmental milestones, loss of
diamond on quadriceps
differential diagnosis
difficulty going down stairs
distal muscle weakness
diurnal variation
dopa responsive dystonia
dysarthria
dyspraxia
dystonia
dystonia, treatment of
dystrophin
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
encephalopathy
epileptic encephalopathy
exercise
exome sequencing
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fever
fibrillations
fine motor function, impaired
foot deformity
foot drop
gait disorder
gait, spastic
gene
gene mutation
gene therapy
genetic neurologic disorders
genetic testing
Gowers maneuver
growth retardation
heart block
heart block, complete
heart murmur
high arched feet
hyperreflexia
hyporeflexia
hypotonia
imbalance
implantable cardioverter defibrillator
influenza A virus
influenza B virus
Krabbe's disease
L-dopa
leukodystrophy
life expectancy
limb-girdle weakness
liver disease
lysosomal storage disease
malignant hyperpyrexia
meningitis, CSF cell count-normal
mental retardation
microcephaly
misdiagnosis
mitochondrial disease
molecular genetics
movement disorder
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myoglobinuria
myopathy
myopathy, quadriceps
myositis
myositis, acute of childhood
myositis, post infectious
neurologic disease, diagnoses of
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
pacemaker, cardiac-transvenous
pain, calf
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinsonism syndrome
pes cavus
positive sharp waves
prognosis
progressive neurologic disorder
proximal muscle atrophy
pyramidal tract dysfunction
Red flags
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
scoliosis
seizure
seizure, children
short stature
sinemet
spastic diplegia
spasticity
steroid therapy, CNS treatment and complications with
sudden death
tandem gait, ataxic
tenderness
toe walking
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tripping
urea-cycle enzymopathies
urine, dark
viral infection
viral myopathy
walking
walking frame
walking, delayed
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
web sites
wheelchair
white matter disease
wide based gait
winging of scapula
workup
Showing articles 300 to 350 of 402 << Previous Next >>

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

Barbiturate-Related Connective Tissue Disorder
Arch Int Med 149:911-914, Mattson,R.H.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Effect of Vitamin E Deficiency on Neurologic Function in Patients with Cystic Fibrosis
J Pediatr 113:637-640, Cynamon,H.A.,et al, 1988

Sensory Form of Acute Polyneuritis
Neurol 38:1728-1731, Dawson,D.M.,et al, 1988

Hand Contractures in Parkinson's Disease
JNNP 51:1221-1223, Kyriakides,T.&Hewer,R.L., 1988

Autoantibodies to Glutamic Acid Decarboxylase in Pt with Stiff-Man Syndr, Epilepsy & Type I Diabetes Mellitus
NEJM 318:1012-1020, Solimena,M.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Atlantoaxial Instability in Down Syndrome:Roentgenographic, Neurologic, & Somatosensory Evoked Potential Studies
J Pediatr 110:515-521, Pueschel,S.M.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Increased Concentrations of Cholestanol & Apolipoprotein B in CSF with Cerebrotendinous Xanthomatosis
NEJM 316:1233-1238, Salen,G.,et al, 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Neurologic Manifestations of Heatstroke at the Mecca Pilgrimage
Neurol 37:1004-1006, Yaqub,B.A., 1987

Critical Illness Polyneuropathy:A Complication of Sepsis and Multiple Organ Failure
Brain 110:819-842, Zochodne,D.W.,et al, 1987

Classification of Peripheral Neuropathy:The Long and the Short of It
Muscle & Nerve 9:711-719986., Sabin,T.J., 1986

Chronic Demyelinating Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Ann Neurol 20:89-91, Argov,Z.,et al, 1986

Magnetic Resonance Imaging in Cerebrotendinous Xanthomatosis
Neurol 36:124-126, Swanson,P.D.&Cromwell,L.D., 1986

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Botulism in an Adult Associated with Food-Borne Intestinal Infection with Clostridium Botulinum
NEJM 315:239-241, 254-2551986., Chia,J.K.,et al, 1986

Neurologic Signs in Senescence
Arch Neurol 42:1154-1157, Jenkyn,L.R.,et al, 1985

Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
NEJM 313:1580-1586, Sokol,R.J.,et al, 1985

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Arch Neurol 42:1008-1010, Katz,D.A.,et al, 1985

Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
Ann Neurol 18:517-518, Pedley,T.A.,et al, 1985

Spinocerebellar Degeneration Associated with a Selective Defect of Vitamin E Absorption
NEJM 313:32-35, Harding,A.E.,et al, 1985

Long-Term Treatment of Cerebrotendinous Xanthomatosis with Chenodeoxycholic Acid
NEJM 311:1649-1652, Berginer,V.M.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984

Severe Neurological Disease Associated with Hyperparathyroidism
Ann Neurol 15:453-456, Patten,B.M.,et al, 1984

Bilateral Adie's Tonic Pupil with Anhidrosis & Hyperthermia
Arch Neurol 41:342-343, Spector,R.H.,et al, 1984

Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Ross Syndrome & Skin Changes
Neurol 32:1041-1042, Heath,P.D.,et al, 1982

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,et al, 1982

Brainstem Encephalitis & The Syndrome Of Miller Fisher
Brain 105:481-495, Al-Din,A.N.,et al, 1982

Transient Areflexia & Quadriplegia Following Metrizamide Myelography
Ann Neurol 12:406-407, Peroutka,S.J.,et al, 1982

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Neurologic Signs In Uncomplicated Aging (Senscence)
Seminars In Neurology, Thieme-Stratton Inc. , New York, N. Y. pp. 21-30, Jenkyn,L.R.&Reeves,A.G., 1981

Neurological Manifestation of Accidental Hypothermia
Ann Neurol 10:384-387, Fischbeck,K.H.,et al, 1981

Primary Lateral Sclerosis
Arch Neurol 38:630-633, Beal,M.F.,et al, 1981

The Acute Sensory Neuronopathy Syndrome:A Distinct Clinical Entity
Ann Neurol 7:354-358, Sterman,A.B.,et al, 1980

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

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

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,et al, 1980

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

The Late Postpatrum Eclampsia Controversy
Obstet Gynecol 55:74-78, Sibai,B.M.,et al, 1980

Cervical Myelopathy after Metrizamide Myelography
BMJ 2:1262-1263, Bastow,M.,et al, 1979



Showing articles 300 to 350 of 402 << Previous Next >>