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Differential
(Click to cross reference)
ankle reflex, absent
areflexia
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
benign essential tremor
Brown-Vialetto-Van Laere syndrome
calf hypertrophy
cardiomyopathy
central core disease
cerebellar atrophy, primary
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
clubfoot as related to neurologic disease
cognition
consanguinity
contractures, joint
corpus callosum, thinning
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
developmental milestones, loss of
differential diagnosis
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
diurnal variation
dopa responsive dystonia
dysarthria
dystonia
endemic area
evoked potentials
facial weakness
failure to thrive
falling
familial
fine motor function, impaired
finger nose finger test
foot deformity
foot drop
gait disorder
gait, waddling
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
hammertoes
hand deformity
hand weakness
hearing loss
high arched feet
hyperreflexia
hyporeflexia
hypotonia
hypotonia, infants
imbalance
incoordination
intrinsic hand muscles, wasting of
kyphoscoliosis, neurologic causes of
L-dopa
leg weakness, bilateral
leprosy
lordosis
malignant hyperpyrexia
microcephaly
mitral valve prolapse
molecular genetics
MRI, abnormal
muscle atrophy, static
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
myopathy
nerve conduction studies
nerve enlargement
nerve hypertrophy
neuropathy
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, peripheral
nystagmus
pain, foot
Parkinson disease
past pointing
pes cavus
polymerase chain reaction
polyneuropathy
polyneuropathy, familial
pons, lesion of
prognosis
progressive neurologic disorder
pseudohypertrophy
pyramidal tract dysfunction
rash
Red flags
renal tubular acidosis
review article
riboflavin transporter deficiency
Romberg's sign
Samoa
scoliosis
scoliosis, neurologic association with
sensory loss
skin, biopsy
skin, lesions in neurologic disorders
steppage gait
toe walking
treatment of neurologic disorder
tremor
tremor, intention
tripping
visual evoked response
walking
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
wheelchair
wide based gait
wrist drop
Showing articles 400 to 450 of 857 << Previous Next >>

Evidence From Proton Magnetic Resonance Spectroscopy for a Metabolic Cascade of Neuronal Damage in Shaken Baby Syndrome
Pediatrics 99:4-14, Haseler,L.J.,et al, 1997

Limb-Shaking Carotid Transient Ischemic Attacks Successfully Treated with Modification of the Antihypertensive Regimen
Arch Neurol 54:904-905, Leira,E.C.,et al, 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Tremor and Other Movement Disorders after Whiplash Type Injuries
JNNP 63:110-112, Ellis,S.J., 1997

High-Frequency Unilateral Thalamic Stimulation in the Treatment of Essential and Parkinsonian Tremor
Ann Neurol 42:292-299, Koller,W.,et al, 1997

Correlation of MRI and Neuropathology in AIDS
JNNP 62:92-95, Everall,I.P.,et al, 1997

Diagnosis of Viral Infections of the Central Nervous System:Clinical Interpretation of PCR Results
Lancet 349:313-317, Jeffery,K.J.M.,et al, 1997

Severe Encephalitis with Rapid Recovery
Lancet 349:470, Tong,C.Y.W.,et al, 1997

Persistent High MR Signal of the Posterior Pituitary Gland in Central Diabetes Insipidus
AJNR 18:1749-1752, Maghnie,M.,et al, 1997

Clozapine in Parkinson's Disase Tremor, Effets of Acute and Chronic Administration
Neurol 49:1587-1590, Bonuccelli,U.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

Relationship Between Human Immunodeficiency Virus-Associated Dementia & Viral Load in Cerebrospinal Fluid & Brain
Ann Neurol 42:689-698, 6751997., McArthur,J.C.,et al, 1997

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Prevalence of Parkinsonian Signs and Associated Mortality in a Community Population of Older People
NEJM 334:71-76, Bennett,D.A.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
Neurol 46:992-998, Brashear,A.,et al, 1996

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Diffuse Lewy Body Disease:Clinical Features in Nine Cases without Coexistent Alzheimer's Disease
JNNP 60:531-538, Hely,M.A.,et al, 1996

Yelling Attacks and Wasted Hands
Lancet 348:238, Bosboom,W.M.J.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Radiologic-Clinical Correlation:One-and-a-Half Syndrome Associated with Cheirooral Syndrome
AJNR 17:1482-1484, Shintani,S.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Post-Traumatic Movement Disorders in Survivors of Severe Head Injury
Neurol 47:1488-1492, Krauss,J.K.,et al, 1996

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996

AIDS in the Elderly:New York City Vital Statistics
J Emerg Med 14:19-23, Gaeta,T.J.,et al, 1996

Thalamic Tremor:Case Reports and Implications of the Tremor-Generating Mechanism
Neurol 46:75-79, Miwa,H.,et al, 1996

Neuroimaging Findings in Patients on Immunosuppressive Therapy:Experience with Tacrolimus Toxicity
AJR 166:683-688, Appignani,B.A.,et al, 1996

AIDS and Cerbrovascular Disease
Stroke 27:538-543, Pinto,A.N., 1996

Familial Migraine with Vertigo and Essential Tremor
Neurol 46:458-460, Baloh,R.W.,et al, 1996

Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
Neurol 47:817-821, Lee,H.C.,et al, 1996

Delayed-Onset Cerebellar Syndrome
Arch Neurol 53:450-454, Louis,E.D.,et al, 1996

Deep Brain Stimulation for Essential Tremor
Neurol 46:1150-1153, Hubble,J.P.,et al, 1996

Late Motor Deficits of Chilean Manganese Miners:A Blinded Control Study
Neurol 47:788-795, Hochberg,F.,et al, 1996

Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
Ann Neurol 40:181-187, Jacobs,B.C.,et al, 1996

Neuroimaging Findings in Patients with AIDS
Clin Inf Dis 22:906-919, Walot,I.,et al, 1996

Neurological Complications of HIV Infection
Lancet 348:445-452, Price,R.W., 1996

HIV Encephalitis Presenting with Severe Generalized Chorea
Neurol 46:1163-1165, Gallo,B.V.,et al, 1996

Quantitation of HIV In Brains of Demented and Nondemented Patients with Acquired Immunodeficiency Syndrome
Ann Neurol 39:392-395, Johnson,R.T.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

Systemic Sclerosis Sine Scleroderma:An Unusual Presentation in Scleroderma Renal Crisis
J Rheumatol 22:557-560, Molina,J.F.,et al, 1995

Brainstem Tumors in Patients with Neurofibromatosis Type 1:A Distinct Clinical Entity
Neurol 45:1897-1902, Molloy,P.T.,et al, 1995

Neurotoxicity in Liver Transplant Recipients with Cyclosporine Immunosuppression
Neurol 45:1962-1964, Wijdicks,E.F.M.,et al, 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995



Showing articles 400 to 450 of 857 << Previous Next >>