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acetylcholine
advances in neurology
Alzheimer's disease
anticholinesterase
areflexia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
auditory evoked brainstem potentials
autonomic dysfunction
Babinski sign
baclofen
blindness
bradykinesia
brainstem, atrophy
CAG repeats
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar vermis
chorea
chromosome 14
chromosome 6
Clinical Pathologic Conference(C.P.C.)
controversies in neurology
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
depression
down-beat nystagmus, primary position of gaze
dysarthria
enzyme, defect
evoked potentials
excitotoxin
familial
fragile-X syndrome
Friedreich's ataxia
gaze palsy, supranuclear
genetic neurologic disorders
genetic screening
genetic testing
glutamate dehydrogenase deficiency
glutamic acid
HLA
hot cross bun sign
huntingtin
Huntington's chorea
hydroxytryptophan L-5(L-5 HTP)
hypoxia
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
L-dopa
life expectancy
macular degeneration
molecular genetics
movement disorder, extrapyramidal
MRI
MRI, abnormal
multiple system atrophy
myelomalacia
myoclonic jerks
myotonia dystrophica
neurologic disease
neurologic disease, diagnoses of
neuropathology
neurotoxin
neurotransmitter
nystagmus
ocular motility, disorders of
ophthalmoplegia
optic atrophy
orthostatic hypotension
palatal myoclonus
Parkinson disease
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
physostigmine
pons, atrophy
pontocerebellar atrophy
prognosis
pseudobulbar palsy
psychological testing
psychological testing, neurologic problems
Purkinje cell
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
retinal degeneration
retinitis pigmentosa
review article
seizure
Shy-Drager syndrome
sleep apnea
sleep pathology and physiology
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
striatonigral degeneration
trazodone
treatment of neurologic disorder
trinucleotide repeats
X-linked bulbospinal neuronopathy
Showing articles 1700 to 1750 of 2477 << Previous Next >>

Duration of Impaired Consciousness in Relation to Side of Lesion After Severe Head Injury
Lancet 1:1001-1003, Levin,H.S.,et al, 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Cerebellar Degeneration in Neuroleptic Malignant Synd:Neuropath & Review of Lit Concerning Heat-Related Nervous Syst Injury
JNNP 52:387-391, Lee,S.,et al, 1989

Cerebellar Atrophy Following Acute Intoxication with Phenytoin
Neurol 39:432-433, Masur,H.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

Neurofibromatosis Type 1 (Recklinghausen's Disease) , Neurologic and Cognitive Assessment
Am J Dis Child 143:833-837, Eldridge,R.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Cerebrovascular Disease & Antiphospholipis Antibodies in SLE, Lupus-Like Dis, & Primary Antiphospholipid Synd
Am J Med 86:391-399, Asherson,R.A.,et al, 1989

Emotionalism after Stroke
BMJ 298:991-994, House,A.,et al, 1989

MR Imaging in Progressive Suupranuclear Palsy and Shy-Drager Syndrome
J Comput Assist Tomogr 13:555-560, Savoiardo,M.,et al, 1989

Frontal Lobe Syndrome in a Patient with Bilateral Globus Pallidus Lesions
Arch Neurol 46:1024-1027, Strub,R.L., 1989

Magnetic Resonance Imaging of Spinal Cord Lesions in Multiple Sclerosis
JNNP 52:459-466, Honig,L.S.&Sheremata,W.A., 1989

Apraxia in Alzheimer's Disease
Neurol 39:664-668, Rapcsak,S.Z.,et al, 1989

Quantitation of Cerebral Atrophy in Preclinical and End-Stage Alzheimer's Disease
Ann Neurol 25:450-459, delaMonte,S.M., 1989

Intermittent Obstructive Hydrocephalus in the Arnold-Chiari Malformation
Ann Neurol 26:401-404, Vrabee,T.R.,et al, 1989

Radiation-Induced Dementia in Patients Cured of Brain Metastases
Neurol 39:789-796, DeAngelis,L.M.,et al, 1989

The Alien Hand Syndrome, Clinical and Postmortem Findings
Arch Neurol 46:456-459, Banks,G.,et al, 1989

Occluded Fourth Ventricle After Multiple Shunt Revisions for Hydrocephalus
Pediatrics 83:981-985, Coker,S.B.&Anderson,C.L., 1989

Management Problems in Acute Hydrocephalus after Subarachnoid Hemorrhage
Stroke 20:747-753, Hasan,D.,et al, 1989

Acute Hydrocephalus After Subarachnoid Hemorrhage
Stroke 20:715-717, Heros,R.C., 1989

Factors Assoc with Hydrocephalus after Subarachnoid Hemorrhage
Arch Neurol 46:744-752, Graff-Redford,N.R.,et al, 1989

Tuberculous Meningitis in Children:Treatment with Isoniazid and Rifampicin for Twelve Months
J Pediatr 114:875-879, Visudhiphan,P.&Chiemchanya,S., 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

A Defect in Mitochondrial Electron-Transport Activity in Leber's Hereditary Optic Neuropathy
NEJM 320:1331-1333, Parker,W.D.,et al, 1989

Apraxia of Eyelid Opening Secondary to Right Hemisphere Infarction
Ann Neurol 25:622-624, Kohnston,J.C.,et al, 1989

Posthemorrhagic Hydrocephalus in High-Risk Preterm Infants:Natural History, Management, & Long-Term Outcome
J Pediatr 114:611-618, Dykes,F.D.,et al, 1989

Neurologic Complications in Long-Standing Nephropathic Cystinosis
Arch Neurol 46:543-548, Fink,J.K.,et al, 1989

Computed Tomography of the Brain in the Diagnosis of and Prognosis in Normal Pressure Hydrocephalus
Neuroradiology 31:160-165, Wikkelso,C.,et al, 1989

Clinical-Pathologic Correlation in Huntington's Disease:A Neuropsychological and Computed Tomography Study
Neurol 39:796-801, Bamford,K.A.,et al, 1989

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

Medical Decisions and Prognostications of Pediatricians for Infants with Meningomyelocele
J Pediatr 113:835-840, Siperstein,G.N.,et al, 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

Symptomatic Hydrocephalus:Initial Findings in Brainstem Gliomas not Detected on Computed Tomographic Scans
Pediatrics 82:733-737, Raffel,C.,et al, 1988

Compressive Mononeuropathy of the Deep Palmar Branch of the Ulnar Nerve in Cyclists
JNNP 51:1588-1590, Hankey,G.J.&Gubbay,S.S., 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Natural History of Fetal Ventriculomegaly
Pediatrics 82:692-697, Hudgins,R.J.,et al, 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Reflex Sympathetic Dystrophy in Children:Treatment with Transcutaneous Electric Nerve Stimulation
Pediatrics 82:728-732, Kesler,R.W.,et al, 1988

Reflex Sympathetic Dystrophy Syndrome in Children and Adolescents, Reports of 18 Cases and Review
Am J Dis Child 142:1325-1330, Silber,T.J.&Majd,M., 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Reversible Brain Shrinkage in Abstinent Alcoholics, Measured by MRI
Neuroradiology 30:385-389, Schroth,G.,et al, 1988



Showing articles 1700 to 1750 of 2477 << Previous Next >>