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acetylcholine
advances in neurology
Alzheimer's disease
anticholinesterase
areflexia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
auditory evoked brainstem potentials
autonomic dysfunction
Babinski sign
baclofen
blindness
bradykinesia
brain atrophy
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
choreoathetosis
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
gait disorder
gaze palsy, supranuclear
gene mutation
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)
hypotonia
hypoxia
imbalance
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
L-dopa
life expectancy
macular degeneration
memory, impairment of
molecular genetics
movement disorder, extrapyramidal
MRI
MRI, abnormal
multiple system atrophy
myelomalacia
myoclonic jerks
myoclonus
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
progressive neurologic disorder
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 150 to 162 of 162 << Previous

Optic Nerve Hypoplasia & Maternal Diabetes Mellitus
Arch Neurol 43:20-25, Nelson,M.,et al, 1986

Colpocephaly:Clinical, Radiologic, & Pathogenetic Aspects
Neurol 35:1594-1598, Herskowitz,J.,et al, 1985

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Leber's Congenital Amaurosis
Arch Neurol 41:204-206, Weinstein,J.M.,et al, 1984

Unilateral Cerebellar Hypoplasia
J Comput Assist Tomogr 7:1077-1078, Mendelsohn,D.B.,et al, 1983

Septo-optic Dysplasia in an Infant of a Diabetic Mother
Arch Neurol 38:590-591, Donat,J.F.G., 1981

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

Idiopathic Inflammatory Orbital Pseudotumor in Childhood
Ophthalmology 88:565-574, Mottow-Lippa,L., et al, 1981

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

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

The Orbit
Arch Ophthalmol 89:152, Trokel,S., 1973

Homonymous Hemioptic Hypoplasia
Br J Ophthalmol 56:537, Hoyt,W.F.,et al, 1972

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968



Showing articles 150 to 162 of 162 << Previous