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addiction, heroin
addiction, heroin-neurologic complications with
adrenergic blocker
adverse drug reaction
airway obstruction
akinetic mute
alpha adrenergic blocker
alpha-fetoprotein
alpha-synuclein
Alzheimer's disease
amyloid angiopathy, cerebral
amyloidosis
amyotrophic lateral sclerosis
anatomy of
anhidrosis
anticonvulsants
anticonvulsants, untoward effects of
apraxia of eye movements
areflexia
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, truncal
atypical
autonomic cardiovascular reflexes
autonomic dysfunction
autonomic dysfunction, acute
autonomic dysfunction, evaluation of
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
baroreceptors
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
biologic markers
bladder dysfunction
blinking
blinking, reduced
botulism
bradykinesia
bradykinesia, facial
brainstem, atrophy
cachexia
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cauda equina, lesion of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
clonidine
cognition
cogwheel rigidty
cold hands sign
constipation
contractures, joint
controversies in neurology
cortical-basal ganglionic degeneration
cough
CPAP
degenerative diseases of CNS
dementia
dementia, frontotemporal
dementia, thalamic
demyelinating disease
developmental retardation
diabetes mellitus
differential diagnosis
dopamine receptor
dopamine receptor, D2
down-beat nystagmus
drooling
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspnea
dystonia
dystonia, face
enzyme, defect
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
falling
familial
fatal familial insomnia
foot numbness
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
gait disorder
gammaglobulin therapy, intravenous
gastrointestinal motility
gaze palsy, supranuclear
gaze palsy, vertical
gene
genetic linkage
genetic neurologic disorders
genetic testing
giant cell arteritis
glutamate dehydrogenase deficiency
grasp reflex
growth hormone
growth retardation
head injury
hemiparesis
Horner's syndrome
hot cross bun sign
human T-lymphotropic virus type I(HTLV-I)
Huntington's chorea
hyperreflexia
hypophonia
hypotonia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinence, fecal
intrathecal medication
Jakob-Creutzfeldt disease
L-dopa
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leukemia
leukoencephalopathy
Lewy body
Lewy body disease, diffuse
life expectancy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
marche a petits pas
masked facies
memory, impairment of
mental retardation
microcephaly
midbrain
midbrain, atrophy
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
midodrine
mimics
Mini Mental Status Examination
misdiagnosis
morning glory sign
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, ADC maps
MRI, contrast enhanced
MRI, diffusion weighted
MRI, functional
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, volumetry
MRS
multiple sclerosis
multiple system atrophy
myoclonus
myoclonus, stimulus sensitive
nerve growth factor
nerve growth stimulating activity
neuroblastoma
neurocutaneous disease
neuroendocrinology
neurofibromatosis 1
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromyelitis optica (Devic's disease)
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, sensory, hereditary
nicotine
nystagmus
ocular motility, disorders of
old age, neurology of
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, total
orbit, tomograms of
orthostatic hypotension
orthostatic hypotension, idiopathic
orthostatic hypotension, treatment of
parasympathetic nervous system
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinson disease, rapid progression
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pathology
pheochromocytoma
pons, atrophy
postural abnormality
practice guidelines
prion disease
procainamide
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
proteinopathy
pupil
pupil, abnormality in neurologic disorders
pure autonomic failure
purple glove syndrome
purple hands
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
quadrigeminal plate
radiation hypersensitivity
rapidly progressing neurologic illness
respirations in CNS disease
respiratory failure
review article
RFC1 gene
rigidity
rigidity, axial
Riley-Day syndrome
Romberg's sign
seizure
sensory ganglia
sensory ganglia, abnormal
sensory loss, leg
sexual behavior, disorder of
sexual dysfunction in neurologic disease
Shy-Drager syndrome
sinemet
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
spinal cord, injury of
spinal cord, injury, sexual dysfunction in
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
stare
stem cell transplantation
striatonigral degeneration
stridor
substantia nigra
sudden death
superior colliculus
sympathetic nervous system
syncope
synucleinopathy
systemic illness
tandem gait, ataxic
tau protein
tauopathy
telangiectases
thalamus, lesion of
tracheostomy
treatment of neurologic disorder
tremor
tremor, cerebellar
trinucleotide repeats
upgaze
upgaze, paralysis of
urinary incontinence
valsalva maneuver
vestibular areflexia
vocal cord paralysis
walking, difficulty with
walking, difficulty with in dark
Wallerian degeneration
weight loss
wheelchair
white matter disease
wide based gait
Showing articles 50 to 71 of 71 << Previous

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Shy-Drager Syndrome Presenting as Isolated Paralysis of Vocal Cord Abductors
BMJ 300:1441, Kew,J.,et al, 1990

Abnormal Respiration and Sudden Death During Sleep in Multiple System Atrophy with Autonomic Failure
Neurol 40:677-679, Munschauer,F.E.,et al, 1990

Positron Emission Tomography in Shy-Drager Syndrome
Ann Neurol 28:101-103, Bhatt,M.H.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
Neurol 40:1241-1245, Chida,K.,et al, 1990

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

Shy-Drager Syndrome and Human T-Lymphotropic Virus Type I Infection
Ann Neurol 25:420-421, Kano,M.,et al, 1989

Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
Ann Neurol 21:419-430, McLeod,J.G.&Tuck,R.R., 1987

Tobacco Intolerance in Multiple System Atrophy
Neurol 36:986-988, Johnsen,J.A.,et al, 1986

Bladder Dysfunction in Progressive Autonomic Failure
BMJ 293:223-224, Kirby,R.S.&Bannister,R., 1986

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Clin. Path. Conference
Multiple-System Atrophy with Parkinsonism, Case 28-13, NEJM 308:1406-1414983., , 1983

Midodrine, A New Agent in the Management of Idiopathic Orthostatic Hypotension & Shy-Drager Syndrome
Mayo Clin Proc 56:429-433, Schirger,A.,et al, 1981

Shy-Drager syndrome:Diagnosis & treatment of cholinergic dysfunction
Neurol 30:805-809, Khurana,R.K.,et al, 1980

Upper Airway Obstruction in the Shy-Drager Syndrome
Ann Neurol 2:83, Israel,R.H., 1977

The Sympathetic-Nervous-System Defect in Primary Orthostatic Hypotension
NEJM 296:293, Ziegler,M.G.,et al, 1977

Nerve Growth Factor (three parts)
NEJM 297:1096, 1149, 1211977., Mobley,W.C.,et al, 1977

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Dysautonomia, Its Significance in Neurologic Disease (Specialty Conference)
Calif Med 117:28, Wichser,J.,et al, 1972



Showing articles 50 to 71 of 71 << Previous