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abdominal distention
abdominal protrusion
abducens nerve paralysis
addiction, heroin
addiction, heroin-neurologic complications with
Addison's disease
adolescent medicine
adverse drug reaction
airway obstruction
akinetic mute
algorithm
alpha-fetoprotein
alpha-synuclein
Alzheimer's disease
amyloid angiopathy, cerebral
amyloidosis
amyotrophic lateral sclerosis
anatomy of
anemia
angiography, cerebral
anti Tr antibodies
anticoagulant, treatment
anticonvulsants
anticonvulsants, untoward effects of
antiphospholipid antibodies
anxiety
apraxia
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
Argyll Robertson pupil
arteritic anterior ischemic optic neuropathy
arteritis, temporal
arthralgia
arthritis
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune cerebellar ataxia
autoimmune disease
autonomic cardiovascular reflexes
autonomic dysfunction
autonomic dysfunction, acute
autonomic dysfunction, evaluation of
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
B 12 deficiency
B12
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Behcet's syndrome
benign essential tremor
biologic markers
bladder dysfunction
blinking
blinking, reduced
bone biopsy
bone pain
bone scanning
botulism
bradykinesia
bradykinesia, facial
BRAF protooncogene
brain atrophy
brain biopsy
brain purpura
brainstem, atrophy
brainstem, lesion of
cachexia
calcification, intracranial
carcinoembryonic antigen
carcinoma
cardiac surgery, neurologic complications with
cardiomyopathy
carotid artery occlusion, intracranial
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, venography
cauda equina, lesion of
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebellum, disease of
cerebral arteries
cerebral cortical atrophy
cerebral edema, vasogenic
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, prevention of
cerebrovascular accident, prognosis in
cerebrovascular accident, recurrent
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, young adult
children
chorea
choreoathetosis
choroidopathy
chromosomal abnormality
chromosome 11
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
clonidine
clubbing of fingers
cognition
cogwheel rigidty
cold hands sign
collateral circulation
complications
confusion
conjunctivitis
consanguinity
constipation
contractures, joint
controversies in neurology
corpus callosum, lesion of
cortical-basal ganglionic degeneration
cotton-wool spots
cough
CPAP
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
craniectomy, decompressive
creatine phosphokinase(CPK)elevated
critical care unit
cryopyrin-associated periodic syndrome
cytokines
D-dimer
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, thalamic
dementia, treatment of
demyelinating disease
depression
dermatitis herpetiformis
developmental retardation
diabetes insipidus
diabetes mellitus
diarrhea
differential diagnosis
difficulty climbing stairs
distal muscle weakness
dopamine receptor
dopamine receptor, D2
down-beat nystagmus
drooling
dural sinus thrombosis
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dystonia
dystonia, face
edema, pedal
edema, periorbital
electroencephalogram, abnormalities of
electromyogram
emergencies, ocular
emotional lability
empty sella
encephalitis
encephalitis, autoimmune
encephalitis, focal
encephalomalacia
encephalopathy
endovascular therapy
enzyme, defect
epidemiology of neurology
episodic disorders
Erdheim-Chester disease
erectile dysfunction
erythema migrans
evidence-based research
extraocular muscle lesion
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial weakness
Factor V Leiden
falling
false negative
false positive
familial
fatal familial insomnia
fatigue
fever
fever, recurrent
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
fine motor function, impaired
fingers, abnormal
fluorescein angiography
foot drop
foot drop, bilateral
foot numbness
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frontal bossing
gadolinium
gait disorder
gait, spastic
gait, waddling
gammaglobulin therapy, intravenous
ganglionitis
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastrointestinal perforation
gastroparesis
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
genital ulcerations
giant cell arteritis
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamate dehydrogenase deficiency
gluten ataxia
gluten sensitivity
gluten-free diet
grasp reflex
growth hormone
growth retardation
Guillain Barre syndrome, differential diagnosis of
hallucination
hallucination, visual
head circumference
head injury
headache
headache, intermittent
headache, severe
hearing loss
hemiparesis
hepatitis
heralding manifestation
histiocytosis
HLA
Horner's syndrome
Horner's syndrome, childhood
hot cross bun sign
Huntington's chorea
hydrocephalus
hyperreflexia
hypertension
hypertrophic intracranial pachymeningitis
hypogonadism
hypophonia
hyporeflexia
hypotension, systemic
hypotonia
iatrogenic neurologic disorders
IgG4-related disease
imbalance
imbalance, postural
immunodeficiency
immunologic disease
immunosuppression
impotence
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinence, fecal
infraorbital nerve
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracerebral hemorrhage
intracranial hypertension, benign
intracranial pressure, increased
intrathecal medication
iridocyclitis
iritis
Jakob-Creutzfeldt disease
keratoconjunctivitis
lacrimal gland enlargement
L-dopa
leg numbness
leg weakness, bilateral
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukemia
leukocytosis
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
Lewy body
Lewy body disease, diffuse
lid
life expectancy
limbic encephalitis
long bone lesion
Lyme disease
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malabsorption
malignant papulosis
marche a petits pas
masked facies
memory, impairment of
meningeal biopsy
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, chronic
mental retardation
mental status, abnormal
methylmalonic aciduria
microcephaly
microinfarcts
midbrain
midbrain, atrophy
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
monoclonal gammopathy
mononeuritis multiplex
morning glory sign
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
moyamoya, adult
MRI
MRI, abnormal
MRI, ADC maps
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, functional
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, mass effect on
MRI, spinal cord
MRI, venography
MRI, volumetry
MRS
multiple organ failure
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myasthenic syndrome
myelopathy
myelopathy, necrotizing
myoclonic jerks
myoclonus
myoclonus, stimulus sensitive
myopathy
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
nausea and vomiting
neurocutaneous disease
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuromyelitis optica (Devic's disease)
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, peripheral
nicotine
non-arteritic antererior ischemic optic neuropathy
nutritional deficiency
nystagmus
ocular motility, disorders of
old age, neurology of
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, total
optic atrophy
optic atrophy, bilateral
optic disc cup
optic disc edema
optic disc ischemia
optic nerve
optic nerve, blood supply of
optic nerve, infarction of
optic neuritis
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, ischemic
optic neuropathy, ischemic, anterior
optic neuropathy, ischemic, posterior
oral contraceptives
oral contraceptives, cerbrovascular disease and
oral ulcerations
orbit, fat
orbit, inflammation in
orbit, lesions of
orbit, pseudotumor of
orbit, tomograms of
orthostatic hypotension
orthostatic hypotension, idiopathic
osteoporosis
Paget's disease
pain, abdominal
pancreatitis
papilledema
paraparesis, spastic
parasympathetic nervous system
paresthesias
paresthesias, hands
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
pars planitis
pathology
pitfalls
plasmacytoma
pleocytosis of cerebrospinal fluid
POEMS syndrome
polymerase chain reaction
polyneuropathy
polyneuropathy, critically ill
pons, atrophy
postoperative neurologic complications
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prethrombotic state
prevention of neurologic disorders
prion disease
procainamide
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
proptosis
protein C deficiency
protein S deficiency
proteinopathy
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
puberty
puberty, delayed
pupil
pupil, abnormality in neurologic disorders
pure autonomic failure
purple glove syndrome
purple hands
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
radiation hypersensitivity
ragged-red fibers
rapidly progressing neurologic illness
rash
recurrent
red eye
remote effect of cancer on the nervous system
renal failure
respirations in CNS disease
respirator
respiratory failure
respiratory tract infection
retina, abnormal
retinal hemorrhages
retinal ischemia
retinal lesion
retinal vasculitis
retinal vasculopathy
retinal vasculopathy with cerebral leukodystrophy
retinopathy
retroperitoneal mass
reversible neurologic disorder
review article
RFC1 gene
rigidity
rigidity, axial
Riley-Day syndrome
risk factors
Romberg's sign
scleritis
sclerosis, bone
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory loss
sensory loss, leg
septicemia
serologic testing
sexual behavior, disorder of
sexual dysfunction in neurologic disease
short stature
Shy-Drager syndrome
sicca syndrome
sinemet
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
skull bone, thickening
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
spirochete infection
stare
stem cell transplantation
steppage gait
steroid therapy, CNS treatment and complications with
striatonigral degeneration
stridor
subdural effusion
subdural hygroma
sudden death
superior sagittal sinus thrombosis
sympathetic nervous system
synucleinopathy
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic lupus erythematosus, neuro-opthal.complications with
tandem gait, ataxic
tau protein
tauopathy
telangiectases
tendonitis
thalamus, lesion of
third nerve palsy
tissue plasminogen activator, intravenous
Tolosa Hunt syndrome
tongue, ulcer
tracheostomy
treatment of neurologic disorder
tremor
tremor, cerebellar
trigeminal nerve, hypertrophy
trigeminal neuralgia
trinucleotide repeats
trochlear nerve palsy
upgaze
upgaze, paralysis of
urinary incontinence
uveitis
vascular endothelial growth factor
vasculitides
vasculopathy
vegetarianism
Vemurafenib
vestibular areflexia
vibratory sensation, abnormal
visual acuity, decreased, monocular
visual field defect
visual field defect, altitudinal
visual loss
visual loss, progressive
visual loss, slow
visual loss, sudden-unilateral
vitamin deficiency
vitiligo
walking, difficulty with
walking, difficulty with in dark
Wallerian degeneration
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
word-finding difficulty
workup
writing
xanthelasma
xerostomia
Showing articles 1900 to 1950 of 2520 << Previous Next >>

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Current Status of Thyrotropin-Releasing Hormone Therapy in Amyotrophic Lateral Sclerosis
Comm. on Health Care Issues, Amer Neuro Assoc, Ann Neurol 22:541-54387., , 1987

A Rating Scale for Amyotrophic Lateral Sclerosis:Description & Preliminary Experience
Ann Neurol 22:328-333, Appel,V.,et al, 1987

Late Denervation in Patients with Antecedent Paralytic Poliomyelitis
NEJM 317:7-12, Cashman,N.R.,et al, 1987

Motor Neuron Disease in the US, 1971 & 1973-1978:Patterns of Mortality & Associated Conditions at Time of Death
Neurol 37:1339-1343, Leone,M.,et al, 1987

Clinincopath Conf
Progressive Muscular Atrophy & Diabetic Neuromuscular Disease, Case 21-1987, NEJM 316:1326-13357., , 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Computed Tomography Abnormalities in Hanging
Neuroradiology 29:297-298, Bianco,F.&Floris,R., 1987

Anti-Purkinje Cell Antibody Producing B-Cell Lines from a Patient with Paraneoplastic Cerebellar Degeneration
Arch Neurol 44:833-837, Tsukamoto,T.,et al, 1987

Anterior Ischaemic Optic Neuropathy in the Acquired Immune Deficiency Syndrome
BMJ 295:696-697, Brack,M.J.,et al, 1987

Unilateral Optic Neuropathy in Non-Hodgkin's Lymphoma
Neurol 37:1563-1564, Lanska,D.J.,et al, 1987

Diagnosis of Thoracic Outlet Syndrome, Value of Sensory & Motor Conduction Studies & Quantitative EMG
Arch Neurol 44:1161-1163, Smith,T.&Trojabor,W., 1987

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

MR Findings in Normal-Pressure Hydrocephalus:Significace & Comparison with Other Forms of Dementia
Jr. , et al, J Comput Assist Tomogr 11:923-93187., Jack,C.R., 1987

Magnetic Resonance Imaging in Temporal Lobe Epilepsy:Pathological Correlations
Ann Neurol 22:341-347, Kuzniecky,R.,et al, 1987

Clinicopath Conf
Malignant Lymphoma, Intravascular, Large-Cell, Immunoblastic type (Malignant Angioendotheliomatosis), , Case86,NEJM 315:874-885,1986., 1986

Cerebral Dominance & Epilepsy Surgery
Editorial, Lancet 2:1318-13191986., , 1986

Magnetic Resonance Imaging in Partial Complex Epilepsy
Arch Neurol 43:869-872, Jabbari,B.,et al, 1986

Clinicopath Conf (Juvenile) Periarteritis Nodosa (Kawasaki Syndrome)
with Involvement of Subcutaneous ( & Cerebral) Arteries, Case 43-1986, NEJM 315:1143-1154, , 1986

Spastic Pure Motor Monoparesis
Ann Neurol 20:638-641, Ashizawa,T.,et al, 1986

Dolichoectatic Basilar Artery:A Review of 23 Cases
Stroke 17:1277-1281, Nishizaki,T.,et al, 1986

Clinicopath Conf
Tuberous Sclerosis, Case 41-1986, NEJM 315:1013-1022986., , 1986

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Alzheimer's Disease, Parkinson's Disease, & Motoneurone Disease:Abiotropic Interaction Between Ageing & Environment
Lancet 2:1067-1068, Calne,D.B.,et al, 1986

Brain Stem Mucormycosis in a Narcotic Addict with Eventual Recovery
Am J Med 80:126-128, Woods,K.F.&Hanna,B.J., 1986

Visual & Auditory Neurotoxicity in Patients Receiving Subcutaneous Deferoxamine Infusions
NEJM 314:869-873, Olivieri,N.F.,et al, 1986

Anticerebellar Antibodies in Serum & Cerebrospinal Fluid with Carcinoma of Lung & Paraneopl Cerebellar Degen
Ann Neurol 19:82-85, Greenlee,J.E.,et al, 1986

Catheter Shunts for Fetal Hydronephrosis & Hydrocephalus, Report of the International Fetal Surgery Registry
NEJM 315:336-340, Manning,F.A.,et al, 1986

Lyme Disease Associated with Optic Neuropathy
Am J Med 81:143-145, Schechter,S.L., 1986

Brain Abscess, A Study of 45 Consecutive Cases
Medicine 65:415-431, Chun,C.H.,et al, 1986

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Slow Resolution of Multifocal Weakness & Fasciculation:A Reversible Motor Neuron Syndrome
Neurol 36:1260-1263, Chad,D.A.,et al, 1986

Motor Neuron Disease & Plasma Cell Dyscrasia
Neurol 36:1429-1436, Shy,M.E.,et al, 1986

Ultrasound Screening for Spina Bifida:Cranial & Cerebellar Signs
Lancet 2:72-74, Nicolaides,K.H.,et al, 1986

Delayed Postirradiation Lower Motor Neuron Syndrome
Ann Neurol 19:308-309, Gallego,J.,et al, 1986

CT Myelography in Spinal Cysticercosis
J Comput Assist Tomogr 10:195-198, Zee,C.,et al, 1986

Hydrocephalic Dementia & Spinal Cord Tumor, Report of a Case & Review of the Literature
Arch Neurol 43:714-718, Feldmann,E.,et al, 1986

Magnetic Resonance Imaging in Intractable Partial Epilepsy:Correlative Studies
Ann Neurol 20:57-62, Sperling,M.R.,et al, 1986

Lathyrism:Evidence for Role of the Neuroexcitatory Aminoacid BOAA
Lancet 2:1066-1067, Spencer,P.S.,et al, 1986

Bilateral Lucency of the Globus Pallidus Complicating Methylmalonic Acidemia
Ann Neurol 20:364-366, Korf,B.,et al, 1986

Antibodies to Brain Proteins in Paraneoplastic Cerebellar Degeneration
Neurol 36:1169-1172, Tanaka,L.,et al, 1986

Primary Amyloidosis with Peripheral Neuropathy & Signs of Motor Neuron Disease
Neurol 36:1125-1127, Abarbanel,J.M.,et al, 1986

Brain Atrophy & Alcoholism
BMJ 292:787, Thomas,P.K., 1986

Peripheral Neuropathy Associated with Dysproteinaemia, Skin Changes, & Endocrinopathy
BMJ 292:1415-1416, Burton,J.L., 1986

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986

Acute Cerebellar Hemorrhage & CT Evidence of Tight Posterior Fossa
Neurol 36:858-860, Weisberg,L.A., 1986

Partial Dorsal Mesencephalic Hemorrhages:Report of Three Cases
Neurol 36:529-533, Sand,J.J.,et al, 1986

Mesencephalic Hemorrhages:Clinical & Computed Tomographic Correlations
Weisberg. L. A. , Neurol 36:713-7166., , 1986



Showing articles 1900 to 1950 of 2520 << Previous Next >>