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acetylcholine
advances in neurology
akinetic mute
algorithm
alien hand syndrome
Alzheimer's disease
anomic aphasia
anticholinesterase
anticonvulsants
anticonvulsants, selection of
antineutrophil cytoplasmic autoantibodies
aphasia
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-motor
apolipoprotein E
apraxia
apraxia of eye movements
apraxia, constructional
apraxia, speech
areflexia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
atypical
auditory evoked brainstem potentials
autonomic dysfunction
axonal degeneration
axonal injury
Babinski sign
baclofen
basal ganglia, degeneration
basal ganglia, lesion, bilateral
Bing-Neel syndrome
blindness
blinking, reduced
brachium pontis
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
Broca's aphasia
burning paresthesia
CAG repeats
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, orbits
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebellum
cerebral cortical atrophy
chemosis
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosome 12
chromosome 14
chromosome 6
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
cobalt toxicity
cognition
color vision, impaired
complications
controversies in neurology
corpus callosum
corpus callosum, atrophy of
cortical-basal ganglionic degeneration
cranial nerve enlargement
cranial nerve palsies
cranial nerve palsy, alternating
degenerative diseases of CNS
dementia
dementia, frontotemporal
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dexterity, impaired
diagnostic criteria
differential diagnosis
diplopia
donut sign
down-beat nystagmus, primary position of gaze
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dyspnea
dyspraxia
dysthyroid ocularmyopathy
dysthyroidism
dystonia
dystonia, focal
edema, periorbital
ejection fraction, abnormal
enzyme, defect
ethics in neurology
evoked potentials
excitotoxin
exophthalmus
extraocular muscle enlargement
extraocular muscle lesion
eye movement, disorders of
eye movement, painful
eye, pain in
falling
familial
fragile-X syndrome
Friedreich's ataxia
frontal behavioral spatial syndrome
fundus, abnormality of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glabellar sign
glioma
globus pallidus, lesion of
glutamate dehydrogenase deficiency
glutamic acid
granulomatosis with polyangiitis
Graves ophthalmopathy
headache
headache, unilateral
hearing loss
hip arthroplasty
HLA
hot cross bun sign
huntingtin
Huntington's chorea
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hyperthyroidism
hypothalamus
hypothalamus, lesion of
hypotonia
hypoxia
ibrutinib
IgG4, serum
IgG4-related disease
imbalance
imbalance, postural
immunotherapy
inattention
incidence
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracranial pressure, increased
Jakob-Creutzfeldt disease
jaw pain
jocularity
Lafora's disease
language disorder in adults
lateral rectus palsy
L-dopa
leukodystrophy
levitation
life expectancy
lobar atrophy
lymphoma
lymphoma involving CNS
macroglobulinemia
macular degeneration
malignant optic glioma of adulthood
masked facies
maxillary nerves
memory, defect of recent
memory, impairment of
meningitis
mental retardation
MERRF syndrome
methotrexate
midbrain
midbrain, atrophy
mimics
misdiagnosis
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, FLAIR
MRI, nodular enhancement
MRI, optic nerve
MRI, orbit
multiple system atrophy
muscle biopsy, extraocular
mutism
myelomalacia
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, stimulus sensitive
myopathy, necrotizing
myopathy, steroid responsive
myositis
myositis, ocular
myotonia dystrophica
necrotizing vasculitis
neuroaxonal degeneration
neurofibromatosis 1
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neurotoxic
neurotoxin
neurotransmitter
nystagmus
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, total
optic atrophy
optic canal
optic canal, enlargement of
optic chiasm, enlarged
optic chiasm, lesion of
optic disc edema
optic glioma
optic nerve sheath enhancement
optic nerve, enhancement
optic nerve, enlarged
optic nerve, lesion of
optic nerve, neoplasm of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, ischemic
optic neuropathy, ischemic, posterior
orbit
orbit, biopsy
orbit, fat
orbit, inflammation in
orbit, lesions of
orbit, mass
orbital apex
orthostatic hypotension
pain
palatal myoclonus
papilledema
paresthesias
paresthesias, feet
Parkinson disease
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, differential diagnosis of
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pathology
perineuritis
perineuritis, optic
perivascular enhancement
personality change
photophobia
photosensitivity, skin
physostigmine
Pick's disease
pleocytosis of cerebrospinal fluid
polymerase chain reaction
pons, atrophy
pons, lesion of
pontocerebellar atrophy
postoperative neurologic complications
postoperative visual loss
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
proptosis
proptosis, unilateral
proteinopathy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
ptosis
Purkinje cell
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
radiation therapy, CNS treatment and complications with
rapidly progressing neurologic illness
rash
release phenomena
retinal degeneration
retinitis pigmentosa
retro-orbital pain
review article
rigidity
rigidity, axial
risk factors
rituximab
saccadic eye movements
saccadic eye movements, abnormal
salivary gland enlargement
scotoma
seizure
seizure, paradoxical
seizure, treatment of
sella turcica, enlargement of
sensorineural hearing loss
sensory loss
sensory loss, cortical
Shy-Drager syndrome
sialadenitis
sinuses, diseases of
sinusitis
sleep apnea
sleep pathology and physiology
speech disorder
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
steroid therapy, CNS treatment and complications with
striatonigral degeneration
subthalamic nucleus
suck reflex
synucleinopathy
tau protein
tauopathy
tram-track sign
trazodone
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
vasculitides
vision, blurred
visual acuity, decreased
visual acuity, decreased, monocular
visual field defect
visual field defect, altitudinal
visual loss
visual loss, progressive
visuospatial disturbance
Waldenstrom's macroglobulinemia
weight loss
Wernicke's aphasia
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 1150 to 1200 of 2361 << Previous Next >>

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

AAEM Case Report#13:Diabetic Amyotrophy
Muscle & Nerve 19:939-945996., Chokroverty,S.&Sander,H.W., 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

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,et al, 1996

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

Anti-Yo-Associated Paraneoplastic Cerebellar Degeneration in a Man with Adenocardinoma of Unknown Origin
Neurol 46:1486-1487, Krakauer,J.,et al, 1996

Motor Neuron Disease:A Paraneoplastic Process Associated with Anti-Hu Antibody and Small-Cell Lung Carcinoma
Ann Neurol 40:112-116, Verma,A.,et al, 1996

Falls and Urinary Incontinence in a 66-Year Old Woman
Lancet 347:1738, Yusuf,S.W.,et al, 1996

Progressive Blurring of Vision in Both Eyes
Lancet 346:1402, Nishioka,T.,et al, 1995

The Hippocampus in Status Epilept:Signal Intensity & Morph Changes with Sequent Fast Spin-Echo MR Imaging
Radiology 194:249-256, Tien,R.D.&Felsberg,G.J., 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Magnetic Resonance Imaging of the Brain in Nonarteritic Ischemic Optic Neuropathy
J Neuro-Ophthalmol 15:158-160, Arnold,A.C.,et al, 1995

Epidemic Optic Neuropathy in Cuba-Clinical Characterization and Risk FActors
NEJM 333:1176-1182, Bern,C.,et al, 1995

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995

MR Findings in Methanol Intoxication
AJNR 16:1783-1786, Gaul,H.P.,et al, 1995

Optic Neuropathy, Headache, & Diplopia with MRI Suggestive of Cerebral Arteritis in Relapsing Polychondritis
J Neuro-Ophthalmol 15:171-175, Massry,G.G.,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

Juvenile Huntington Disease:CT and MR Features
AJNR 16:1405-1412, Ho,V.B.,et al, 1995

Surgical Treatment of Temporal Lobe Epilepsy:Clinical, Radiological and Histopathological Findings in 178 Patients
JNNP 58:666-673, Zentner,J.,et al, 1995

Bilaterally Symmetric Hippocampi and Surgical Outcome, Jack
Neurol 45:1353-1358, Jr,C.R.,et al, 1995

Hippocampal Volumetrics Differentiate Pts with Temporal Lobe Epilepsy & Extratemporal Lobe Epil
Arch Neurol 52:819-824, Gilmore,R.L.,et al, 1995

Preoperative MRI Predicts Outcome of Temporal Lobectomy:An Actuarial Analysis
Neurol 45:1358-1363, 12481995., Berkovic,S.F.,et al, 1995

Comparison of Ictal SPECT and Interictal PET in the Presurgical Evaluation of Temporal Lobe Epielspy
Ann Neurol 37:738-745, Ho,S.S.,et al, 1995

Neurologic Abnormalities in Murderers
Neurol 45:1641-1647, Blake,P.Y.,et al, 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Clinicopath Conf
Multiple Myeloma with Bilateral Carpal Tunnel Syndrome Probably Due to Secondary Amyloid Deposit, Ca, e38-1995,NEJM 333:1625-1630,1995., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Pineal Parenchymal Tumors:CT and MR Features
J Comput Assist Tomogr 19:509-517, Chiechi,M.V.,et al, 1995

High Resolution MRI of Anterior Visual Pathway in Pts with Optic Neuropathies Using Fast Spin Echo & Phased Array Local Coils
JNNP 58:562-569, Gass,A.,et al, 1995

Multiple System Atrophy presenting as Parkinsonism:Clinical Features and Diagnostic Criteria
JNNP 59:144-151, Albanese,A.,et al, 1995

Stereotactic Ventral Pallidotomy for Parkinson's Disease
Neurol 45:753-761, Dogali,M.,et al, 1995

Bilateral Ulnar Handcuff Neuropathies with Segmental Conduction Block
Muscle & Nerve 18:1021-1023995., Satkunam,L.&Zochodne,D., 1995

Complications with Shunts in Adults with Spina Bifida
BMJ 311:286-287, Tomlinson,P.&Sugarman,I.D., 1995

The Predictive Value of CSF Dynamic Tests in Patients with the Idiopathic Adult Hydrocephalus Syndrome
Arch Neurol 52:783-789, Malm,J.,et al, 1995

Tourette's Syndrome:A Model Neuropsychiatric Disorder
JAMA 273:498-501, Hyde,T.M.&Weinberger,D.R., 1995

Decreased Hippocampal Volume Asymmetry on MRIs in Nondemented Elderly Subjects Carrying the Apolipoprotein E-4 Allele
Neurol 45:391-392, Soininen,H.,et al, 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Some Specific Clinical Features Differentiate Multiple System Atrophy (Striatonigral Variety) from Parkinson's Disease
Arch Neurol 52:294-298, Colosimo,C.,et al, 1995

Clinical/Metabolic Correlations in Multiple System Atrophy, A PET Study
Arch Neurol 52:179-185, Perani,D.,et al, 1995

Different of Multi Syst Atrophy from Idiopathic Parkinson's Disease Using Proton MR Spectroscopy
Ann Neurol 37:204-210, Davie,C.A.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995



Showing articles 1150 to 1200 of 2361 << Previous Next >>