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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 1300 to 1350 of 2361 << Previous Next >>

Hippocampal Sclerosis in Children with Intractable Temporal Lobe Epilepsy:Detection with MR Imaging
AJR 161:1045-1048, Grattan-Smith,J.D.,et al, 1993

Diagnosis of Medial Temporal Lobe Seizure Onset:Relative Specificity and Sensitivity of Quantitative MRI
Neurol 43:2117-2124, Spencer,S.S.,et al, 1993

Hallervorden-Spatz Disease with Bilat Invol of Globus Pallidus & Substantia Nigra:MR Demonstra
J Comput Assist Tomogr 17:961-963, Porter-Grenn,L.,et al, 1993

Clinicopath Conf
Acquired Demyelinating Neuropathy, ? CIDP, ? Motor Neuropathy with Multifocal Conduction Blocks, Cas, 41-1EJM 329:1182-1190,1993., 1993

MRI Pallidal Hyperintensity & Brain Atrophy in Cirrhotic Pts:2 Different MRI Patterns of Clin Deterior?
Neurol 43:2570-2573, Kulisevsky,J.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

The Motor Disorder of Multiple System Atrophy
JNNP 56:1239-1242, Quinn,N.P.&Marsden,C.D., 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

Spinal Cord MRI Using Multi-Array Coils and Fast Spin Echo, II. Findings in Multiple Sclerosis
Neurol 43:2632-2637, Kidd,D.,et al, 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Communicating Hydrocephalus, Basilar Invagination, and Other Neurologic Features in Osteogenesis Imperfecta
Neurol 43:2603-2608, Charnas,L.R.&Marini,J.C., 1993

Choroid Plexus Infection in Cerebral Toxoplasmosis in AIDS Patients
Neurol 43:2035-2040, Falangola,M.F.&Petito,C.K., 1993

Neurosurgical Management of the Acquired Immunodeficiency Syndrome
West J Med 158:249-253, Andrews,B.T.&Kenefick,T.P., 1993

MRI in Acute Transverse Myelopathy
Neuroradiology 35:221-226, Holtas,S.,et al, 1993

Facial Asymmetry, Hippocampal Pathology, & Remote Symptomatic Seizures:A Temporal Lobe Epileptic Syndrome
Neurol 43:725-727, Cascino,G.D.,et al, 1993

Update on Surgical Treatment of the Epilepsies, Second Intern Palm Desert Conf on Surgical Trtm of Epilepsies (1992)
Neurol 43:1612-1617, Engel,J.Jr., 1993

Early Childhood Prolonged Febrile Convulsions, Atrophy & Sclerosis of Mesial Struc & Temporal Lobe Epilepsy:An MRI Study
Neurol 43:1083-1087, Cendes,F.,et al, 1993

Magnetic Resonance Imaging in Childhood Intractable Partial Epilepsies:Pathologic Correlations
Neurol 43:681-687, Kuzniecky,R.,et al, 1993

Detection of Hippocampal Pathology in Intractable Partial Epilepsy
Neurol 43:1793-1799, Jackson,G.D.,et al, 1993

Measurement of Whole Temporal Lobe and Hippocampus for MR Volumetry:Normative Data
Neurol 43:2006-2010, Bhatia,S.,et al, 1993

Frequency and Characteristics of Visual Field Deficits after Surgery for Mesial Temporal Sclerosis
Neurol 43:1235-1238, Tecoma,E.S.,et al, 1993

Collosal Disconnection in Multiple Sclerosis
Neurol 43:1243-1245, Schnider,A.,et al, 1993

Single-Photon Emission Computed Tomographic Investigation of Patients with Motor Neuron Disease
Neurol 43:1569-1573, Abe,K.,et al, 1993

Spinal Fluid Cells and Protein in Amyotrophic Lateral Sclerosis
Arch Neurol 50:489-491, Norris,F.H.,et al, 1993

The Natural History of Amyotrophic Lateral Sclerosis
Neurol 43:1316-1322, Ringel,S.P.,et al, 1993

Poliomyelitis:Hyperintensity of the Anterior Horn Cells on MRI Images of the Spinal Cord
AJR 161:863-865, Malzberg,M.S.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993

Multiple System Atrophy & Prog Supranuc Palsy, Dimin Striatal D2 Dopamine Receptor Act by SPECT
Arch Neurol 50:513-516, vanRoyen,E.,et al, 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Embolic Cerebral Infarction:MR Findings in the First 3 Hours AFter Onset
AJR 160:1077-1082, Shimosegawa,E.,et al, 1993

Cerebellar Infarction, Clinical and Anatomic Observations in 66 Cases
Stroke 24:76-83, Kase,C.S.,et al, 1993

Funct'l Import of Ventric Enlarge & Cortical Atrophy in Healthy Subj & Alcoholics:PET, MR, & Neuropsych Testing
Radiology 186:59-65, Wang,G.,et al, 1993

Pick's Disease Versus Alzheimer's Disease:A Comparison of Clinical Characteristics
Neurol 43:289-292, Mendez,M.F.,et al, 1993

Clinicopath Conf
Cysticercosis Involving Basal Cisterns of Brain, Case 8-1993, NEJM 328:566-573993., , 1993

Callosal Atrophy with Reduced Cortical Oxygen Metabolism in Carotid Artery Disease
Stroke 24:88-93, Yamauchi,H.,et al, 1993

The Visual Variant of Alzheimer's Disease, A Clinicopathologic Case Study
Neurol 43:305-313, Levine,D.N.,et al, 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993



Showing articles 1300 to 1350 of 2361 << Previous Next >>