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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 1050 to 1100 of 2361 << Previous Next >>

Longitudinal Change in Basal Ganglia Volume in Patients with Huntington's Disease
Neurol 48:394-399, Aylward,E.H.,et al, 1997

Medial Temporal Lobe Volumetrics in Traumatic Brain Injury
AJNR 18:25-28, Jack,C.R.,et al, 1997

Midline Cerebral Morphometry Distinguishes Frontotemporal Dementia and Alzheimer's Disease
Neurol 48:978-985, Kaufer,D.I.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Frontotemporal Dementia and Early Alzheimer Disease:Differentiation with Frontal Lobe H-1 MR Spectroscopy
Radiology 203:829-836, Ernst,T.,et al, 1997

Clinical and Radiologic Findings in Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
AJNR 18:751-757, Cory,R.C.,et al, 1997

A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
Neurol 49:878-881, Stojsavljevic,N.,et al, 1997

Quadriceps Weakness and Osteoarthritis of the Knee
Ann Int Med 127:97-104, 1541997., Slemenda,C.,et al, 1997

Rapid Spongiform Degeneration of the Cerebrum and Cerebellum in Creutzfeldt-Jakob Encephalitis:Serial MR Findings
AJNR 18:583-586, Tzeng,B-C.,et al, 1997

Neuro-Ophthalmic Manifestations of Lyme Disease
J Neuro-Ophthalmol 17:108-121, Balcer,L.J.,et al, 1997

Generalised Motor Neuron Disease as an Unusual Manifestation of Borrelia Burgdorferi Infection
JNNP 63:257-258, Hemmer,B.,et al, 1997

Clinicopath Conf
Acute Critical-Illness Myopathy, with Loss of Myosin Filaments, ? Induced by Steroid, Case 11-1997,, EJM 379-1088,1997., 1997

Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997

ALS Standard of Care Consensus
Neurol 48 (Suppl 4) :S33-S37997., Miller,R.G.,et al, 1997

Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
Ann Int Med 127:450-453, Aboussouan,L.S.,et al, 1997

Practice Advisory on the Trtm of ALS with Riluzole
Quality Standards Subcommittee of the AAN, Neurol 49:657-6591997., , 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Lymphoproliferative Disorders and Motor Neuron Disease:An Update
Neurol 48:1671-1678, Gordon,P.H.,et al, 1997

Hepatoerythropoietic Porphyria:Neuroimaging Findings
AJNR 18:1557-1560, Berenguer,J.,et al, 1997

Optic Atrophy and Cerebral Infarcts Caused by Methanol Intoxication:MRI
Neuroradiology 39:192-194, Hsu,H.H.,et al, 1997

Spinal Pseudoathetosis:A Rare, Forgotten Syndrome, With a Review of Old and Recent Descriptions
Neurol 49:432-437, Ghika,J.&Bogousslavsky,J., 1997

Clinicopath Conf
Hodgkin's Disease, Paraneoplastic Cerebellar Degeneration, Case 21-1997, NEJM 337:115-12297., , 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

What is the Accuracy of the Clinical Diagnosis of Multiple System Atrophy
Arch Neurol 54:937-944, Litvan,I.,et al, 1997

Distinction of Idiopathic Parkinson's Dis from Multi-Syst Atrophy by Stim of Growth-Hormone Release w Clonidine
Lancet 349:1877-1881, Kimber,J.R.,et al, 1997

Cordarone (Amiodarone)
Product Insert, Wyeth-Ayerst Laboratories, June 1997., , 1997

Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
Muscle & Nerve 20:347-351997., Pringle,C.E.,et al, 1997

Anticedents of Cerebral Palsy in a Multicenter Trial of Indomethacin for Intraventricular Hemorrhage
Arch Pediatr Adolesc Med 151:580-585, Allan,W.C.,et al, 1997

Postoperative Cerebral Edema Occurring in Children with Slit Ventricles
Pediatrics 99:625-630, Eldredge,E.,et al, 1997

Preliminary Results of Linear Accelerator Radiosurgery for Acoustic Schwannomas
J Neurosurg 85:1013-1019, Mendenhall,W.M.,et al, 1997

Ischemic Lesion Volumes in Acute Stroke by Diffusion-Weighted MRI Correlate with Clinical Outcome
Ann Neurol 42:164-170, Lovblad,K-O.,et al, 1997

Clinical Characteristics of Patients with Motor Disability Due to Conversion Disorder:A Prospective Study
JNNP 63:83-88, Binzer,M.,et al, 1997

Etiology and Early Prognosis of Newly Diagnosed Partial Seizures in Adults
Neurol 49:753-757, Van Paesschen,W.,et al, 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
Neurol 49:1243-1246, 11961997., Stevanin,G.,et al, 1997

Symmetrical Necrosis of Globus Pallidus with Severe Gait Disturbance in a Patient with Myelodysplastic Syndrome Given Allogeneic Marrow Transplantation
Ann Hematol 75:235-237, Rabitsch,W.,et al, 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Bilirubin Metabolism and Kernicterus
Adv Pediatr 44:173-229, Gourley,G.R., 1997

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

MR Imaging of the Meninges, Part II, Neoplastic Disease
Radiology 201:605-612, Fukui,M.B.,et al, 1996

Refractory Epilepsy:Comparison of MR Imaging, CT, and Histopathologic Findings in 117 Patients
Radiology 201:97-105, Bronen,R.A.,et al, 1996

Reversible Signal Abnormalities in the Hippocampus and Neocortex after Prolonged Seizures
AJNR 17:1725-1731, Chan,S.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Motor Neuron Disease with Parkinsonism
Arch Neurol 53:987-991, Qureshi,A.I.,et al, 1996



Showing articles 1050 to 1100 of 2361 << Previous Next >>