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advances in neurology
akinetic mute
algorithm
alien hand syndrome
Alzheimer's disease
anomic aphasia
anticonvulsants
anticonvulsants, selection of
aphasia
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-motor
apolipoprotein E
apraxia
apraxia of eye movements
apraxia, constructional
apraxia, speech
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
Babinski sign
basal ganglia, degeneration
basal ganglia, lesion, bilateral
blinking, reduced
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, lesion of
Broca's aphasia
CAG repeats
CAT scan, emission, abnormal
cerebellar atrophy, primary
cerebellar vermis
cerebral cortical atrophy
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosome 12
Clinical Pathologic Conference(C.P.C.)
cognition
controversies in neurology
corpus callosum
corpus callosum, atrophy of
cortical-basal ganglionic degeneration
degenerative diseases of CNS
dementia
dementia, frontotemporal
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
dexterity, impaired
diagnostic criteria
differential diagnosis
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dyspraxia
dystonia
dystonia, focal
ethics in neurology
eye movement, disorders of
falling
familial
fragile-X syndrome
Friedreich's ataxia
frontal behavioral spatial syndrome
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus, lesion of
huntingtin
Huntington's chorea
hyperreflexia
hypotonia
imbalance
imbalance, postural
inattention
incidence
intellectual deficit
Jakob-Creutzfeldt disease
jocularity
Lafora's disease
language disorder in adults
L-dopa
leukodystrophy
levitation
lobar atrophy
masked facies
memory, defect of recent
memory, impairment of
meningitis
mental retardation
MERRF syndrome
midbrain
midbrain, atrophy
mimics
misdiagnosis
molecular genetics
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
multiple system atrophy
mutism
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, stimulus sensitive
myotonia dystrophica
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, total
Parkinson disease
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, differential diagnosis of
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
pathology
personality change
Pick's disease
polymerase chain reaction
pontocerebellar atrophy
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
proteinopathy
psychiatric problems in neurologic disorders
psychological testing
rapidly progressing neurologic illness
release phenomena
review article
rigidity
rigidity, axial
risk factors
saccadic eye movements
saccadic eye movements, abnormal
seizure
seizure, paradoxical
seizure, treatment of
sensory loss
sensory loss, cortical
speech disorder
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
striatonigral degeneration
subthalamic nucleus
suck reflex
synucleinopathy
tau protein
tauopathy
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
visuospatial disturbance
Wernicke's aphasia
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 1050 to 1100 of 2224 << Previous Next >>

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Visual Loss after Neurosurgical Repair of Paraclinoid Aneurysms
Ophthalmol 102:905-910, Rizzo,J.F.,III, 1995

Extrapyramidal Symptoms in a BMT Recipient with Hyperintense Basal Ganglia and Elevated Manganese
Bone Marrow Transplantation 15:989-992, Fredstrom,S.,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

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Reversible Dementia and Apparent Brain Atrophy During Valproate Therapy
Ann Neurol 38:687-691, Papazian,O.,et al, 1995

Quantitative Hippocampal MRI and Intractable Temporal Lobe Epilepsy
Neurol 45:2233-2240, vanPaesschen,W.,et al, 1995

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

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

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Bilateral Simultaneous Optic Neuropathy in Adults:Clinical, Imaging, Serological, and Genetic Studies
JNNP 58:70-74, Morrissey,S.P.,et al, 1995

Optic Nerve Decompr Surg for Nonarter Anterior Ischemic Optic Neuropathy (NAION) Not Effective & May Be Harmful
JAMA 273:625-632, 6661995., Kelman,S.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,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

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 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

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Magnetic Resonance Angiography in the Diagnosis of Deep Cerebral Venous Thrombosis
J Stroke Cerebrovasc Dis 5:29-32, Finelli,P.F.,et al, 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995

On Politics and Health:An Epidemic of Neurologic Disease in Cuba
Ann Int Med 122:530-533, Roman,G.C., 1995

Neurofibromatosis Type 1:Pathologic Substrate of High-Signal-Intensity Foci in the Brain
Radiology 195:721-724, DiPaolo,D.P.,et al, 1995

MR Findings in Adult-Onset Adrenoleukodystrophy
AJNR 16:1227-1237, Kumar,A.J.,et al, 1995

Neurosurgical Management of Cerebellar Haematoma and Infarct
JNNP 59:287-292, Mathew,P.,et al, 1995

Thalamic Hemorrhage:A Prospective Study of 100 Patients
Stroke 26:964-970, Kumral,E.,et al, 1995

Binswanger's Disease-Revisited
Neurol 45:626-633, Caplan,L.R., 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
J Comput Assist Tomogr 19:635-638, Engelbrecht,V.,et al, 1995

Multiple Sclerosis in the Spinal Cord, MR Appearance and Correlation with Clinical Parameters
Radiology 195:725-732, Tartaglino,L.M.,et al, 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995



Showing articles 1050 to 1100 of 2224 << Previous Next >>