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accomodation, abnormal

achilles tendon, enlarged

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

adverse drug reaction

alien hand syndrome

Alzheimer's disease

amyotrophic lateral sclerosis

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, negative

anticholinergic drugs

antiviral agents

aphasia, classification of

aphasia, progressive, primary

ataxia, cerebellar

ataxia, frontal

ataxia, hereditary

ataxia, progressive

autoimmune disease

bacterial infection

bacterial infection, CNS

basal ganglia, degeneration

behavior modification

behavioral disorder

Bell's phenomenon

blinking, reduced

brainstem, lesion of

calcium antagonist

carbon monoxide poisoning

CAT scan, abnormal

CAT scan, angiography

cerebellar atrophy, primary

cerebellar degeneration

cerebellum, disease of

cerebral cortical atrophy

cerebrospinal fluid, abnormal

cerebrospinal fluid, drainage of

cerebrospinal fluid, elevated protein of

cerebrovascular accident

cerebrovascular accident, young adult

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

concentration, impaired

contractures, joint

convergence, impaired

conversion reaction

corpus callosum

corpus callosum, lesion of

cortical-basal ganglionic degeneration

Coxiella burnetti

crying, pathologic

cryopyrin-associated periodic syndrome

cystatin C mutation

degenerative diseases of CNS

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, subcortical

demyelinating disease

developmental retardation

diagnostic criteria

differential diagnosis

digital subtraction angiography

disability, neurological

disconnection syndrome

dopamine agonist

drug induced neurologic disorders

dysdiadochokinesia

electroencephalogram, abnormalities of

electroencephalogram, triphasic delta waves

encephalitis, brainstem

encephalitis, human immunodeficiency virus type 1

encephalitis, viral

encephalopathy, delayed

episodic disorders

Erdheim-Chester disease

eye movement, disorders of

fever, recurrent

finger nose finger test

Friedreich's ataxia

frontal behavioral spatial syndrome

frontal bossing

frontal lobe, atrophy

frontal lobe, behavior with disease of

frontal lobe, pathologic signs of

frontotemporal dementia, behavioral variant

gait, festinating

gaze palsy, vertical

genetic neurologic disorders

genetic testing

hallucination, visual

head circumference

headache, awakened by

headache, awakening with

headache, bifrontal

headache, occipital

headache, recurrent

headache, severe

highly active antiretroviral therapy

hip flexor weakness

human immunodeficiency virus type 1

hydrocephalus, normal pressure

hydrocephalus, normal pressure, etiology

hypertrophic intracranial pachymeningitis

hypometric saccades

hypomyelination

imbalance, postural

immune reconstitution inflammatory syndrome

immunosuppression

immunosuppressive agents

incontinence, fecal

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

jaw jerk, abnormal

kinesia paradoxica

lacunar infarction

laughing, pathologic

leg weakness, bilateral

Legionnaires'disease

marche a petits pas

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, neurologic aspects and complications of

mental status, abnormal

middle cerebellar peduncle, lesion

motor dysfunction

motor neuron disease

movement disorder

movement disorder, extrapyramidal

movement disorder, psychogenic

MRI, angiography

MRI, contrast enhanced

MRI, contrast enhanced, high dose

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, high signal intensity of basal ganglia

MRI, nodular enhancement

multimodal neuroimaging

multiple system atrophy

nausea and vomiting

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuropathy, demyelinating

next-generation sequencing

nystagmus, gaze-evoked

nystagmus, upbeating on upgaze

ocular motility, disorders of

old age, neurology of

opportunistic infection, CNS

optic atrophy, bilateral

paraparesis, spastic

Parkinson disease

Parkinson disease, diagnosis

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

PAS positive material in the brain

pathologic reflex

patient information and support

Pelizaeus Merzbacher

perivascular enhancement

Persistent postural-perceptual dizziness

personality change

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polymerase chain reaction, false negative

pons, lesion of

posterior leukoencephalopathy syndrome

precipitating factors

progressive multifocal leucoencephalopathy

progressive neurologic disorder

progressive supranuclear palsy

proprioception, abnormal

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

pupil, light reflex, abnormal

reflex, cutaneous

release phenomena

respiratory tract infection

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

rickettsial organism

selective serotonin reuptake inhibitors

sensorineural hearing loss

serologic testing

serotonin norepinephrine reuptake inhibitors

shunt procedure, ventricular

shunt procedure, ventricular-complications of

single photon emission computed tomography

skin, lesions in neurologic disorders

skull bone, thickening

slow virus infection of CNS

speech disorder

splenium of corpus callosum

spongy degeneration of brain

startle myoclonus

startle reaction

steroid therapy, CNS treatment and complications with

stooped posture

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcortical U fibers

systemic illness

systemic lupus erythematosus

tandem gait, ataxic

temporal lobe, atrophy

thrombocytopenia

tongue, fasciculations of

transient neurologic deficit

treatment of neurologic disorder

tremor, resting

upgaze, paralysis of

urinary incontinence

vasospasm, cerebral

ventriculostomy

vibratory sensation, abnormal

viral infection

viral infection, CNS

visual impairment

voice, abnormality of

walking, difficulty with

weakness, generalized

white matter disease

wide based gait

Showing articles 750 to 800 of 1411 << Previous Next >>

An Emotional 13-Year Old Girl
Lancet 348:1000, Kanabar,D.J.,et al, 1996

Gait Disorders in Older Adults
J Am Geriatr Soc 44:434-452, Alexander,N.B., 1996

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Herpes Zoster Ophthalmicus
Neurol 45(suppl)s50-s51, Pavan-Langston, D., 1995

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

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

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,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

Leukoencephalopathy with Swelling & A Discrepantly Mild Clinical Course in Eight Children
Ann Neurol 37:324-334, van der Knaap,M.S.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Improvement of Paraneoplastic Opsoclonus-Myoclonus After Protein A Column Therapy
NEJM 332:192, Nitschke,M.,et al, 1995

Permanent Hemiparesis Due to Partial Status Epilepticus
Neurol 45:187-188, Borchert,L.D.&Labar,D.R., 1995

Pharyngeal Sensation and Gag Reflex in Healthy Subjects
Lancet 345:487-488, Davies,A.E.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Neuroradiologic Aspects of Chester-Erdheim Disease
AJNR 16:735-740, Caparros-Lefebvre,D.,et al, 1995

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 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

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

A Single-Photon Emission Computed Tomographic Study of Anosognosia in Alzheimer's Disease
Arch Neurol 52:415-420, Starkstein,S.E.,et al, 1995

Syndromes of Pontine Base Infarction:A Clinical-Radiological Correlation Study
Stroke 26:950-955, Kim,J.S.,et al, 1995

Clinical and Topographical Range of Callosal Infarction:A Clinical and Radiological Correlation Study
JNNP 59:238-242, Giroud,M.&Duman,R., 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 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

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Headache at Stroke Onset:The Lausanne Stroke Registry
JNNP 58:490-492, Kumral,E.,et al, 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Neuroblastoma-Associated Opsoclonus-Myoclonus Treated with IVIgG
J Pediatr 127:328-329, Petruzzi,M.J.&deAlarcon,P.A., 1995

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

Ependymomas of the Posterior Cranial Fossa:CT and MRI Findings
Neuroradiology 37:238-243, Tortori-Donati,P.,et al, 1995

Isolated Third-Nerve Palsy Associated with Frontal Sinus Mucocele
J Neuro-Ophthalmol 15:105-108, Ehrenpreis,S.J.&Biedlingmaier,J.F., 1995

Clinicopath Conf
Ganglioneuroblastoma of Adrenal Gland, Opsoclonus-Myoclonus-Ataxia Syndrome, Paraneoplastic, Case 27, 199EJM 333:579-586,1995., 1995

'Anesthesia Paresthetica':Nitrous Oxide-Induced Cobalamin Deficiency
Neurol 45:1608-1610, 14351995., Kinsella,L.J.&Green,R., 1995

Neurological Multisystem Manifestation in Multiple Symmetric Lipomatosis:A Clinical and Electrophysiological Study
Muscle & Nerve 18:693-698995., Naumann,M.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Midcervical Central Cord Syndrome:Numb & Clumsy Hands Due to Midline Cervical Disc Protrusion at C3-4 Intervert Level
JNNP 58:607-613, Nakajima,M.&Hirayama,K., 1995

Reversible Downbeat Nystagmus and Ataxia in Felbamate Intoxication
Neurol 45:845, Hwang,T.L.,et al, 1995

The Syndrome of Frontal Lobe Epilepsy:Characteristics and Surgical Management
Neurol 45:780-787, Laskowitz,D.T.,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

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Showing articles 750 to 800 of 1411 << Previous Next >>