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abdominal cramps

abdominal reflex, absent

acute disseminated encephalomyelitis

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

Alexanders disease

Alexanders disease, adult onset

aminoacidopathies

amnestic syndrome

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, prognosis

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angina pectoris

anti MAG antibodies

antispasticity drugs

ataxia, cerebellar

attention deficit disorder with hyperactivity

autonomic dysfunction

basal ganglia, infarction

basal ganglia, lesion of

behavioral disorder

benign essential tremor

beta adrenergic blocker

bladder dysfunction

bone marrow transplantation

brainstem, infarction of

brainstem, lesion of

burning paresthesia

calcification, intracranial

Canavan's disease

CAT scan, abnormal

CAT scan, demyelinating disease

CAT scan, serial

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral infarction

cerebral infarction, small, deep

cerebral infarction, subcortical

cerebral ischemia

cerebral venous infarction

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, immunoglobulins of

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

cerebrovascular disease, cardiovascular disease with

Charcot-Marie-Tooth

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

congenital malformation

congestive heart failure

corneal dystrophy

cortical blindness

cortical blindness, transient

crying, pathologic

cyst, porencephalic

deep gray nuclei

degenerative diseases of CNS

dementia, cerebrovascular disease causing

dementia, presenile

dementia, subcortical

dementia, thalamic

demyelinating disease

dentate nuclei, lesion of

diabetes mellitus

diagnostic criteria

differential diagnosis

disability, neurological

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dystonia musculorum deformens

electrical sensation

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

emotional lability

encephalitis, viral

encephalomalacia

encephalopathy, metabolic

evoked potentials

exercise intolerance

Fabry's disease

facial nerve palsy

facial weakness

facial weakness, bilateral

gamma amino butyric acid

gamma amino butyric acid-mimetic drug

gamma knife therapy

gangliosidosis GM2

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

Gilles de la Tourette syndrome

glutaric acidemia

granular osmiphilic material

hearing loss, bilateral

heavy metal intoxication

hemianopia, transient

hemiparesis, transient

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatolenticular degeneration(Wilson's disease)

holoprosencephaly

homovanillic acid

hormone replacement

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

hyperthyroidism

hypoxic encephalopathy

iatrogenic neurologic disorders

intellectual deficit

intellectual deterioration

interferon beta 1-a

interferon beta 1-b

intrathecal antispasticity drugs

Krabbe's disease

lactic acidemia

lacunar infarction

laughing, pathologic

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

leukoencephalopathy

leukoencephalopathy, differential diagnosis

level of consciousness, decreased

Lhermitte's sign

lipid storage disorder of CNS

low birth weight

magnetic susceptibility

malformation, CNS, congenital

maple syrup urine disease

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

microhemorrhage, intracerebral

mitochondrial disease

motor neuron disease

movement disorder

MRI, CAT scan compared to

MRI, complications with

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, paramagnetic effect

MRI, spinal cord

MRI, T1 weighted high signal foci

multiple sclerosis

multiple sclerosis, asymptomatic

multiple sclerosis, chronic progressive

multiple sclerosis, clinical patterns

multiple sclerosis, conjugal

multiple sclerosis, diagnosis of

multiple sclerosis, differential diagnosis of

multiple sclerosis, etiology of

multiple sclerosis, familial

multiple sclerosis, linoleic acid in

multiple sclerosis, misdiagnosis

multiple sclerosis, parental transmission

multiple sclerosis, pathogenesis

multiple sclerosis, prognosis

multiple sclerosis, risk factors for

multiple sclerosis, spinal form

multiple sclerosis, treatment of

myelin basic protein gene

myelinolysis, extrapontine

myelitis, longitudinal

myelitis, transverse

myelopathy, chronic progressive

myocardial infarction

nausea and vomiting

neurogenic bladder

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuropathy, peripheral

neurotransmitter

obsessive-compulsive disorder

occipital lobe, infarction

occipital lobe, lesion of

old age, neurology of

optic atrophy, bilateral

optic atrophy, hereditary

optic nerve, hypoplasia of

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

palatal myoclonus

paraparesis, spastic

paraparesis, spastic, tropical

paratrigeminal syndrome

Parkinson disease

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

PAS positive material in the brain

Pelizaeus Merzbacher

periventricular leukomalacia

phenylketonuria

phenylketonuria, adult onset

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

polymerase chain reaction

pons, lesion of

posterior cerebral artery territory infarction

posterior leukoencephalopathy syndrome

premature infant

prevention of neurologic disorders

primary lateral sclerosis

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

pyramidal tract dysfunction

quality of life

radiation therapy, stereotactic

ragged-red fibers

regional enteritis

reversible neurologic disorder

Riley-Day syndrome

Rosenthal fibers

Sandhoff's disease

Schilder's disease

scotoma, central

seizure, children

seizure, neonatal

sensorineural hearing loss

sick sinus syndrome

skin, lesions in neurologic disorders

spasticity, treatment of

speech disorder

speech, loss of

spinal cord, injury of

spinal cord, injury, management of

spinal cord, lesion of

spontaneous remission

steroid therapy, CNS treatment and complications with

stimulation, deep brain

symmetric brain lesions

systemic lupus erythematosus

tardive dyskinesia

Tay-Sachs disease

temporal lobe, lesion, bilateral

thalamic tumors

thalamic tumors, bilateral

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

tongue, impaired movements of

top of the basilar syndrome

transient ischemic attack

transient ischemic attack, recurrent

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

ulcerative colitis

urinary frequency

urinary incontinence

urinary urgency

vasospasm, cerebral

vertigo, episodic

very long chain fatty acids

viral infection

viral infection, CNS

vision loss, sequential

visual acuity, decreased

visual evoked response

visual loss, progressive

visual loss, sudden

visual loss, transient

walking, difficulty with

water channel antibodies

Wernicke's encephalopathy

white matter disease

Showing articles 1250 to 1300 of 5493 << Previous Next >>

Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis
Neurol 44:2253-2257, Chance,P.F.,et al, 1994

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

Neuroanatomy of Fragile X Syndrome:The Temporal Lobe
Neurol 44:1317-1324, Reiss,A.L.,et al, 1994

The Hidden Costs of Medicolegal Abuses in Neurology
Arch Neurol 51:650-652, Scheinberg,P., 1994

Turcot's Syndrome:Evidence for Linkage to the Adenomatous Polyposis Coli (APC) Locus
neurol 44:1083-1086, Lasser,D.M.,et al, 1994

Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutations in Multiple Sclerosis
Ann Neurol 36:109-112, Kellar-Wood,H.,et al, 1994

Uhthoff's Symptom in Disorders of the Anterior Visual Pathways
Neurol 44:1036-1038, Lepore,F.E., 1994

A Sproadic Form of Hereditary Neuropathy with Liability to Pressure Palsies:Clin, Electrodiag & Molecular Genetic Findings
Neurol 44:753-755, Reisecker,F.,et al, 1994

Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
Neurol 44:823-828, Aylward,E.H.,et al, 1994

The Use of Brain Magnetic Resonance Imaging in Multiple Sclerosis
Arch Neurol 51:505-516, Goodkin,D.E.,et al, 1994

Benign Form of Multiple Sclerosis:MRI Evidence for Less Frequent and Less Inflammatory Disease Activity
JNNP 57:1070-1072, Kidd,D.,et al, 1994

Quantitative Brain MRI Lesion Load Predicts the Course of Clinically Isolated Syndromes Suggestive of Multiple Sclerosis
Neurol 44:635-641, Felippi,M.,et al, 1994

Extent of Pontine Pyramidal Tract Wallerian Degeneration and Outcome after Supratentorial Hemorrhagic Stroke
Stroke 25:1207-1210, Fukui,K.,et al, 1994

A Brief History of the Use of Interferons as Treatment of Multiple Sclerosis
Arch Neurol 51:1245-1252, Jacobs,L.&Johnson,K.P., 1994

Tizanidine Treatment of Spasticity Caused by Multiple Sclerosis:Results of a Double-Blinded, Placebo-Controlled Trial
Neurol 44:S34-S43, Smith,C.,et al, 1994

A Double-Blind, Placebo-Controlled Trial of Tizanidine in the Treatment of Spasticity Caused by Multiple Sclerosis
Neurol 44:S70-S78, Barnes,M.P.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Takayasu Arteritis
Ann Int Med 120:919-929, Kerr,G.S.,et al, 1994

Movement Disorders Following Lesions of the Thalamus or Subthalamic Region
Mov Disord 9:493-507, Lee,M.S. &Marsden, C.D., 1994

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

Correlation Between Magnetic Resonance Imaging Findings and Lesion Development in Chronic, Active Multiple Sclerosis
Ann Neurol 34:661-669, Katz,D.,et al, 1993

Functional and Magnetic Resonance Imaging Correlates of Callosal Involvement in Multiple Sclerosis
Arch Neurol 50:1077-1082, Pelletier,J.,et al, 1993

X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome
Lancet 342:1197-1200, Murphy,D.G.M.,et al, 1993

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

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

The Effect of Corticosteroids for Acute Optic Neuritis on the Subsequent Development of Multiple Sclerosis
NEJM 329:1764-1769, 1808-18101993., Beck,R.W.,et al, 1993

Effect of Brain Irradiation on Demyelinating Lesions
Neurol 43:2105-2112, Peterson,K.,et al, 1993

End-State Alzheimer's Disease:Glasgow Coma Scale and the Neurologic Examination
Arch Neurol 50:1309-1315, Benesch,C.G.,et al, 1993

Seizures Due to Multiple Sclerosis:Seven Patients with MRI Correlations
JNNP 56:1317-1320, Thompson,A.J.,et al, 1993

Sudden Hearing Loss as the Initial Monosymptom of Multiple Sclerosis
Neurol 43:2703-2705, Drulovic,B.,et al, 1993

Methylprednisolone in Multiple Sclerosis:A Comparison of Oral with Intravenous Therapy at Equivalent High Dose
JNNP 56:1219-1220, Alam,S.M.,et al, 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

Trauma and Multiple Sclerosis:A Population-Based Cohort Study from Olmsted County, Minnesota
Neurol 43:1878-1882, 18711993., Siva,A.,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

Pheochromocytomas, Multiple Endocrine Neoplasia Type 2, and Von Hippel-Lindau Disease
NEJM 329:1531-1538, Neumann,H.P.H.,et al, 1993

Brain Magnetic Resonance Imaging in Acute Optic Neuritis, Experience of the Optic Neuritis Study Group
Arch Neurol 50:841-846, Beck,R.W.,et al, 1993

Congruous Quadrantanopia and Optic Radiation Lesion
Neurol 43:1430-1432, Borruat,F.X.,et al, 1993

The Accuracy of Magnetic Resonance Imaging in Patients with Suspected Multiple Sclerosis
JAMA 269:3146-3151, Mushlin,A.I.,et al, 1993

Assessment of MRI Criteria for a Diagnosis of MS
Neurol 43:905-909, Offenbacher,H.,et al, 1993

Clinical Worsening in MS is Associated with Incr'd Freq & Area of Gadopenetate Dimeglumine-enhancing MRI Lesions
Ann Neurol 33:480-489, Smith,M.E.,et al, 1993

Transverse Myelitis, Retrosp Analy of 33 Cases, with Diff Cases Assoc with MS & Parinfectious Events
Arch Neurol 50:532-535, Jeffery,D.R.,et al, 1993

Functional Abilities at Age 4 Years of Children Born Before 29 Weeks of Gestation
BMJ 306:1715-1718, Johnson,A.,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

Systemic Histiocytosis Presenting as Multiple Sclerosis
Ann Neurol 33:549-554, Smith,M.E.,et al, 1993

Recovery of Functional Status After Stroke, A Postrehabilitation Follow-up Study
Stroke 24:200-250, Ferrucci,L.,et al, 1993

Showing articles 1250 to 1300 of 5493 << Previous Next >>