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abdominal x-ray

adverse drug reaction

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

amyloid angiopathy, cerebral

angiitis, granulomatous of CNS

angiitis, isolated of CNS

antibodies to measles

anticonvulsants

anticonvulsants, selection of

antithyroid antibodies

aphasia, progressive

arm swing, reduced

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autoimmune disease

autonomic dysfunction

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, lesion, bilateral

behavioral disorder

biologic markers

Borrelia miyamotoi infection

brain biopsy, false negative

brainstem, atrophy

brainstem, lesion of

calcification, intracranial

CAT scan, abnormal

CAT scan, chest

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

celiac disease, adult

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar plaques, amyloid

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebral vasculature

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

cherry red spot-myoclonus syndrome

chewing movements

chorea, familial

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

color vision, impaired

coma, sudden onset

congenital infection, CNS

congenital paresis

cortical blindness

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

crying, pathologic

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, differential diagnosis of

dementia, familial

dementia, presenile

dementia, rapidly progressive

dementia, transmissible

dementia, treatment of

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

developmental milestones, loss of

diabetes mellitus

diagnostic criteria

dialysis dementia

differential diagnosis

doll's head maneuver

downward deviation of eyes

Dravet syndrome

dysdiadochokinesia

dyssynergia cerebellaris myoclonica

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electroencephalogram, video monitoring with

electron microscopy

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, autoimmune

encephalopathy, acute

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

enterovirus infection of CNS

episodic disorders

episodic neurologic deficits

episodic unconsciousness

exome sequencing

extralimbic encephalitis

eye movement, disorders of

eye movement, painful

faciobrachial dystonic seizure

failure to thrive

fatal familial insomnia

fine motor function, impaired

finger nose finger test

flaccid paralysis

gamma amino butyric acid receptor antibody

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

globus pallidus, lesion of

glutamic acid decarboxylase, antibody

gluten sensitivity

gluten-free diet

glycine receptor antibodies

granular osmiphilic material

growth retardation

hallucination, visual

hand-foot-mouth disease

hemianopia, homonymous

hemimyoclonic jerks

hepatosplenomegaly

heralding manifestation

hyperammonemic encephalopathy

hyperthyroidism

hypoglycorrhachia

hypometric saccades

imbalance, postural

immunohistochemistry

immunosuppression

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, eosinophilic intranuclear

inclusion bodies, intracytopasmic

insular cortex, lesion

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral of CNS

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

juvenile paresis

Kearns-Sayre syndrome

lactic acidemia

Lafora's disease

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

leucine rich glioma inactivated 1 antibodies

leukocyte enzyme abnormality

leukoencephalopathy

life expectancy

limbic encephalitis

mediastinum, mass of

memory, defect of recent

memory, impairment of

meningitis, aseptic

meningitis, neutrophilic

meningitis, treatment of

meningoencephalitis

mental retardation

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

motor neuron disease

motor neuron disease, misdiagnosis

movement disorder

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, spinal cord

MRI, sulcal hyperintensity

MRI, susceptibility weighted

multinucleated giant cell

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myelitis, longitudinal

myelitis, transverse

myoclonic ataxia

myoclonic jerks

myoclonus, cortical

myoclonus, epilepsy

myoclonus, multifocal

myoclonus, segmental

myoclonus, stimulus sensitive

myoclonus, treatment of

myoclonus-ataxia syndrome

myopathy, mitochondrial

nausea and vomiting

neuroendocrinology

neurologic complications

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, ataxia, retinitis pigmentosa

next-generation sequencing

NMDA antagonists

ophthalmoplegia

ophthalmoplegia, progressive external

opsoclonus-myoclonus syndrome

optic atrophy, hereditary

optic neuropathy

oral ulcerations

ornithine transcarbamylase deficiency

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

paraparesis, spastic

Parkinsonism syndrome

paroxysmal neurologic deficits

PAS positive material in the brain

persistent vegetative state

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polymerase chain reaction

pontocerebellar atrophy

potassium channel antibodies

progressive encephalomyelitis with rigidity syndrome

progressive infantile poliodystrophy

progressive myoclonic epilepsy

progressive neurologic disorder

progressive pallidum atrophy

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, acute

pursuit eye movements, abnormal

pyruvate metabolism, abnormality of

ragged-red fibers

Ramsay Hunt syndrome

rapidly progressing neurologic illness

real-time quaking-induced conversion

REM sleep behavior disorder

remote effect of cancer on the nervous system

respiratory failure

retro-orbital pain

reversible neurologic disorder

rubella encephalitis

rubella encephalitis, progressive

rubella syndrome

saccadic eye movements, abnormal

seizure, children

seizure, drug resistance

seizure, intractable

seizure, paradoxical

seizure, teenager

seizure, treatment of

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

sleep pathology and physiology

slow virus infection of CNS

speech disorder

spinal cord, lesion of

spinocerebellar ataxia

spirochete infection

spongy degeneration of brain

square wave jerks

startle myoclonus

startle reaction

status epilepticus

status epilepticus, intractable

steroid therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

symmetric brain lesions

systemic illness

tandem gait, ataxic

temporal lobe, lesion

temporal lobe, lesion, bilateral

temporalis muscle wasting

teratoma, ovarian

thalamus, lesion of-bilateral

toxins, nervous system

transient neurologic deficit

transplacental virus infections

treatment of neurologic disorder

tremor, postural

trichopoliodystrophy

uncal herniation

unconsciousness

unconsciousness, episodic

unconsciousness, transient

Unverricht-Lundborg disease

upgaze, paralysis of

urea-cycle enzymopathies

viral infection

viral infection, CNS

viral isolation

vision, blurred

vision, blurred, monocular

visuospatial disturbance

walking, difficulty with

weakness, acute

weakness, focal

weakness, generalized

white matter disease

white matter disease, subcortical

wide based gait

word-finding difficulty

Showing articles 300 to 350 of 5574 << Previous Next >>

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

Miliary Metastasis to the Brain:Clinical & Radiologic Features
Neurol 37:1817-1818, Floeter,M.K.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Seizures & Myoclonus in Patients with Alzheimer's Disease
Neurol 36:1226-1230, Hauser,W.A.,et al, 1986

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Meperidine-Associated Myoclonus & Seizures in Long-Term Hemodialysis Patients
Ann Neurol 14:593, Hochman,M.S., 1983

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Valproate & Clonazepam in the Treatment of Severe Progressive Myoclonus Epilepsy
Arch Neurol 39:236-238, Iivanainen,M.,et al, 1982

Neurologic Complications of Primary Sjogren's Syndrome
Medicine 61:247-257, Alexander,E.L.,et al, 1982

Valproic Acid, Treatment of Myoclonus in Dyssynergia Cerebellaris Myoclonica
Arch Neurol 39:527-528, Sommerville,E.R.,et al, 1982

Cephaloridine Encephalopathy
BMJ 283:409-410, Taylor,R.,et al, 1981

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Myoclonic Seizures Following Chlorambucil Overdose
Jr. , Ann Neurol 9:191-194981., Byrne,T.N., 1981

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Valproic Acid
NEJM 302:661-666, Brown,T.R., 1980

Neurologic Prognosis after Cardiopulmonary Arrest:III. Seizure Activity
Neurol 30:1292-1297, Snyder,B.D.,et al, 1980

Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
Arch Neurol 37:634-636, Weiss,G.M.,et al, 1980

Lafora Disease:Diagnosis by Liver Biopsy
Ann Neurol 8:409-415, Nishimura,R.N.,et al, 1980

Clin. Path. Conference
Lymphoplasmacytic Intersitial Pneumonitis, Progressive Multifocal Leukoencephalopathy. Case Record 1, -10,NEJM 302:795,1980., 1980

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Microangiopathy of the Brain & Retina
Neurol 29:313-316, Susac,J.O.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Imipramine in Absence & Myoclonic-astatic Seizures
Neurol 28:953-957, Fromm,G.H.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Drug Therapy, Clonazepam
NEJM 299:812-816, Brown,T.R., 1978

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Serotonin & Myoclonic Seizures
NEJM 296:101, Munsat,T.L., 1977

Long-term Therapy of Myoclonus & Other Neurologic Disorders with L-5-Hydroxytryptophan & Carbidopa
NEJM 296:70, VanWoert,M.H.,et al, 1977

Neurologic Manifestations in Sarcoidosis
Ann Int Med 87:336, Delaney,P., 1977

CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977

CT Scanning & Diagnosis of Adrenoleukodystrophy
Neurol 27:884, Greenberg,H.S.,et al, 1977

Sodium Valproate & Clonazepam in the Treatment of Intractable Epilepsy
Arch Neurol 34:14, Lance,W.,et al, 1977

Clonazepam & Branchial Myoclonus
Ann Neurol 1:306, Gledhill,R.F., 1977

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

A Fatal Encephalopathy in Chronic Haemodialysis Patients
Lancet 764, Burks,J.S.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Acquired Toxoplasmosis
Arch Neurol 32:335, Townsend,J.,et al, 1975

Acute Areflexic Paralysis
Arch Neurol 32:706, Furlan,A.J.,et al, 1975

Levodopa-Induced Myoclonus
Arch Neurol 32:331-334, Klawans,H.L., 1975

Showing articles 300 to 350 of 5574 << Previous Next >>