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acoustic nerve, vestibular division of

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

advances in neurology

adverse drug reaction

Alexanders disease

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, pathogenesis

aneurysm, intracranial

aneurysm, intracranial, familial

anterior horn cell disease

antiviral agents

apolipoprotein E

arrhythmia, cardiac

ataxia, cerebellar

ataxia, hereditary

auditory evoked brainstem potentials

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

brainstem, dysfunction

brainstem, lesion of

cafe au lait spots

CAT scan, abdomen

CAT scan, abnormal

caudate nucleus, lesion of, bilateral

cavernous hemangioma

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebral embolism

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, young adult

chromosomal abnormality

congenital heart disease

congenital myopathy

contractures, joint

cranial nerve tumor

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

dementia, presenile

dentatorubral-pallidoluysian atrophy

developmental retardation

differential diagnosis

dopa responsive dystonia

drug induced neurologic disorders

dystonia, children

Ehlers-Danlos syndrome

encephalitis, autoimmune

Fabry's disease

facial weakness, bilateral

fibromuscular dysplasia

fragile-X syndrome

Friedreich's ataxia

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

GLUT1 deficiency syndrome

glutamate dehydrogenase deficiency

hemoglobin abnormality, neurologic complications of

hereditary hemorrhagic telangiectasia(HHT)

high arched palate

highly active antiretroviral therapy

history of neurology

human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus, treatment of

hypoglycorrhachia

hypotonia, infants

immune reconstitution inflammatory syndrome

inborn errors of metabolism

intellectual deficit

interferon beta 1-a

interferon beta 1-b

intracerebral hemorrhage

intracerebral hemorrhage, young adult

islet cell tumor

learning disability

learning disability, in children

Legius syndrome

lenticular nucleus, lesion of, bilateral

life expectancy

long bone lesion

lumbar puncture

macular degeneration

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

meningioma, familial

meningioma, multiple

mental retardation

migraine, hemiplegic

mitral valve prolapse

molecular genetics

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, paramagnetic effect

multiple sclerosis

multiple sclerosis, clinical patterns

multiple sclerosis, diagnosis of

multiple sclerosis, pathogenesis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, Duchenne

myasthenia gravis

myasthenia gravis, familial incidence of

myasthenic syndrome

myoclonic jerks

myotonia dystrophica

nemaline rod myopathy

neoplasm, peripheral nerve

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-familial occurrence

nerve growth factor

neurocutaneous disease

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuromuscular disease, electrodiagnosis of

neuronal degeneration

next-generation sequencing

ocular motility, disorders of

ophthalmoplegia

palatal myoclonus

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal exertion-induced dyskinesia

patient information and support

pheochromocytoma

polycythemia, primary

practice guidelines

precocious puberty

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

progressive neurologic disorder

protein C deficiency

pseudoxanthoma elasticum

pyramidal tract dysfunction

recombinant DNA

repetitive nerve stimulation

respiratory failure

retinal degeneration

retinitis pigmentosa

rigid spine syndrome

Riley-Day syndrome

root lesion, nerve

Rosenthal fiber encephalopathy

Rosenthal fibers

scoliosis, neurologic association with

seizure, children

seizure, familial

seizure, neonatal

seizure, petit mal

sensory ganglia

sensory ganglia, abnormal

shunt procedure, ventricular

Shy-Drager syndrome

sickle cell disease

skin, lesions in neurologic disorders

skull x-ray, abnormal

skull x-ray, bony defect on

slit lamp examination

speech disorder

spinal cord degeneration

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, neoplasm, extramedullary intradural

spinal cord, neoplasm, intramedullary

spinal cord, neoplasm, neurofibroma

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

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

SPRED1 mutation

striatal encephalitis

survival motor neuron gene

symmetric brain lesions

third ventricle

thrombocytopenia

tongue, fasciculations of

treatment of neurologic disorder

trinucleotide repeats

tuberous sclerosis

type 1 muscle fiber

urinary catecholamines

ventriculostomy

ventriculostomy, endoscopic

Von Hippel Lindau

walking, difficulty with

weakness, generalized

weakness, progressive

X-linked bulbospinal neuronopathy

Showing articles 1500 to 1550 of 2452 << Previous Next >>

Mononeuritis Multiplex Associated with Cryoglobulinemia in HIV Infection
Neurol 42:2103-2105, Stricker,R.B.,et al, 1992

Primary Cerebral Lymphoma in Patients with AIDs:MR Findings in 17 Cases
AJR 159:841-847, Cordoliani,Y.,et al, 1992

Efficacy of Cytarabine in Progressive Multifocal Leucoencephalopathy in AIDS
Lancet 339:306, Nicoli,F.,et al, 1992

Progressive Multifocal Leukoencephalopathy in HIV-1-Infected Children
AIDS 6:837-841, Berger,J.R.,et al, 1992

Tuberculous Meningitis in Patients With and Without Human Immunodeficiency Virus Infection
Am J Med 93:520-524, Dube,M.P.,et al, 1992

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992

Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia
NEJM 327:1069-1074, Bilous,R.W.,et al, 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Familial Alzheimer's Disease:Second Gene Locus Located, Markers for Familial Disease May be Available
BMJ 305:1108-1109, Mullan,M., 1992

Screening for von Hippel-Lindau Disease by DNA Polymorphism Analysis
JAMA 267:1226-1231, Glenn,G.M.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Toxoplasmosis with Early Intracerebral Hemorrhage in a Patient with the Acquired Immunodeficiency Syndrome
Neurol 42:436-438, Trenkwalder,P.,et al, 1992

Treatment of Toxoplasmic Encephalitis in Patients with AIDS, Pyrimethamine & Clindamycin vs. Pyrimethamine & Sulfadiazine
Ann Int Med 116:33-43, Dannemann,B.,et al, 1992

Toxicity of Clindamycin as Prophylaxis for AIDS-Associated Toxoplasmic Encephalitis
Lancet 339:333-334, Jacobson,M.A.,et al, 1992

Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
Arch Neurol 49:170-173, Malik,S.,et al, 1992

A Study of Twins and Stroke
Stroke 23:221-223, Brass,L.M.,et al, 1992

Clinicopath Conf
Huntington's Diseae, Case2-1992, NEJM 326:117-125992., , 1992

The Chiari Type I Malformation in Two Monozygotic Twins and First-Degree Relatives
Ann Neurol 31:220-222, Stovner,L.J.,et al, 1992

Hypomelanosis of Ito
Editorial, Lancet 339:651-6521992., , 1992

Relapsing and Remitting Human Immunodeficiency Virus-Associated Leukoencephalomyelopathy
Ann Neurol 31:34-38, Berger,J.R.,et al, 1992

Cognitive and Motor Development in Infants at Risk for Human Immunodeficiency Virus
Am J Dis Child 146:218-222, Aylward,E.H.,et al, 1992

Meningoencephalitis in a Neonate Congenitally Infected with Human Immunodeficiency Virus Type 1
J Pediatr 120:93-95, Srugo,I.,et al, 1992

Recurrent Encephalopathy and Seizures in a US Native with HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis
Neurol 42:658-661, Smith,C.R.,et al, 1992

Neurological and Neuropsychological Performance in HIV Seropositive Men Without Symptoms
JNNP 55:143-148, McAllister,R.H.,et al, 1992

Cortically Evoked Motor Responses in Patients with Xp22. 3-Linked Kallmann's Syndrome and in Female Gene Carriers
Ann Neurol 31:299-304, Danek,A.,et al, 1992

Toxoplasma Encephalitis in Patients with the Acquired Immunodeficiency Syndrome
Medicine 71:224-239, Renold,C.,et al, 1992

Central Pain from Cerebral Abscess:Thalamic Syndrome in AIDS Patients with Toxoplasmosis
Neurol 42:1107-1109, Gonzales,G.R.,et al, 1992

Hyperdense CT Foci in Treated AIDS Toxoplasmosis Encephalitis:MR and Pathologic Correlation
J Comput Assist Tomogr 16:372-375, REvel,M.P.,et al, 1992

Low-Dose Trimethoprim-Sulfamethoxazole Prophylaxis for Toxoplasmic Encephalitis in Patients with AIDS
Ann Int Med 117:106-111, 163-1641992., Carr,A.,et al, 1992

Efficacy of Atovaquone in Treatment of Toxoplasmosis in Patients with AIDS
Lancet 340:637-638, Kovacs,J.A., 1992

Intracranial Tuberculosis in AIDS:CT and MRI Findings
et al Neuroradiology 34:11-14, Villoria,M.F., 1992

The Diagnostic Utility of Elevation in Cerebrospinal Fluid B2-Microglobulin in HIV-1 Dementia
Neurol 42:1707-1712, McArthur,J.C.,et al, 1992

Asymptomatic HIV Infection Does Not Cause EEG Abnormalities:Results from the Multicenter AIDS Cohort Study (MACS)
Neurol 42:1214-1219, Nuwer,M.R.,et al, 1992

Event-Related Potentials in Human Immunodeficiency Virus Infection
Arch Neurol 49:396-400, Messenheimer,J.A.,et al, 1992

Improvement of Motor Performance of HIV-Positive Patients Under AZT Therapy
Neurol 42:891-896, Arendt,G.,et al, 1992

Plasma Vitamin B12 Level as a Potential Cofactor in Studies of HIV Type 1-Related Cognitive Changes
Arch Neurol 49:501-506, Beach,R.S.,et al, 1992

Epidemiology of Human Immunodeficincy Virus Encephalopathy in the United States
Neurol 42:1472-1476, Janssen,R.S.,et al, 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Fibromyalgia Syndrome in Patients Infected with Human Immunodeficiency Virus
Am J Med 92:368-374, Simms,R.W.,et al, 1992

Midbrain Myasthenia:Fatigable Ptosis, 'Lid Twitch'Sign, and Ophthalmoparesis From a Dorsal Midbrain Glioma
Neurol 42 917-919, Ragge,N.K.&Hoyt,W.F., 1992

Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome
NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992

The Ethical Role of Neurologists in the AIDS Epidemic
Report of Ethics and Humanities Subcommittee of the American Academy of Neurology, Neurol 42:1116-11, 71992., 1992

Familial Cluster Headache:Occurrence in Three Generations
Neurol 42:1399-1400, Spierings,E.L.H.&Vincent,A.J.P.E., 1992

Migraine:Theories of Pathogenesis
Lancet 339:1202-1207, Blau,J.N., 1992

Detection of JC Virus DNA in Peripherl Lymphocytes from PTs with & Without Progressive Multifocal Leukoencephalopathy
Ann Neurol 31:454-462, Tornatore,C.,et al, 1992

Showing articles 1500 to 1550 of 2452 << Previous Next >>