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Differential
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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 1750 to 1800 of 2452 << Previous Next >>

Utility of the VDRL Test in HIV-Seropositive Patients
NEJM 322:271, Drabick,J.J.&Tramont,E.C., 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

Cerebral Mass Lesions in Patients with AIDS
BMJ 301:226-228, , 1990

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

MR Imaging of Acute Transverse Myelitis and AIDS Myelopathy
J Comput Assist Tomogr 14:46-50, Barakos,J.A.,et al, 1990

Early HIV-1 Infection and the AIDS Dementia Complex
Neurol 40:323-326, Sidtis,J.J.&Price,R.W., 1990

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

Neurosyphilis in the Patient Infected with Human Immunodeficiency Virus, Editorial
Ann Neurol 27:211-213, Davis,L.E., 1990

Neurosyphilis in AIDS Patients:Initial CSF VDRL May be Negative
Neurol 40:541-543, Feraru,E.R.,et al, 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Clinicopath Conf
Primary CNS Lymphoma with AIDS, Am J Med 88:169-1761990., , 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

A Large Kindred with Autosomal Dominant Parkinson's Disease
Ann Neurol 27:276-282, Golbe,L.I.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation
NEJM 322:28-32, 541990., Krivit,W.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Primary Intracranial CNS Lymphoma:MR Manifestations
AJNR 10:725-729, Schwaighofer,B.W.,et al, 1989

Cerebral Venous Thrombosis and Dual Primary Infection with Human Immunodeficiency Virus and Cytomegalovirus
JNNP 52:1010-1016, Meyohas,M-C.,et al, 1989

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

Progressive Multifocal Leukoencephalopathy in Patients with AIDS:Appearance on MR Images
Radiology 173:517-529, Mark,A.S.&Atlas,S.W., 1989

Lumbosacral Plexopathy Secondary to Perirectal Abscess in a Patient with HIV Infection
Neurol 39:1400-1401, Holtzman,D.M.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Declining Incidence of AIDS Dementia Complex after Introduction of Zidovudine Treatment
BMJ 299:819-821, Portegies,P.,et al, 1989

Neuropathological Changes in Early HIV-1 Dementia
Ann Neurol 26:681-684, McArthur,J.C.,et al, 1989

Neuropathology of HIV Infection in Haemophiliacs:Comparative Necropsy Study
BMJ 299:1312-1315, Esiri,M.M.,et al, 1989

Spinal Cord Toxoplasmosis in AIDS
Neurol 39:1552-1553, Herskovitz,S.,et al, 1989

Association of Painful Peripheral Neuropathy in AIDS with Cytomegalovirus Infection
Lancet 2:937-941, Fuller,G.N.,et al, 1989

Low Prevalence of Neurological and Neuropsych Abn in Healthy HIV-1-Infected Indiv
Ann Neurol 26:601-611, McArthur,J.C.,et al, 1989

Neurological and Neuropsych Manif of HIV-1:Assoc with ARC not Aympto HIV-1 Infection
Ann Neurol 26:592-600, Janssen,R.S.,et al, 1989

Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989

Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
Am J Med 87:481-483, Panegyres,P.K.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989

Tourette's Syndrome:Current Concepts
Neurol 39:1625-1630, Kurland,R., 1989

A New Sign of Neurofibromatosis on Magnetic Resonance Imaging of Children
Arch Neurol 46:1222-1224, Goldstein,S.M.,et al, 1989

Optic Gliomas in Children with Neurofibromatosis Type 1
J Pediatr 114:788-792, Listernick,R.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Evaluation of the Policy of Empiric Treatment of Suspected Toxoplasma Encephalitis in Patients with AIDS
Am J Med 86:521-527, Cohn,J.A.,et al, 1989

Clinicopath Conf
Somatostatin-Rich Carcinoid Tumor (Somotostatinoma) of Duodenum, vonRecklinghausen's Disease, Case 1, -198JM 320:996-1004,1989., 1989

Cytomegalovirus Infection of Laryngeal Nerve Presenting as Hoarseness in Pts with Acquired Immunodeficiency Syndrome
Am J Med 86:108-110, Small,P.M.,et al, 1989

Hereditary Sensory Neuropathy with Deafness:A Familial Multisystem Atrophy
Neurol 39:244-248, Horoupian,D.S., 1989

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Showing articles 1750 to 1800 of 2452 << Previous Next >>