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Differential
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aciduria

acoustic nerve, vestibular division of

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

adrenal mass

advances in neurology

adverse drug reaction

Alexanders disease

algorithm

Alzheimer's disease

Alzheimer's disease, early onset

Alzheimer's disease, familial

Alzheimer's disease, familial, late onset

Alzheimer's disease, pathogenesis

amniocentesis

amyloidosis

aneurysm

aneurysm, intracranial

aneurysm, intracranial, familial

anterior horn cell disease

auditory evoked brainstem potentials

autoantibodies

autoimmune basal ganglia encephalitis

autoimmune disease

autonomic dysfunction

baclofen

basal ganglia, lesion of

basal ganglia, lesion, bilateral

blindness

brainstem, dysfunction

caudate nucleus, lesion of, bilateral

cavernous hemangioma

CD4 counts

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebral embolism

cerebral palsy

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, young adult

children

chorea

chromosomal abnormality

congenital heart disease

creatine phosphokinase(CPK)elevated

deafness

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

dentatorubral-pallidoluysian atrophy

developmental retardation

diet

differential diagnosis

DNA probes

dopa responsive dystonia

drug induced neurologic disorders

Ehlers-Danlos syndrome

electromyogram

encephalitis, autoimmune

facial weakness, bilateral

familial

fasciculation

fibromuscular dysplasia

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

GLUT1 deficiency syndrome

glutamate dehydrogenase deficiency

hamartoma

headache

hearing loss

hemoglobin abnormality, neurologic complications of

hereditary hemorrhagic telangiectasia(HHT)

high arched palate

highly active antiretroviral therapy

history of neurology

HLA

homocystinuria

human immunodeficiency virus type 1

huntingtin

Huntington's chorea

hydrocephalus

hydrocephalus, treatment of

immune reconstitution inflammatory syndrome

inborn errors of metabolism

intracerebral hemorrhage

intracerebral hemorrhage, young adult

learning disability, in children

Legius syndrome

lenticular nucleus, lesion of, bilateral

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

mitral valve prolapse

movement disorder, extrapyramidal

MRI, paramagnetic effect

MRI, spine

multiple sclerosis

multiple sclerosis, clinical patterns

multiple sclerosis, diagnosis of

multiple sclerosis, pathogenesis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, Duchenne

myasthenia gravis

myasthenia gravis, familial incidence of

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

neurofibroma

neurofibromatosis 1

neurofibromatosis 2

neurofibromatosis 2, presymptomatic

neurofibromin

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neuromuscular disease, electrodiagnosis of

neuronal degeneration

neuropathology

neuropathy

neurotomy

next-generation sequencing

NF1 gene

nusinersen

nystagmus

ocular motility, disorders of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal exertion-induced dyskinesia

patient information and support

pheochromocytoma

polycythemia, primary

practice guidelines

preclinical

precocious puberty

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

presenilin-1 gene

presenilin-2 gene

prognosis

progressive neurologic disorder

protein C deficiency

pruritus

pseudarthrosis

pseudoxanthoma elasticum

Purkinje cell

pyramidal tract dysfunction

recombinant DNA

repetitive nerve stimulation

Rosenthal fiber encephalopathy

Rosenthal fibers

schwannoma

scoliosis

scoliosis, neurologic association with

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

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

steroid

striatal encephalitis

survival motor neuron gene

symmetric brain lesions

third ventricle

thrombocytopenia

tinnitus

tongue, fasciculations of

treatment of neurologic disorder

trinucleotide repeats

tuberous sclerosis

type 1 muscle fiber

ubiquilin 1

urinary catecholamines

ventriculostomy

ventriculostomy, endoscopic

Von Hippel Lindau

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

X-linked bulbospinal neuronopathy

Showing articles 950 to 1000 of 2452 << Previous Next >>

Cryptococcus Meningoencephalitis in AIDS:Parenchymal and Meningeal Forms
Neuroradiology 41:129-133, Berkefeld,J.,et al, 1999

Getting a Grip on the Myotonic Dystrophies
Neurol 52:12-13, Thornton,C.A.&Ashizawa,T., 1999

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Influence of Human Immunodeficiency Virus 1 Infection and Degree of Immunosuppression in the Clinical Characteristics and Outcome of Infective Endocarditis in Intravenous Drug Users
Arch Int Med 158:2043-2050, Ribera,E.,et al, 1998

Dual Infective Pathology in Patients with Cryptococcal meningitis
Neurol 51:1213-1215, Silber,E.,et al, 1998

Central Nervous System Infection with Listeria Monocytogenes
Medicine 77:313-316, Mylonakis,E.,et al, 1998

A 29-Year-Old Man with Multiple Sclerosis
JAMA 280:1432-1439, Rudick,R.A., 1998

Neutralizing Antibodies to Interferon B-1a and Interferon B-1b in MS Patients are Cross-Reactive
Neurol 51:1698-1702, Khan,O.A. & Dhib-Jalbut,S., 1998

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Lipodystrophy Associated with an HIV-Protease Inhibitor
NEJM 339:1296, Carr,A.&Cooper,D.A., 1998

Buffalo Hump in a Patient with the Acquired Immunodeficiency Syndrome
NEJM 339:1297, Aboulafia,D.M.&Bundow,D., 1998

Incidence of Dilated Cardiomyopathy and Detection of HIV in Myocardial Cells of HIV-Positive Patients
NEJM 339:1093-1099,1153, Barbaro,G.,et al, 1998

Amelioration of Flulike Symptoms at the Onset of Interferon B-1b Therapy in Multiple Sclerosis by Low-Dose Oral Steriods is Related to a Decrease in Interleukin-6 Induction
Ann Neurol 44:682-685, Martinez-Caceres,E.M.,et al, 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
Lancet 352:1892-1897, Labauge,P.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
Stroke 29:2507-2510, Ludemann,P.,et al, 1998

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

Interferon B Therapy for Multiple Sclerosis
Lancet 352:1486-1487, Goodkin,D.E., 1998

Interferons in the Treatment of Multiple Sclerosis,Do They Prevent the Progression of the Disease?
Arch Neurol 55:1578-1580,1583, Rice,G.&Ebers,G, 1998

Interferons Should be Used to Treat Most Patients with MS
Arch Neurol 55:1581-1583, Herndon,R.M.&Jacobs,L, 1998

Randomised Double-Blind Placebo-Controlled Study of Interferon B-1a in Relapsing/Remitting Multiple Sclerosis
Lancet 352:1498-1504,1486, PRISMS, 1998

Placebo-Controlled Multicentre Randomised Trial of Interferon B-1b in Treatment of Secondary Progressive Multiple Sclerosis
Lancet 352:1491-1497,1486, European Study Group on Interferon B-1b in Seconda, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Localization of the Giant Axonal Neuropathy Gene to Chromosome 16q24
Ann Neurol 43:143-148, Flanigan,K.M.,et al, 1998

Numb Chin Syndrome as the Initial Manifestation of HIV Infection
Neurol 50:511-512, Benito-Leon,J.,et al, 1998

Magnetic Resonance Imaging Lesion Analysis in Neurofibromatosis Type 1
Arch Neurol 55:500-505, DiMario,F.J.&Ramsby,G., 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Rate of Pregnancy-Related Relapse in Multiple Sclerosis
NEJM 339:285-291, 3391998., Confavreux,C.,et al, 1998

Synergistic Immunomod Effects of Interferon-Beta1b & Phosphodiesterase Inhib Pentoxifylline in Pts with Relapsing-Remit MS
Ann Neurol 44:27-34, 71998., Weber,F.,et al, 1998

Effects of Copolymer-1 on Serial Gadolinium-Enhanced MRI in Relapsing Remitting Multiple Sclerosis
Neurol 50:1127-1133, Mancardi,G.L.,et al, 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

Genetic Studies on Chromosome 12 in Late-Onset Alzheimer Disease
JAMA 280:619-622, 6521998., Wu,W.S.,et al, 1998

Evidence for an Alzheimer Disease Susceptability Locus on Chromosome 12 and for Further Locus Heterogeneity
JAMA 280:614-618, 6521998., Rogaeva,E.,et al, 1998

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

Variable Progression of HIV-Associated Dementia
Neurol 50:1814-1820, Bouwman,F.H.,et al, 1998

HIV-Protease Inhibitors
NEJM 338:1281-1292, Flexner,C., 1998

Optic Neuritis Heralding Varicella Zoster Virus Retinitis in a Patient with Acquired Immunodeficiency Syndrome
Ann Neurol 43:534-536, Meenken,C.,et al, 1998

Neuropathy in Diffuse Infiltrative Lymphocytosis Syndrome
Neurol 50:1041-1044, 8551998., Gherardi,R.K.,et al, 1998

Cerebral Aneurysmal Arteriopathy in Childhood AIDS
Neurol 51:560-565, Dubrovsky,T.,et al, 1998

Low-Dose Steroids Reduce Flu-Like Symptoms at the Initiation of INFB-1b in Relapsing-Remitting MS
Neurol 50:1910-1912, Rio,J.,et al, 1998

Incidence and Significance of Neutralizing Antibodies to Interferon Beta-1a in Multiple Sclerosis
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Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

Failure of Cytarabine in Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
NEJM 338:1345-1351, 13781998., , 1998

Mass Effect in Progressive Multifocal Leukoencephalopathy
Arch Neurol 55:1148-1149, Finelli,P.F., 1998

Showing articles 950 to 1000 of 2452 << Previous Next >>