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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 900 to 950 of 2452 << Previous Next >>

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Brain Biopsy in Patients with Acquired Immunodeficiency Syndrome, Diagnostic Value, Clinical Performance, and Survival Time
Arch Int Med 159:2590-2596, Hornef,M.W.,et al, 1999

Treatment of Attention-Deficit-Hyperactivity Disorder
NEJM 340:780-788, Elia,J.,et al, 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

Population Based Cost Utility Study of Interferon Beta-1b in Secondary Progressive Multiple Sclerosis
BMJ 319:1529-1533, Forbes,R.B.,et al, 1999

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Interferon-B-1a in Relapsing-Remitting Multiple Sclerosis:Effect on Hypointense Lesion Volume on T1 Weighted Images
JNNP 67:579-584, Gasperini,C.,et al, 1999

MR Findings in AIDS-Associated Myelopathy
AJNR 20:1412-1416,1387, Chong,J.,et al, 1999

A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
Ann Neurol 46:671-678, Peiffer,A.,et al, 1999

Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
Ann Neurol 46:794-798, Nygaard,T.G.,et al, 1999

Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
Neurol 53:1180-1183, Plaster,N.M.,et al, 1999

Neurologic Manifestations of AIDS in Older Adults
Infect Dis Clin Practice 8:179-185, Finelli,P.F.,et al, 1999

Neurology and the Skin
JNNP 66:417-430, Hurko,O.&Provost,T.T., 1999

Proton Magnetic Resonance Spectroscopy Pattern of Progressive Multifocal Leukoencephalopathy in AIDS
JNNP 66:520-523, Iranzo,A.,et al, 1999

Prospective Study of New-Onset Seizures in Patients with Human Immunodeficiency Virus Infection
Arch Neurol 56:609-612, Pascual-Sedano,B.,et al, 1999

Primary Intracranial Neoplasms in Patients with HIV
Neurol 52:1648-1651, Blumenthal,D.T.,et al, 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Hyperintense Basal Ganglia on T1-Weighted MR Imaging
AJR 172:1109-1115, Lai,P.H.,et al, 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

Linkage of Proximal Myotonic Myopathy to Chromosome 3q
Neurol 52:170-171,12, Ricker,K.,et al, 1999

Epstein-Barr Virus in Monitoring the Response to Therapy of Acquired Immunodeficiency-Related Primary Central Nervous System Lymphoma
Ann Neurol 5:259-261, Antinori,A.,et al, 1999

Value of Combined Approach with Thallium-201 Single-Proton Emission Computed Tomography and Epstein-Barr Virus DNA Polymerase Chain Reaction in CSF for the Diagnosis of AIDS-Related Primary CNS Lympho
J Clin Oncol 17:554-560, Antinori,A.,et al, 1999

Parkinson Disease in Twins,An Etiologic Study
JAMA 281:341-346,376, Tanner,C.M.,et al, 1999

Ibuprofen Treatment Versus Gradual Introduction of Interferon B-1b in patients with MS
Neurol 52:1893-1895, Rice,G.P.A.,et al, 1999

Neurological Complications of Neurofibromatosis Type 1 in Adulthood
Brain 122:473-481, Creange,A.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
Neurol 53:629-631, Weil,S.,et al, 1999

Magnetic Resonance Imaging Results of the PRISMS Trial:A Randomized, Double-Blind, Placebo-Controlled Study of Interferon-B1a in Relapsing-Remitting Multiple Scleroosis
Ann Neurol 46:197-206, Li,D.K.B.,et al, 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Evidence of Interferon B-1a Dose Response In Relapsing-Remitting MS, The OWIMS Study
Neurol 53:679-686, The Once Weekly Interferon for MS Study Group (OWI, 1999

Highly Active Antiretroviral Therapy Reverses Brain Metabolite Abnormalities in Mild HIV Dementia
Neurol 53:782-789, Chang,L.,et al, 1999

Disease-Modifying Drugs for Relapsing-Remitting Multiple Sclerosis and Future Directions for Multiple Sclerosis Therapeutics
Arch Neurol 56:1079-1084, Rudick,R.A., 1999

Importance of Dural Ectasia in Phenotypic Assessment of Marfan's Syndrome
Lancet 354:910-913, 878, Fattori,R.,et al, 1999

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

New Developments in the Neurobiology of the Tuberous Sclerosis Complex
Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999

Treatment Recommendations for Interferon-B in Multiple Sclerosis
JNNP 67:561-566, Polman,C.H.,et al, 1999

Multiple Sclerosis, Side Effects of Interferon Beta Therapy and Their Management
Neurol 53:1622-1627, Walther,E.U.&Hohlfeld,R., 1999

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

The Roussy-Levy Family:From the Original Description to the Gene
Ann Neurol 46:770-773, Plante-Bordeneuve,V.,et al, 1999

Neuropsychological Status in Multiple Sclerosis after Treatment with Glatiramer
Arch Neurol 56:319-324, Weinstein,A.,et al, 1999

Paroxysmal Dyskinesias in Patients with HIV Infection
Neurol 52:109-114, Mirsattari,S.M.,et al, 1999

Severe Anaphylaxis with Recombinant Interferon Beta
Neurol 52:425, Corona,T.,et al, 1999

Radiation-Induced Cerebral Vasculopathy in Children with Neurofibromatosis and Optic Pathway Glioma
Ann Neurol 45:393-396, Grill,J.,et al, 1999

Herpes Varicella Zoster Encephalitis in Immunocompromised Patients
Neurol 52:193-195, Weaver,S.,et al, 1999

Cerebral Tumor-Like American Trypanosomiasis in Acquired Immunodeficiency Syndrome
Ann Neurol 45:403-406, Pagano,M.A.,et al, 1999

HAART Improves Prognosis in HIV-Associated Progressive Multifocal Leukoencephalopathy
Neurol 52:623-625,440, Clifford,D.B.,et al, 1999

Multiple Sclerosis,Therapeutic Update
Arch Neurol 56:277-280, Tselis,A.C.&Lisak,R.P., 1999

Progressive Multifocal Leukoencephalopathy and Human Immunodeficiency Virus-associated White Matter Lesions in AIDS:Magnetization Transfer MR Imaging
Radiology 210:539-543, Ernst,T.,et al,, 1999

Isolated,Chronic,Epilepsia Partialis Continua in an HIV-Infected Patient
Arch Neurol 56:111-114, Bartolomei,F.,et al, 1999

Showing articles 900 to 950 of 2452 << Previous Next >>