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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
antiviral agents
apolipoprotein E
APP
APP gene
areflexia
arrhythmia, cardiac
astrocytoma
ataxia
ataxia, cerebellar
ataxia, hereditary
atrial myxoma
audiogram
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
brainstem, lesion of
cafe au lait spots
CAG repeats
carcinoma
cardiomyopathy
CAT scan, abdomen
CAT scan, abnormal
cataracts
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
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cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, young adult
children
chorea
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 21
chromosome 22
chromosome 4
chromosome 5
chromosome 6
chromosome 9
coagulopathy
congenital heart disease
congenital myopathy
constipation
contractures, joint
cranial nerve tumor
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
dysarthria
dyskinesia
dystonia
dystonia, children
Ehlers-Danlos syndrome
electromyogram
encephalitis, autoimmune
encephalopathy
endoscopy
enzyme, defect
ependymoma
Fabry's disease
facial weakness, bilateral
familial
fasciculation
fibromuscular dysplasia
fragile-X syndrome
Friedreich's ataxia
gadolinium
gene
gene mutation
gene therapy
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genetic diagnosis, prenatal
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genetic neurologic disorders
genetic screening
genetic testing
glioma
GLUT1
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
hypertension
hypoglycorrhachia
hyporeflexia
hypotonia
hypotonia, infants
immune reconstitution inflammatory syndrome
inborn errors of metabolism
intellectual deficit
interferon
interferon beta 1-a
interferon beta 1-b
intracerebral hemorrhage
intracerebral hemorrhage, young adult
iris, abnormal
iron, brain
islet cell tumor
karyotyping
ketogenic diet
learning disability
learning disability, in children
Legius syndrome
lenticular nucleus, lesion of, bilateral
life expectancy
Lisch nodules
long bone lesion
lordosis
lumbar puncture
lymphoma
macrocephaly
macular degeneration
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
meningioma
meningioma, familial
meningioma, multiple
mental retardation
merlin
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
MRI
MRI, abnormal
MRI, muscle
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
myasthenic syndrome
myoclonic jerks
myopathy
myotonia dystrophica
neck weakness
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
ophthalmoplegia
optic atrophy
optic glioma
palatal myoclonus
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
respiratory failure
retinal degeneration
retinitis pigmentosa
review article
RFLPs
rigid spine syndrome
Riley-Day syndrome
root lesion, nerve
Rosenthal fiber encephalopathy
Rosenthal fibers
schwannoma
scoliosis
scoliosis, neurologic association with
screening
seizure
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
SMN1 gene
spasticity
speech disorder
spinal cord
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
web sites
white freckles
Wood's light
workup
X-linked bulbospinal neuronopathy
Showing articles 800 to 850 of 2452 << Previous Next >>

Randomized, Comparative Study of Interferon B-1a Treatment Regimens in MS
Neurol 59:1496-1506,1482, Panitch,H.,et al, 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Familial Temporal Lobe Epilepsy with Febrile Seizures
Neurol 58:1429-1433, Depondt,C.,et al, 2002

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

Interferon Beta-1a for Early Multiple Sclerosis: CHAMPS Trial Subgroup Analyses
Ann Neurol 51:481-490, Beck,R.W.,et al, 2002

Progression to Neuropsychological Impairment in Human Immunodeficiency Virus Infection Predicted by Elevated Cerebrospinal Fluid Levels of Human Immunodeficiency Virus RNA
Arch Neurol 59:923-928,909, Ellis,R.J.,et al, 2002

Interferon Beta but not Glatiramer Acetate Therapy Aggravates Headaches in MS
Neurol 59:636-639, Pollmann,W.,et al, 2002

Benefit of Interferon B-1a on MSFC Progression in Secondary Progressive MS
Neurol 59:679-687, Cohen,J.A.,et al, 2002

Superior Saittal Sinus Thrombosis and HIV
Ann Int Med 137:375, Karin,M.S.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Expression of p53 and Prognosis in Children With Malignant Gliomas
NEJM 346:420-427, Pollack,I.F.,et al, 2002

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

An Open-Label Trial of Combination Therapy With Interferon B-1a and Oral Methotrexate in MS
Neurol 58:314-317, Calabresi,P.A.,et al, 2002

Disease Modifying Therapies in Multiple Sclerosis
Neurol 58:169-178, Goodin,D.S.,et al, 2002

Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency
J Pediatr 140:242-246, Wolf,B.,et al, 2002

Recurrent Stroke as a Manifestation of Primary Angiitis of the Central Nervous System in a Patient Infected With Human Immunodeficiency Virus
Arch Neurol 59:468-473, Nogueras,C.,et al, 2002

Abnormal Cobalamin-dependent Transmethylation in AIDS-associated Myelopathy
Neurol 58:730-735, Di Rocco,A.,et al, 2002

Disease-Modifying Therapy in Multiple Sclerosis: Strategies for Optimizing Management
The Neurologist 8:227-236, Frohman,E.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Holmes Tremor Following Midbrain Toxoplasma Abscess: Clinical Features and Treatment of a Case
Park Rel Dis 8:177-180, Pezzini, A.,et al, 2002

HIV-Related Movement Disorders, Epidemiology, Pathogenesis and Management
CNS Drugs 16:663-668, Cardoso,F., 2002

Hypertrophic Cardiomyopathy A Systematic Review
JAMA 287:1308-1320, Maron, B.J., 2002

Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
J Am Coll Cardiol 39:301-307, Maron,B.J.,et al, 2002

Primary Lymphoma of the Pituitary: An Emerging Clinical Entity
J Clin Endocrinol Metab 86:4567-4575, Giustina,A.,et al, 2001

The Effect of IFNB-1b on the Evolution of Enhancing Lesions in Secondary Progressive MS
Neurol 57:2185-2190, Brex,P.A.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Parkinsonism as the Presenting Manifestation of HIV Infection: Improvement on HAART
Neurol 56:278-279, Hersh,B.P.,et al, 2001

Amyotrophic Lateral Sclerosis
NEJM 344:1688-1700, Rowland,L.P. & Shneider,N.A., 2001

Effect of Early Interferon Treatment on Conversion to Definite Multiple Sclerosis: A Randomised Study
Lancet 357:1576-1582,1547, Comi,G.,et al, 2001

Association Between Migraine and Endothelin Type A Receptor (ETA-231 A/G) Gene Polymorphism
Neurol 56 :1273-1277, Tzourio,C.,et al, 2001

Fulminant Liver Failure During Interferon Beta Treatment of Multiple Sclerosis
Neurol 56:1416, Yoshida,E.M.,et al, 2001

Randomized Controlled Trial of Interferon-beta-1a in Secondary Progressive MS
Neurol 56:1496-1504, Secondary Progressive Efficacy Clinical Trial of R, 2001

Randomized Controlled Trial of Interferon-beta-1a in Secondary Progressive MS
Neurol 56:1505-1513, Li,D.K.B.,et al, 2001

Impact of the Human Genome Projects and Identification of a Stroke Gene
Stroke 32:1239-1241, Alberts,M.J., 2001

Hereditary Benign Chorea
Neurol 57:106-110, Fernandez,M.,et al, 2001

The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel
NEJM 345:17-24,57, Ducros,A.,et al, 2001

Fits and Strokes
Lancet 358:120, Sharma,P.,et al, 2001

PRISMS-4: Long-Term Efficacy of Interferon-B-1a in Relapsing MS
Neurol 56:1628-1636,1620, The PRISMS Study Group, 2001

Coma in a Young Anorexic Woman
Lancet 357:1944, Blans,M.J.,et al, 2001

Measurement of Antibodies to Interferon Beta in Patients With Multiple Sclerosis
Arch Neurol 58:1299-1300,1301, Pachner,A.R., 2001

The Significance of Neutralizing Antibodies in Patients With Multiple Sclerosis Treated With Interferon Beta
Arch Neurol 58:1297-1298,1301, Rice,G., 2001

Brain Abscess Due to Listeria Monocytogenes, Five Cases and a Review of the Literature
Medicine 80:223-235, Eckburg,P.B.,et al, 2001

An ALS-Like Syndrome with New HIV Infection and Complete Response to Antiretroviral Therapy
Neurol 57:1094-1097,945, MacGowan,D.J.L.,et al, 2001

Reversible ALS-Like Disorder in HIV Infection
Neurol 57:995-1001,945, Moulignier,A.,et al, 2001

Clinical and Genetic Aspects of Distal Myopathies
Muscle Nerve 24:1440-1450, Saperstein,D.S.,et al, 2001

Acute Disseminated Encephalomyelitis as Manifestation of Primary HIV Infection
Neurol 57:1493-1496, Narciso,P.,et al, 2001

Complete Genomic Screen in Parkinson Disease
JAMA 286:2239-2244, Scott,W.K.,et al, 2001



Showing articles 800 to 850 of 2452 << Previous Next >>